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If no cells are available for analysis, no analysis charges will be incurred. \n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":3,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2791,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":3,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8372,"DictMethodologyId":173,"TdTestInfoSpecificId":3,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":3,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"5 days per week","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":32157,"SpecialInstructions":"One formalin-fixed, paraffin embedded block containing representative tissue OR unstained 4 μm tissue sections on electrostatically charged slides containing representative tumor. Tissue must be fixed in formalin NOT B5 or PREFER fixative\n","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":130,"DictSpTypeName":"Slide (s), unstained","DictSpVolumeId":160,"DictSpVolumeName":"2 slides","TdTestInfoSpecificId":3,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":30278,"Description":"FFPE tissue blocks and slides from FFPE specimens are stable at ambient temperatures","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":3,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":3,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2845,"LISCode":"FUNGSC","PrimaryName":"Yeast Screen","LISName":"Yeast Screen","EMRName":"Yeast Screen","EMRCode":"SQFUNGSC","LOINC":"580-1","RecommendedUse":"Recovery and identification of yeast infections from oral and vaginal specimens. All other specimens have alternative test codes. \n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6787,"Aka":"Culture, Rapid Growing Yeast ","TdTestInfoCommonId":2845},{"Id":6788,"Aka":"Yeast Screen","TdTestInfoCommonId":2845},{"Id":14413,"Aka":"Candidiasis","TdTestInfoCommonId":2845},{"Id":14414,"Aka":"Oral Candida","TdTestInfoCommonId":2845},{"Id":14415,"Aka":"Vaginal yeast","TdTestInfoCommonId":2845},{"Id":14416,"Aka":"Vulvovaginitis","TdTestInfoCommonId":2845},{"Id":14417,"Aka":"Yeast culture","TdTestInfoCommonId":2845}],"TdBillingCommons":[{"Id":9795,"CptCode":"87102","Quantity":1,"Tmid":"30600065","CclTechComponentPrice":54.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2845,"IsBeakerData":false},{"Id":18682,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2845,"IsBeakerData":false},{"Id":18683,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2845,"IsBeakerData":false},{"Id":18684,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2845,"IsBeakerData":false},{"Id":18690,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2845,"IsBeakerData":false},{"Id":19374,"CptCode":"87015","Quantity":1,"Tmid":"30606300","CclTechComponentPrice":43.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Fluid Concentration","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2845,"IsBeakerData":false}],"TdIncludes":[{"Id":25918,"TestName":"Specimens may include some pre-processing steps to aid in recovery of yeast","Rank":1,"TdTestInfoCommonId":2845}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2845,"SpecialInfo":"Specimens are plated on special fungal media for recovery, isolation and identification of yeast. Cultures are only held for 7 days. This is adequate time to culture yeast organisms but if fastidious yeast or filamentous mold infections are suspected fungal culture and smear (FCULSM) should be ordered by contacting the lab/medical director. Susceptibility testing on isolated recovered from vaginal and oral samples must be separately requested when clinically indicated. These requests can be made by calling lab client services or by calling the lab/medical director. Additional CPT codes may be applicable for recovery and identification of yeast - 87102 Fungal culture, 87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing, 87186 - Fungal susceptibility testing for yeast by request only.\n","ClinicalInfo":"This test can be utilized to determining etiology of infectious vaginitis, monitoring therapeutic efficacy for vaginitis and/or management of chronic recurring disease. Diagnosis can be challenging as yeast are part of the normal vaginal and oral flora. Clinical factors such as clinical symptoms and signs consistent with disease should be considered. In cases of recurrent infections where development of resistance is suspected, susceptibility testing can be requested by contacting lab client services and/or the lab/medical director.  \n","ClinicalReference":"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. ","ClinicalLimitation":"Yeast especially Candida species are part of the normal vaginal and oral flora. Significance of recovery and identification of yeast from these sites requires clinical correlation. 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Secretions from the mucosal membrane of the vaginal vault should be collected with a moist E-swab. If fungal infections other than Candida species are suspected, fungal culture and smear should be ordered and required pre-approval for this specimen source by contacting the lab/medical director.","LogicalOperation":null,"DictSpContainerId":130,"DictSpContainerName":"E Swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":38,"DictSpVolumeName":"Swab","TdTestInfoSpecificId":5,"IsBeakerData":false},{"Id":678313,"SpecialInstructions":"Urine: Preferred collection is 3 ml urine in a BD gray top preservative tube. Alternatively, collect 50 ml of first morning void in sterile container. Patient prep: Usual preparation for clean mid-void urine. 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When conducting ear swabs, employing aseptic technique is crucial; gently rotate the E-swab within the canal for optimal sampling.","LogicalOperation":null,"DictSpContainerId":130,"DictSpContainerName":"E Swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":24,"DictSpTypeName":"Other","DictSpVolumeId":38,"DictSpVolumeName":"Swab","TdTestInfoSpecificId":5,"IsBeakerData":false},{"Id":678327,"SpecialInstructions":"Eye: Eye swabs are permissible, with an extended holding period of 28 days to facilitate the recovery of fungal organisms. However, for heightened sensitivity in detection, scrapings and fluids from the eye should be prioritized and submitted as a Fungal Culture and Smear (FCULSM). 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However, in cases where only a yeast infection is suspected and obtaining tissue or fluid samples isn't feasible due to the location of the infection, a swab may be used to recover yeast.","LogicalOperation":null,"DictSpContainerId":130,"DictSpContainerName":"E Swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":24,"DictSpTypeName":"Other","DictSpVolumeId":38,"DictSpVolumeName":"Swab","TdTestInfoSpecificId":5,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16297,"Description":"7 days\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":5,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16298,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":5,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16299,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":5,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":5,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false}]},{"Id":2870,"LISCode":"GENTRA","PrimaryName":"Gentamicin, Random","LISName":"Gentamicin, Random","EMRName":"Gentamicin Random","EMRCode":"SQGENTRA","LOINC":"3664-0","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":14522,"CptCode":"80170","Quantity":1,"Tmid":"30100310","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"GENTAMICIN ASSAY","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2870,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2870,"SpecialInfo":"Do not collect in a gel separator tube. \n\nUtilized for collections outside of trough (pre-dose) or peak levels (post-dose). 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","ClinicalInfo":"Synovial fluid:\nSynovial fluid glucose measurement may be useful in classifying various joint disorders.  A concurrent plasma glucose measurement should be performed to determine the (glucose plasma) – (glucose synovial fluid) difference, which is normally = 10.0 mg/dL.  Artificial lowering of synovial fluid glucose, due to glycolytic action of leukocytes, may result from analyses that occur more than one hour from the time of collection.\n\nReference:\n1.\tCLSI. Analysis of Body Fluids in Clinical Chemistry; Approved Guideline. CLSI document C49-A. 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Clinical Correlation is required. Medical director may be contacted should interpretation be needed. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":3,"DictIntendedFor":null,"TdAlias":[{"Id":10028,"Aka":"Epstein-Barr Virus Antibody Panel","TdTestInfoCommonId":2694}],"TdBillingCommons":[{"Id":12995,"CptCode":"86665","Quantity":2,"Tmid":"30200505","CclTechComponentPrice":82.00,"CclProfComponentPrice":null,"TestNameForCdm":"EBV-VCA IFA IGG","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2694,"IsBeakerData":false},{"Id":12996,"CptCode":"86664","Quantity":1,"Tmid":"30200495","CclTechComponentPrice":69.00,"CclProfComponentPrice":null,"TestNameForCdm":"EBV-NA IFA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2694,"IsBeakerData":false}],"TdIncludes":[{"Id":19010,"TestName":"EBV Ab IgG","Rank":1,"TdTestInfoCommonId":2694},{"Id":19011,"TestName":"EBV Ab IgM","Rank":2,"TdTestInfoCommonId":2694},{"Id":19013,"TestName":"EBV Ab NA","Rank":3,"TdTestInfoCommonId":2694}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2694,"SpecialInfo":null,"ClinicalInfo":"","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":25,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2694,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":25,"IsStat":false,"Comments":null,"DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13281,"DictMethodologyId":164,"TdTestInfoSpecificId":25,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":25,"DictDaysPerformedId":47,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Fri","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":39420,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":25,"IsBeakerData":false},{"Id":39421,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":25,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22555,"Description":"24 hours\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":25,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22556,"Description":"7 days\n","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":25,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22557,"Description":"14 days\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":25,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":25,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2696,"LISCode":"EBVNA","PrimaryName":"EBV Antibody to Nuclear Antigen","LISName":"EBV NA Antibody","EMRName":"Antibody Epstein-Barr Nuclear Antigen","EMRCode":"SQEBVNA","LOINC":"31372-6","RecommendedUse":"Please see Clinical Info. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":10027,"Aka":"Epstein Barr Virus NA Antibody","TdTestInfoCommonId":2696}],"TdBillingCommons":[{"Id":12993,"CptCode":"86664","Quantity":1,"Tmid":"30200495","CclTechComponentPrice":69.00,"CclProfComponentPrice":null,"TestNameForCdm":"EBV-NA IFA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2696,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2696,"SpecialInfo":"Avoid hemolysis.\nAvoid multiple freeze thaw cycles.","ClinicalInfo":"EBV nuclear antigen (EBNA-1) IgG typically appears from several weeks to several months after primary EBV infection and may remain elevated for life but it may become equivocal or undetectable in certain immunocompromised individuals. The final interpretation should be done in the context of other EBV serology panel results.      ","ClinicalReference":"","ClinicalLimitation":"Assay performance has not been established for immunocompromised or immunosuppressed patients.\nAssay performance has not been established for cord blood, neonatal specimens or infants.\nThere is a possibility of assay cross-reactivity with specimens containing anti E-coli antibody.\nAssay performance has not been established for the diagnosis of nasopharyngeal carcinoma, Burkitt's lymphoma, other EBV-associated lymphomas, and other EBV associated diseases other than EBV related mononucleosis.\nTesting should not be performed as a screening procedure for the general population. It should only be performed when clinical evidence suggests the diagnosis of EBV-associated infectious mononucleosis.\nIf the marker is negative and exposure to EBV is suspected, a second sample should be collected and tested no less than one-two weeks later.\nIn cases of equivocal results, a second freshly collected sample should be obtained and tested.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":27,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2696,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":27,"IsStat":false,"Comments":"","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13284,"DictMethodologyId":164,"TdTestInfoSpecificId":27,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":27,"DictDaysPerformedId":47,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Fri","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":39413,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":27,"IsBeakerData":false},{"Id":39414,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":27,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22549,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":27,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22550,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":27,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22551,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":27,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":27,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2698,"LISCode":"EBVQNT","PrimaryName":"Epstein-Barr Virus (EBV) DNA, Quantitative PCR, Plasma","LISName":"Epstein-Barr Virus (EBV) DNA, Quantitative PCR, Plasma","EMRName":"Epstein-Barr Virus (EBV) DNA, Quantitative PCR, Plasma","EMRCode":"SQEBVQNT","LOINC":"47982-4","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14561,"Aka":"EBVQNT","TdTestInfoCommonId":2698},{"Id":14562,"Aka":"SQEBVQNT","TdTestInfoCommonId":2698},{"Id":14563,"Aka":"viral load","TdTestInfoCommonId":2698},{"Id":14564,"Aka":"PTLD","TdTestInfoCommonId":2698},{"Id":14565,"Aka":"EBV DNA","TdTestInfoCommonId":2698},{"Id":14566,"Aka":"EBVDNA","TdTestInfoCommonId":2698}],"TdBillingCommons":[{"Id":16595,"CptCode":"87799","Quantity":1,"Tmid":"30600705","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Quantification, Epstein-Barr Virus","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2698,"IsBeakerData":false}],"TdIncludes":[{"Id":26295,"TestName":"EBV DNA","Rank":1,"TdTestInfoCommonId":2698},{"Id":26296,"TestName":"EBV DNA (IU/mL)","Rank":2,"TdTestInfoCommonId":2698},{"Id":26297,"TestName":"EBV DNA (log IU/mL)","Rank":3,"TdTestInfoCommonId":2698}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2698,"SpecialInfo":"","ClinicalInfo":"Epstein-Barr virus (EBV) is a common viral pathogen that can cause disease in transplant recipients through reactivation of latent virus or through a new primary infection, especially in EBV-negative transplant recipients who receive grafts from EBV-positive donors. For these patients, the most severe form of EBV-related disease is post-transplant lymphoproliferative disorder (PTLD), which results from uncontrolled proliferation of lymphocytes, typically B cells. Early identification of primary EBV infections and DNA level monitoring can support prompt therapeutic intervention to prevent progression to EBV-related disease. cobas EBV is an FDA-approved in vitro nucleic acid amplification test for the quantitation of Epstein-Barr virus (EBV) DNA in human EDTA plasma. cobas EBV is intended for use as an aid in the management of EBV in transplant patients. In patients undergoing monitoring of EBV, serial DNA measurements can be used to indicate the need for potential treatment changes and to assess response to treatment. The results from cobas EBV are intended to be read and analyzed by a qualified licensed healthcare professional in conjunction with clinical signs and symptoms and relevant laboratory findings. Negative test results do not preclude EBV infection or EBV disease. Test results must not be the sole basis for patient management decisions. cobas EBV is not intended for use as a screening test for donors of blood or blood products or human cells, tissues, and cellular and tissue-based products (HCT/Ps). The assay is a quantitative PCR assay that targets highly-conserved regions of the EBV located in the EBV EBNA-1 gene and the EBV BMRF gene, and is reported out in international units (IU/mL). The linear range of the assay is 35.0 to 100,000,000 IU/mL (1.54 - 8.00 log IU/mL). The lower limit of detection of the assay is 18.8 IU/mL.","ClinicalReference":"1. Styczynski J, van der Velden W, Fox CP, Engelhard D, de la Camara R, Cordonnier C, Ljungman P; Sixth European Conference on Infections in Leukemia, a joint venture of the Infectious Diseases Working Party of the European Society of Blood and Marrow Transplantation (EBMT-IDWP), the Infectious Diseases Group of the European Organization for Research and Treatment of Cancer (EORTC-IDG), the International Immunocompromised Host Society (ICHS) and the European Leukemia Net (ELN). Management of Epstein-Barr Virus infections and post-transplant lymphoproliferative disorders in patients after allogeneic hematopoietic stem cell transplantation: Sixth European Conference on Infections in Leukemia (ECIL-6) guidelines. Haematologica. 2016 Jul;101(7):803-11. doi: 10.3324/haematol.2016.144428. PMID: 27365460\n2. U.S. Food and Drug Administration (FDA). De Novo Evaluation of Automatic Class III Designation for cobas EBV DEN200015. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/reviews/DEN200015.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Recommendations regarding monitoring EBV viral load post-transplant and medically relevant EBV DNA thresholds vary among transplant type and transplant institutions. While elevated EBV viral load may suggest post-transplant lymphoproliferative disorders (PTLD), the diagnosis of PTLD is made based on histological evaluation of tissue biopsy. PTLD may be present without detectable EBV viral load, and an increase in EBV viral load is not necessarily diagnostic of PTLD. As with any molecular test, mutations within the target regions of cobas EBV could affect primer and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus. Due to the potential for variability in EBV DNA measurements across different EBV assays, it is recommended that the same device be used for the serial quantitation of EBV DNA when managing individual patients.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":28,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2698,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":28,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13729,"DictMethodologyId":482,"TdTestInfoSpecificId":28,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":28,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51783,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":28,"IsBeakerData":false},{"Id":51784,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma. Aliquots must be made from specimen prior to testing in any lab outside of Molecular Microbiology, and must be placed in a sterile aliquot tube.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":28,"IsBeakerData":false},{"Id":678987,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":28,"IsBeakerData":false},{"Id":678988,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":217,"DictSpContainerName":"Pink KEDTA","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":28,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29753,"Description":"6 days for plasma separated from whole blood within 24 hours;\n24 hours for whole blood unspun/unseparated\n","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":28,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29754,"Description":"24 hours for plasma or for whole blood unspun/unseparated","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":28,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29755,"Description":"6 months for plasma if separated from whole blood and aliquoted into a secondary tube within 24 hours (plasma cannot be frozen in PPT tubes)\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":28,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":28,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2700,"LISCode":"ECHINO","PrimaryName":"Echinococcus Ab, IgG","LISName":"Echinococcus Ab, IgG","EMRName":"Echinococcus Ab, IgG","EMRCode":"SQECHINO","LOINC":"9656-0","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":9463,"CptCode":"86682","Quantity":1,"Tmid":"30201185","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"HELMINTH, NES","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2700,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2700,"SpecialInfo":"Contaminated, heat-inactivated, grossly hemolyzed, or severely lipemic specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Patients with collagen vascular diseases, hepatic cirrhosis, schistosomiasis, and other parasitic infections can produce false-positive results. There is a strong cross-reaction between echinococcosis and cysticercosis-positive sera. Seroconversion between acute and convalescent sera is considered strong evidence of recent infection. 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If needed repeat step 3 to remove extraneous red blood cells.\n5.\tTransfer serum into a second properly labeled plastic tube. Store at 2-8°C for at least 72 hours to precipitate the cryoglobulins. 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Substituted: Creatinine is less than 2mg/dL and the Specific gravity is less than 1.003 or greater than or equal to 1.020. 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Grossly hemolyzed or lipemic serum or specimens should\nbe avoided.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":129,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2444,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":129,"IsStat":false,"Comments":"","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11920,"DictMethodologyId":161,"TdTestInfoSpecificId":129,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":129,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":46815,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":129,"IsBeakerData":false},{"Id":46816,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":138,"DictSpVolumeName":"0.25 mL","TdTestInfoSpecificId":129,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26765,"Description":"1 day","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":129,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26766,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":129,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26767,"Description":"1 year, up to 2 freeze thaw cycles","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":129,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":129,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2447,"LISCode":"CAROT","PrimaryName":"Carotene","LISName":"Carotene","EMRName":"Carotene Serum","EMRCode":"SQCAROT","LOINC":"2053-7","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":12139,"Aka":"Beta Carotene","TdTestInfoCommonId":2447},{"Id":12140,"Aka":"Carotene, Serum Total","TdTestInfoCommonId":2447}],"TdBillingCommons":[{"Id":14954,"CptCode":"82380","Quantity":1,"Tmid":"30100835","CclTechComponentPrice":36.00,"CclProfComponentPrice":null,"TestNameForCdm":"CAROTENE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2447,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2447,"SpecialInfo":"Patient Preparation: 12 hour fast prior to collection is preferred, but not required. CRITICAL: Protect from light during collection, storage, and shipment, and use amber transport tubes. Separate specimens must be submitted when multiple tests  are ordered. Unacceptable conditions: Any specimen other than serum, hemolyzed or icteric specimens. This test is New York DOH approved. ","ClinicalInfo":"Use to assess fat malabsorption.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":130,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2447,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":130,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11847,"DictMethodologyId":188,"TdTestInfoSpecificId":130,"DictMethodology":{"Id":188,"Name":"Spectrophotometry (S)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":130,"DictDaysPerformedId":32,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Thu, Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":46493,"SpecialInstructions":"CRITICAL: Protect specimen from light during collection, storage and shipment. Transfer 3 mL serum into amber transport tube. Separate specimens MUST be submitted when multiple tests are ordered. Draw 2 tubes to ensure adequate volume.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":130,"IsBeakerData":false},{"Id":46494,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":11,"DictSpVolumeName":"0.6 mL","TdTestInfoSpecificId":130,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26561,"Description":"After separation from cells: 1 month","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":130,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26562,"Description":"After separation from cells: 4 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":130,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26563,"Description":"After separation from cells: Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":130,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":130,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2452,"LISCode":"STCATH","PrimaryName":"Cathartic Laxative, Stool","LISName":"Cathartic Lax Stool","EMRName":"Stool Cathartic Laxative","EMRCode":"SQSTCATH","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":12234,"Aka":"Laxatives","TdTestInfoCommonId":2452}],"TdBillingCommons":[{"Id":15057,"CptCode":"83735","Quantity":1,"Tmid":"30121635","CclTechComponentPrice":195.00,"CclProfComponentPrice":null,"TestNameForCdm":"STCATH Assay of magnesium","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2452,"IsBeakerData":false},{"Id":15058,"CptCode":"84100","Quantity":1,"Tmid":"30102665","CclTechComponentPrice":165.00,"CclProfComponentPrice":null,"TestNameForCdm":"%STCATH PHOSPOROUS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2452,"IsBeakerData":false}],"TdIncludes":[{"Id":22501,"TestName":"Magnesium","Rank":1,"TdTestInfoCommonId":2452},{"Id":22502,"TestName":"Phosphorus","Rank":2,"TdTestInfoCommonId":2452}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2452,"SpecialInfo":"Specimens for elemental testing should be collected in certified metal-free containers. Elevated results for elemental testing may be caused by environmental contamination\nat the time of specimen collection and should be interpreted accordingly.","ClinicalInfo":"Useful for compliance or abuse monitoring of laxative(s). It is recommended that unexpected elevated results be verified by testing another specimen. Magnesium concentrations in stool water above the normal levels of 0.7-1.2 mg/mL have been indicative of surreptitious abuse of magnesium containing laxatives. Laboratory calculated stool magnesium normal is approximately 0.5-10 mg/g (Based on the reported range of magnesium eliminated per day in stool and the range of stool mass per day in adults). Not for clinical diagnostic purposes.\nPhosphorus concentration in stool water averaged 1.8 +/- 0.3 mg/mL (ranged from 0.3-4.2 mg/mL) following administration of 105 mmol of sodium phosphate. Laboratory calculated stool phosphorus is approximately 1.4-22 mg/g (Based on the reported range of phosphorius eliminated per day in stool and the range of stool mass per day in adults). Not for clinical diagnostic purposes.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":131,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2452,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":131,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11941,"DictMethodologyId":7,"TdTestInfoSpecificId":131,"DictMethodology":{"Id":7,"Name":"Inductively Coupled Plasma/Optical Emission Spectrometry (ICP/OES)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":131,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":202,"DictDaysPerformed":"Mon - 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Reporting limit: Desacetyl Bisacodyl (Bisacodyl diphenol): 5.0 ng/mL, Rhein: 5.0 ng/mL, Emodin: 5.0 ng/mL, Aloe-Emodin: 5.0 ng/mL.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":132,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2453,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":132,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9138,"DictMethodologyId":54,"TdTestInfoSpecificId":132,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":132,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":104,"DictDaysPerformed":"Mon - Sun","DictReported":"8 - 9 days"},"TdSpecimenRequirements":[{"Id":35263,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":132,"IsBeakerData":false},{"Id":35264,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":86,"DictSpVolumeName":"1.2 mL","TdTestInfoSpecificId":132,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19916,"Description":"2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":132,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19917,"Description":"30 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":132,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19918,"Description":"30 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":132,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":132,"TestCode":null,"IsReportable":false,"DictVendorId":76,"DictVendor":{"Id":76,"Name":"National Med Serv Inc","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2449,"LISCode":"PLCAT","PrimaryName":"Catecholamines, Fractionated, Plasma","LISName":"Catecholamines, Fractionated, Plasma","EMRName":"Catecholamines, Fractionated, Plasma","EMRCode":"SQPLCAT","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":11667,"CptCode":"82384","Quantity":1,"Tmid":"30100845","CclTechComponentPrice":126.00,"CclProfComponentPrice":null,"TestNameForCdm":"CATECHOLAMINE FRACT PL","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2449,"IsBeakerData":false}],"TdIncludes":[{"Id":16718,"TestName":"Norepinephrine","Rank":1,"TdTestInfoCommonId":2449},{"Id":16719,"TestName":"Epinephrine","Rank":2,"TdTestInfoCommonId":2449},{"Id":16720,"TestName":"Dopamine","Rank":3,"TdTestInfoCommonId":2449}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2449,"SpecialInfo":"Patient should be calm and seated for 15 minutes prior to collection. Alternately, patient may be calm and supine for 30 minutes prior to collection. Drugs and medications may affect results and should be discontinued for 72 hours prior to specimen collection, if possible. CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered. This test is New York state approved. Unacceptable conditions: Serum, or urine.  ","ClinicalInfo":"Not recommended for evaluation of pheochromocytoma or paraganglioma. Use to evaluate clinical symptoms of excess catecholamine secretion. Small increases in catecholamines (less than 2 times the upper reference limit) are usually the result of physiological stimuli, drugs, or improper specimen collection. Significant elevation of one or more catecholamines (2 or more times the upper reference limit) can result from a neuroendocrine tumor. Measurement of plasma or urine fractionated metanephrines should be used for assessment of suspected pheochromocytoma or paraganglioma. Lower catecholamine concentrations are observed in specimens collected from supine adults. Medications may interfere with catecholamines and metabolites. The effect of drugs on catecholamine results may not be predictable. Children, particularly those under 2 years of age, often show an elevated catecholamine response to stress. ","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":134,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2449,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":134,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13471,"DictMethodologyId":54,"TdTestInfoSpecificId":134,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":134,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":35154,"SpecialInstructions":"Patient should be calm and seated for 15 minutes or supine for 30 minutes prior to collection. Collect 2 tubes. Centrifuge, aliquot and freeze within one hour of collection. Refrigerated centrifuge is preferred but not required. 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Results obtained with different assay methods or kits cannot be used interchangeably. Measurements of CEA have been shown to be clinically relevant in the management of patients with colorectal, breast, lung, prostatic, pancreatic, and ovarian carcinomas. Smokers may have slightly elevated levels of CEA. 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This testing can rule out celiac disease with high negative predictive value (NPV) of 95 - 100% depending on the ethnic background.\n\n\nReferences: \n1. Koskinen L, Romanos J, Kaukinen K, et al. Cost-effective HLA typing with tagging SNPs predicts celiac disease risk haplotypes in the Finnish, Hungarian, and Italian populations. Immunogenetics. 2009 Apr;61(4):247-56.\n2. Sollid LM. Coeliac disease: dissecting a complex inflammatory disorder. Nat Rev Immunol. 2002 Sep;2(9):647-55.\n3. Liu E, Lee HS, Aronsson CA, et al. Risk of pediatric celiac disease according to HLA haplotype and country. 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If a factor VIII inhibitor is suspected, this assay should be ordered in addition to Factor VIII inhibitor level if porcine factor VIII is a therapeutic option.  Factor VIII inhibitor: Inhibitor titers < 5 Bethesda units are considered low titer inhibitors; those > or = 5 Bethesda units are considered high titer inhibitors. 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For EDTA plasma, utilize BKQUAN.","ClinicalInfo":"BK virus (BKV) is a common viral pathogen that can cause polyoma virus nephropathy in kidney transplant patients. It is also associated with hemorrhagic cystitis in immunocompromised patients, especially in hematopoietic stem cell transplant recipients. cobas BKV is an FDA-approved in vitro nucleic acid amplification test for the quantitation of BK virus (BKV) DNA in human EDTA plasma and urine stabilized in cobas PCR Media. In EDTA plasma, cobas BKV is intended for use as an aid in the management of BKV in transplant patients. In patients undergoing monitoring of BKV in EDTA plasma, serial DNA measurements can be used to indicate the need for potential treatment changes and to assess viral response to treatment. In urine stabilized in cobas PCR Media, cobas BKV is intended for use as an aid in the management of BKV in transplant patients. The results from cobas BKV are intended to be read and analyzed by a qualified licensed healthcare professional in conjunction with clinical signs and symptoms and relevant laboratory findings. Test results must not be the sole basis for patient management decisions. The assay is a quantitative PCR assay that targets highly-conserved regions of the BKV located in the BKV small t-antigen region and the BKV VP2 region, and is reported out in international units (IU/mL). The linear range of the assay in urine is 200 to 100,000,000 IU/mL (2.30 - 8.00 log IU/mL). The lower limit of detection of the assay in urine is 12.2 IU/mL.\n","ClinicalReference":"1. Hirsch HH, Randhawa PS; AST Infectious Diseases Community of Practice. BK polyomavirus in solid organ transplantation-Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice. Clin Transplant. 2019 Sep;33(9):e13528. doi: 10.1111/ctr.13528. Epub 2019 Apr 10. PMID: 30859620.\n2. U.S. Food and Drug Administration (FDA). 510(k) Substantial Equivalence Determination Decision Summary K203220. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/reviews/K203220.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Recommendations regarding monitoring BKV viral load post-transplant and medically relevant BKV DNA thresholds vary among transplant type and transplant institutions. As with any molecular test, mutations within the target regions of cobas BKV could affect primer and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus. 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The correct volume of urine has been added when the fluid level is between the two black lines on the tube label.\n","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":310,"IsBeakerData":false},{"Id":33830,"SpecialInstructions":"The minimum volume of urine accepted is 1 mL.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":310,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19032,"Description":"24 hours for neat urine; 90 days for urine stabilized in cobas PCR media","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":310,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19033,"Description":"24 hours for neat urine; 90 days for urine stabilized in cobas PCR media","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":310,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":310,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2356,"LISCode":"BKQUAN","PrimaryName":"BK Virus (BKV) DNA, Quantitative PCR, Plasma","LISName":"BK Virus (BKV) DNA, Quantitative PCR, Plasma","EMRName":"BK Virus (BKV) DNA, Quantitative PCR, Plasma","EMRCode":"SQBKQUAN","LOINC":"41479-7","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14537,"Aka":"BKQUAN","TdTestInfoCommonId":2356},{"Id":14538,"Aka":"SQBKQUAN","TdTestInfoCommonId":2356},{"Id":14539,"Aka":"viral load","TdTestInfoCommonId":2356},{"Id":14540,"Aka":"BKVAN","TdTestInfoCommonId":2356},{"Id":14541,"Aka":"polyomavirus","TdTestInfoCommonId":2356},{"Id":14542,"Aka":"PVAN","TdTestInfoCommonId":2356},{"Id":14543,"Aka":"BKV DNA","TdTestInfoCommonId":2356},{"Id":14544,"Aka":"BKVDNA","TdTestInfoCommonId":2356}],"TdBillingCommons":[{"Id":16451,"CptCode":"87799","Quantity":1,"Tmid":"30606745","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Quantification, BK Virus","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2356,"IsBeakerData":false}],"TdIncludes":[{"Id":26285,"TestName":"BKV DNA","Rank":1,"TdTestInfoCommonId":2356},{"Id":26286,"TestName":"Plasma BKV DNA (IU/mL)","Rank":2,"TdTestInfoCommonId":2356},{"Id":26287,"TestName":"Plasma BKV DNA (log IU/mL)","Rank":3,"TdTestInfoCommonId":2356}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2356,"SpecialInfo":"BKQUAN should only be utilized for EDTA plasma. For urine, utilize UBKQT.","ClinicalInfo":"BK virus (BKV) is a common viral pathogen that can cause polyoma virus nephropathy in kidney transplant patients. It is also associated with hemorrhagic cystitis in immunocompromised patients, especially in hematopoietic stem cell transplant recipients. cobas BKV is an FDA-approved in vitro nucleic acid amplification test for the quantitation of BK virus (BKV) DNA in human EDTA plasma and urine stabilized in cobas PCR Media. In EDTA plasma, cobas BKV is intended for use as an aid in the management of BKV in transplant patients. In patients undergoing monitoring of BKV in EDTA plasma, serial DNA measurements can be used to indicate the need for potential treatment changes and to assess viral response to treatment. In urine stabilized in cobas PCR Media, cobas BKV is intended for use as an aid in the management of BKV in transplant patients. The results from cobas BKV are intended to be read and analyzed by a qualified licensed healthcare professional in conjunction with clinical signs and symptoms and relevant laboratory findings. Test results must not be the sole basis for patient management decisions. The assay is a quantitative PCR assay that targets highly-conserved regions of the BKV located in the BKV small t-antigen region and the BKV VP2 region, and is reported out in international units (IU/mL). The linear range of the assay in EDTA plasma is 21.5 to 100,000,000 IU/mL (1.33 - 8.00 log IU/mL). The lower limit of detection of the assay in EDTA plasma is 21.5 IU/mL.\n","ClinicalReference":"1. Hirsch HH, Randhawa PS; AST Infectious Diseases Community of Practice. BK polyomavirus in solid organ transplantation-Guidelines from the American Society of Transplantation Infectious Diseases Community of Practice. Clin Transplant. 2019 Sep;33(9):e13528. doi: 10.1111/ctr.13528. Epub 2019 Apr 10. PMID: 30859620.\n2. U.S. Food and Drug Administration (FDA). 510(k) Substantial Equivalence Determination Decision Summary K203220. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/reviews/K203220.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Recommendations regarding monitoring BKV viral load post-transplant and medically relevant BKV DNA thresholds vary among transplant type and transplant institutions. As with any molecular test, mutations within the target regions of cobas BKV could affect primer and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus. Due to the potential for variability in BKV DNA measurements across different BKV assays, it is recommended that the same device be used for the serial quantitation of BKV DNA when managing individual patients.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":311,"ActiveDate":"2010-08-02T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2356,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":311,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13726,"DictMethodologyId":482,"TdTestInfoSpecificId":311,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":311,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51383,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":311,"IsBeakerData":false},{"Id":51384,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma. 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Results obtained with different methods or kits cannot be used interchangeably.\n\nPatients taking a biotin dose of up to 5 mg/day should refrain from taking biotin for 4 hours prior to sample collection. Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.  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","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":10006,"Aka":"Cancer Antigen 19-9","TdTestInfoCommonId":2412},{"Id":10007,"Aka":"Carbohydrate Antigen 19-9","TdTestInfoCommonId":2412}],"TdBillingCommons":[{"Id":12973,"CptCode":"86301","Quantity":1,"Tmid":"30200730","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"IMMUNOASSY TUMOR CA 19-9","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2412,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2412,"SpecialInfo":"\nThe CA 19-9 Antigen test was performed using the Beckman Coulter Unicel DXI paramagnetic particle chemiluminescent immunoassay method. Results obtained with different assay methods or kits cannot be used interchangeably.","ClinicalInfo":"Cancer antigen 19-9 test is used as an aid in monitoring response to treatment or recurrence in patients with established pancreatic, hepatobiliary, or gastrointestinal malignancies. ","ClinicalReference":"","ClinicalLimitation":"Patients taking a Biotin dose of up to 5 mg/day should refrain from taking Biotin for 1 hour prior to sample collection. Patients taking a Biotin dose > 5 mg/day to 10 mg/day should refrain from taking Biotin for 2 hours prior to sample collection. Patients taking a Biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken. 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Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result. \n","ClinicalInfo":"Diagnosis of adrenal disorders","ClinicalReference":"","ClinicalLimitation":"During metyrapon tests, 11 deoxycortisol levels are elevated. \nFalsely elevated cortisol values may be determined due to cross reactions.\n\nIn samples from patients who have been treated with prednisolone, 6-alpha-Methylprednisolone or prednisone, falsely elevated concentrations of cortisol may be determined.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":372,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2574,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":372,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12178,"DictMethodologyId":185,"TdTestInfoSpecificId":372,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":372,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":9,"DictDaysPerformed":"Sun - Sat","DictReported":"24 hours"},"TdSpecimenRequirements":[{"Id":47896,"SpecialInstructions":"Indicate collection time on specimen.","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Grossly hemolyzed, icteric, lipemic or heparinized specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Screen, diagnose, and monitor diseases associated with excess or deficient cortisol production. To convert to nmol/L, multiply ug/dL by 27.6.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":373,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2575,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":373,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6945,"DictMethodologyId":394,"TdTestInfoSpecificId":373,"DictMethodology":{"Id":394,"Name":"Equilibrium Dialysis","Description":null},"TdTestInfoSpecific":null},{"Id":6946,"DictMethodologyId":265,"TdTestInfoSpecificId":373,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":373,"DictDaysPerformedId":55,"DictHoursPerformedId":null,"DictReportedId":68,"DictDaysPerformed":"Sun, Tue, Thu, Fri","DictReported":"3 - 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Swab must be completely saturated to ensure sufficient volume for testing. Collection should follow ARUP instructions provided with Salivette. Record collection time on container and requisition. Do not centrifuge Salivette. Full Salivette device must be returned: blue stopper, swab, insert, and tube. Patient Preparation: Do not collect specimen within 60 minutes after eating a meal, within 12 hours after consuming alcohol, immediately after brushing teeth, using mouthwash, or after any activity that may cause gums to bleed. Avoid using lipstick, ChapStick, and other lip items prior to sample collection. Avoid use of exogenous sources of cortisol (e.g., topical or oral hydrocortisone) or similar products during collection to reduce contamination. Rinse mouth thoroughly with water 10 minutes before collecting specimen. Recommended collection time is between 11:00 p.m. - 1:00 a.m.","LogicalOperation":null,"DictSpContainerId":74,"DictSpContainerName":"Swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":61,"DictSpTypeName":"Saliva","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":375,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16354,"Description":"3 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":375,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16355,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":375,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16356,"Description":"6 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":375,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":375,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2579,"LISCode":"COXIGG","PrimaryName":"Coxiella Burnetii IgG Abs","LISName":"Coxiella IgG Abs","EMRName":"Antibody Coxiella burnetii IgG Phase 1&2","EMRCode":"SQCOXIGG","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":10852,"Aka":"Coxiella Burnetii IgG Phase 1&2","TdTestInfoCommonId":2579},{"Id":10853,"Aka":"Q-Fever IgG","TdTestInfoCommonId":2579},{"Id":13982,"Aka":"C. burnetii Ab IgG, Phase I and II with Reflex to Titer\t","TdTestInfoCommonId":2579}],"TdBillingCommons":[{"Id":14078,"CptCode":"86638","Quantity":2,"Tmid":"30202505","CclTechComponentPrice":115.00,"CclProfComponentPrice":null,"TestNameForCdm":"COXIELLA BURNETII IGG X2","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2579,"IsBeakerData":false}],"TdIncludes":[{"Id":20516,"TestName":"IgG Phase 1","Rank":1,"TdTestInfoCommonId":2579},{"Id":20517,"TestName":"IgG Phase 2","Rank":2,"TdTestInfoCommonId":2579}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2579,"SpecialInfo":"Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. If either C. Burnetii Abs IgG Phase I and/or Phase II result is indeterminate or positive, then titer(s) will be added at an additional cost. Contaminated, hemolyzed, or severely lipemic specimens are unacceptable. This test is New York DOH approved. \n","ClinicalInfo":"Useful to confirm infectious agent as C. burnetii (Q-fever) in symptomatic patients. Testing of acute and convalescent sera is recommended. Single phase II IgG titers of 1:256 and greater are considered evidence of C. burnetii infection at some time prior to the date of the serum specimen. Phase I antibody titers of 1:16 and greater are consistent with chronic infection or convalescent phase of Q-fever. 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Label specimens plainly as 'acute' or 'convalescent.' Cerebrospinal fluid (CSF) or plasma will be rejected. Contaminated, hemolyzed, or severely lipemic specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Single positive antibody titers of greater than or equal to 1:80 may indicate past or current infection. Seroconversion or an increase in titers between acute and convalescent sera of at least fourfold is considered strong evidence of current or recent infection.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":378,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2583,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":378,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10873,"DictMethodologyId":309,"TdTestInfoSpecificId":378,"DictMethodology":{"Id":309,"Name":"Serum Neutralization Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":378,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":49,"DictDaysPerformed":"Mon - Fri","DictReported":"7 - 13 days"},"TdSpecimenRequirements":[{"Id":51956,"SpecialInstructions":"Parallel testing is preferred, and convalescent specimens must be received within 30 days from receipt of acute specimens. Label specimens plainly as 'acute' or 'convalescent.' Separate serum from cells ASAP or within 2 hours of collection and transfer into a standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":378,"IsBeakerData":false},{"Id":51957,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":378,"IsBeakerData":false},{"Id":51958,"SpecialInstructions":"Parallel testing is preferred, and convalescent specimens must be received within 30 days from receipt of acute specimens. Label specimens plainly as 'acute' or 'convalescent.' Separate serum from cells ASAP or within 2 hours of collection and transfer into a standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":378,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":24097,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":378,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24098,"Description":"1 year (Avoid repeated freeze/thaw cycles)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":378,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24099,"Description":"48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":378,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":378,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2609,"LISCode":"CAD","PrimaryName":"Cryptococcus antigen screen and titer by LFA","LISName":"Cryptococcus antigen screen and titer by LFA","EMRName":"Cryptococcus antigen screen and titer by LFA","EMRCode":"SQCAD","LOINC":"43228-6","RecommendedUse":"Aiding in the diagnosis of cryptococcosis","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6793,"Aka":"Antigen Detection, Cryptococcus","TdTestInfoCommonId":2609},{"Id":6794,"Aka":"CAD","TdTestInfoCommonId":2609},{"Id":14441,"Aka":"Cerebrospinal fluid","TdTestInfoCommonId":2609},{"Id":14442,"Aka":"Cryptococcus","TdTestInfoCommonId":2609},{"Id":14443,"Aka":"CSF fungal","TdTestInfoCommonId":2609},{"Id":14444,"Aka":"serum, Cryptococcus","TdTestInfoCommonId":2609}],"TdBillingCommons":[{"Id":9805,"CptCode":"87899","Quantity":1,"Tmid":"30601440","CclTechComponentPrice":104.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, CAD","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2609,"IsBeakerData":false},{"Id":19390,"CptCode":"87899","Quantity":1,"Tmid":"30201515","CclTechComponentPrice":104.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, CAD Titer","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2609,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2609,"SpecialInfo":"The Cryptococcal antigen lateral flow assay is a dipstick immunochromatographic assay. The test utilizes specimen wicking up the membrane to interact with capture gold-conjugated anti-CrAG antibodies. The antibody-antigen complex continues to wick up the membrane and interact with test line which has the immobilized anti-CrAg monoclonal antibodies. The antibody-antigen complex forms a visible line at the \"test line\". In order to report a test positive, a visible line is also needed at the \"control line\" which ensures proper migration of the specimen through the membrane. Thus, positive test results will create two lines (test and control), negative test results will only form one line (control). Test may result as invalid if a control line does not develop. Semi-quantitative titration procedures are employed with an initial positive or if there is an extremely faint line to rule out false negative results from high titer specimens (hook effect/postzone)\n\nIf Cryptococcal Antigen Detection is positive, a titer will be performed at an additional charge with CPT code 87899 applied.\nIf Cryptococcal Antigen Detection is positive in CSF, fungal culture CSF will be reflexed. ","ClinicalInfo":"Cryptococcus species are typically acquired by the pulmonary route and have a predilection for CNS infections. CSF is the specimen of choice for detection of cryptococcal meningitis in adults. Cryptococcus antigen test on serum and CSF specimens is a rapid and sensitive diagnostic method for detection of Cryptococcal infections. Declining titers may indicate regression of infection. However, monitoring titers to cryptococcal antigen should not be used as a test of cure or to guide treatment decisions. Low-level titers may persist for extended periods of time following appropriate therapy and resolution of infection\n","ClinicalReference":"Perfect JR, Dismukes WE, Dromer F, et al: Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2010 Feb 1;50(3):291-322\n\"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. \"\n\n","ClinicalLimitation":"Testing is limited CSF and serum specimens only. Antigen screen (positive/negative) are performed across all shifts, Cryptococcus titer results are only performed during 7am-4pm. CSF specimens submitted for initial diagnosis that test positive by the lateral flow assay, should also be submitted for routine fungal culture. Culture can aid in differentiating between the 2 common Cryptococcus species causing disease (Cryptococcus neoformans and Cryptococcus gattii) and can be used for antifungal susceptibility testing, if necessary. CAD test should not be used as a screening procedure for the general population. This test should not be used as a test of cure or to guide treatment decisions. Bloody lumbar puncture and/or contamination of the cerebrospinal fluid (CSF) specimen with serum, other yeast infections such as Trichosporon may lead to a positive Cryptococcus antigen result. CAD titers can be utilised to monitor therapy but titers acquired by different assays are not interchangeable; titers acquired by lateral flow assay may be higher than other antigen assays such as agglutination tests. Extremely high concentrations of cryptococcal antigen can result in negative CAD results. If high burden is suspected, sample may be diluted to resolve false negative. Please call the lab/medical director in such instances. \n","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":379,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2609,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":379,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13212,"DictMethodologyId":328,"TdTestInfoSpecificId":379,"DictMethodology":{"Id":328,"Name":"Line Immunoassay (INNO-LIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":379,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":77,"DictDaysPerformed":"Sun - Sat","DictReported":"1 day"},"TdSpecimenRequirements":[{"Id":28614,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":5,"DictSpVolumeName":"0.1 mL","TdTestInfoSpecificId":379,"IsBeakerData":false},{"Id":678358,"SpecialInstructions":"Sterile technique should be used to collect specimen to decrease contamination issues. FUNCSF order is suggested in recovering Cryptococcus from clinical specimen with consistently low titers and in cases where susceptibility testing may be indicated. \n","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":379,"IsBeakerData":false},{"Id":678359,"SpecialInstructions":"Serum should be separated as soon as possible after collection by centrifuging. Grossly hemolysed samples may cause false positive results and will be rejected.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":379,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16310,"Description":"7 days (72 hours preferred for Cryptococcus Antigen test)","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":379,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16311,"Description":"Indefinitely","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":379,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31008,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":379,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":379,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":2844,"PrimaryName":"Fungal CSF culture and CAD","IsRequired":false}]},{"Id":2610,"LISCode":"CRYSPO","PrimaryName":"Cryptosporidia, Cyclospora and Cystoisospora Examination","LISName":"Cryptosporidia/Cyclospora Stain Exam","EMRName":"Cryptosporidia/Cyclospora Stain Exam","EMRCode":"SQCRYSPO","LOINC":"20781-1","RecommendedUse":"In individuals presenting with persistent diarrhea or risk factors for Cryptosporidium, Cyclospora or Cystoisospora infections; Immunocompromised patients, HIV, primary immunodeficiency or history of transplant. Consider ordering if exposure to infectious agent during an outbreak. For suspicion of Cryptosporidium, the antigen test OVAPSC is recommended. This test does not detect other common infectious parasites that cause diarrhea; order OVAP.","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6090,"Aka":"Cyclospora Examination","TdTestInfoCommonId":2610},{"Id":6091,"Aka":"Cystoisospora Examination","TdTestInfoCommonId":2610},{"Id":6092,"Aka":"Ova and parasite for Cryptosporidia","TdTestInfoCommonId":2610},{"Id":14296,"Aka":"CLB","TdTestInfoCommonId":2610},{"Id":14297,"Aka":"Coccidia","TdTestInfoCommonId":2610},{"Id":14298,"Aka":"Coccidiaan like bodies","TdTestInfoCommonId":2610},{"Id":14299,"Aka":"Cryptosporidia","TdTestInfoCommonId":2610},{"Id":14300,"Aka":"Cryptosporidium","TdTestInfoCommonId":2610},{"Id":14301,"Aka":"Cyclospora","TdTestInfoCommonId":2610},{"Id":14302,"Aka":"Cystoisospora","TdTestInfoCommonId":2610},{"Id":14303,"Aka":"Isospora","TdTestInfoCommonId":2610},{"Id":14304,"Aka":"Modified acid fast parasites","TdTestInfoCommonId":2610},{"Id":14305,"Aka":"Stool test","TdTestInfoCommonId":2610},{"Id":14306,"Aka":"STUL kit","TdTestInfoCommonId":2610}],"TdBillingCommons":[{"Id":8711,"CptCode":"87015","Quantity":1,"Tmid":"30606300","CclTechComponentPrice":44.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Fluid Concentration","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2610,"IsBeakerData":false},{"Id":8712,"CptCode":"87207","Quantity":1,"Tmid":"31200245","CclTechComponentPrice":39.00,"CclProfComponentPrice":null,"TestNameForCdm":"Smear, Parasite Special Stain","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2610,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2610,"SpecialInfo":"Recommend sending a complete STUL kit for submission of all outpatient specimens for any additional add-on testing. ","ClinicalInfo":"Cryptosporidia, Cyclospora and Cystoisospora are protozoan parasites that cause infection in the intestinal tract resulting in diarrhea amongst other symptoms such as abdominal pain, weight loss. Infections can be self limited but can also cause prolonged infection depending on the exposure, age and immune compromise of the host.  Transmission is via ingestion of fecally contaminated food or water. Waterborne transmission through swimming pools is a common route for exposure in outbreaks of Cryptosporidiosis. Due to the small size (Cryptosporidium and Cyclospora) and inability to be stained by trichrome stain, a modified acid-fast stain is required to detect these organisms. ","ClinicalReference":"","ClinicalLimitation":"Due to intermittent shedding of parasites a single negative test does not rule out a parasitic infection. Recommend testing 3 different stool specimens collected in separate containers on different days (over 5-7 days), preferably at different times of day. This test does not detect other common infectious parasites that cause diarrhea; consider ordering OVAP (other parasites) and MICSPO (for microsporidia). The gastrointestinal pathogen panel (STGIPI) is a molecular test that can also be performed to detect Cryptosporidium and Cyclospora along with other common infectious causes of persistent diarrhea. 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STUL kit can be purchased via oracle #1570140. Refer to Stool collection guide (https://clevelandcliniclabs.com/our-laboratories/laboratory-medicine/microbiology/plmi-collection-guidelines-resources/stool-specimen-collection-guide/)","LogicalOperation":null,"DictSpContainerId":46,"DictSpContainerName":"EcoFix fixative","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":4,"DictSpCollectionTemperatureName":"Refrigerated","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":52,"DictSpTypeName":"Stool","DictSpVolumeId":244,"DictSpVolumeName":"Complete to fill line","TdTestInfoSpecificId":380,"IsBeakerData":false},{"Id":677575,"SpecialInstructions":"Unpreserved stool should be submitted to the lab in a securely tightened sterile screw-top container and should be limited to inpatient settings due to a significantly shorter stability window. Use of non-standard (eg. food containers) is discouraged. Refer to Stool collection guide (https://clevelandcliniclabs.com/our-laboratories/laboratory-medicine/microbiology/plmi-collection-guidelines-resources/stool-specimen-collection-guide/)","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":4,"DictSpCollectionTemperatureName":"Refrigerated","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":52,"DictSpTypeName":"Stool","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":380,"IsBeakerData":false},{"Id":678095,"SpecialInstructions":"Body fluids (including but not limited to GI aspirates, respiratory secretions, CSF) should be submitted to the lab in a securely tightened sterile screw-top container. A minimum volume of 0.5ml needed, however larger volumes (1-10ml) are concentrated to increase sensitivity of detection. For CSF specimens, consider reaching out to the lab or microbiology medical director prior to collection.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":4,"DictSpCollectionTemperatureName":"Refrigerated","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":48,"DictSpTypeName":"Fluid, body","DictSpVolumeId":55,"DictSpVolumeName":"0.5 mL - 10 mL","TdTestInfoSpecificId":380,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":14392,"Description":"Stool - Preserved: 2 months; Unpreserved: Preferred within 6 hours, acceptable within 12 hours. 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Separate serum from cells within 2 hours of collection and transfer into standard aliquot tube. 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Heparinized specimens and tissues in optimal cutting temperature compound are unacceptable. This test is New York DOH approved. ","ClinicalInfo":"Use to detect adenovirus groups A-F; does not quantify viral load.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":425,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2038,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":425,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12028,"DictMethodologyId":480,"TdTestInfoSpecificId":425,"DictMethodology":{"Id":480,"Name":"Real-Time Polymerase Chain Reaction (RT-PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":425,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":47270,"SpecialInstructions":"Transfer to standard aliquot tube and freeze.","LogicalOperation":"Or","DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47275,"SpecialInstructions":"Transfer to standard aliquot tube and freeze.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47278,"SpecialInstructions":"All specimen types except tissue","LogicalOperation":"Or","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47279,"SpecialInstructions":"Specimen source required","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":59,"DictSpTypeName":"Sputum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47280,"SpecialInstructions":"Transfer tissue to sterile container and freeze immediately. 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Do not send tissues in optimal cutting temperature compound.","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":53,"DictSpTypeName":"Tissue","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47281,"SpecialInstructions":"Specimen source required","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":150,"DictSpTypeName":"Bronch (BAL)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47282,"SpecialInstructions":"Specimen source required","LogicalOperation":"Or","DictSpContainerId":113,"DictSpContainerName":"Viral Transport Media","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":34,"DictSpTypeName":"Nasopharyngeal swab","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":47283,"SpecialInstructions":"Specimen source required","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":678934,"SpecialInstructions":"Do not freeze.","LogicalOperation":"Or","DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":678935,"SpecialInstructions":"Conjunctival swabs in viral transport media are acceptable for testing with a disclaimer.","LogicalOperation":"Or","DictSpContainerId":113,"DictSpContainerName":"Viral Transport Media","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":1,"DictSpTypeName":"Conjunctival","DictSpVolumeId":38,"DictSpVolumeName":"Swab","TdTestInfoSpecificId":425,"IsBeakerData":false},{"Id":678936,"SpecialInstructions":"Transfer to standard aliquot tube and freeze.","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":425,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27046,"Description":"24 hours (whole blood, plasma, serum, BAL, CSF, swab, sputum); 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Nocardia spp. will grow from AFB cultures. Stain results are reported within 24 hours of specimen receipt. Cultures are incubated for 6 weeks; negative cultures are updated weekly.  Extended incubation or special requests require consultation with a medical director. Do not put special instructions in order comments. Providers are notified of initial positive smear or culture results and any identification of M. tuberculosis. \n\nSpecimen collection methods should minimize contamination with respiratory, skin or urogenital flora. If specimen transport is delayed by more than 2 hours, specimens should be refrigerated. When collecting in the outpatient setting, patients should be sent home with a pre-labeled container. Instruct patients to record collection date/time on the labeled container and refrigerate the specimen until submission. Due to the small volume collected and hydrophobicity of mycobacteria, swabs are suboptimal for recovery, and will be rejected. Exceptions require medical director approval. If a swab must be used, E swab is preferred.\n\nBoth source and body site should be provided with orders. Specimens from all skin sites and those from the extremities are cultured at both 37°C and 30°C to optimize recovery of M. marinum, M. haemophilum and some rapidly growing mycobacteria.  In Epic, the “Rule-out” drop down feature may be used when ordering to notify the laboratory if species with special growth requirements are in the differential.\n\nMycobacteria and Nocardia spp. from positive cultures are identified using a combination of MALDI TOF and/or sequencing methods. Susceptibility testing is performed on all M. tuberculosis, Nocardia species and M. kansasii.  Other susceptibility testing is performed on request, if clinically significant. The clarithromycin microbroth dilution test is incubated 14 days to detect phenotypic inducible resistance in rapidly growing mycobacteria. Molecular testing for erm(41) which mediates inducible resistance to clarithromycin is performed for M. abscessus species. Deletions in erm(41) prevent inducible clarithromycin resistance and are present in M. abscessus subsp. massiliense.\n\nMultiple identification procedures may be required. The following CPT codes are billed as applicable: Cepheid PCR 87556 87798, Additional stain testing 87206, MALDI-TOF 87118, Sequencing 87153, and Susceptibility Testing 87186.\n\n","ClinicalInfo":"Culture is performed to identify infection due to mycobacteria. Negative cultures do not rule-out infection. Multiple cultures (three) are generally performed to optimize sensitivity and to help determine the clinical significance of pulmonary infection with non-tuberculous mycobacteria. Clinical presentation, radiographic findings and histopathology should be evaluated in conjunction with culture data. (PMID: 32797222).\n\nFor patients in whom a diagnosis of pulmonary M. tuberculosis is in the differential, PCR is recommended on at least one respiratory specimen, and may be ordered on up to two specimens collected at least eight hours apart, including one first-morning sputum. Sensitivity of PCR for smear positive, culture positive TB is 97%; sensitivity for smear-negative, culture positive TB is 67%. (PMID 31173647).\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":427,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2042,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":427,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10548,"DictMethodologyId":224,"TdTestInfoSpecificId":427,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null},{"Id":10551,"DictMethodologyId":260,"TdTestInfoSpecificId":427,"DictMethodology":{"Id":260,"Name":"Stain","Description":null},"TdTestInfoSpecific":null},{"Id":13274,"DictMethodologyId":229,"TdTestInfoSpecificId":427,"DictMethodology":{"Id":229,"Name":"DNA Sequencing","Description":null},"TdTestInfoSpecific":null},{"Id":13275,"DictMethodologyId":537,"TdTestInfoSpecificId":427,"DictMethodology":{"Id":537,"Name":"Matrix-assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) Mass Spectrometry ","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":427,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":140,"DictDaysPerformed":"Sun - Sat","DictReported":"7 weeks"},"TdSpecimenRequirements":[{"Id":40655,"SpecialInstructions":"Larger volumes improve recovery. Collect BAL, wash, or aspirate into sputum trap or sterile cup. Volume:  at least 10 mL (preferred). Place bronchial brush in sterile, leak-proof tube or cup with enough non-bacteriostatic sterile saline to cover the brush (1-10 ml). ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":7,"DictSpTypeName":"Bronchoscopy specimen","DictSpVolumeId":24,"DictSpVolumeName":"10 mL","TdTestInfoSpecificId":427,"IsBeakerData":false},{"Id":40656,"SpecialInstructions":"Larger volumes improve recovery.  Volume 5-10 mL (preferred). ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":14,"DictSpTypeName":"Aspirate, tracheal","DictSpVolumeId":24,"DictSpVolumeName":"10 mL","TdTestInfoSpecificId":427,"IsBeakerData":false},{"Id":40657,"SpecialInstructions":"Biopsy material from the periphery of a cutaneous lesion. Tissue may be kept moist with a small amount (1-3 ml) of sterile saline. Send a separate portion for histopathology using sterile technique. Tissue in formalin is unacceptable for culture. 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Volume: 5 mL (preferred); 1 mL minimum.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":59,"DictSpTypeName":"Sputum","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":427,"IsBeakerData":false},{"Id":40659,"SpecialInstructions":"Aspirate pleural, pericardial, peritoneal, or synovial fluid using sterile technique after skin disinfection or during surgical procedure. Transfer fluid to sterile tube or cup.  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Patient Preparation: Usual preparation for clean-catch mid-void urine collection.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":98,"DictSpVolumeName":"40 mL","TdTestInfoSpecificId":427,"IsBeakerData":false},{"Id":40664,"SpecialInstructions":"Culture yield is increased with larger specimen volumes. Specimen volumes between 0.5 and 2 mL will be processed with a disclaimer. 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Blood cultures for AFB should ideally be drawn prior to administration of antimicrobials. Patient Preparation: Wipe off venipuncture site using a 70% alcohol pad. Apply Chloraprep to the skin over the selected venipuncture site and apply using up and down and back and forth strokes for a full 30 seconds.  Allow the site to dry completely for 30 - 60 seconds. Swab septum of  Myco/F bottle using 70% alcohol. Draw 5 ml into the Myco/ F bottle.  After inoculation, clean septum with 70% alcohol.  Transport to Microbiology promptly. Glass containers may not be transported using the pneumatic tube system.  ","ClinicalInfo":"An AFB Culture only test should be  performed to identify an infection due to mycobacteria in blood or bone marrow specimens. Broth medium will be utilized for culturing blood or bone marrow sites.  Identification of positive cultures will be performed utilizing current methodologies. Susceptibility testing will be performed on significant isolates. A single negative culture does not rule out the presence of a mycobacterial infection.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":428,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2043,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":428,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10794,"DictMethodologyId":224,"TdTestInfoSpecificId":428,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":428,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":81,"DictDaysPerformed":"7 days a week","DictReported":"9 weeks"},"TdSpecimenRequirements":[{"Id":41545,"SpecialInstructions":"Minimum for blood.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":428,"IsBeakerData":false},{"Id":41547,"SpecialInstructions":"Draw 1-2 mL bone marrow using a heparinized syringe. Transfer to a sodium or lithium heparin tube.","LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":76,"DictSpVolumeName":"1 - 2 mL","TdTestInfoSpecificId":428,"IsBeakerData":false},{"Id":678192,"SpecialInstructions":"Draw 1-2 mL bone marrow with heparinized syringe. 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Do not overfill.","LogicalOperation":null,"DictSpContainerId":120,"DictSpContainerName":"Myco/F Lytic Bottle","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":151,"DictSpTypeName":"Blood","DictSpVolumeId":46,"DictSpVolumeName":"3 - 5 mL","TdTestInfoSpecificId":428,"IsBeakerData":false},{"Id":678194,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":151,"DictSpTypeName":"Blood","DictSpVolumeId":24,"DictSpVolumeName":"10 mL","TdTestInfoSpecificId":428,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23899,"Description":"<72 hrs","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":428,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23900,"Description":"<72 hrs","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":428,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23901,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":428,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":428,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":4587,"PrimaryName":"Mold Susceptibility One Drug","IsRequired":false},{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3399,"PrimaryName":"Organism Identification, Mold","IsRequired":false},{"TdTestInfoCommonId":3400,"PrimaryName":"Organism Identification, Nocardia","IsRequired":false},{"TdTestInfoCommonId":3401,"PrimaryName":"Organism Identification, Yeast","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false},{"TdTestInfoCommonId":6959,"PrimaryName":"Antimicrobial Susceptibility, Mycobacterium tuberculosis Primary Panel","IsRequired":false}]},{"Id":2067,"LISCode":"ALKISO","PrimaryName":"Alkaline Phosphatase Isoenzymes","LISName":"Alk Phos Isoenzymes","EMRName":"Alkaline Phosphatase Isoenzymes Blood","EMRCode":"SQALKISO","LOINC":"","RecommendedUse":"The test is used to determine alkaline phosphatase isoenzyme fractions and estimated concentrations. 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Macrohepatic isoenzyme of alkaline phosphatase can be seen in the context of viral hepatitis, alcoholic cirrhosis, metastatic liver disease, and other liver diseases. It may also occasionally be seen in healthy individuals. Clinical correlation is required.","ClinicalReference":"","ClinicalLimitation":"High concentrations of phosphate, oxalate, citrate and cyanide will inhibit alkaline phosphatase (ALP) activity. Excess glycine may inhibit ALP activity by complexing Mg2+.  EDTA inhibits some of the isoenzymes of ALP. Do not use as an anticoagulant.  Several drugs cause an enzymatic imbalance which may change the ALP level. 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Patients who have B or O blood group and are secretors may have an elevated ALP about two hours after a fatty meal. Age and sex of patient are necessary for interpretation of results.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":6,"DictSpCollectionTemperatureName":"N/A","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":430,"IsBeakerData":false},{"Id":38498,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":16,"DictSpVolumeName":"1.5 mL","TdTestInfoSpecificId":430,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21986,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":430,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21987,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":430,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21988,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":430,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":430,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2068,"LISCode":"APBONE","PrimaryName":"Alkaline Phosphatase, Bone Specific","LISName":"Alk Phos Bone Spec","EMRName":"Alkaline Phosphatase Bone Specific","EMRCode":"SQAPBONE","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13228,"CptCode":"84080","Quantity":1,"Tmid":"30109595","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"ALK-P BONE SPECIFIC","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2068,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2068,"SpecialInfo":"Critical frozen. Grossly hemolyzed specimens will be rejected. Urine is unacceptable. This test is New York DOH approved.","ClinicalInfo":"Liver alkaline phosphatase can affect the measurement of bone specific alkaline phosphatase in this assay. 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The LGV strains of C. trachomatis are not included in this assay.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":508,"ActiveDate":"2012-10-30T00:00:00","CreatedOn":"2012-10-30T00:00:00","CreatedById":326,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4674,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":508,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10593,"DictMethodologyId":34,"TdTestInfoSpecificId":508,"DictMethodology":{"Id":34,"Name":"Semi-Quantitative Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":508,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Mon - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":40847,"SpecialInstructions":"Separate serum from cells within 2 hours of collection and transfer into a standard aliquot tube.\r\nParallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. 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Label specimens plainly as acute or convalescent. 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If the sample submitted was collected during the acute-phase of illness, submit a marked convalescent sample within 25 days for paired testing.","ClinicalInfo":"Differentiate between Chlamydophila species (C. psittaci, C. pneumoniae). Differentiate early IgM response to infection from persistent low-level titer. Because of cross-reactivity, a C. pneumoniae-specific reaction will exhibit titers two-fold or greater than C. trachomatis or C. psittaci serology. Seroconversion, a fourfold or greater rise in antibody titer between acute and convalescent sera, is considered strong evidence of recent infection.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":509,"ActiveDate":"2012-10-30T00:00:00","CreatedOn":"2012-10-30T00:00:00","CreatedById":326,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4675,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":509,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11831,"DictMethodologyId":34,"TdTestInfoSpecificId":509,"DictMethodology":{"Id":34,"Name":"Semi-Quantitative Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":509,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon - Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":46427,"SpecialInstructions":"Separate serum from cells within 2 hours of collection.\r\nParallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. 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If IgG sensitization is detected, depending on the clinical situation, eluate testing for new red cell alloantibodies may be required.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":532,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2279,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":532,"IsStat":false,"Comments":"","DictPerformingLabId":18,"DictPerformingLab":{"Id":18,"Name":"Blood Bank (x46539)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12787,"DictMethodologyId":251,"TdTestInfoSpecificId":532,"DictMethodology":{"Id":251,"Name":"Agglutination","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":532,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":72,"DictDaysPerformed":"Sun - Sat","DictReported":"4 hours"},"TdSpecimenRequirements":[{"Id":50572,"SpecialInstructions":"Do not use serum separator tubes.","LogicalOperation":null,"DictSpContainerId":22,"DictSpContainerName":"EDTA (Pink)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":25,"DictSpVolumeName":"6 mL","TdTestInfoSpecificId":532,"IsBeakerData":false},{"Id":50573,"SpecialInstructions":"Do not use serum separator tubes.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":532,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28999,"Description":"2 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":532,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29000,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":532,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29001,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":532,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":532,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2282,"LISCode":"NEUTR","PrimaryName":"Granulocyte Antibodies","LISName":"Granulocyte Abs","EMRName":"Granulocyte Abs","EMRCode":"SQNEUTR","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8106,"Aka":"Anti-Neutrophil Antibody","TdTestInfoCommonId":2282},{"Id":8107,"Aka":"Neutrophil Antibody","TdTestInfoCommonId":2282},{"Id":8108,"Aka":"Neutrophil-Associated Antibodies","TdTestInfoCommonId":2282}],"TdBillingCommons":[{"Id":10629,"CptCode":"86021","Quantity":1,"Tmid":"30200070","CclTechComponentPrice":218.00,"CclProfComponentPrice":null,"TestNameForCdm":"AB ID LEUKO AB","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2282,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2282,"SpecialInfo":"This test is New York DOH approved. Ship frozen on dry ice.","ClinicalInfo":"Neutrophil-associated antibodies may cause neutropenia in various autoimmune disorders including Felty syndrome, SLE and drug-induced neutropenia. Febrile transfusion reactions and isoimmune neonatal neutropenia may also be caused by antibodies to neutrophil-specific antigens or HLA antigens. A positive result on this test is not definitive for specific anti-neutrophil antibodies, since anti-HLA antibodies and immune complexes may also cause a positive result. The results of this test should be correlated to clinical history and other data.\nCirculating antibodies in patient's serum are measured by flow cytometry after incubation with normal neutrophils. Values greater than 2 standard deviations of a normal control population are interpreted as \"weakly positive\" and greater than 3 standard deviations as \"positive.\"\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":533,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2282,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":533,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":533,"DictDaysPerformedId":30,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Mon, Thu","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":31881,"SpecialInstructions":"Remove serum from cells ASAP or within 2 hours of collection. Transfer serum to standard aliquot tube and freeze. Ship frozen on dry ice.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":533,"IsBeakerData":false},{"Id":31882,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":533,"IsBeakerData":false},{"Id":31883,"SpecialInstructions":"Remove serum from cells ASAP or within 2 hours of collection. Transfer serum to standard aliquot tube and freeze. Ship frozen on dry ice. 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All positive specimens (OD>= 0.400) will have confirmatory platelet aggregation testing (PLHEPP or PLLMWP) ordered and charged. If Heparin Induced Thrombocytopenia is due to low molecular weight heparin (LMWH), contact the lab at 216-444-2519.","ClinicalInfo":"Test to detect IgG anti-PF4/heparin antibodies, observed in patients with heparin-induced thrombocytopenia.  OD > = 0.400 with positive heparin confirmation step suggests presence of anti-PF4/heparin antibody, but does not  confirm a diagnosis of heparin-induced thrombocytopenia (HIT), which should include clinical findings.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":534,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2285,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":534,"IsStat":false,"Comments":null,"DictPerformingLabId":19,"DictPerformingLab":{"Id":19,"Name":"Manual Lab (x42519)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12096,"DictMethodologyId":170,"TdTestInfoSpecificId":534,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":534,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":77,"DictDaysPerformed":"Sun - Sat","DictReported":"1 day"},"TdSpecimenRequirements":[{"Id":47593,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":534,"IsBeakerData":false},{"Id":47596,"SpecialInstructions":"Separate plasma from cells ASAP.","LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. 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Serum not preferred, as it cannot be used for positive confirmatory reflex test.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":534,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27230,"Description":"Remove plasma from cells ASAP. Plasma good for 4 hours ambient.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":534,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27231,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":534,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27232,"Description":"2 weeks","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":534,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":534,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":556,"Title":"Testing for Heparin-Induced Thrombocytopenia","FileName":"anti-platelet-81311","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":2285,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[{"TdTestInfoCommonId":3482,"PrimaryName":"Platelet Antibody/Heparin","IsRequired":false}]},{"Id":2313,"LISCode":"ASGCSF","PrimaryName":"Aspergillus galactomannan CSF","LISName":"Aspergil galac, CSF","EMRName":"Aspergillus galactomannan CSF","EMRCode":"SQASGCSF","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13994,"CptCode":"87305","Quantity":1,"Tmid":"30601710","CclTechComponentPrice":165.00,"CclProfComponentPrice":null,"TestNameForCdm":"ASPERGILLUS GALACT SERUM","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2313,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2313,"SpecialInfo":"Specimens that are too viscous to pipette will be rejected.","ClinicalInfo":"Two or more consecutive positive results should be obtained from separately collected specimens before the patient is considered to have a positive Aspergillus antigen test. Antifungal therapy may reduce the assay's sensitivity. False positive results can be caused by: Piperacillin-tazobactam and a few other antibiotics; Plasmalyte and other fluids containing sodium gluconate,   infection with Penicillium, Alternaria,Paecilomyces, Fusarium, Histoplasma, or  Blastomyces.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":535,"ActiveDate":"2012-10-18T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2313,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":535,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11027,"DictMethodologyId":161,"TdTestInfoSpecificId":535,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":535,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon - Fri","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":42457,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":535,"IsBeakerData":false},{"Id":42459,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":13,"DictSpVolumeName":"0.8 mL","TdTestInfoSpecificId":535,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":24429,"Description":"5 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":535,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24430,"Description":"5 months","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":535,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24431,"Description":"48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":535,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":535,"TestCode":null,"IsReportable":false,"DictVendorId":75,"DictVendor":{"Id":75,"Name":"MiraVista Diagnostics","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2314,"LISCode":"ASPCLP","PrimaryName":"Aspirin/Clopidogrel Resistance (Aggregation) Panel","LISName":"ASP/CLO Resist Pnl","EMRName":"Aspirin/Clopidogrel Resistance Panel","EMRCode":"SQASPCLP","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":3,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13777,"CptCode":"85576","Quantity":2,"Tmid":"30500780","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"*BLOOD PLT AGGREGATION EA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2314,"IsBeakerData":false}],"TdIncludes":[{"Id":20153,"TestName":"ADP Aggregation","Rank":1,"TdTestInfoCommonId":2314},{"Id":20154,"TestName":"Arach Max Aggreg","Rank":2,"TdTestInfoCommonId":2314}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2314,"SpecialInfo":"Do not spin the tubes.  The sample must be delivered to the Manual Hematology-Coagulation laboratory within 3 hours of collection.  Please indicate the precise antiplatelet therapy that the patient is receiving at the time of testing (i.e. aspirin dose, clopidogrel (PLAVIX) dose).  Test will not be performed if the platelet count is less than 100,000/uL.  3.2% sodium citrate is the preferred anticoagulant recommended by the NCCLS.","ClinicalInfo":"This test is recommended for monitoring the inhibitory effect of aspirin or clopidogrel. It should not be ordered to diagnose intrinsic platelet dysfunction. 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Female patients - sit on toilet with legs apart and spread labia with one hand. First void in toilet and then, continuing to void, hold specimen container in “midstream” to collect sample. Male patients - retract foreskin if uncircumcised. First void in toilet and then, continuing to void, hold specimen container in “midstream” to collect sample. \nIndwelling (foley) catheter or suprapubic tube (SPT): Perform hand hygiene. Clamp drainage tubing a minimum of 12 inches below the sampling port. Allow 30 min for urine to fill the tubing to slightly above sampling port. After performing hand hygiene, apply clean gloves. Clean the entry port with alcohol (scrub for 20 s). Wait for port to dry. Perform urine collection from sampling port using the BD Vacutainer Luer-Lok Access Device. Position device over center of sampling port. Push it on and rotate clockwise until it fits securely. Push C&S Preservative Tube over the holder portion of Access Device. 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Shake tube vigorously to mix sample. If both a UA (red/yellow) and C&S tube (gray top) are being collected, transfer urine to C&S tube first. Urine specimens are processed based on whether the specimen was collected with an invasive (straight catheter, suprapubic aspirate, cystoscopy) or noninvasive (midstream clean catch, indwelling catheter, stoma) method. A low colony count is performed on urine specimens collected via invasive methods. Normal flora from the urethra, vagina and perineum often contaminate urine specimens. Quantitation of bacteria helps to distinguish contaminated specimens from those representing infection. The most common uropathogens are normal intestinal flora organisms such as Escherichia coli, Klebsiella spp. Enterobacter spp., Proteus spp. and Enterococcus spp. The level of work up is based on the specimen type, number of different organisms growing, and the quantity of potential uropathogens in relation to urogenital flora. If culture is positive, identification will be performed on clinically significant organisms at an additional charge. Identification CPT codes that may apply include: 87077, 87088, 87106, 87107, 87153. Antimicrobial susceptibilities are performed when indicated, and the following CPT codes may apply: 87181, 87184, 87185, 87186.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":620,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3853,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":620,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7543,"DictMethodologyId":224,"TdTestInfoSpecificId":620,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":620,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":106,"DictDaysPerformed":"Sun - 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Separate serum from cells within 1 hour of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":8,"DictSpCollectionTemperatureName":"Place specimen on ice after draw.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":635,"IsBeakerData":false},{"Id":679728,"SpecialInstructions":"Critical Refrigerated. Patient should fast for 12 hours and abstain from alcohol for 24 hours prior to collection. Separate plasma from cells within 1 hour of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Separate plasma from cells within 1 hour of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":8,"DictSpCollectionTemperatureName":"Place specimen on ice after draw.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":635,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":13121,"Description":"After separation from cells: Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":635,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13122,"Description":"After separation from cells: 1 month","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":635,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13123,"Description":"After separation from cells: 1 year","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":635,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":635,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3881,"LISCode":"B12","PrimaryName":"Vitamin B12","LISName":"Vitamin B12","EMRName":"Cobalamin/Vitamin B12 Serum","EMRCode":"SQB12","LOINC":"2132-9","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":14946,"CptCode":"82607","Quantity":1,"Tmid":"30003540","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"VIT B-12","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3881,"IsBeakerData":true}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3881,"SpecialInfo":"A fasting sample is preferred but not required. \n\nPatients taking a biotin dose of up to 5 mg/day should refrain from taking biotin for 4 hours prior to sample collection. Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.  Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.\n","ClinicalInfo":"Vitamin B12 (cobalamin) is important for maintaining metabolism, brain and nervous system functions, and the formation of red blood cells. Vitamin B12 is not produced by the human body, so it must be obtained through eating animal proteins such as meat, dairy, or eggs. Although the body can store sufficient vitamin B12 reserves for 2 to 5 years, deficiency can develop due to extended nutritional insufficiency among strict vegetarians, vegans, or elderly patients with limited diets. Vitamin B12 deficiency is also caused by malabsorption issues such as pernicious anemia or underlying disorders or damage to the stomach, small bowel, or pancreas. \n\nTesting for vitamin B12 is performed to detect deficiency and monitor vitamin B12 therapy. Symptoms of vitamin B12 deficiency include macrocytic megaloblastic anemia, peripheral neuropathy, glossitis, hyperreflexia, ataxia, poor coordination, deficient proprioception, affective behavioral disorder, weakness, and fatigue. Some patients may show the neurological or psychiatric defects without anemia, particularly the elderly.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":636,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3881,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":636,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11839,"DictMethodologyId":185,"TdTestInfoSpecificId":636,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":636,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":46448,"SpecialInstructions":"Submit in original tube or aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":636,"IsBeakerData":false},{"Id":46449,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":636,"IsBeakerData":false},{"Id":46450,"SpecialInstructions":"Submit in original tube or aliquot into CCL aliquot tube ","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.  Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.\n","ClinicalInfo":"Evaluation of deficiencies, therapy","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":637,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3882,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":637,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8702,"DictMethodologyId":185,"TdTestInfoSpecificId":637,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":637,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":33519,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":637,"IsBeakerData":false},{"Id":33520,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":637,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":18858,"Description":"Unacceptable","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":637,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18859,"Description":"24 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":637,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18860,"Description":"2 months, freeze once, protect from light","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":637,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":637,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3884,"LISCode":"VITB6","PrimaryName":"Vitamin B6/Pyridoxin","LISName":"Vitamin B6/Pyridoxin","EMRName":"Vitamin B6/Pyridoxin","EMRCode":"SQVITB6","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9295,"Aka":"P 5-P","TdTestInfoCommonId":3884},{"Id":9296,"Aka":"Pyridoxal Phosphate","TdTestInfoCommonId":3884},{"Id":9297,"Aka":"Pyridoxine","TdTestInfoCommonId":3884},{"Id":9298,"Aka":"Vitamin B6 (Pyridoxal 5-Phosphate)","TdTestInfoCommonId":3884}],"TdBillingCommons":[{"Id":12210,"CptCode":"84207","Quantity":1,"Tmid":"30102795","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"VITAMIN B6 PLASMA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3884,"IsBeakerData":false}],"TdIncludes":[{"Id":25597,"TestName":"Vitamin B6 (Pyridoxal 5-Phosphate)","Rank":1,"TdTestInfoCommonId":3884}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3884,"SpecialInfo":"Collect specimen after an overnight fast. Whole blood will be rejected. Specimens not protected from light, or icteric specimens are unacceptable. Separate specimens must be submitted when multiple tests are ordered. This test is New York DOH approved. ","ClinicalInfo":"Use for nutritional assessment of vitamin B6. The biologically active form of vitamin B6, pyridoxal 5-phosphate, is measured in this assay. Pyridoxal 5-phosphate measured in a specimen collected following an 8 hour or overnight fast accurately indicates vitamin B6 nutritional status. Non-fasting specimen concentration reflects recent vitamin intake.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":639,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3884,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":639,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13513,"DictMethodologyId":265,"TdTestInfoSpecificId":639,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":639,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":36875,"SpecialInstructions":"Collect after an overnight fast. Separate plasma from cells within 1 hour of collection and freeze. Protect specimen from light. Use amber transport tubes. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":221,"DictSpContainerName":"Green NaHep NOGEL","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":639,"IsBeakerData":false},{"Id":36876,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":639,"IsBeakerData":false},{"Id":36877,"SpecialInstructions":"Collect after an overnight fast. 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Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":639,"IsBeakerData":false},{"Id":36881,"SpecialInstructions":"Collect after an overnight fast. Separate serum from cells within 1 hour of collection and freeze. Protect specimen from light. Use amber transport tubes. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":639,"IsBeakerData":false},{"Id":677823,"SpecialInstructions":"Collect after an overnight fast. Separate plasma from cells within 1 hour of collection and freeze. Protect specimen from light. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":196,"DictSpContainerName":"Green LiHep Nogel","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":639,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20950,"Description":"After separation from cells: 2 months","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":639,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20951,"Description":"After separation from cells: 1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":639,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20952,"Description":"After separation from cells: 3 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":639,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":639,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3885,"LISCode":"VITC","PrimaryName":"Vitamin C","LISName":"Vitamin C","EMRName":"Vitamin C","EMRCode":"SQVITC","LOINC":"1903-4","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8364,"Aka":"Ascorbic Acid","TdTestInfoCommonId":3885}],"TdBillingCommons":[{"Id":11064,"CptCode":"82180","Quantity":1,"Tmid":"30101775","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"TRANSFERRIN BLOOD","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3885,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3885,"SpecialInfo":"Thawing and refreezing of the specimen and exposure to light will result in decreased Vitamin C concentration. EDTA plasma, whole blood, body fluids, and grossly hemolyzed specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Useful to evaluate scurvy, Vitamin C deficiency or ascorbic acid metabolism. Vitamin C concentrations lower than 11 umol/L indicate deficiency. Concentrations between 11 and 23 umol/L are consistent with a moderate risk of deficiency due to inadequate tissue stores. Vitamin C concentration is reported as micromoles per liter (umol/L). To convert concentration to milligrams per deciliter (mg/dL), multiply the result by 0.0176.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":640,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3885,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":640,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8647,"DictMethodologyId":167,"TdTestInfoSpecificId":640,"DictMethodology":{"Id":167,"Name":"High Performance Liquid Chromatography (HPLC)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":640,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":16,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 7 days"},"TdSpecimenRequirements":[{"Id":33303,"SpecialInstructions":"Protect specimen from light. Centrifuge ASAP or within 1 hour of collection. 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Although sunlight exposure to skin may provide adequate levels of vitamin D, minimal or no sun exposure and low dietary vitamin D intake commonly results in hypovitaminosis D (vitamin D deficiency).\n\n25-Hydroxy vitamin D [25(OH)D], the principal circulating form of vitamin D in plasma, is the most reliable measure of overall vitamin D status even though it is biologically inactive. Testing for 25(OH)D is useful in ruling out vitamin D deficiency as a cause of hypocalcemia, rickets, or osteomalacia, as well as in securing a differential diagnosis of hypercalcemia that could be indicative of excess parathyroid hormone, sarcoidosis, some forms of lymphoma, or other disorders. Testing for 25(OH)D is also useful in diagnosing intestinal malabsorption and vitamin D deficiency or intoxication, including the following: distinguishing between vitamin D-dependent and vitamin D-resistant rickets, monitoring the vitamin D status of patients with chronic renal failure, and monitoring therapeutic response in patients being treated for vitamin D-related disorders.\n\nDecreased 25-hydroxy vitamin D levels indicate an insufficiency or deficiency due to poor diet, decreased exposure to the sun, malabsorption of vitamin D, or liver and kidney diseases. When associated with hypercalcemia, there may be hypersensitivity to vitamin D, as in sarcoidosis.","ClinicalReference":"","ClinicalLimitation":"Values of 25-hydroxy vitamin D can vary with exposure to sunlight, which may be affected by the season of the year and geographic location. There are also variations depending on skin pigmentation, age, and during menstrual cycles, particularly at the time of ovulation. 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The DNAse B test is more reliable in the detection of anti-streptococcal antibodies following Group A Streptococcal Pyoderma.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":778,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2294,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":778,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6498,"DictMethodologyId":243,"TdTestInfoSpecificId":778,"DictMethodology":{"Id":243,"Name":"Immunoturbidometric Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":778,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":24419,"SpecialInstructions":"Submit in original tube or aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":778,"IsBeakerData":false},{"Id":24420,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":778,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":13834,"Description":"2 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":778,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13835,"Description":"8 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":778,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13836,"Description":"6 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":778,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":778,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2295,"LISCode":"AT3ASY","PrimaryName":"Antithrombin  Assay","LISName":"Antithrombin","EMRName":"Antithrombin  Assay","EMRCode":"SQAT3ASY","LOINC":"27811-9","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":11175,"Aka":"AT Assay","TdTestInfoCommonId":2295}],"TdBillingCommons":[{"Id":14321,"CptCode":"85300","Quantity":1,"Tmid":"30500125","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"ANTITHROMBIN 3","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2295,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2295,"SpecialInfo":"3.2% sodium citrate is the preferred anticoagulant recommended by CLSI. Formerly called Antithrombin III Assay.","ClinicalInfo":"(1) Evaluation of the hypercoagulable state to detect congenital and acquired antithrombin deficiency.(2) Useful in diagnosing disseminated intravascular coagulation.(3) Following the response to therapy with antithrombin concentrates.(4) Evaluation of heparin resistance.  Patients with antithrombin levels < 65% may have an inadequate clinical response to heparin. Heparin therapy decreases levels to a variable degree.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":779,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2295,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":779,"IsStat":false,"Comments":null,"DictPerformingLabId":19,"DictPerformingLab":{"Id":19,"Name":"Manual Lab (x42519)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11330,"DictMethodologyId":235,"TdTestInfoSpecificId":779,"DictMethodology":{"Id":235,"Name":"Chromogenic","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":779,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":43883,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":779,"IsBeakerData":false},{"Id":43886,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. Blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":779,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":25200,"Description":"4 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":779,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25201,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":779,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25202,"Description":"14 days at -20 C; 6 months at -70 C","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":779,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":779,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2297,"LISCode":"APC","PrimaryName":"APC Resistance","LISName":"APC Resistance","EMRName":"APC Resistance","EMRCode":"SQAPC","LOINC":"48591-2","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":11189,"Aka":"Activated Protein C Resistance","TdTestInfoCommonId":2297}],"TdBillingCommons":[{"Id":14360,"CptCode":"85307","Quantity":1,"Tmid":"30500155","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"APC RESISTANCE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2297,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2297,"SpecialInfo":"3.2% sodium citrate is the preferred anticoagulant recommended by CLSI. Patient should not be on heparin therapy or DTI therapy.","ClinicalInfo":"Evaluation of hypercoagulable states and thrombotic disease. Factor V Leiden PCR assay can be used to confirm APC resistance due to factor V Leiden.  Ratios less than 2.07 suggest APC - resistance.  High heparin concentrations (> 1 U/mL)  and direct thrombin inhibitor drugs may interfere with test results. Lupus anticoagulant and other coagulation inhibitors may also interfere with test results.  Causes of APC resistance other than abnormalities of factor V may not be detected by this assay as all factors except factor V are replaced in the assay.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":781,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2297,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":781,"IsStat":false,"Comments":"","DictPerformingLabId":19,"DictPerformingLab":{"Id":19,"Name":"Manual Lab (x42519)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11347,"DictMethodologyId":237,"TdTestInfoSpecificId":781,"DictMethodology":{"Id":237,"Name":"Clotting Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":781,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":44011,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":781,"IsBeakerData":false},{"Id":44014,"SpecialInstructions":"Collection tube must be filled to total fill volume.  Inadequately filled tubes will be rejected. Invert to mix 3-4 times. Non-Testing Sites: Centrifuge sample; Aliquot plasma into a separate tube and label with Epic Beaker labels. Specimens should be frozen (-20C or colder).","LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. Blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":21,"DictSpTransportTemperatureName":"Centrifuge, aliquot and freeze ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":781,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":25240,"Description":"Main Campus: ACCEPTABLE for Whole Blood. (Must be delivered ambient to testing lab less than 4 hours post collection). Non-Testing Sites: UNACCEPTABLE.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":781,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25241,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":781,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25242,"Description":"For Non-Testing Sites: Frozen Plasma is ACCEPTABLE. Centrifuge sample, then aliquot plasma into a separate tube and label with Epic Beaker label. Specimen should be frozen (-20 C or colder) and is stable for 2 months.","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":781,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":781,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2298,"LISCode":"APOEG","PrimaryName":"Apolipoprotein E (APOE) Genotyping, Cardiovascular Risk","LISName":"APO E Genotype","EMRName":"APOE Genotype - Cardiovascular Risk","EMRCode":"SQAPOEG","LOINC":"21619-2","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":12615,"Aka":"Apolipoprotein E (Condon 112 &158)","TdTestInfoCommonId":2298}],"TdBillingCommons":[{"Id":15790,"CptCode":"81401","Quantity":1,"Tmid":"30107625","CclTechComponentPrice":116.00,"CclProfComponentPrice":null,"TestNameForCdm":"APOEG TEST","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2298,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2298,"SpecialInfo":"This test is not recommended for nonsymptomatic patients under 18 years of age. Plasma, serum and frozen specimens in glass collection tubes will be rejected. This test is New York DOH approved.","ClinicalInfo":"Background Information for Apolipoprotein E (APOE) Genotyping, Cardiovascular Risk\nCharacteristics: Hyperlipoproteinemia III (HPL III) is characterized by increased cholesterol and triglyceride levels, presence of B-VLDL, xanthomas, and premature vascular disease including coronary heart disease (CHD) and peripheral artery disease.\nIncidence of HPL III: Approximately 1 in 5,000.\nInheritance of HPL III: Multifactorial; greater than 90 percent of affected individuals are homozygous for the e2 allele but other factors such as diabetes and hypothyroidism also play a large role in development of disease.\nPenetrance: 1 to 5 percent of individuals homozygous for the e2 will develop HPL III.\nCause: 2 copies of the e2 allele provides supporting evidence for a diagnosis of HPL III in a symptomatic individual but e2 homozygosity is neither necessary nor sufficient for HPL III. Variants Tested: APOE gene alleles, e2 (c.388T, p.130Cys and c.526C>T, p.Arg176Cys), e3 (c.388T, p.130Cys and c.526C, p.176Arg ), e4 (c.388T>C, p.Cys130Arg and c.526C, p.176Arg).\nClinical Sensitivity: 90 percent of individuals with HPL III are homozygous for the e2 variant.\nMethodology: Polymerase chain reaction (PCR) and fluorescence monitoring using hybridization probes.\nAnalytical Sensitivity and Specificity: 99 percent.\nLimitations: Only the e2, e3 and e4 variants will be detected. Rare isoforms of APOE will not be detected. If rare alleles are suspected, phenotyping by isoelectric focusing may be indicated. 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If an elevated result is suspected to be due to contamination, confirmation with a second specimen collected in a certified trace element-free tube is recommended.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":787,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2307,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":787,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9234,"DictMethodologyId":178,"TdTestInfoSpecificId":787,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":787,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":35587,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and non-essential over-the-counter medications (upon the advice of their physician) and avoid shellfish and seafood for 48 to 72 hours. Send blood in original collection tube.","LogicalOperation":null,"DictSpContainerId":37,"DictSpContainerName":"EDTA (Royal blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":26,"DictSpVolumeName":"7 mL","TdTestInfoSpecificId":787,"IsBeakerData":false},{"Id":35588,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":787,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20155,"Description":"Indefinitely","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":787,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20156,"Description":"Indefinitely ","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":787,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20157,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":787,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":787,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":404,"Title":"Heavy Metal Requisition ","FileName":"HeavyMetalRequisitionDemographicForm","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":2307,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":2308,"LISCode":"ARSHR","PrimaryName":"Arsenic, Hair","LISName":"Arsenic Hair","EMRName":"Hair Arsenic","EMRCode":"SQARSHR","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":14493,"CptCode":"82175","Quantity":1,"Tmid":"30109245","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"ARSENIC HAIR OR NAILS","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2308,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2308,"SpecialInfo":"Patient demographics (Heavy Metals) form is required to meet State Health Department requirements. Specimen source is required.","ClinicalInfo":"Toxicity-arsenic poisoning. Hair arsenic levels above 1.00 mcg/g dry weight indicate excessive exposure. It is normal for some arsenic to be present in hair. 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Cut hair near scalp, at least 3 inches long and the width of a pencil. Do not apply tape to hair. 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Specimen must be received 1 day prior to assay day for processing.  Frozen or ambient samples or samples with preservatives are unacceptable. Indicate total volume on requisition. ","ClinicalInfo":"Screening test for metachromatic leukodystrophy. Leukocytes are the preferred screening specimen for metachromatic leukodystrophy. Due to the use of artificial substrate, this test does not reliably pick up carriers. 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Please correlate with vaccination history if applicable. Equivocal results cannot exclude non-specific reactivity or recent or past exposure to Rubella virus including vaccination. Equivocal result may also be seen due to waning immunity to Rubella virus or presence of passively-transferred antibodies. Please correlate with patient’s history.        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Please label specimen plainly as 'acute' or 'convalescent'. Contaminated, heat-inactivated, icteric, or grossly hemolyzed specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Not recommended as a stand-alone test. Testing immediately post-exposure is of no value without a later convalescent specimen. While the presence of IgM antibodies suggests current or recent infection, low levels of IgM antibodies may occasionally persist for more than 12 months post-infection or immunization. The magnitude of the measured result is not indicative of the amount of antibody present.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":871,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3643,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":871,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7528,"DictMethodologyId":407,"TdTestInfoSpecificId":871,"DictMethodology":{"Id":407,"Name":"Semi-Quantitative Chemiluminescent Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":871,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":28344,"SpecialInstructions":"Allow specimen to clot at room temperature. Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":871,"IsBeakerData":false},{"Id":28345,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":871,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16135,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":871,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16136,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":871,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16137,"Description":"After separation from cells: 1 year (Avoid repeated freeze/thaw cycles)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":871,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":871,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3645,"LISCode":"SALI","PrimaryName":"Salicylate","LISName":"Salicylate","EMRName":"Salicylate Serum","EMRCode":"SQSALI","LOINC":"4024-6","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12276,"Aka":"Acetylsalicylic Acid","TdTestInfoCommonId":3645},{"Id":12277,"Aka":"Aspirin Level","TdTestInfoCommonId":3645},{"Id":12278,"Aka":"Salicylic Acid","TdTestInfoCommonId":3645}],"TdBillingCommons":[{"Id":15110,"CptCode":"80179","Quantity":1,"Tmid":"30120965","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"SALICYLATE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3645,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3645,"SpecialInfo":"Main and other sites: Do not collect in a gel separator tube","ClinicalInfo":"Therapeutic range for anti-pyretic: 3.0-10.0 mg/dL.\nTherapeutic range for anti-inflammatory/rheumatic fever: 15.0-30.0 mg/dL.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":872,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3645,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":872,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11987,"DictMethodologyId":182,"TdTestInfoSpecificId":872,"DictMethodology":{"Id":182,"Name":"Enzymatic","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":872,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":47086,"SpecialInstructions":"Do not collect in a gel separator tube. 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Centrifuge and transfer plasma/serum to a CCL tube and refrigerate.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":872,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26936,"Description":"After separation from cells: 3 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":872,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26937,"Description":"After separation from cells: 2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":872,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26938,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":872,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":872,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3641,"LISCode":"APLPCR","PrimaryName":"PML :: RARA Detection by RT-PCR, Quantitative","LISName":"PML :: RARA Detection by RT-PCR, Quantitative","EMRName":"PML :: RARA Detection by RT-PCR, Quantitative","EMRCode":"SQAPLPCR","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":15167,"Aka":"AMPL' APL","TdTestInfoCommonId":3641},{"Id":15168,"Aka":"APL MRD","TdTestInfoCommonId":3641},{"Id":15169,"Aka":"APL Post-consolidation therapy testing","TdTestInfoCommonId":3641},{"Id":15170,"Aka":"PML-RARA fusion types, A, B, B variant","TdTestInfoCommonId":3641},{"Id":15171,"Aka":"PML-RARA long, short, variable types","TdTestInfoCommonId":3641},{"Id":15172,"Aka":"PML-RARA S, L, V forms","TdTestInfoCommonId":3641},{"Id":15173,"Aka":"PML::RARA fusion types","TdTestInfoCommonId":3641},{"Id":15174,"Aka":"PML::RARA fusion types, A, B, B variant","TdTestInfoCommonId":3641},{"Id":15175,"Aka":"PML::RARA long, short, variable types","TdTestInfoCommonId":3641},{"Id":15176,"Aka":"PML::RARA S, L, V forms","TdTestInfoCommonId":3641},{"Id":15177,"Aka":"PML_RARA fusion types","TdTestInfoCommonId":3641},{"Id":15178,"Aka":"Quantitative PML","TdTestInfoCommonId":3641},{"Id":15179,"Aka":"t(15;17)","TdTestInfoCommonId":3641}],"TdBillingCommons":[{"Id":15197,"CptCode":"81315","Quantity":1,"Tmid":"30100485","CclTechComponentPrice":590.00,"CclProfComponentPrice":null,"TestNameForCdm":"APLPCR RTPCR TEST","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3641,"IsBeakerData":false}],"TdIncludes":[{"Id":26925,"TestName":"PML::RARA Translocation, Source","Rank":1,"TdTestInfoCommonId":3641},{"Id":26926,"TestName":"PML::RARA Translocation, Result","Rank":2,"TdTestInfoCommonId":3641},{"Id":26927,"TestName":"\tPML::RARA Translocation, NCN","Rank":3,"TdTestInfoCommonId":3641}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3641,"SpecialInfo":"CRITICAL REFRIGERATED. Severely hemolyzed or clotted specimens will be rejected.","ClinicalInfo":"Use to detect and quantitate PML::RARA fusion transcripts in individuals with acute promyelocytic leukemia. Use to monitor minimal residual disease and assess the risk of disease relapse. ","ClinicalReference":"","ClinicalLimitation":"Testing is not New York state approved.\nThis test detects fusion types 1, 2, and 3; it does NOT identify which transcript is detected.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":873,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3641,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":873,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12060,"DictMethodologyId":219,"TdTestInfoSpecificId":873,"DictMethodology":{"Id":219,"Name":"Reverse Transcription/Polymerase Chain Reaction (RT/PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":873,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":25,"DictDaysPerformed":"Varies","DictReported":"3 - 10 days"},"TdSpecimenRequirements":[{"Id":47454,"SpecialInstructions":"Critical refrigerated. Specimen must be delivered to Cleveland Clinic Laboratories by 3 p.m. EST on the day of collection. DO NOT collect the day before or the day of a major holiday. Separate specimens must be submitted when multiple tests are ordered. 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'Pre' and 'post' vaccine specimens may be submitted separately or together and post specimens must be received within 60 days from receipt of the pre specimens. Label specimens plainly as 'pre-vaccine' and 'post-vaccine.' 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Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and nonessential over-the-counter medications (upon the advice of their physician). Specimens collected or transported in tubes other than royal blue (EDTA) or trace element-free transport tube will be rejected. Clotted specimens will be rejected. This test is New York DOH approved. ","ClinicalInfo":"Blood thallium levels reflect recent exposure as thallium has a biological half-life of approximately 2 to 4 days. Blood levels greater than 100 µg/L are considered toxic and greater than 300 µg/L indicate severe ingestion. After severe thallium poisonings, reported symptoms have varying times of onset and include gastroenteritis, multi-organ failure and neurologic injury. Peripheral neuropathy and alopecia are well-documented effects of acute and chronic exposure. Human health effects from low-level thallium exposure are unknown. 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If contamination concerns exist due to elevated levels of blood thallium, confirmation with a second specimen collected in a certified metal-free tube is recommended.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":958,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3766,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":958,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9576,"DictMethodologyId":178,"TdTestInfoSpecificId":958,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":958,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":36916,"SpecialInstructions":"Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and non-essential over-the-counter medications (upon the advice of their physician). Send blood in original collection tube.","LogicalOperation":null,"DictSpContainerId":37,"DictSpContainerName":"EDTA (Royal blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":26,"DictSpVolumeName":"7 mL","TdTestInfoSpecificId":958,"IsBeakerData":false},{"Id":36917,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":958,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20974,"Description":"Indefinitely","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":958,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20975,"Description":"Indefinitely","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":958,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20976,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":958,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":958,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3767,"LISCode":"UTHAL","PrimaryName":"Thallium, Urine","LISName":"Thallium, Urine","EMRName":"Thallium, Urine","EMRCode":"SQUTHAL","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12554,"CptCode":"83018","Quantity":1,"Tmid":"30109860","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"TOXIC METAL, QUANT EA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3767,"IsBeakerData":false}],"TdIncludes":[{"Id":18113,"TestName":"Thallium, Urine per volume","Rank":5,"TdTestInfoCommonId":3767},{"Id":18114,"TestName":"Thallium, Urine per 24 hour","Rank":6,"TdTestInfoCommonId":3767},{"Id":18116,"TestName":"Creatinine, Urine per volume","Rank":3,"TdTestInfoCommonId":3767},{"Id":18117,"TestName":"Creatinine, Urine per 24 hour","Rank":4,"TdTestInfoCommonId":3767},{"Id":25218,"TestName":"Hours Collected","Rank":1,"TdTestInfoCommonId":3767},{"Id":25219,"TestName":"Total Volume ","Rank":2,"TdTestInfoCommonId":3767},{"Id":25220,"TestName":"Thallium, Urine - ratio to CRT","Rank":7,"TdTestInfoCommonId":3767}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3767,"SpecialInfo":"Patient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function. Collection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected.  Elevated results may be due to skin or collection- related contamination, including the use of collection containers that are not certified to be trace - element free. Confirmation with a second specimen collected in a certified trace element-free container is recommended if an elevated result is suspected to be due to contamination. This test is New York DOH approved.","ClinicalInfo":"This test may be useful as a biomarker of chronic thallium exposure. Urinary thallium levels may reflect recent or chronic exposure, and the presence of thallium in urine after acute exposure may persist for up to several weeks. Concentrations less than 5 µg/L are unlikely to cause adverse health effects while concentrations greater than 500 µg/L have been associated with clinical poisoning. After severe thallium poisoning, reported symptoms have varying times of onset and include gastroenteritis, multi-organ failure and neurologic injury. Peripheral neuropathy and alopecia are well-documented effects of acute and chronic exposure. 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Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":7,"DictSpCollectionTemperatureName":"Refrigerate during collection.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":56,"DictSpTypeName":"Urine, 24-hour (well-mixed)","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":959,"IsBeakerData":false},{"Id":38006,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":959,"IsBeakerData":false},{"Id":38007,"SpecialInstructions":"Patient Prep: High concentrations of iodine may interfere with testing. 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Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":959,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21682,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":959,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21683,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":959,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21684,"Description":"1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":959,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":959,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3768,"LISCode":"THEO","PrimaryName":"Theophylline","LISName":"Theophylline","EMRName":"Aminophylline/Theophylline","EMRCode":"SQTHEO","LOINC":"4049-3","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":12209,"Aka":"Aminophylline","TdTestInfoCommonId":3768},{"Id":12210,"Aka":"Elixophyllin","TdTestInfoCommonId":3768}],"TdBillingCommons":[{"Id":15027,"CptCode":"80198","Quantity":1,"Tmid":"30100390","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"THEOPHYLLINE ASSAY","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3768,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3768,"SpecialInfo":"Do not collect in a gel separator tube. 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If IFA patterns suggest amphiphysin Ab, amphiphysin immunoblot is performed at an additional cost. If IFA patterns suggest ANNA-1 Ab, ANNA-1 immunoblot is performed at an additional cost. If IFA patterns suggest ANNA-2 Ab, ANNA-2 immunoblot is performed at an additional cost. If IFA patterns suggest PCA-1 Ab, PCA-1 immunoblot is performed at an additional cost. If IFA patterns suggest PCA-Tr Ab, PCA-Tr immunoblot is performed at an additional cost. If client requests or if IFA patterns suggest CRMP-5-IgG, CRMP-5-IgG Western blot is performed at an additional cost. If IFA patterns suggest GAD65 Ab, GAD65 Ab RIA is performed at an additional cost. If IFA patterns suggest NMDA-R, NMDA-R Ab CBA and/or NMDA-R Ab IF Titer Assay is performed at an additional cost. If IFA patterns suggest AMPA-R, AMPA-R Ab CBA and/or AMPA-R Ab IF Titer Assay is performed at an additional cost. If IFA patterns suggest GABA-B-R, GABA-B-R Ab CBA and/or GABA-B-R Ab IF Titer Assay is performed at an additional cost. If IFA patterns suggest DPPX, DPPX Ab CBA and DPPX Ab titer are performed at an additional cost. If IFA patterns suggest mGluR1, mGluR1 Ab CBA and mGluR1 Ab titer are performed at an additional cost. If CRMP IFA is positive, ACh receptor binding Ab, CRMP-5-IgG Western blot will be performed at an additional cost. Testing should be requested in cases of subacute basal ganglionic disorders (chorea, Parkinsonism), cranial neuropathies (especially loss of vision, taste, or smell) and myelopathies. If VGKC >0.00, LGI1-IgG CBA, S (Leucine-Rich Glioma Inactivated Protein-1 IgG, Serum) and CASPR2-IgG CBA, S (Contactin-Associated Protein-Like-2-IgG, Serum) are performed at an additional cost. Neuron-restricted patterns of IgG staining that do not fulfill criteria for amphiphysin, ANNA-1, ANNA-2, ANNA-3, AGNA-1, PCA-1, PCA-2, PCA-Tr, or CRMP-5-IgG may be reported as \"unclassified antineuronal IgG.\" Complex patterns that include non-neuronal elements may be reported as \"uninterpretable.\" Provide relevant clinical information and name, phone number, address, and email of ordering provider. Patient Prep: For optimal antibody detection, it is recommended to collect the specimen prior to initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will be dependent upon the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held for 1 week and assayed if sufficiently decayed, or canceled if radioactivity remains. Patient should have no general anesthetic or muscle-relaxant drugs in the previous 24 hours. Causes for specimen rejection: Grossly hemolyzed, grossly lipemic, grossly icteric.","ClinicalInfo":"Note: Titers lower than 1:240 are detectable by recombinant CRMP-5 Western blot analysis. CRMP-5 WB will be done on request on stored serum (held 4 weeks). This supplemental testing is recommended in cases of chorea, vision loss, cranial neuropathy, and myelopathy. Call Cleveland Clinic Client Services at 216-444-5755 and ask them to call the Mayo Neuroimmunology Lab at 800-533-1710 to request CRMP-5 Western blot. This test should not be requested on patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. 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This test is New York DOH approved.","ClinicalInfo":"The presence of PM/Scl-100 IgG antibody along with a positive ANA IFA nucleolar pattern is associated with connective tissue diseases such as polymyositis (PM), dermatomyositis (DM), systemic sclerosis (SSc), and polymyositis/systemic sclerosis overlap syndrome. The clinical relevance of PM/Scl-100 IgG antibody with a negative ANA IFA nucleolar pattern is unknown. PM/Scl-100 is the main target epitope of the PM/Scl complex, although antibodies to other targets not detected by this assay may occur.  \n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1048,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3491,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1048,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13546,"DictMethodologyId":406,"TdTestInfoSpecificId":1048,"DictMethodology":{"Id":406,"Name":"Immunoblot (IB), Qualitative","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1048,"DictDaysPerformedId":66,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Tue, Thu, Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":24021,"SpecialInstructions":"Transfer 1 mL serum into standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1048,"IsBeakerData":false},{"Id":24022,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1048,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":13592,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1048,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13593,"Description":"After separation from cells: 1 month (avoid repeated freeze/thaw cycles)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1048,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13594,"Description":"After separation from cells: 14 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1048,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1048,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3495,"LISCode":"PNHPNL","PrimaryName":"PNH Panel by FCM","LISName":"PNH Panel by FCM","EMRName":"FCM Paroxysmal Nocturnal Hemoglobinuria","EMRCode":"SQPNHPNL","LOINC":"55164-8","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":10918,"Aka":"Flow Panel for Paroxysmal Nocturnal Hemoglobinuria","TdTestInfoCommonId":3495}],"TdBillingCommons":[{"Id":14124,"CptCode":"88184","Quantity":1,"Tmid":"31101715","CclTechComponentPrice":145.00,"CclProfComponentPrice":null,"TestNameForCdm":"ADDITIONAL MARKERS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3495,"IsBeakerData":true},{"Id":14125,"CptCode":"88185","Quantity":2,"Tmid":"31100075","CclTechComponentPrice":73.00,"CclProfComponentPrice":null,"TestNameForCdm":"ADDITIONAL MARKERS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3495,"IsBeakerData":true},{"Id":18145,"CptCode":"88187","Quantity":1,"Tmid":"88187","CclTechComponentPrice":null,"CclProfComponentPrice":238.00,"TestNameForCdm":"Flow interp 2-8 markers","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3495,"IsBeakerData":false}],"TdIncludes":[{"Id":24709,"TestName":"PNH Granulocyte clone","Rank":1,"TdTestInfoCommonId":3495},{"Id":24710,"TestName":"PNH RBC Clone-Partial Ag Loss (Type II) ","Rank":2,"TdTestInfoCommonId":3495},{"Id":24711,"TestName":"PNH RBC Clone-Complete Ad Loss (Type III)","Rank":3,"TdTestInfoCommonId":3495},{"Id":24712,"TestName":"Sum of PNH RBC Clones (Type II + Type III)","Rank":4,"TdTestInfoCommonId":3495},{"Id":24713,"TestName":"Interpretation","Rank":5,"TdTestInfoCommonId":3495},{"Id":24714,"TestName":"Reviewed by","Rank":6,"TdTestInfoCommonId":3495}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3495,"SpecialInfo":"Do not draw on Fridays, weekends or holidays. Specimens greater than 48 hours old will be rejected.","ClinicalInfo":"The presence of paroxysmal nocturnal hemoglobinuria (PNH) clones in the erythrocyte and granulocyte populations is assessed in this procedure. For erythrocytes antibodies to Glycophorin A are used to specifically gate red cells and PNH clones are identified by lack of CD59 expression. For granulocytes, CD15 and CD 33 are used to specifically gate granulocytes. The PNH-type granulocytes are then identified by lack of expression of CD24 and lack of reactivity to Fluorescent Aerolysin (FLAER). The lower limit of detection for this assay is 0.01% PNH-type cells. The presence of a PNH clone occurs in classical hemolytic PNH, generally at levels above 1%. PNH clones may be seen in other disorders such as aplastic anemia and myelodysplastic syndrome. Thus, these results must be put in context of the clinical findings.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":1051,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3495,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1051,"IsStat":false,"Comments":"-If the sum of TYPE III + TYPE II RBC clones is greater than 1 then, TYPE III, TYPE II and the sum of both will be reported.\n-If the sum of TYPE III + TYPE II RBC clones is less than 1, then only TYPR III RBC clone will be reported.\n-Interpretation will be reported has \"positive\", \"low positive\" or \"negative\"","DictPerformingLabId":2,"DictPerformingLab":{"Id":2,"Name":"Flow Cytometry (x40042)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13119,"DictMethodologyId":401,"TdTestInfoSpecificId":1051,"DictMethodology":{"Id":401,"Name":"Flow Cytometry (FC)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1051,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":677397,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":1051,"IsBeakerData":false},{"Id":678789,"SpecialInstructions":"Peripheral blood samples to be delivered to the flow cytometry lab within 24 hours of draw time. Samples greater than 48 hours old will be rejected. Do not draw on Fridays, weekends or holidays.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":25,"DictSpCollectionTemperatureName":"Ambient or Refrigerated","DictSpTransportTemperatureId":25,"DictSpTransportTemperatureName":"Ambient or Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":1051,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":24745,"Description":"48 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1051,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24746,"Description":"48 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1051,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24747,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1051,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1051,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":525,"Title":"High Sensitivity Flow Cytometry for Paroxysmal Nocturnal Hemoglobinuria","FileName":"HighSensitivityFlowCytometry_0724","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":3495,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":3498,"LISCode":"UPBG","PrimaryName":"Porphobilinogen (PBG), Urine, Screen","LISName":"Porphobilinogen (PBG), Urine, Screen","EMRName":"Porphobilinogen (PBG), Urine, Screen","EMRCode":"SQUPBG","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":5068,"Aka":"PBG","TdTestInfoCommonId":3498}],"TdBillingCommons":[{"Id":7390,"CptCode":"84106","Quantity":1,"Tmid":"30101525","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"PORPHOBILINOGEN UR SCN","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3498,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3498,"SpecialInfo":"Instruct patient to deliver urine ASAP upon collection.","ClinicalInfo":"Rule out porphyrias","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":1052,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3498,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1052,"IsStat":false,"Comments":null,"DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":5636,"DictMethodologyId":281,"TdTestInfoSpecificId":1052,"DictMethodology":{"Id":281,"Name":"Spectrophotometry, Watson-Schwartz","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1052,"DictDaysPerformedId":2,"DictHoursPerformedId":null,"DictReportedId":12,"DictDaysPerformed":"Wed","DictReported":"1 - 8 days"},"TdSpecimenRequirements":[{"Id":21077,"SpecialInstructions":"First morning void.  Protect from light.","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":24,"DictSpVolumeName":"10 mL","TdTestInfoSpecificId":1052,"IsBeakerData":false},{"Id":21078,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1052,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":11903,"Description":"Stable protected and unprotected from light for 24 hours.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1052,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":11904,"Description":"1 month","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1052,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":11905,"Description":"1 week","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1052,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1052,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3500,"LISCode":"UPBGQT","PrimaryName":"Porphobilinogen, Urine Quant","LISName":"PBG Urine Quant","EMRName":"PBG Urine Quant","EMRCode":"SQUPBGQT","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8405,"Aka":"PBG, Urine","TdTestInfoCommonId":3500}],"TdBillingCommons":[{"Id":18840,"CptCode":"82570","Quantity":1,"Tmid":"30122335","CclTechComponentPrice":23.00,"CclProfComponentPrice":null,"TestNameForCdm":"Creatinine, Ur (LabCorp Porphobilinogen, Qn, Random Ur)","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3500,"IsBeakerData":false},{"Id":18841,"CptCode":"84110","Quantity":1,"Tmid":"30105880","CclTechComponentPrice":178.00,"CclProfComponentPrice":null,"TestNameForCdm":"Porphobilinogen, Qn, Random Ur","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3500,"IsBeakerData":false}],"TdIncludes":[{"Id":26117,"TestName":"Porphobilinogen, Qn, Random Ur\t","Rank":1,"TdTestInfoCommonId":3500},{"Id":26118,"TestName":"Creatinine, U\t","Rank":2,"TdTestInfoCommonId":3500},{"Id":26119,"TestName":"PBG/Creatinine Ratio\t","Rank":3,"TdTestInfoCommonId":3500}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3500,"SpecialInfo":"Patient should avoid excessive fluid intake. Do not collect first morning void or after 8pm. Protect from light.","ClinicalInfo":"This test is useful to rule out acute intermittent porphyria (AIP) and other acute attack types of porphyrias associated with neurologic and/or psychiatric symptoms. If testing for an acute porphyria, please consider ordering PBG, Screen (SQUPBG). If testing for a cutaneous porphyria, please consider ordering Porphyrins, Urine (SQUPORFR). If testing for erythropoietic porphyria, please consider ordering Total Erythrocyte Porphyrins (SQPROPOR).","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1053,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3500,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1053,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13656,"DictMethodologyId":295,"TdTestInfoSpecificId":1053,"DictMethodology":{"Id":295,"Name":"Chromatography","Description":null},"TdTestInfoSpecific":null},{"Id":13657,"DictMethodologyId":188,"TdTestInfoSpecificId":1053,"DictMethodology":{"Id":188,"Name":"Spectrophotometry (S)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1053,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":116,"DictDaysPerformed":"Varies","DictReported":"4 - 7 days"},"TdSpecimenRequirements":[{"Id":33450,"SpecialInstructions":"Patient should avoid excessive fluid intake. Do not collect first morning void or after 8pm. Protect from light. Transfer aliquot to amber transport tube and freeze.","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":1053,"IsBeakerData":false},{"Id":33451,"SpecialInstructions":"Does not allow for repeat testing.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1053,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":18810,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1053,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18811,"Description":"24 hours (protected from light)","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1053,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18812,"Description":"1 month (protected from light)","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1053,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1053,"TestCode":null,"IsReportable":false,"DictVendorId":71,"DictVendor":{"Id":71,"Name":"LabCorp","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3504,"LISCode":"SPORPH","PrimaryName":"Porphyrins, Total, Plasma or Serum","LISName":"Porphyrins, Total, Plasma or Serum","EMRName":"Porphyrins, Total, Plasma or Serum","EMRCode":"SQSPORPH","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":1980,"CptCode":"84311","Quantity":1,"Tmid":"30106295","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"PORPHYRINS SERUM TOTAL","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3504,"IsBeakerData":false}],"TdIncludes":[{"Id":25642,"TestName":"Porphyrins, Total, Plasma/Serum\t","Rank":1,"TdTestInfoCommonId":3504},{"Id":25643,"TestName":"Porphyrins, Total, Plasma/Serum, Interp.\t","Rank":2,"TdTestInfoCommonId":3504}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3504,"SpecialInfo":"Protect from light during collection, storage and shipment. Hemolyzed samples and frozen whole blood are unacceptable. This test is New York DOH approved.","ClinicalInfo":"This test is useful to monitor porphyria cutanea tarda (PCT) and to confirm diagnosis of suspected variegate porphyria (VP) and erythropoietic protoporphyria (EPP).\nIf testing for an acute porphyria, please consider ordering PBG, Screen (SQUPBG). If testing for a cutaneous porphyria, please consider ordering Porphyrins, Urine (SQUPORFR). If testing for erythropoietic porphyria, please consider ordering Total Erythrocyte Porphyrins (SQPROPOR).","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1054,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3504,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1054,"IsStat":false,"Comments":null,"DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":1507,"DictMethodologyId":211,"TdTestInfoSpecificId":1054,"DictMethodology":{"Id":211,"Name":"Fluorometry (FLM)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1054,"DictDaysPerformedId":54,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Sun, Tue, Thu","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":6305,"SpecialInstructions":"Protect specimen from light during collection, storage, and shipment. Separate serum from cells ASAP or within 1 hour of collection. 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Separate plasma from cells ASAP or within 1 hour of collection. Transfer plasma to amber transport tube.","LogicalOperation":"Or","DictSpContainerId":28,"DictSpContainerName":"Sodium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1054,"IsBeakerData":false},{"Id":677859,"SpecialInstructions":"Protect specimen from light during collection, storage, and shipment. Separate plasma from cells ASAP or within 1 hour of collection. 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Do not collect in a gel separator tube.  Centrifuge and transfer plasma/serum to a CCL tube and transport refrigerated.","LogicalOperation":"Or","DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1074,"IsBeakerData":false},{"Id":38295,"SpecialInstructions":"Collect immediately prior to next dose.  Do not collect in a gel separator tube.  Centrifuge and transfer plasma/serum to a CCL tube and transport refrigerated.","LogicalOperation":"Or","DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1074,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21860,"Description":"After separation from cells: 48 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1074,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21861,"Description":"After separation from cells: 30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1074,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21862,"Description":"After separation from cells: 7 days","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1074,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1074,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3534,"LISCode":"PROC","PrimaryName":"Procainamide/NAPA","LISName":"Procainamide/NAPA","EMRName":"Procainamide and N-Acetylprocainamide","EMRCode":"SQPROC","LOINC":"3983-4","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":3729,"Aka":"N-Acetylprocainamide","TdTestInfoCommonId":3534},{"Id":3730,"Aka":"Pronestyl","TdTestInfoCommonId":3534}],"TdBillingCommons":[{"Id":5274,"CptCode":"80192","Quantity":1,"Tmid":"30109785","CclTechComponentPrice":45.00,"CclProfComponentPrice":null,"TestNameForCdm":"PROCAINAMIDE/NAPA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3534,"IsBeakerData":false}],"TdIncludes":[{"Id":6867,"TestName":"N Acetylprocainamide","Rank":1,"TdTestInfoCommonId":3534},{"Id":6868,"TestName":"Procainamide","Rank":2,"TdTestInfoCommonId":3534}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3534,"SpecialInfo":"Collect immediately prior to next dose. Do not use serum separator tubes.","ClinicalInfo":"The commonly expected therapeutic range for the sum of NAPA and Procainamide is 5-30 ug/mL. However, the concentration of NAPA is dependent on many factors, including; time of last procainamide dose, mode of administration, concomitant drug therapy, sample condition, time of sample collection and individual variations in absorption, biotransformation, distribution and excretion. Therapeutic ranges are provided only as a guide for interpretation along with other clinical symptoms and patient history.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1075,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3534,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1075,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13211,"DictMethodologyId":161,"TdTestInfoSpecificId":1075,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1075,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Mon - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":14800,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1075,"IsBeakerData":false},{"Id":14801,"SpecialInstructions":"Collect immediately prior to next dose. Do not use plasma separator tubes.","LogicalOperation":null,"DictSpContainerId":24,"DictSpContainerName":"Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1075,"IsBeakerData":false},{"Id":14802,"SpecialInstructions":"Collect immediately prior to next dose. 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Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.  Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.\n","ClinicalInfo":"Fertility diagnosis for detection of ovulation and assessment of the luteal phase.\n\nFemale reference ranges/interpretive guidelines:\n\nMenstrual cycle Progesterone reference ranges:\nFollicular: < 1.0 ng/mL\nOvulation: < 12.1 ng/mL\nLuteal: 1.8 to 23.9 ng/mL\n\nPregnancy Progesterone reference ranges vary by gestational period:\nFirst trimester: 11.0 to 44.3 ng/mL\nSecond trimester: 25.4 to 83.4 ng/mL\nThird trimester:  58.7 to 214 ng/mL\n\nPost-menopausal Progesterone: < 0.5 ng/mL\n\nReference:\n1. Progesterone (Progesterone III) [package insert V 1.0 English]. Roche Diagnostics, Indianapolis, IN; October 2015.\n\nPediatric references:\n\nReference ranges were not locally established for pediatric patients.  The normal values are based on the following source: CALIPER Pediatric Reference Intervals. www.sickkids.ca/caliperproject/index.html. The Hospital for Sick Children (SickKids). 1999-2016: Toronto, Canada. Accessed on November 15, 2016.\n\nFor females ages 0 to 3 days and males ages 0 to 29 days: Reference ranges for female patients under 4 days old and male patients under 30 days old have not been established.  Cutoffs are based on normal values for infants up to one year of age.  Source: CALIPER Pediatric Reference Intervals. www.sickkids.ca/caliperproject/index.html. The Hospital for Sick Children (SickKids). 1999-2016: Toronto, Canada. Accessed on November 15, 2016.\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1076,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3536,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1076,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11538,"DictMethodologyId":185,"TdTestInfoSpecificId":1076,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1076,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":44843,"SpecialInstructions":"Submit in original tube or aliquot into CCL aliquot tube.","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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This may be related to the distribution of adipose tissue where omental fat vs. subcutaneous fat, which differs between genders, may have different leptin production rates. Its role in metabolism, insulin sensitivity, as a potential therapeutic modality for weight loss, as well as, involvement in endocrine function are still under investigation.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1114,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3201,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1114,"IsStat":false,"Comments":null,"DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7641,"DictMethodologyId":433,"TdTestInfoSpecificId":1114,"DictMethodology":{"Id":433,"Name":"Quantitative Chemiluminescent Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1114,"DictDaysPerformedId":30,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Mon, Thu","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":28751,"SpecialInstructions":"Patient should fast overnight prior to collection ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1114,"IsBeakerData":false},{"Id":28752,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":1114,"IsBeakerData":false},{"Id":28753,"SpecialInstructions":"Patient should fast overnight prior to collection ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1114,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16399,"Description":"After separation from cells: 1 day","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1114,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16400,"Description":"After separation from cells: 2 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1114,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16401,"Description":"After separation from cells: 2 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1114,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1114,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3205,"LISCode":"LCMIS","PrimaryName":"Leukocyte Cytochemistry","LISName":"Cytochem Misc LC","EMRName":"Cytochem Misc LC (Lab Ordered)","EMRCode":"SQLCMIS","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":1551,"CptCode":"88319","Quantity":1,"Tmid":null,"CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":null,"SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3205,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3205,"SpecialInfo":"Indicate stain(s) desired on test request form. Charge is per stain.  Prior consultation is required to determine stain(s) to be performed.  Call Client Services at 444-5755.","ClinicalInfo":"Differential diagnosis of leukemia","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1115,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3205,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1115,"IsStat":false,"Comments":null,"DictPerformingLabId":17,"DictPerformingLab":{"Id":17,"Name":"Manual Lab (x42507)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":1204,"DictMethodologyId":213,"TdTestInfoSpecificId":1115,"DictMethodology":{"Id":213,"Name":"Microscopy","Description":null},"TdTestInfoSpecific":null},{"Id":1205,"DictMethodologyId":260,"TdTestInfoSpecificId":1115,"DictMethodology":{"Id":260,"Name":"Stain","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1115,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":5088,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":1115,"IsBeakerData":false},{"Id":5089,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1115,"IsBeakerData":false},{"Id":5090,"SpecialInstructions":"Peripheral blood and/or bone marrow smears","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":130,"DictSpTypeName":"Slide (s), unstained","DictSpVolumeId":45,"DictSpVolumeName":"Four","TdTestInfoSpecificId":1115,"IsBeakerData":false},{"Id":5091,"SpecialInstructions":"Bone marrow","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1115,"IsBeakerData":false},{"Id":5092,"SpecialInstructions":"Peripheral blood","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1115,"IsBeakerData":false}],"TdSpecimenStabilities":[],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1115,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3207,"LISCode":"LEVET","PrimaryName":"Levetiracetam","LISName":"Levetiracetam","EMRName":"Levetiracetam (Keppra) Blood","EMRCode":"SQLEVET","LOINC":"30471-7","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":10256,"Aka":"Keppra","TdTestInfoCommonId":3207}],"TdBillingCommons":[{"Id":13439,"CptCode":"80177","Quantity":1,"Tmid":"30104205","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"LEVETIRACETAM/KEPPRA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3207,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3207,"SpecialInfo":"Collect specimen immediately prior to next dose. Remove plasma/serum from whole blood as soon as possible, preferably within 1 hour after collection. Hydrolysis of levetiracetam may occur in the presence of whole blood.  Levetiracetam samples that are not separated from red cells within 48 hours of collection or hemolyzed samples not analyzed within 48 hours are rejected and credited.\n\nThis test is not suitable for patients receiving treatment with the drug brivaracetam (Briviact).  The drug causes an interference that may lead to falsely elevated levetiracetam results.\nBrivaracetam (Briviact) interferes with measurements of levetiracetam (Keppra) in the levetiracetam assay. Patients undergoing a switch in drug therapy involving Keppra and Briviact should not be monitored for levetiracetam using the assay. Brivaracetam is a chemical analog of levetiracetam. They are structurally similar and thus immunochemical crossreactivity is possible.  The circulating half-life of each drug is approximately 8 to 9 hours. Sufficient time should be allowed for clearance \nprior to using the Levetiracetam Assay.  Please contact Client Services at 216-444-5755 for suitable testing.\n","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":1117,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3207,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1117,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10579,"DictMethodologyId":161,"TdTestInfoSpecificId":1117,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1117,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":40786,"SpecialInstructions":" Do not use tubes containing cell separator gel. Centrifuge and transfer serum/plasma to a clean, tightly sealed tube as soon as possible after collection. Refrigerate sample for transport. \r\n","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1117,"IsBeakerData":false},{"Id":40787,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1117,"IsBeakerData":false},{"Id":40788,"SpecialInstructions":" Do not use tubes containing cell separator gel. Centrifuge and transfer serum/plasma to a clean, tightly sealed tube as soon as possible after collection. Refrigerate sample for transport. ","LogicalOperation":null,"DictSpContainerId":15,"DictSpContainerName":"EDTA (Navy Blue)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1117,"IsBeakerData":false},{"Id":40789,"SpecialInstructions":" Do not use tubes containing cell separator gel. Centrifuge and transfer serum/plasma to a clean, tightly sealed tube as soon as possible after collection. Refrigerate sample for transport. 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","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1117,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23395,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1117,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23396,"Description":"1 month","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1117,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1117,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3208,"LISCode":"LH","PrimaryName":"LH","LISName":"LH","EMRName":"LH/Luteinizing Hormone Serum","EMRCode":"SQLH","LOINC":"10501-5","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13518,"Aka":"Luteinizing Hormone","TdTestInfoCommonId":3208},{"Id":13519,"Aka":"Luteinizing Hormone","TdTestInfoCommonId":3208}],"TdBillingCommons":[{"Id":16292,"CptCode":"83002","Quantity":1,"Tmid":"30001530","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"GONADOTROPIN LH","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3208,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3208,"SpecialInfo":"Patients taking a biotin dose of up to 5 mg/day should refrain from taking biotin for 4 hours prior to sample collection. Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.  Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.\n","ClinicalInfo":"Values vary widely during the different phases of the menstruating woman.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1118,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3208,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1118,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12877,"DictMethodologyId":185,"TdTestInfoSpecificId":1118,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1118,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":50874,"SpecialInstructions":"Submit in original tube or aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Contaminated, hemolyzed, or severely lipemic specimens will be rejected. This test is New York DOH approved.","ClinicalInfo":"NMDA receptor antibody is found in a subset of patients with autoimmune limbic encephalitis and may occur with or without associated tumor. Decreasing antibody levels may be associated with therapeutic response. In addition, positive results have been reported in patients with nonautoimmune phenotypes. A negative test result does not rule out a diagnosis of autoimmune limbic encephalitis. Results should be interpreted in correlation with the patients clinical history and other laboratory findings. Serum testing should be paired with CSF testing for improved diagnostic sensitivity.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1141,"ActiveDate":"2012-05-01T00:00:00","CreatedOn":"2012-02-24T00:00:00","CreatedById":412,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4560,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1141,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13193,"DictMethodologyId":554,"TdTestInfoSpecificId":1141,"DictMethodology":{"Id":554,"Name":"Semi-Quantitative Cell-Based Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1141,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":19792,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1141,"IsBeakerData":false},{"Id":19793,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":161,"DictSpVolumeName":"0.15 mL","TdTestInfoSpecificId":1141,"IsBeakerData":false},{"Id":679691,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1141,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":11082,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1141,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":11083,"Description":"After separation from cells: 1 year","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1141,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":11084,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1141,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1141,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":4691,"PrimaryName":"N-methyl-D- Aspartate Receptor Antibody, IgG, Titer (Bill Only)","IsRequired":false}]},{"Id":3232,"LISCode":"LMWHEP","PrimaryName":"LMW Anti Xa Assay","LISName":"LMW Anti Xa Assay","EMRName":"LMW Anti Xa Assay","EMRCode":"SQLMWHEP","LOINC":"32684-3","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12091,"Aka":"Low Molecular Weight Heparin Assay","TdTestInfoCommonId":3232},{"Id":12092,"Aka":"Low Molecular Weight Heparin Assay Blood","TdTestInfoCommonId":3232}],"TdBillingCommons":[{"Id":14892,"CptCode":"85520","Quantity":1,"Tmid":"30501110","CclTechComponentPrice":81.00,"CclProfComponentPrice":null,"TestNameForCdm":"ANTIXA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3232,"IsBeakerData":false}],"TdIncludes":[{"Id":25531,"TestName":"LMW Anti Xa Assay","Rank":1,"TdTestInfoCommonId":3232}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3232,"SpecialInfo":"3.2% sodium citrate is the preferred anticoagulant recommended by CLSI.\n\nPatient samples should be centrifuged by the laboratory < 1 hour from collection time to prevent falsely decreased Low Molecular Weight Anti Xa values due to heparin neutralization by in vitro release of platelet factor 4. Samples that are centrifuged > 1 and < 4 hours from collection will have the following comment attached: Interpret with caution. Sample centrifuged greater than 1 hour from collection time. According to Clinical and Laboratory Standards Institute guidelines, results could be falsely decreased due to heparin neutralization by in vitro release of platelet factor 4. Suggest correlation with clinical findings and redraw if indicated.","ClinicalInfo":"Used in monitoring patients on low molecular weight heparin.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1142,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3232,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1142,"IsStat":false,"Comments":"","DictPerformingLabId":7,"DictPerformingLab":{"Id":7,"Name":"Auto Lab (x45477)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11791,"DictMethodologyId":235,"TdTestInfoSpecificId":1142,"DictMethodology":{"Id":235,"Name":"Chromogenic","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1142,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":72,"DictDaysPerformed":"Sun - Sat","DictReported":"4 hours"},"TdSpecimenRequirements":[{"Id":46262,"SpecialInstructions":"Collection tube must be filled to total fill volume. Inadequately filled tubes will be rejected. Non Testing Sites: Centrifuge within one hour of collection , aliquot platelet poor plasma into a separate tube with Epic Beaker label, freeze plasma at -20C, send frozen plasma to Main Campus on dry ice. ","LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. 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Inadequately filled tubes will be rejected. Non Testing Sites: Centrifuge within one hour of collection , aliquot platelet poor plasma into a separate tube with Epic Beaker label, freeze plasma at -20C, send frozen plasma to Main Campus on dry ice. ","LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. Blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":21,"DictSpTransportTemperatureName":"Centrifuge, aliquot and freeze ASAP.","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":205,"DictSpVolumeName":"1.8","TdTestInfoSpecificId":1142,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26405,"Description":"Centrifuge within one hour of phlebotomy and test or freeze platelet poor plasma within four hours. 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Patient preparation: Discontinue heparin therapy for 2 days prior to collection. If tests are abnormal, the following tests may be ordered and billed: PTT Mixing Study (85730),  Factor II (85210),  Factor V (85220), Factor VII (85230), Factor X (85260), Von Willebrand Factor Antigen (85246), Ristocetin Co-factor (85245), Factor IX Assay (85250), Factor XI Assay (85270), Factor XII Assay (85280), Reptilase Time (85635), D-Dimer (85379), Fibrinogen Ag (85385), Fibrinogen Activity (85384), Bethesda Assay (85335), Factor VIII Chromogenic (85240), Antithrombin Assay (85300), Protein C Functional (85303), Protein S Clottable (85306), and APC Resistance (85307).  Sample must be accompanied by the completed Clinical History Form for Hemostasis and Thrombosis Evaluation.","ClinicalInfo":"Evaluation of acquired hypercoagulable states and detection of Lupus anticoagulant and Antiphospholipid antibodies","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1143,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3238,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1143,"IsStat":false,"Comments":"","DictPerformingLabId":17,"DictPerformingLab":{"Id":17,"Name":"Manual Lab (x42507)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11338,"DictMethodologyId":233,"TdTestInfoSpecificId":1143,"DictMethodology":{"Id":233,"Name":"Refer to individual components","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1143,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"Mon - Fri","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":43960,"SpecialInstructions":"Serum","LogicalOperation":"and","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":1143,"IsBeakerData":false},{"Id":43961,"SpecialInstructions":"Plasma","LogicalOperation":"and","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":18,"DictSpVolumeName":"2.5 mL","TdTestInfoSpecificId":1143,"IsBeakerData":false},{"Id":43964,"SpecialInstructions":null,"LogicalOperation":"And","DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1143,"IsBeakerData":false},{"Id":43965,"SpecialInstructions":"Collection tubes must be filled to total fill volume. Inadequately filled tubes will be rejected. Non-testing sites: Centrifuge samples; Aliquot plasma into a separate tube and label with Epic Beaker labels. Specimens should be frozen (-20C or colder). Indicate on each tube as plasma. ","LogicalOperation":"And","DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. Blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":21,"DictSpTransportTemperatureName":"Centrifuge, aliquot and freeze ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1143,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":25216,"Description":"4 hours - Main campus: ACCEPTABLE for Whole Blood. (Must be delivered ambient to testing lab less than 4 hours post collection.) Non-Testing Sites: UNACCEPTABLE.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1143,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25217,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1143,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25218,"Description":"For Non-Testing sites, Frozen Plasma is ACCEPTABLE. (Centrifuge samples, then aliquot plasma into a separate tube and label with Epic Beaker labels. Specimens should be frozen at -20° C and they are stable for 2 weeks. Specimens frozen at -70° C are stable for up to 6 months.","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1143,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1143,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":535,"Title":"Clinical History Form for Hemostasis and Thrombosis Evaluation","FileName":"Clinical-History-Form-for-Hemostasis-Thrombosis-Evaluation","DictDocumentFormatId":1,"DictDocumentTypeId":4,"TdTestInfoCommonId":3238,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":4,"Name":"Patient Info Sheet","Description":null,"FolderName":"PatientInfoSheet","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[{"TdTestInfoCommonId":2743,"PrimaryName":"Factor II Assay","IsRequired":false},{"TdTestInfoCommonId":2745,"PrimaryName":"Factor V Assay","IsRequired":false},{"TdTestInfoCommonId":2749,"PrimaryName":"Factor X Assay","IsRequired":false},{"TdTestInfoCommonId":2345,"PrimaryName":"Bethesda Inhibitor","IsRequired":false},{"TdTestInfoCommonId":3896,"PrimaryName":"Von Willebrand Factor Antigen","IsRequired":false},{"TdTestInfoCommonId":2744,"PrimaryName":"Factor IX Assay","IsRequired":false},{"TdTestInfoCommonId":6263,"PrimaryName":"Factor VIII Chromogenic - DO NOT USE","IsRequired":false},{"TdTestInfoCommonId":2295,"PrimaryName":"Antithrombin  Assay","IsRequired":false},{"TdTestInfoCommonId":2297,"PrimaryName":"APC Resistance","IsRequired":false},{"TdTestInfoCommonId":3547,"PrimaryName":"Protein C  Functional","IsRequired":false},{"TdTestInfoCommonId":3555,"PrimaryName":"Protein S Clottable","IsRequired":false},{"TdTestInfoCommonId":6656,"PrimaryName":"VWF GPIbM Activity","IsRequired":false},{"TdTestInfoCommonId":2750,"PrimaryName":"Factor XI Assay","IsRequired":false},{"TdTestInfoCommonId":2751,"PrimaryName":"Factor XII Assay","IsRequired":false},{"TdTestInfoCommonId":5816,"PrimaryName":"APTT Incubated Mixing Add On","IsRequired":false},{"TdTestInfoCommonId":2641,"PrimaryName":"D-Dimer","IsRequired":false},{"TdTestInfoCommonId":2776,"PrimaryName":"Fibrinogen Antigen","IsRequired":false},{"TdTestInfoCommonId":3609,"PrimaryName":"Reptilase Time","IsRequired":false}]},{"Id":3244,"LISCode":"LYMEWB","PrimaryName":"Lyme Western Blot","LISName":"Lyme Ab Panel WBlot","EMRName":"Antibody Lyme Panel Western Blot","EMRCode":"SQLYMEWB","LOINC":"","RecommendedUse":"Lyme western blot (immunoblot) is used as an aid in diagnosis of Lyme disease only where Lyme antibody screen test is positive. 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Results obtained with different assay methods or kits cannot be used interchangeably.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1158,"ActiveDate":"2012-03-12T00:00:00","CreatedOn":"2012-03-08T00:00:00","CreatedById":233,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4570,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1158,"IsStat":false,"Comments":null,"DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":2546,"DictMethodologyId":170,"TdTestInfoSpecificId":1158,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1158,"DictDaysPerformedId":59,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Tue","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":10384,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1158,"IsBeakerData":false},{"Id":10386,"SpecialInstructions":"Collect one serum separator tube. Separate serum from cells within 2 hours of collection.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1158,"IsBeakerData":false},{"Id":10387,"SpecialInstructions":"Collect one red top tube. Separate serum from cells within 2 hours of collection.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1158,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":6142,"Description":"After separation from cells: 1 day","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1158,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":6143,"Description":"After separation from cells: 1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1158,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":6144,"Description":"After separation from cells: 3 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1158,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1158,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3268,"LISCode":"MEASLG","PrimaryName":"Measles IgG Antibody","LISName":"Measles IgG Antibody","EMRName":"Measles IgG Antibody","EMRCode":"SQMEASLG","LOINC":"7962-4","RecommendedUse":"Determination of immune status, response to Measles vaccine, confirmation of positive Measles IgM result post infection.  ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13424,"CptCode":"86765","Quantity":1,"Tmid":"30200675","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"MEASLES-RUBEOLA IGG AB","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3268,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3268,"SpecialInfo":"Avoid using hemolyzed, lipemic or bacterially contaminated sera. ","ClinicalInfo":"The test may be used for determination of immune status, response to Measles vaccine, confirmation of positive Measles IgM result post infection. This test does not detect neutralizing antibodies and some individuals with past history of Measles vaccination may test negative using this test. It is typically used as a surrogate of immunity virus. ","ClinicalReference":"","ClinicalLimitation":"Bacterial contamination or heat inactivation of the specimens may affect the test result.\n","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1161,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3268,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1161,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10569,"DictMethodologyId":52,"TdTestInfoSpecificId":1161,"DictMethodology":{"Id":52,"Name":"Immunochemiluminometric Assay (ICMA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1161,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":40757,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1161,"IsBeakerData":false},{"Id":40758,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1161,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23379,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1161,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23380,"Description":"9 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1161,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23381,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1161,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1161,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3269,"LISCode":"MEAIGM","PrimaryName":"Measles (Rubeola) Antibody, IgM","LISName":"Measles (Rubeola) Antibody, IgM","EMRName":"Measles (Rubeola) Antibody, IgM","EMRCode":"SQMEAIGM","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":1471,"Aka":"Rubeola Antibody IgM","TdTestInfoCommonId":3269}],"TdBillingCommons":[{"Id":1640,"CptCode":"86765","Quantity":1,"Tmid":"30201365","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"MEASLES-RUBEOLA IGM AB","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3269,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":3269,"SpecialInfo":"Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimens plainly as \"acute\" or \"convalescent.\" Separate serum from cells within 2 hours of collection. This test is New York DOH approved.","ClinicalInfo":"False-negative results are possible if the specimen was collected too soon after exposure. Molecular testing may be helpful. False positive results are possible. ","ClinicalReference":null,"ClinicalLimitation":"Bacterially contaminated, heat-inactivated, hemolyzed, icteric, lipemic, or turbid specimens are unacceptable.","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":1162,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3269,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1162,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13919,"DictMethodologyId":34,"TdTestInfoSpecificId":1162,"DictMethodology":{"Id":34,"Name":"Semi-Quantitative Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1162,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Mon - Fri","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":5343,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1162,"IsBeakerData":false},{"Id":5344,"SpecialInstructions":"Separate serum from cells within 2 hours of collection. Transfer 0.5 mL serum to a standard transport tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1162,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":5953,"Description":"After separation from cells: 48 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1162,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":5954,"Description":"After separation from cells: 2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1162,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":5955,"Description":"After separation from cells: 1 month","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1162,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1162,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3277,"LISCode":"MERC2","PrimaryName":"Mercury, Blood","LISName":"Mercury, Blood","EMRName":"Mercury Blood","EMRCode":"SQMERC2","LOINC":"5685-3","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":11810,"CptCode":"83825","Quantity":1,"Tmid":"30111150","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"MERCURY QUANT","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3277,"IsBeakerData":false}],"TdIncludes":[{"Id":26768,"TestName":"Mercury, Whole Blood","Rank":1,"TdTestInfoCommonId":3277}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3277,"SpecialInfo":"Patient demographics (Heavy Metals) form is required to meet State Health Department requirements. Indications: Toxicity-Mercury poisoning. Patient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and non-essential over-the-counter medications (upon the advice of their physician), and avoid shellfish and seafood for 48 - 72 hours. Specimens collected or transported in tubes other than royal blue (EDTA) or trace element-free transport tubes will be rejected. Clotted specimens are not acceptable. This test is New York DOH approved.","ClinicalInfo":"Preferred test for the assessment of acute mercury exposure. Blood mercury levels predominantly reflect recent exposures, and they are most useful in the diagnosis of acute poisoning as blood mercury concentrations rise sharply and fall rapidly over several days after ingestion. Blood concentrations in unexposed individuals rarely exceed 20 ug/L. The reference interval relates to inorganic mercury concentrations. Dietary and nonoccupational exposure to organic mercury forms may contribute to an elevated total mercury result. Clinical presentation after toxic exposure to organic mercury may include dysarthria, ataxia and constricted vision fields with mercury blood concentrations from 20 to 50 ug/L. Elevated results may be due to skin- or collection-related contamination, including the use of tubes that are not certified to be trace element free. If an elevated result is suspected to be due to contamination, confirmation with a second specimen collected in a certified trace element-free tube is recommended. Mercury is volatile; concentration may decrease over time.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1164,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3277,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1164,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9238,"DictMethodologyId":178,"TdTestInfoSpecificId":1164,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1164,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":35597,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and non-essential over-the-counter medications upon the advice of their physician and avoid shellfish and seafood for 48 to 72 hours. Send blood in original collection tube.","LogicalOperation":null,"DictSpContainerId":37,"DictSpContainerName":"EDTA (Royal blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":26,"DictSpVolumeName":"7 mL","TdTestInfoSpecificId":1164,"IsBeakerData":false},{"Id":35598,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1164,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20164,"Description":"1 week","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1164,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20165,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1164,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20166,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1164,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1164,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":407,"Title":"Heavy Metal Requisition ","FileName":"HeavyMetalRequisitionDemographicForm","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":3277,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":3278,"LISCode":"UMERC3","PrimaryName":"Mercury, Urine 24 Hour","LISName":"Mercury, Urine 24 Hour","EMRName":"Mercury, Urine 24 Hour","EMRCode":"SQUMERC3","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9564,"Aka":"Hg, Urine 24 Hour","TdTestInfoCommonId":3278}],"TdBillingCommons":[{"Id":12556,"CptCode":"83825","Quantity":1,"Tmid":"30109565","CclTechComponentPrice":79.00,"CclProfComponentPrice":null,"TestNameForCdm":"MERCURY URINE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3278,"IsBeakerData":false}],"TdIncludes":[{"Id":18118,"TestName":"Mercury, Urine per volume","Rank":5,"TdTestInfoCommonId":3278},{"Id":18119,"TestName":"Mercury, Urine per 24 hour","Rank":6,"TdTestInfoCommonId":3278},{"Id":18120,"TestName":"Mercury, Urine ratio to creatinine","Rank":7,"TdTestInfoCommonId":3278},{"Id":18121,"TestName":"Creatinine, Urine per volume","Rank":3,"TdTestInfoCommonId":3278},{"Id":18122,"TestName":"Creatinine, Urine per 24 hour","Rank":4,"TdTestInfoCommonId":3278},{"Id":25202,"TestName":"Hours Collected","Rank":1,"TdTestInfoCommonId":3278},{"Id":25203,"TestName":"Total Volume","Rank":2,"TdTestInfoCommonId":3278}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3278,"SpecialInfo":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, nonessential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. High concentrations of iodine may interfere with testing. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected. Elevated results may be due to skin or collection-related contamination, including the use of collection containers that are not certified to be trace element-free. Confirmation with a second specimen collected in a certified trace-element free container is recommended if an elevated result is suspected to be due to contamination. This test is New York DOH approved.","ClinicalInfo":"This test may be useful in the assessment of acute or chronic elemental or inorganic mercury exposure and/or in monitoring chelation therapy. Urinary mercury levels predominantly reflect acute or chronic elemental or inorganic mercury exposure. Urine concentrations in unexposed individuals are typically less than 10 µg/L. 24 hour urine concentrations of 30 to 100 µg/L may be associated with subclinical neuropsychiatric symptoms and tremor while concentrations greater than 100 µg/L can be associated with overt neuropsychiatric disturbances and tremors. 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Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). 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This result is not valid for patients who have received GLUCARPIDASE (carboxypeptidase G2) as a high dose rescue therapy.  Alternative Methotrexate testing is available by send-out for patients on glucarpidase.\n\nReferences:\nWidemann, B.C., Adamson, P.C. (2006). Understanding and Managing Methotrexate Nephrotoxicity. 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","ClinicalInfo":"Microsporidia are considered obligate intracellular parasites that have since been classified within fungi. Transmission routes include ingestion, inhalation or direct inoculation of infective spores. Immunocompromised population specifically patients with AIDS or history of transplant. Infections in immunocompetent individuals have also been reported. Clinical manifestations of microsporidiosis is diverse and can vary with the causal species. Enterocytozoon bieneusi and Encephalitozoon intestinalis are the most common microsporidian species infecting humans and cause gastrointestinal symptoms including diarrhea, fever, malaise and weight loss. Infections in extraintestinal sites is possible and dissemination of infection to other sites have been reported. Microscopy is unable to differentiate and provide a species level identification. 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STUL kit can be purchased via oracle #1570140. Refer to Stool collection guide (https://clevelandcliniclabs.com/our-laboratories/laboratory-medicine/microbiology/plmi-collection-guidelines-resources/stool-specimen-collection-guide/)","LogicalOperation":null,"DictSpContainerId":46,"DictSpContainerName":"EcoFix fixative","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":4,"DictSpCollectionTemperatureName":"Refrigerated","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":52,"DictSpTypeName":"Stool","DictSpVolumeId":244,"DictSpVolumeName":"Complete to fill line","TdTestInfoSpecificId":1175,"IsBeakerData":false},{"Id":11852,"SpecialInstructions":"Unpreserved stool should be submitted to the lab in a securely tightened sterile screw-top container and should be limited to inpatient settings due to a significantly shorter stability window. Use of non-standard (eg. food containers) is discouraged. Refer to Stool collection guide (https://clevelandcliniclabs.com/our-laboratories/laboratory-medicine/microbiology/plmi-collection-guidelines-resources/stool-specimen-collection-guide/)","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":4,"DictSpCollectionTemperatureName":"Refrigerated","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":52,"DictSpTypeName":"Stool","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1175,"IsBeakerData":false},{"Id":678088,"SpecialInstructions":"Body fluids (including but not limited to GI aspirates, respiratory secretions, CSF) should be submitted to the lab in a securely tightened sterile screw-top container. A minimum volume of 0.5ml needed, however larger volumes (1-10ml) are concentrated to increase sensitivity of detection. 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Culture is recommended if the relevant specimen type is not validated for a molecular assay or if susceptibility testing is desired.                                                                                                                                                                                           If culture is positive, identification will be performed at an additional charge. Identification CPT codes that may apply include: 87077, 87153. Antimicrobial susceptibilities are performed when requested, and CPT code 87185 would apply. ","ClinicalInfo":"Because of the labile nature of the organism, a negative culture does not rule out N. gonorrhoeae infection. Specimens are screened for N. gonorrhoeae only. Overgrowth by normal microbiota may make it impossible to rule out N. gonorrhoeae. False negative results may occur with delayed transport. 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Abnormal mannose-binding protein concentrations have been found in patients with infectious disorders such as tuberculosis, hepatitis B, and in autoimmune disorders including recurrent spontaneous abortion and systemic lupus erythematosis.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1181,"ActiveDate":"2012-04-20T00:00:00","CreatedOn":"2012-04-16T00:00:00","CreatedById":393,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4590,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1181,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12054,"DictMethodologyId":170,"TdTestInfoSpecificId":1181,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1181,"DictDaysPerformedId":59,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Tue","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":47431,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection. 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Transfer serum to standard aliquot tube and freeze. 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Specimens not protected from light will be rejected. If tube other than a gel-barrier tube is used, transfer separated serum or plasma to a plastic transport tube. \nGrossly lipemic, hemolyzed or icteric specimens will be rejected","ClinicalInfo":"Neopterin, a pyrazolopyridine compound, is produced by macrophages after induction by interferon gamma and serves as a marker of cellular immune system activation. Measurable levels of neopterin have been detected in both the serum and urine of patients suffering from various types of malignancies(1) and viral infections. Changes in neopterin concentrations in serum or urine can predict complications such as graft rejection in organ transplant recipients. Elevated neopterin levels are found in autoimmune disorders such as rheumatoid arthritis and systemic lupus erythematosus (SLE). Neopterin levels can be used as prognostic predictors for certain types of malignancies. Measurement of neopterin levels has particular value for monitoring patients infected with HIV. Neopterin is eliminated primarily in the urine, so evaluation of urinary neopterin levels may be useful in assessing activation of the cellular immunity system even in the absence of typical clinical symptoms, since a correlation has been observed with the course of diseases involving cellular immunity activation and urinary neopterin levels.\n \n1. Werner ER, Bichler A, Daxenbichler G, et al. Determination of neopterin in serum and urine. Clin Chem. 1987 Jan; 33(1):62-66. 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Results obtained with different methods or kits cannot be used interchangeably. Results cannot be interpreted as absolute evidence of the presence or absence of malignant disease.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":1214,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3362,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1214,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12924,"DictMethodologyId":174,"TdTestInfoSpecificId":1214,"DictMethodology":{"Id":174,"Name":"Immunoassay (IA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1214,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":51911,"SpecialInstructions":"Separate from cells within 1 hour of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1214,"IsBeakerData":false},{"Id":51912,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1214,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29341,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1214,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29342,"Description":"1 week","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1214,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29343,"Description":"1 year (Avoid repeated freeze/thaw cycles)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1214,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1214,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3363,"LISCode":"NSE","PrimaryName":"Neuron-Specific Enolase, Serum","LISName":"Neuron Spec Enolase","EMRName":"Neuron Specific Enolase","EMRCode":"SQNSE","LOINC":"15060-7","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":16611,"CptCode":"83520","Quantity":1,"Tmid":"30205035","CclTechComponentPrice":126.00,"CclProfComponentPrice":null,"TestNameForCdm":"NERUON SPEC ENOLASE, SER","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3363,"IsBeakerData":true}],"TdIncludes":[{"Id":24688,"TestName":"Neuron-Specific Enolase, Serum","Rank":1,"TdTestInfoCommonId":3363}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3363,"SpecialInfo":"Plasma specimens are unacceptable. Hemolyzed specimens will be rejected.","ClinicalInfo":"Use as a tumor marker for evaluation of neuroendocrine tumors. This assay is performed using the BRAHMS NSE Kryptor Immunoassay. Results obtained with different assay methods or kits cannot be used interchangeably. 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Centrifuge within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1215,"IsBeakerData":false},{"Id":51836,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1215,"IsBeakerData":false},{"Id":51837,"SpecialInstructions":"Allow specimen to clot completely at room temperature. Separate serum from cells within 2 hours and transfer into standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1215,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29786,"Description":"1 year (Avoid repeated freeze/thaw cycles) ","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1215,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29787,"Description":"1 week","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1215,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29788,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1215,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1215,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3365,"LISCode":"ANCA","PrimaryName":"Neutrophil Cytoplasmic Antibody","LISName":"Anti-Neutro.Cyto.Ab","EMRName":"ANCA/Anti Neutrophil Cytoplasmic Ab Bld","EMRCode":"SQANCA","LOINC":"","RecommendedUse":"This test is used as an aid in diagnosis of patients with autoimmune vasculitidies. The final interpretation should be done in conjunction with Myeloperoxidase and Proteinase-3 test results and clinical correlation.     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Also present in Polyarthritis Nodosa and other vasculitides.  Atypical indirect immunofluorescence may be seen with inflammatory bowel disease and a common mediated liver disease, usually in the P-ANCA pattern","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1216,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3365,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1216,"IsStat":false,"Comments":"","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13069,"DictMethodologyId":77,"TdTestInfoSpecificId":1216,"DictMethodology":{"Id":77,"Name":"Indirect Immunofluorescence Assay (IFA) ","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1216,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":51663,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1216,"IsBeakerData":false},{"Id":51664,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1216,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29671,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1216,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29672,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1216,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29673,"Description":"30 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1216,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1216,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3366,"LISCode":"UNI24","PrimaryName":"Nickel, Urine 24 Hour","LISName":"Nickel, Urine 24 Hour","EMRName":"Nickel, Urine 24 Hour","EMRCode":"SQUNI24","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":9316,"CptCode":"83885","Quantity":1,"Tmid":"30102535","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"NICKEL URINE 24HR","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3366,"IsBeakerData":false}],"TdIncludes":[{"Id":13790,"TestName":"Nickel, Urine - per volume","Rank":5,"TdTestInfoCommonId":3366},{"Id":13791,"TestName":"Nickel, Urine - per 24h","Rank":6,"TdTestInfoCommonId":3366},{"Id":13792,"TestName":"Nickel, Urine - ratio to CRT","Rank":7,"TdTestInfoCommonId":3366},{"Id":25198,"TestName":"Hours Collected","Rank":1,"TdTestInfoCommonId":3366},{"Id":25199,"TestName":"Total Volume","Rank":2,"TdTestInfoCommonId":3366},{"Id":25200,"TestName":"Creatinine, Urine - per volume","Rank":3,"TdTestInfoCommonId":3366},{"Id":25201,"TestName":"Creatinine, Urine - per 24h","Rank":4,"TdTestInfoCommonId":3366}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3366,"SpecialInfo":"Patient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, nonessential over-the-counter medications (upon the advice of their physician). High concentrations of iodine may interfere with testing. Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected.  Elevated results may be due to skin or collection-related contamination, including the use of collection containers that are not certified to be trace element-free. 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Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours. Collection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). 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Passive exposure to tobacco: Nicotine concentration: < 2 ng/mL; Cotinine concentration: < 8 ng/mL. Unexposed non-tobacco user or Abstinent user for > 2 weeks: Nicotine concentration: < 2 ng/mL; Cotinine concentration: < 2 ng/mL. 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This test is New York DOH approved. ","ClinicalInfo":"This test is designed to evaluate recent use of nicotine-containing products. Passive and active exposure cannot be discriminated definitively, although a cutoff of 100 ng/mL cotinine is frequently used for surgery qualification purposes. For smoking cessation programs or compliance testing, the absence of expected drug(s) and/or drug metabolite(s) may indicate non-compliance, inappropriate timing of specimen collection relative to drug administration, poor drug absorption, diluted/adulterated urine, or limitations of testing. The concentration value must be greater than or equal to the cutoff to be reported as positive. Anabasine is included as a biomarker of tobacco use, versus nicotine replacement. Interpretive questions should be directed to the laboratory. 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Significantly abnormal excretion rates may be associated with severe stress due to multiple trauma, head injury, sepsis, or extensive burns. CAUTION: Measurement of both urine and fecal nitrogen is necessary for the accurate determination of nitrogen balance. 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Positive HBsAg confirmatory assay indicates active infection with Hepatitis B Virus. The test may also remain positive up to a few weeks after administration of Hepatitis B vaccine. Clinical correlation is required. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":14999,"CptCode":"87341","Quantity":1,"Tmid":"30200895","CclTechComponentPrice":60.00,"CclProfComponentPrice":null,"TestNameForCdm":"HEPATITIS HBSAG CONF","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2989,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2989,"SpecialInfo":"This test should be preceded by a positive HBsAg screening assay.**Not intended for use in screening blood, plasma, or tissue donors.**Performance has not been established for the use of cadaveric specimens or the use of body fluids other than human serum.**","ClinicalInfo":"The test is only performed in reflex to a positive/reactive HBsAg screen assay. Positive HBsAg confirmatory assay indicates active infection with Hepatitis B Virus. The test may also remain positive up to a few weeks after administration of Hepatitis B vaccine. Clinical correlation is required. ","ClinicalReference":"","ClinicalLimitation":"Criteria for rejection: Heat inactivated, pooled, grossly hemolyzed, obvious microbial contamination.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1226,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2989,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1226,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11895,"DictMethodologyId":396,"TdTestInfoSpecificId":1226,"DictMethodology":{"Id":396,"Name":"Chemiluminescent Microparticle Immunoassay (CMIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1226,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Sun - 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Patients with chronic HBV infection are at high risk of long-term complications of infection, including chronic hepatitis, cirrhosis, and hepatocellular carcinoma. cobas HBV is an FDA-approved in vitro nucleic acid amplification test for the quantitation of hepatitis B virus (HBV) DNA in human EDTA plasma or serum of HBV-infected individuals. This test is intended for use as an aid in the management of patients with chronic HBV infection undergoing anti-viral therapy. The test can be used to measure HBV DNA levels at baseline and during treatment to aid in assessing response to treatment. The results from cobas HBV must be interpreted within the context of all relevant clinical and laboratory findings. The cobas HBV is not intended for use as a screening test for the presence of HBV in blood or blood products or as a diagnostic test to confirm the presence of HBV infection. The assay is a quantitative PCR that targets highly conserved regions of HBV and is reported out in international units (IU/mL). The linear range of the assay is 10 to 1,000,000,000 IU/mL (1.00 - 9.00 log IU/mL). The lower limit of detection of the assay is 2.7 IU/mL in EDTA plasma and 2.4 IU/mL in serum.","ClinicalReference":"1. Terrault NA, Lok ASF, McMahon BJ, Chang KM, Hwang JP, Jonas MM, Brown RS Jr, Bzowej NH, Wong JB. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Hepatology. 2018 Apr;67(4):1560-1599. doi: 10.1002/hep.29800. PMID: 29405329.\n2. U.S. Food and Drug Administration (FDA). Premarket Approval Summary of Safety and Effectiveness Data P150014. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/pdf15/P150014B.pdf.\n","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Though rare, mutations within the highly conserved regions of a viral genome covered by cobas HBV, may affect primers and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus.\n","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1228,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2990,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1228,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13731,"DictMethodologyId":482,"TdTestInfoSpecificId":1228,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1228,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51416,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR,  CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false},{"Id":51417,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma/serum. Aliquots must be made from specimen prior to testing in any lab outside of Molecular Microbiology, and must be placed in a sterile aliquot tube.\n","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false},{"Id":51418,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false},{"Id":51419,"SpecialInstructions":"Collect serum according to standard protocol. Separate serum by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HCQPCR.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false},{"Id":678990,"SpecialInstructions":"Collect serum according to standard protocol. Centrifuge (at 1,100 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HCQPCR.","LogicalOperation":null,"DictSpContainerId":127,"DictSpContainerName":"SST (Speckled or Tiger Top)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false},{"Id":678991,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":217,"DictSpContainerName":"Pink KEDTA","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1228,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29529,"Description":"24 hours for plasma/serum or for whole blood unspun/unseparated\t","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1228,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29530,"Description":"6 days for plasma/serum separated from whole blood within 24 hours; \n24 hours for whole blood unspun/unseparated","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1228,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29531,"Description":"12 weeks for plasma/serum if separated from whole blood and aliquoted into a secondary tube within 24 hours (plasma/serum cannot be frozen in PPT/SST tubes)\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1228,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1228,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2991,"LISCode":"AHBE","PrimaryName":"Hepatitis Be Antibody","LISName":"HepatitisBe Antibody","EMRName":"Hepatitis Be Antibody","EMRCode":"SQAHBE","LOINC":"13953-5","RecommendedUse":"This test should only be used in patients with a previously known and/or concurrent positive HBsAg result. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12647,"Aka":"Hepatitis B envelope Antibody, Serum","TdTestInfoCommonId":2991},{"Id":12648,"Aka":"Hepatitis Be VIrus Antibody","TdTestInfoCommonId":2991}],"TdBillingCommons":[{"Id":15818,"CptCode":"86707","Quantity":1,"Tmid":"30201225","CclTechComponentPrice":59.00,"CclProfComponentPrice":null,"TestNameForCdm":"HEPATITIS BE ANTIBODY","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2991,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2991,"SpecialInfo":"Bacterial contamination or heat inactivation of the specimen may affect the test result, do not heat inactivate sera.","ClinicalInfo":"This test should only be used in patients with a previously known and/or concurrent positive HBsAg result. Along with HBeAg test, Hepatitis B e antibody test is used for monitoring the natural history of Hepatitis B virus infection and\nprognostication. Clinical correlation is required. ","ClinicalReference":"","ClinicalLimitation":"This assay is not approved for use in screening blood, plasma or tissue donors. This assay is not designed to test body fluids other than human serum.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1229,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2991,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1229,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12487,"DictMethodologyId":164,"TdTestInfoSpecificId":1229,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1229,"DictDaysPerformedId":30,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Mon, Thu","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":48896,"SpecialInstructions":"Separate serum from cells as soon as possible. Transfer serum to standard aliquot tube and refrigerate.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1229,"IsBeakerData":false},{"Id":48897,"SpecialInstructions":"Minimum volume will not allow for repeat or additional testing. Sending of 0.5ml is preferred when possible.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1229,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28135,"Description":"7 days, after separation from cells ","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1229,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28136,"Description":"14 days, after separation from cells  (Up to six freeze/thaw cycles are acceptable)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1229,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28137,"Description":"4 days, after separation from cells","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1229,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1229,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2992,"LISCode":"HBEAG","PrimaryName":"Hepatitis Be Antigen","LISName":"Hepatitis Be Antigen","EMRName":"Hepatitis Be Antigen","EMRCode":"SQHBEAG","LOINC":"13954-3","RecommendedUse":"Please see clinical info","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9480,"Aka":"Hepatitis Be Virus Antigen","TdTestInfoCommonId":2992}],"TdBillingCommons":[{"Id":12416,"CptCode":"87350","Quantity":1,"Tmid":"30600395","CclTechComponentPrice":77.00,"CclProfComponentPrice":null,"TestNameForCdm":"HEPATITIS BE ANTIGEN","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2992,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2992,"SpecialInfo":"If Lav tube - Separate plasma from cells within 2 hours of collection.","ClinicalInfo":"HBeAg test should only be done in patients with positive HBsAg result and be used as an aid to determine the level of infectiousness and for monitoring chronic Hepatitis B activity over time as an important prognostic test. HBeAg may test negative in HBV-infected individuals with precore or basal core promoter mutations. Anti-HBe antibody test should be considered in conjunction with HBeAg test.  ","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1230,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2992,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1230,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9736,"DictMethodologyId":164,"TdTestInfoSpecificId":1230,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1230,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Fri","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":37584,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1230,"IsBeakerData":false},{"Id":37587,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1230,"IsBeakerData":false},{"Id":37589,"SpecialInstructions":"Separate plasma from cells within 2 hours of collection.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1230,"IsBeakerData":false},{"Id":678055,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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HCV RNA testing, if indicated, will determine if there is active HCV infection. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":15001,"CptCode":"86803","Quantity":1,"Tmid":"30211700","CclTechComponentPrice":62.00,"CclProfComponentPrice":null,"TestNameForCdm":"*HEP C AB","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2995,"IsBeakerData":false}],"TdIncludes":[{"Id":22434,"TestName":"Hepatitis C Antibody","Rank":1,"TdTestInfoCommonId":2995}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2995,"SpecialInfo":"If HCV antibody is positive will reflex to a quantitative HCV RNA.**Not intended for use in screening blood, plasma, or tissue donors. **Assay performance characteristics have not been established for newborns, infants, children, or populations of immunocompromised or immunosuppressed patients. **Performance has not been established for the use of cadaveric specimens or the use of body fluids other than human serum.","ClinicalInfo":"The test is used to investigate the evidence of past or current infection with Hepatitis C Virus. HCV RNA testing, if indicated, will determine if there is active HCV infection. ","ClinicalReference":"","ClinicalLimitation":"Criteria for rejection: Heat inactivated, pooled, grossly hemolyzed, obvious microbial contamination.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1232,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2995,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1232,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11897,"DictMethodologyId":396,"TdTestInfoSpecificId":1232,"DictMethodology":{"Id":396,"Name":"Chemiluminescent Microparticle Immunoassay (CMIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1232,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":46711,"SpecialInstructions":"Separate plasma from cells within 6 hours of collection.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1232,"IsBeakerData":false},{"Id":46712,"SpecialInstructions":"Centrifuge SST tube within 6 hours of collection","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1232,"IsBeakerData":false},{"Id":46714,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1232,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26696,"Description":"3 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1232,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26697,"Description":"14 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1232,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26698,"Description":"7 days","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1232,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1232,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":2998,"PrimaryName":"Hepatitis C Virus (HCV) RNA, Quantitative PCR, Plasma/Serum","IsRequired":false}]},{"Id":2998,"LISCode":"HCQPCR","PrimaryName":"Hepatitis C Virus (HCV) RNA, Quantitative PCR, Plasma/Serum","LISName":"Hepatitis C Virus (HCV) RNA, Quantitative PCR, Plasma/Serum","EMRName":"Hepatitis C Virus (HCV) RNA, Quantitative PCR, Plasma/Serum","EMRCode":"SQHCQPCR","LOINC":"20416-4 ","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14577,"Aka":"HCQPCR","TdTestInfoCommonId":2998},{"Id":14578,"Aka":"hep c","TdTestInfoCommonId":2998},{"Id":14579,"Aka":"SQHCQPCR","TdTestInfoCommonId":2998},{"Id":14580,"Aka":"HCV RNA","TdTestInfoCommonId":2998},{"Id":14581,"Aka":"HCVRNA","TdTestInfoCommonId":2998},{"Id":14582,"Aka":"viral load","TdTestInfoCommonId":2998}],"TdBillingCommons":[{"Id":16455,"CptCode":"87522","Quantity":1,"Tmid":"30600535","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Quantification, Hepatitis C Virus ","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2998,"IsBeakerData":false}],"TdIncludes":[{"Id":26304,"TestName":"HCV RNA","Rank":1,"TdTestInfoCommonId":2998},{"Id":26305,"TestName":"HCV RNA (IU/mL)","Rank":2,"TdTestInfoCommonId":2998},{"Id":26306,"TestName":"HCV RNA (log IU/mL)","Rank":3,"TdTestInfoCommonId":2998}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2998,"SpecialInfo":"","ClinicalInfo":"HCV is a single stranded, positive sense RNA virus, which can be transmitted by blood and blood products. Detection of antibodies to HCV (anti-HCV) indicates prior exposure to hepatitis C but does not distinguish between cleared or active infection. Detection of HCV RNA with the detection of anti-HCV identifies an active hepatitis C infection. The results of HCV RNA testing together with other biochemical and clinical information, may be used to confirm an active HCV infection, measure the level of virus in the blood and assist in HCV prevention counseling medical care and treatment decision making. cobas HCV is an FDA-approved in vitro nucleic acid amplification test for both the detection and quantitation of hepatitis C virus (HCV) RNA, in human EDTA plasma or serum, of HCV antibody positive or HCV infected individuals. Specimens containing HCV genotypes 1 to 6 are validated for detection and quantitation in the assay. cobas HCV is intended for use as an aid in the diagnosis of HCV infection in the following populations: individuals with antibody evidence of HCV with evidence of liver disease, individuals suspected to be actively infected with HCV antibody evidence, and individuals at risk for HCV infection with antibodies to HCV. Detection of HCV RNA indicates that the virus is replicating and therefore is evidence of active infection. cobas HCV is intended for use as an aid in the management of HCV infected patients undergoing anti viral therapy. The assay can be used to measure HCV RNA levels at baseline during treatment, at the end of and at the end of follow up of treatment to determine sustained or non sustained viral response. The results must be interpreted within the context of all relevant clinical and laboratory findings. cobas HCV has not been approved for use as a screening test for the presence of HCV in blood or blood products. The assay is a quantitative PCR that targets highly-conserved regions of HCV and is reported out in international units (IU/mL). The linear range of the assay is 15 to 100,000,000 IU/mL (1.18 - 8.00 log IU/mL). The lower limit of detection of the assay is 15 IU/mL.","ClinicalReference":"1. AASLD-IDSA. Recommendations for testing, managing, and treating hepatitis C. Accessed July 5, 2024. http://www.hcvguidelines.org.\n2. Cartwright EJ, Patel P, Kamili S, Wester C. Updated Operational Guidance for Implementing CDC’s Recommendations on Testing for Hepatitis C Virus Infection. MMWR Morb Mortal Wkly Rep 2023;72:766–768. DOI: http://dx.doi.org/10.15585/mmwr.mm7228a2.\n3. U.S. Food and Drug Administration (FDA). Premarket Approval Summary of Safety and Effectiveness Data P150015. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/pdf15/P150015B.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Though rare, mutations within the highly conserved regions of a viral genome covered by cobas HCV may affect primer and/or probe binding resulting in the under quantitation of virus or failure to detect the presence of virus. Our laboratory accepts remnant specimens previously tested for anti-HCV from select other laboratories, in accordance with reflex testing algorithms recommended by the Centers for Disease Control (https://www.cdc.gov/mmwr/volumes/72/wr/mm7228a2.htm). This is associated with a small risk of carryover contamination, which may lead to rare cases of false positive results. In this setting, if results are discordant with clinical history/presentation or other lab findings, it is recommended to submit a dedicated specimen for repeat HCV RNA testing.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1233,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2998,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1233,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13011,"DictMethodologyId":482,"TdTestInfoSpecificId":1233,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1233,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51410,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample can only be shared with AHCV1B, HSVPCR, VZVPCR, HEPGEN, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1233,"IsBeakerData":false},{"Id":51411,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma/serum. Aliquots must be made from specimen prior to testing in any lab outside of Molecular Microbiology, and must be placed in a sterile aliquot tube.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1233,"IsBeakerData":false},{"Id":51413,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HSVPCR, VZVPCR, HEPGEN, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n\n","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1233,"IsBeakerData":false},{"Id":678992,"SpecialInstructions":"Collect serum according to standard protocol. Separate serum by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HEPGEN, or HBVDNU.\n\n","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1233,"IsBeakerData":false},{"Id":678993,"SpecialInstructions":"Collect serum according to standard protocol. Centrifuge (at 1,100 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HEPGEN, or HBVDNU.\n","LogicalOperation":null,"DictSpContainerId":127,"DictSpContainerName":"SST (Speckled or Tiger Top)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1233,"IsBeakerData":false},{"Id":678994,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. 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This test is New York DOH approved.","ClinicalInfo":"Order this assay only when patient has an acute or chronic hepatitis B infection. This test detects total antibodies (IgG and IgM) to the hepatitis Delta agent. 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If Hepatitis B Surface Antigen is initially reactive, a Hepatitis B Surface Antigen Confirmation will be ordered and charged.","ClinicalInfo":"To assess or rule out a remote history of viral Hepatitis B or C. Methodology not approved for donor testing.  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HSV causes about 5–10% of all encephalitis cases, and is one of the most common causes of identified sporadic encephalitis globally. HSV-1 encephalitis is more common in adults; and HSV-2 encephalitis is more common in neonates. Clinical features involved with HSV encephalitis include fever, hemicranial headache, language and behavioral abnormalities, memory impairment, and seizures. HSV can also be associated with meningitis. Nucleic acid amplification testing of CSF specimens has greatly increased the ability to diagnose infections of the CNS, especially viral infections caused by the herpesviruses. \n\nThe FDA-cleared DiaSorin Molecular Simplexa HSV 1 & 2 Direct  is a multiplex qualitative real-time PCR assay that targets HSV-1 and HSV-2 DNA polymerase genes, and is intended for use as an aid in the diagnosis of HSV-1 and HSV-2 infections of the CNS. For encephalitis patients with a negative herpes simplex PCR result, consideration should be given to repeating the test 3–7 days later for patients demonstrating a compatible clinical syndrome or temporal lobe localization on neuroimaging. This standalone HSV-1 and HSV-2 PCR test has been shown to have greater analytic sensitivity for HSV detection as compared to large multiplex panels, and should be considered for patients with high pre-test probability of HSV encephalitis.","ClinicalReference":"Vaugon E, Mircescu A, Caya C, Yao M, Gore G, Dendukuri N, Papenburg J. Diagnostic accuracy of rapid one-step PCR assays for detection of herpes simplex virus-1 and -2 in cerebrospinal fluid: a systematic review and meta-analysis. Clin Microbiol Infect. 2022 Dec;28(12):1547-1557. doi: 10.1016/j.cmi.2022.06.004. Epub 2022 Jun 17. PMID: 35718347.","ClinicalLimitation":"Negative results do not preclude HSV-1 or HSV-2 infection and should not be used as the sole basis for treatment or other patient management decisions, especially if performed very early in the course of illness. For encephalitis patients with a negative herpes simplex PCR result, consideration should be given to repeating the test 3–7 days later for patients demonstrating a compatible clinical syndrome or temporal lobe localization on neuroimaging. As with other tests, false-positive results may occur. Repeat testing or testing with a different device may be indicated in some settings. A positive result by this test cannot rule out infections caused by other viral or bacterial pathogens. Viral nucleic acids may persist in vivo independent of virus viability. 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Results between different Histoplasma assays cannot be compared.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1253,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3029,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1253,"IsStat":false,"Comments":"","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12068,"DictMethodologyId":161,"TdTestInfoSpecificId":1253,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1253,"DictDaysPerformedId":63,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Tue, Fri","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":47495,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1253,"IsBeakerData":false},{"Id":47496,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1253,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27163,"Description":"2 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1253,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27164,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1253,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27165,"Description":"60 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1253,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1253,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":651,"Title":"Histoplasma Galactomannan Antigen Test","FileName":"HistoplasmaGalactomannanAntigenTest","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":3029,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":3030,"LISCode":"SHISTO","PrimaryName":"Histoplasma Antigen Quantitative by EIA, Serum","LISName":"Histoplasma Antigen Quantitative by EIA, Serum","EMRName":"Histoplasma Antigen Quantitative by EIA, Serum","EMRCode":"SQSHISTO","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":15211,"CptCode":"87385","Quantity":1,"Tmid":"30201485","CclTechComponentPrice":149.00,"CclProfComponentPrice":null,"TestNameForCdm":"HISTOPLASMA CAPSULA AG","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3030,"IsBeakerData":false}],"TdIncludes":[{"Id":25891,"TestName":"Histoplasma Antigen, Serum","Rank":1,"TdTestInfoCommonId":3030},{"Id":25892,"TestName":"Histoplasma Antigen, Serum Interp\t","Rank":2,"TdTestInfoCommonId":3030}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3030,"SpecialInfo":"","ClinicalInfo":"The quantitative range of this assay is 0.19-60.0 ng/mL. Antigen concentrations less than 0.19ng/mL ;greater than 60.0 ng/mL fall outside the linear range of the assay and cannot be accurately quantified.\n\nThis EIA test should be used in conjunction with other diagnostic procedures, including microbiological culture, histological examination of biopsy samples, serology and/or radiographic evidence, to aid in the diagnosis of histoplasmosis.\n\nCross-reactivity with Blastomyces dermatiditis, Coccidioides immitis, and possibly Talaromyces marneffei have been observed with this EIA. Other clinically and geographically relevant endemic mycoses should be considered in the case of a positive test result.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1254,"ActiveDate":"2015-09-29T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3030,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1254,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12067,"DictMethodologyId":161,"TdTestInfoSpecificId":1254,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1254,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":47483,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1254,"IsBeakerData":false},{"Id":47484,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":86,"DictSpVolumeName":"1.2 mL","TdTestInfoSpecificId":1254,"IsBeakerData":false},{"Id":47490,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1254,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27160,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1254,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27161,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1254,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27162,"Description":"1 month","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1254,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1254,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5834,"LISCode":"NUCBLD","PrimaryName":"DNA Extraction Blood","LISName":"DNA Extract Blood","EMRName":"DNA Extraction Blood","EMRCode":"SQNUCBLD","LOINC":"","RecommendedUse":"","DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13636,"CptCode":"81479","Quantity":1,"Tmid":"","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5834,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5834,"SpecialInfo":"Specimens will be available for 3 years from the date of collection. To order testing on this specimen for Cleveland Clinic patients, please place an Epic order for DNA and RNA for Clinical Testing (SQNUCADD). To order for patients outside of the Cleveland Clinic system, please request DNA and RNA for Clinical Testing, order code NUCADD.  Note: Only DNA will be extracted from blood samples. If additional paperwork is required for testing, please send completed forms via secure email to DNASendOuts@ccf.org","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1255,"ActiveDate":"2020-01-07T00:00:00","CreatedOn":"2019-11-05T14:20:00","CreatedById":20,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5834,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1255,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10736,"DictMethodologyId":203,"TdTestInfoSpecificId":1255,"DictMethodology":{"Id":203,"Name":"Extraction (EXT)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1255,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":null,"DictDaysPerformed":"5 days per week","DictReported":null},"TdSpecimenRequirements":[{"Id":41358,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":151,"DictSpTypeName":"Blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1255,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23757,"Description":"Transport within 48 hours.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1255,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23758,"Description":"Refrigerated specimens are acceptable.","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1255,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23759,"Description":"Will be rejected.","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1255,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1255,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3038,"LISCode":"HIVRNA","PrimaryName":"Human Immunodeficiency Virus 1 (HIV-1) RNA, Quantitative PCR, Plasma","LISName":"Human Immunodeficiency Virus 1 (HIV-1) RNA, Quantitative PCR, Plasma","EMRName":"Human Immunodeficiency Virus 1 (HIV-1) RNA, Quantitative PCR, Plasma","EMRCode":"SQHIVRNA","LOINC":"20447-9","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13753,"Aka":"HIV RNA","TdTestInfoCommonId":3038},{"Id":13754,"Aka":"HIV RNA","TdTestInfoCommonId":3038},{"Id":14567,"Aka":"HIVRNA","TdTestInfoCommonId":3038},{"Id":14568,"Aka":"SQHIVRNA","TdTestInfoCommonId":3038},{"Id":14569,"Aka":"viral load","TdTestInfoCommonId":3038},{"Id":14570,"Aka":"AIDS","TdTestInfoCommonId":3038}],"TdBillingCommons":[{"Id":16604,"CptCode":"87536","Quantity":1,"Tmid":"30600565","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Quantification, HIV-1","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3038,"IsBeakerData":false}],"TdIncludes":[{"Id":26298,"TestName":"HIV-1 RNA","Rank":1,"TdTestInfoCommonId":3038},{"Id":26299,"TestName":"HIV-1 RNA (copies/mL)","Rank":2,"TdTestInfoCommonId":3038},{"Id":26300,"TestName":"HIV-1 RNA (log copies/mL)","Rank":3,"TdTestInfoCommonId":3038}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3038,"SpecialInfo":"","ClinicalInfo":"Human immunodeficiency virus (HIV) is the etiologic agent of acquired immunodeficiency syndrome (AIDS). Quantitative measurements of HIV viremia in the plasma have shown that higher virus levels are correlated with more rapid clinical progression of HIV disease. Furthermore, nearly two decades of clinical research have established that reductions in plasma virus levels with the use of antiretroviral therapy (ART) significantly decrease the risk of clinical progression, including death, development of AIDS, opportunistic infections, and HIV-associated morbidity. HIV viral load is also predictive of the risk of transmission of HIV, and randomized controlled clinical trials have established that early initiation of ART with suppression of the viral load reduces HIV transmission by 96%. cobas HIV-1 is an in vitro nucleic acid amplification test for the quantitation of human immunodeficiency virus type 1 (HIV-1) in EDTA plasma of HIV-1-infected individuals. This test is intended for use in conjunction with clinical presentation and other laboratory markers for the clinical management of HIV-1 infected patients. The test can be used to assess patient prognosis by measuring the baseline HIV-1 level or to monitor the effects of antiretroviral therapy by measuring changes in HIV-1 RNA levels during the course of antiretroviral treatment. This assay is not intended for use as a screening test for the presence of HIV-1 in donated blood or plasma or as a diagnostic test to confirm the presence of HIV-1 infection. The assay is a quantitative PCR assay that targets highly-conserved regions of the HIV-1 genome including the HIV-1 gag gene and the HIV-1 LTR region, and is reported out in copies/mL. The linear range of the assay is 20 to 10,000,000 copies/mL (1.30 - 7.00 log copies/mL). The lower limit of detection of the assay is 13.2 copies/mL.","ClinicalReference":"1. Centers for Disease Control and Prevention. HIV screening and testing. Accessed July 5, 2024. https://www.cdc.gov/hiv/guidelines/testing.html.\n2. U.S. Food and Drug Administration (FDA). Cobas HIV-1 Roche Molecular Systems Instructions for Use PMA BP150262. Accessed July 5, 2024. https://www.fda.gov/vaccines-blood-biologics/approved-blood-products/cobas-hiv-1.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Though rare, mutations within the highly conserved regions of a viral genome covered by cobas HIV-1 may affect primers and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus. Samples from subjects under 19 years of age were not evaluated. False positive results have been reported in patients with history of chimeric antigen receptor (CAR) T cell immunotherapy using lentiviral vectors, which can cross react with assay targets (PMID: 31694968). This assay does not detect HIV-2.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1257,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3038,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1257,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13730,"DictMethodologyId":482,"TdTestInfoSpecificId":1257,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1257,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51803,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1257,"IsBeakerData":false},{"Id":51804,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma. Aliquots must be made from specimen prior to testing in any lab outside of Molecular Microbiology, and must be placed in a sterile aliquot tube.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1257,"IsBeakerData":false},{"Id":51805,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. 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Patients who are taking methotrexate, carbamazepine, phenytoin, nitrous oxide, anticonvulsants, or 6-azauridine triacetate may have elevated levels of homocysteine due to their effect on the pathway.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1265,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3058,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1265,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9101,"DictMethodologyId":182,"TdTestInfoSpecificId":1265,"DictMethodology":{"Id":182,"Name":"Enzymatic","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1265,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":35111,"SpecialInstructions":"Centrifuge and separate plasma/serum from cells less than one hour after collection. If collected in a non-gel separator tube, centrifuge and transfer plasma/serum to a CCL tube and refrigerate.","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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If collected in a non-gel separator tube, centrifuge and transfer plasma/serum to a CCL tube and refrigerate.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":8,"DictSpCollectionTemperatureName":"Place specimen on ice after draw.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1265,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19820,"Description":"After separation from cells: 4 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1265,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19821,"Description":"After separation from cells: 4 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1265,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19822,"Description":"After separation from cells: 10 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1265,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1265,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":3060,"LISCode":"UHVA","PrimaryName":"Homovanillic Acid (HVA), 24 Hour Urine","LISName":"Homovanillic Acid (HVA), 24 Hour Urine","EMRName":"Homovanillic Acid (HVA), 24 Hour Urine","EMRCode":"SQUHVA","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13618,"Aka":"HVA, Urine","TdTestInfoCommonId":3060}],"TdBillingCommons":[{"Id":16430,"CptCode":"83150","Quantity":1,"Tmid":"30108945","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"HOMOVANILLIC ACID URINE","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":3060,"IsBeakerData":false}],"TdIncludes":[{"Id":24539,"TestName":"Creatinine, Urine per volume","Rank":1,"TdTestInfoCommonId":3060},{"Id":24540,"TestName":"Creatinine, Urine per day","Rank":2,"TdTestInfoCommonId":3060},{"Id":24541,"TestName":"HVA per volume","Rank":3,"TdTestInfoCommonId":3060},{"Id":24542,"TestName":"HVA ratio to Creatinine","Rank":4,"TdTestInfoCommonId":3060},{"Id":24543,"TestName":"HVA per 24 hours","Rank":5,"TdTestInfoCommonId":3060}],"TdLaboratoryCommon":{"TdTestInfoCommonId":3060,"SpecialInfo":"Indicate total volume. This test is New York DOH approved.","ClinicalInfo":"Moderately elevated HVA (homovanillic acid) may be caused by a variety of factors such as essential hypertension, intense anxiety, intense physical exercise, and numerous drug interactions (including some over-the-counter medications and herbal products). Medications that may interfere with catecholamines and their metabolites include amphetamines and amphetamine-like compounds, appetite suppressants, bromocriptine, buspirone, caffeine, chlorpromazine, clonidine, disulfiram, diuretics (in doses sufficient to deplete sodium), epinephrine, glucagon, guanethidine, histamine, hydrazine derivatives, imipramine, levodopa (L-dopa, Sinemet(R)), lithium,\nMAO inhibitors, melatonin, methyldopa (Aldomet(R)), morphine, nitroglycerin, nose drops, propafenone (Rythmol), radiographic agents, rauwolfia alkaloids (Reserpine), and vasodilators. The effects of some drugs on catecholamine metabolite results may not be predictable.\nInterpretive Data: Homovanillic acid (HVA) results are expressed as a ratio to creatinine excretion (mg/g CRT). No reference interval is available for results reported in units of mg/L. Slight or moderate increases in catecholamine metabolites may be due to extreme anxiety, essential hypertension, intense physical exercise, or drug interactions. Significant increase of one or more catecholamine metabolites (several times the upper reference limit) is associated with an increased probability of a secreting neuroendocrine tumor. Per 24h calculations are provided to aid interpretation for collections with a duration of 24 hours and an average daily urine volume. For specimens with notable deviations in collection time or volume, ratios of analytes to a corresponding urine creatinine concentration may assist in result interpretation.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1266,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":3060,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1266,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12992,"DictMethodologyId":54,"TdTestInfoSpecificId":1266,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1266,"DictDaysPerformedId":53,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun, Tue - 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Alternative test codes available for these specimen sources. Various identification are utilised and susceptibility testing performed as appropriate. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6100,"Aka":"Culture for mold","TdTestInfoCommonId":2840},{"Id":6101,"Aka":"Culture for yeast","TdTestInfoCommonId":2840},{"Id":14405,"Aka":"Fungal culture","TdTestInfoCommonId":2840},{"Id":14406,"Aka":"Fungus culture","TdTestInfoCommonId":2840},{"Id":14407,"Aka":"Mold","TdTestInfoCommonId":2840},{"Id":14408,"Aka":"Mold culture","TdTestInfoCommonId":2840},{"Id":14409,"Aka":"Mould","TdTestInfoCommonId":2840},{"Id":14410,"Aka":"Mycology","TdTestInfoCommonId":2840},{"Id":14411,"Aka":"Yeast","TdTestInfoCommonId":2840},{"Id":14412,"Aka":"Yeast culture","TdTestInfoCommonId":2840}],"TdBillingCommons":[{"Id":8719,"CptCode":"87102","Quantity":1,"Tmid":"30600065","CclTechComponentPrice":54.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18669,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18670,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18671,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18672,"CptCode":"87176","Quantity":1,"Tmid":"30600215","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Tissue Homogenization","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18673,"CptCode":"87015","Quantity":1,"Tmid":"30606300","CclTechComponentPrice":43.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Fluid Concentration","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":18676,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":19261,"CptCode":"87186","Quantity":1,"Tmid":"30608565","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Phoenix","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false},{"Id":19262,"CptCode":"87186","Quantity":1,"Tmid":"30608555","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Vitek","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2840,"IsBeakerData":false}],"TdIncludes":[{"Id":25917,"TestName":"Specimens may include some pre-processing steps such as concentration and use of mucolytic agents to aid in the recovery of fungal organisms. ","Rank":1,"TdTestInfoCommonId":2840}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2840,"SpecialInfo":"Fungal smears - direct detection of fungi from clinical specimens will NOT be performed. Please order FCULSM if fungal smears are needed. Clinical specimens for fungal cultures are processed and plated on selective fungal media to optimize recovery of fungal organisms. Cultures are incubated for 28 days; negative results are auto-updated daily. Any fungal organisms recovered will be isolated and identified by various methods. Yeast from respiratory specimen will be ruled for Cryptococcus species and Candida auris and will be reported with minimal ID (Yeast not Cryptococcus); full genus and species ID will only be reported if clinically indicated and requested by clinicians.  Additional CPT codes may be applicable for recovery and identification of fungal organisms - 87176sub- Tissue processing, 87015 - concentration of specimen, 87102 Fungal culture, 87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing. Fungal susceptibility testing for yeast recovered ONLY from sterile sites will be performed automatically (CPT 87186). Yeast susceptibility testing is determined by colorimetric microdilution broth. A standardized inoculation of test organism is incubated with appropriate dilutions of antifungal agents; minimum inhibitory concentration (MIC) are determined by inhibition of growth at the lowest antifungal concentration. MIC are determined and interpreted according to CLSI standards. For yeasts recovered from non-sterile sites are performed in-house by request only - by contacting the lab. Filamentous mold susceptibility testing is a send-out test and can be requested by contacting the lab. Additional billing is applied for sequencing, identification, and susceptibility testing. CPT codes vary based on methodology.","ClinicalInfo":"For optimal recovery of organisms - specimen should be collected using sterile technique, reduce contamination and transported immediately to the microbiology laboratory. Isolation and identification of fungi in the clinical laboratory can help guide patient care. However, fungi can be pathogens, colonizers and/or contaminants. Clinical correlation with patient symptoms is necessary to determine significance of recovered organism. If specific fungi are suspected the \"rule out\" feature in Epic can be utilized. If fungal smears are needed order FCULSM; for fungal blood cultures HISTCL; for CSF order FUNCSF; for dermal samples of hair, skin and nail order ACFSC or FHSNSM (with smear); for candidiasis on vaginal and oral samples order fungal screen FUNGSC.","ClinicalReference":"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. \nAshbee HR: General approaches for direction detection and identification of fungi. In: Carroll KC, Pfaller MA, Landry ML, et al, eds. Manual of Clinical Microbiology. 12th ed. Vol 1. ASM Press; 2019:2035-2055","ClinicalLimitation":"Not all fungal organisms recovered in cultures may be significant; clinical correlation needed to determine significance.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1407,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2840,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1407,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6768,"DictMethodologyId":224,"TdTestInfoSpecificId":1407,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1407,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":148,"DictDaysPerformed":"Sun - Sat","DictReported":"6 weeks"},"TdSpecimenRequirements":[{"Id":678301,"SpecialInstructions":"Biopsy specimens should be collected in a sterile screw-top container with a small amount of sterile saline to prevent specimen from drying out. Specimens from periphery of a cutaneous lesion for recovery of fungal organisms. Specimen for Histopathology should be collected and sent separately. ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":53,"DictSpTypeName":"Tissue","DictSpVolumeId":112,"DictSpVolumeName":"1 - 5 g","TdTestInfoSpecificId":1407,"IsBeakerData":false},{"Id":678302,"SpecialInstructions":"Specimen source is required for processing. Larger volumes are preferred to improve recovery of fungal organisms. Specimen should be collected using sterile technique in a leakproof sterile screw-top container. If specimen volumes are small especially from lesion aspirates- instilling a small volume of sterile saline may aid collection. Specimen may be submitted in a sterile syringe only after removing needle and capping. Swabs are not preferred for fungal cultures; E-swabs are ONLY acceptable for hard-to-collect specimen sources such as ear canal. Specimen for Histopathology should be collected and sent separately.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":48,"DictSpTypeName":"Fluid, body","DictSpVolumeId":43,"DictSpVolumeName":"1-2 mL min (prefer 20-50 mL)","TdTestInfoSpecificId":1407,"IsBeakerData":false},{"Id":678303,"SpecialInstructions":"Corneal scrapings may be submitted in a sterile container but due to the scarcity of material, it is preferred that non-inhibitory fungal plates such as Potato Dextrose Agar (PDA) be inoculated at time of collection. Scrapings should be placed in two or three places on the plate, using an X or C shaped motion. Vitreous fluid may be submitted in a sterile container. If irrigation fluid used to aid in collection submit entire collection to aid in recovery of fungal organisms. ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":11,"DictSpTransportTemperatureName":"See note","DictSpTypeId":154,"DictSpTypeName":"Eye","DictSpVolumeId":154,"DictSpVolumeName":"Variable","TdTestInfoSpecificId":1407,"IsBeakerData":false},{"Id":678304,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1407,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":14407,"Description":"72 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1407,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14408,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1407,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14409,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1407,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1407,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":2045,"PrimaryName":"AFB Susceptibility","IsRequired":false},{"TdTestInfoCommonId":4587,"PrimaryName":"Mold Susceptibility One Drug","IsRequired":false},{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3397,"PrimaryName":"Organism Identification, AFB","IsRequired":false},{"TdTestInfoCommonId":3400,"PrimaryName":"Organism Identification, Nocardia","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false}]},{"Id":2841,"LISCode":"FCULSM","PrimaryName":"Fungal Culture and Smear (Non Dermal)","LISName":"Fungal Culture and Smear (Non Dermal)","EMRName":"Fungal Culture and Smear (Non Dermal)","EMRCode":"SQFCULSM","LOINC":"","RecommendedUse":"Diagnosing fungal infection from clinical specimens EXCEPT - dermal, vaginal/oral, CSF and blood cultures. Alternative test codes available for these specimen sources. Various identification are utilised and susceptibility testing performed as appropriate. \n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6097,"Aka":"Fungus Culture and Calofluor White Stain","TdTestInfoCommonId":2841},{"Id":6098,"Aka":"Fungus Culture and KOH Prep","TdTestInfoCommonId":2841},{"Id":6099,"Aka":"Fungus Culture and KOH Preparation","TdTestInfoCommonId":2841},{"Id":14418,"Aka":" Yeast culture","TdTestInfoCommonId":2841},{"Id":14419,"Aka":"Calcofluor stain","TdTestInfoCommonId":2841},{"Id":14420,"Aka":"Fungal culture","TdTestInfoCommonId":2841},{"Id":14421,"Aka":"Fungal smear","TdTestInfoCommonId":2841},{"Id":14422,"Aka":"Fungal stain","TdTestInfoCommonId":2841},{"Id":14423,"Aka":"KOH stain","TdTestInfoCommonId":2841},{"Id":14424,"Aka":"Mold culture","TdTestInfoCommonId":2841},{"Id":14425,"Aka":"Mycology","TdTestInfoCommonId":2841},{"Id":14426,"Aka":"Yeast","TdTestInfoCommonId":2841}],"TdBillingCommons":[{"Id":18692,"CptCode":"87102","Quantity":1,"Tmid":"30600065","CclTechComponentPrice":54.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18693,"CptCode":"87206","Quantity":1,"Tmid":"30600265","CclTechComponentPrice":35.00,"CclProfComponentPrice":null,"TestNameForCdm":"Smear, Fungal Fluorescent","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18694,"CptCode":"87176","Quantity":1,"Tmid":"30600215","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Tissue Homogenization","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18695,"CptCode":"87015","Quantity":1,"Tmid":"30606300","CclTechComponentPrice":43.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Fluid Concentration","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18698,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18699,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18700,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false},{"Id":18706,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2841,"IsBeakerData":false}],"TdIncludes":[{"Id":25919,"TestName":"Specimens may include some pre-processing steps such as concentration and use of mucolytic agents to aid in the recovery of fungal organisms. ","Rank":1,"TdTestInfoCommonId":2841}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2841,"SpecialInfo":"Fungal smears are performed directly on specimen using a Calcofluor white stain that nonspecifically binds chitin in the cell wall of fungi. Fluorescent microscopy is utilised to detect and report as yeast and/or hyphae present. CPT code: 87206. Clinical specimens for fungal cultures are processed and plated on selective fungal media to optimize recovery of fungal organisms. Cultures are incubated for 28 days; negative results are auto-updated daily. Any fungal organisms recovered will be isolated and identified by various methods. Yeast from respiratory specimen will be ruled for Cryptococcus species and Candida auris and will be reported with minimal ID (Yeast not Cryptococcus); full genus and species ID will only be reported if clinically indicated and requested by clinicians.  Additional CPT codes may be applicable for recovery and identification of fungal organisms - 87176- Tissue processing, 87015 - concentration of specimen, 87102 Fungal culture, 87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing. Fungal susceptibility testing for yeast recovered ONLY from sterile sites will be performed automatically (CPT 87186). Yeast susceptibility testing is determined by colorimetric microdilution broth. A standardized inoculation of test organism is incubated with appropriate dilutions of antifungal agents; minimum inhibitory concentration (MIC) are determined by inhibition of growth at the lowest antifungal concentration. MIC are determined and interpreted according to CLSI standards. For yeasts recovered from non-sterile sites are performed in-house by request only - by contacting the lab. Filamentous mold susceptibility testing is a send-out test and can be requested by contacting the lab.","ClinicalInfo":"For optimal recovery of organisms - specimen should be collected using sterile technique, reduce contamination and transported immediately to the microbiology laboratory. Isolation and identification of fungi in the clinical laboratory can help guide patient care. However, fungi can be pathogens, colonizers and/or contaminants. Clinical correlation with patient symptoms is necessary to determine significance of recovered organism. If specific fungi are suspected the \"rule out\" feature in Epic can be utilised. If fungal smears are needed order FCULSM; for fungal blood cultures HISTCL; for CSF order FUNCSF; for dermal samples of hair, skin and nail order  ACFSC or FHSNSM (with smear); for candidiasis on vaginal and oral samples order fungal screen FUNGSC.","ClinicalReference":"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. \n","ClinicalLimitation":"Not all fungal organisms recovered in cultures may be significant; clinical correlation needed to determine significance.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1408,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2841,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1408,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6766,"DictMethodologyId":224,"TdTestInfoSpecificId":1408,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null},{"Id":6767,"DictMethodologyId":260,"TdTestInfoSpecificId":1408,"DictMethodology":{"Id":260,"Name":"Stain","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1408,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":148,"DictDaysPerformed":"Sun - Sat","DictReported":"6 weeks"},"TdSpecimenRequirements":[{"Id":678338,"SpecialInstructions":"Biopsy specimens should be collected in a sterile screw-top container with a small amount of sterile saline to prevent specimen from drying out. Specimens from periphery of a cutaneous lesion for recovery of fungal organisms. Specimen for Histopathology should be collected and sent separately. ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":53,"DictSpTypeName":"Tissue","DictSpVolumeId":112,"DictSpVolumeName":"1 - 5 g","TdTestInfoSpecificId":1408,"IsBeakerData":false},{"Id":678339,"SpecialInstructions":"Specimen source is required for processing. Larger volumes are preferred to improve recovery of fungal organisms. Specimen should be collected using sterile technique in a leakproof sterile screw-top container. If specimen volumes are small especially from lesion aspirates- instilling a small volume of sterile saline may aid collection. Specimen may be submitted in a sterile syringe only after removing needle and capping. Swabs are not preferred for fungal cultures; E-swabs are ONLY acceptable for hard-to-collect specimen sources such as ear canal. Specimen for Histopathology should be collected and sent separately.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":48,"DictSpTypeName":"Fluid, body","DictSpVolumeId":43,"DictSpVolumeName":"1-2 mL min (prefer 20-50 mL)","TdTestInfoSpecificId":1408,"IsBeakerData":false},{"Id":678340,"SpecialInstructions":"Corneal scrapings may be submitted in a sterile container but due to the scarcity of material, it is preferred that non-inhibitory fungal plates such as Potato Dextrose Agar (PDA) be inoculated at time of collection. Scrapings should be placed in two or three places on the plate, using an X or C shaped motion. Vitreous fluid may be submitted in a sterile container. If irrigation fluid used to aid in collection submit entire collection to aid in recovery of fungal organisms. ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":11,"DictSpCollectionTemperatureName":"See note","DictSpTransportTemperatureId":11,"DictSpTransportTemperatureName":"See note","DictSpTypeId":154,"DictSpTypeName":"Eye","DictSpVolumeId":154,"DictSpVolumeName":"Variable","TdTestInfoSpecificId":1408,"IsBeakerData":false},{"Id":678341,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1408,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":14404,"Description":"72 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1408,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14405,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1408,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14406,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1408,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1408,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3400,"PrimaryName":"Organism Identification, Nocardia","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false},{"TdTestInfoCommonId":2045,"PrimaryName":"AFB Susceptibility","IsRequired":false},{"TdTestInfoCommonId":4587,"PrimaryName":"Mold Susceptibility One Drug","IsRequired":false},{"TdTestInfoCommonId":3397,"PrimaryName":"Organism Identification, AFB","IsRequired":false}]},{"Id":2843,"LISCode":"FUNSUS","PrimaryName":"Yeast Susceptibility Testing","LISName":"Yeast Susceptibility Testing","EMRName":"Yeast Susceptibility Testing","EMRCode":"SQFUNSUS","LOINC":null,"RecommendedUse":"Used to determine the in vitro susceptibility of yeast organisms to select antifungal agents","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":964,"Aka":"Yeast MIC","TdTestInfoCommonId":2843},{"Id":2672,"Aka":"Yeast Susceptibility","TdTestInfoCommonId":2843},{"Id":15033,"Aka":"Amphotericin B","TdTestInfoCommonId":2843},{"Id":15034,"Aka":"Anidulafungin","TdTestInfoCommonId":2843},{"Id":15035,"Aka":"Azoles","TdTestInfoCommonId":2843},{"Id":15036,"Aka":"Caspofungin","TdTestInfoCommonId":2843},{"Id":15037,"Aka":"Cresemba","TdTestInfoCommonId":2843},{"Id":15038,"Aka":"Echinocandin","TdTestInfoCommonId":2843},{"Id":15039,"Aka":"Fluconazole","TdTestInfoCommonId":2843},{"Id":15040,"Aka":"Isavuconazole","TdTestInfoCommonId":2843},{"Id":15041,"Aka":"Itraconazole","TdTestInfoCommonId":2843},{"Id":15042,"Aka":"Micafungin","TdTestInfoCommonId":2843},{"Id":15043,"Aka":"Posaconazole","TdTestInfoCommonId":2843},{"Id":15044,"Aka":"Rezafungin","TdTestInfoCommonId":2843},{"Id":15045,"Aka":"Rezzayo","TdTestInfoCommonId":2843},{"Id":15046,"Aka":"Susceptibility testing","TdTestInfoCommonId":2843},{"Id":15047,"Aka":"Voriconazole","TdTestInfoCommonId":2843}],"TdBillingCommons":[{"Id":1127,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2843,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2843,"SpecialInfo":"Yeast susceptibility testing requires a pure, actively growing culture; mixed or non-viable isolates may lead to invalid results. Accurate species-level identification is essential, as clinical breakpoints vary by species. Testing may be delayed or limited if identification is not provided or not ordered concurrently. The standard antifungal panel does not include 5-fluorocytosine —if susceptibility to this agent  is clinically necessary, please contact the laboratory. MIC interpretations are based on the most recent CLSI guidelines. For antifungal agents lacking established breakpoints, only the MIC value is reported without categorical interpretation. As always, susceptibility results should be interpreted in the context of the patient’s clinical condition, site of infection, and therapeutic considerations, since MIC values alone may not fully predict treatment outcomes.","ClinicalInfo":"This test determines the antifungal susceptibility of rapidly growing, non-fastidious yeast isolates—including Candida and Cryptococcus—to a comprehensive panel of antifungal agents. It is performed on pure yeast cultures to support clinical decision-making and guide patient management.\nSusceptibility testing follows Clinical and Laboratory Standards Institute (CLSI) guidelines, using established breakpoints and interpretive criteria. The antifungal agents tested include amphotericin B, anidulafungin, caspofungin, fluconazole, isavuconazole, itraconazole, micafungin, posaconazole, rezafungin, and voriconazole. Note that 5-fluorocytosine is not included in this panel. Fluconazole and Micafungin will be reported routinely, Amphotericin B will be reported dependent on source. Other antifungals will be reported based on resistance seen to routinely reported antifungals or by request.\nTesting is performed using the TREK Sensititre™ YeastOne™ YO11 colorimetric microdilution broth method. Each susceptibility plate is pre-loaded with standardized concentrations of antifungal agents and a colorimetric growth indicator. After inoculating the plate with a standardized yeast suspension and incubating at 35°C for 24 to 48 hours (up to 72hours for Cryptococcus species), minimum inhibitory concentrations (MICs) are determined. MICs are identified as the lowest concentration of each antifungal agent that prevents visible yeast growth, as indicated by the absence of color change in the test medium. MIC values are interpreted using clinical breakpoints to categorize isolates as susceptible, intermediate, susceptible-dose dependent, or resistant, in accordance with current guidelines from the Clinical and Laboratory Standards Institute (CLSI).\n\nWhen CLSI has not established clinical breakpoints for a specific antifungal agent, only the MIC value is reported without an interpretive category. For further information on MIC interpretation and methodology, consult the most recent CLSI documents related to antifungal susceptibility testing of yeasts.","ClinicalReference":"Pappas PG, Kauffman CA, Andes DR, et al. Clinical Practice Guideline for the Management of Candidiasis: 2016 Update by the Infectious Diseases Society of America. Clin Infect Dis. 2016;62(4):e1-e50\n\nCLSI. Performance standards for antifungal susceptibility testing of yeast, 3rd ed. CLSI supplement M27M44S. Clinical Laboratory Standards Institute; 2022.  \n\nCLSI. Reference Method for Broth Dilution Antifungal Susceptibility Test of Yeasts, 4th ed. CLSI standard M27. Clinical Laboratory Standards Institute; 2017.  ","ClinicalLimitation":"Antifungal susceptibility results do not always correlate with clinical outcomes, as factors like immune status, infection site, drug pharmacokinetics, and biofilm presence can influence treatment success. CLSI breakpoints are limited to select yeast species and antifungal agents; for others, only MIC values are reported without interpretation. Some yeast species, show variable or dose-dependent susceptibility, complicating interpretation. Testing is performed under standardized conditions and may not reflect in vivo environments and evaluation of MIC may be impacted by methodology. Biofilm-related resistance is not assessed, and results from mixed or contaminated cultures may be unreliable. Additionally, the 24–48 hour turnaround time may delay therapy decisions. Results should be interpreted in the context of the full clinical picture.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1410,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2843,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1410,"IsStat":false,"Comments":null,"DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":871,"DictMethodologyId":111,"TdTestInfoSpecificId":1410,"DictMethodology":{"Id":111,"Name":"Microtiter Dilution","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1410,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":149,"DictDaysPerformed":"Sun - Sat","DictReported":"11 days"},"TdSpecimenRequirements":[{"Id":3632,"SpecialInstructions":"The organism must be in pure culture and actively growing. Do not submit mixed cultures.\nSpecimen source is required. Organism identification is also required unless a concurrent identification test has been ordered. If an organism identification is not provided an, organism identification, yeast (OIDYEA) will be ordered. ","LogicalOperation":null,"DictSpContainerId":18,"DictSpContainerName":"Agar slant","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":21,"DictSpTypeName":"Isolate of organism","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":1410,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":4839,"Description":"Preferred","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1410,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":4840,"Description":"Acceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1410,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":4841,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1410,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1410,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2844,"LISCode":"FUNCSF","PrimaryName":"Fungal CSF culture and CAD","LISName":"Fungal CSF culture ","EMRName":"Fungal CSF culture and CAD","EMRCode":"SQFUNCSF","LOINC":"11475-1","RecommendedUse":"Diagnosing fungal infection from cerebrospinal fluid (CSF) by culture and Cryptococcus antigen detection (CAD)\n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6789,"Aka":"Culture, Fungus CSF and Cryptococcus Antigen Detec","TdTestInfoCommonId":2844},{"Id":14429,"Aka":"Cerebrospinal fluid","TdTestInfoCommonId":2844},{"Id":14430,"Aka":"Cryptococcus","TdTestInfoCommonId":2844},{"Id":14431,"Aka":"Cryptococcus Ag Titer","TdTestInfoCommonId":2844},{"Id":14432,"Aka":"Cryptococcus antigen","TdTestInfoCommonId":2844},{"Id":14433,"Aka":"CSF fungal","TdTestInfoCommonId":2844},{"Id":14437,"Aka":"Mycology","TdTestInfoCommonId":2844},{"Id":14440,"Aka":"Cryptococcal antigen detection","TdTestInfoCommonId":2844}],"TdBillingCommons":[{"Id":9796,"CptCode":"87102","Quantity":1,"Tmid":"30600065","CclTechComponentPrice":55.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18721,"CptCode":"87015","Quantity":1,"Tmid":"30606300","CclTechComponentPrice":44.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Fluid Concentration","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18722,"CptCode":"87015","Quantity":1,"Tmid":"30608585","CclTechComponentPrice":40.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Cytospin","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18725,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18726,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18727,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":18733,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":93.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":19407,"CptCode":"87899","Quantity":1,"Tmid":"30601440","CclTechComponentPrice":105.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, CAD","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2844,"IsBeakerData":false},{"Id":19408,"CptCode":"87899","Quantity":1,"Tmid":"30201515","CclTechComponentPrice":105.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, CAD Titer","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":2844,"IsBeakerData":false}],"TdIncludes":[{"Id":25921,"TestName":"Specimens may include some pre-processing steps such as concentration to aid in the recovery of fungal organisms and Cryptococcal antigen detection","Rank":1,"TdTestInfoCommonId":2844}],"TdLaboratoryCommon":{"TdTestInfoCommonId":2844,"SpecialInfo":"Clinical specimens for fungal cultures are processed and plated on selective fungal media to optimize recovery of fungal organisms. Cultures are incubated for 28 days; negative results are auto-updated daily. Any fungal organisms recovered will be isolated and identified by various methods.  Additional CPT codes may be applicable for recovery and identification of fungal organisms -  87015 - concentration of specimen, 87102 Fungal culture, 87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing. Fungal susceptibility testing for yeast ONLY will be performed (CPT 87186). Yeast susceptibility testing is determined by colorimetric microdilution broth. A standardized inoculation of test organism is incubated with appropriate dilutions of antifungal agents; minimum inhibitory concentration (MIC) are determined by inhibition of growth at the lowest antifungal concentration. MIC are determined and interpreted according to CLSI standards. Filamentous mold susceptibility testing is a send-out test and can be requested by contacting the lab. \n","ClinicalInfo":"Fungal cultures are not routinely performed on CSF due to the low probability of fungal infections except Cryptococcus species which have a predilection for CNS infections. CSF is the specimen of choice for detection of cryptococcal meningitis in adults and Candida meningitis in children. Cryptococcus antigen test will always be performed on CSF specimens as it is a rapid and sensitive diagnostic method for detection of Cryptococcal meningitis. Declining titers may indicate regression of infection. However, monitoring titers to cryptococcal antigen should not be used as a test of cure or to guide treatment decisions. Low-level titers may persist for extended periods of time following appropriate therapy and resolution of infection","ClinicalReference":"Perfect JR, Dismukes WE, Dromer F, et al: Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2010 Feb 1;50(3):291-322\nWestblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. \n","ClinicalLimitation":"CSF specimens submitted for initial diagnosis that test positive by the lateral flow assay, should also be submitted for routine fungal culture. Culture can aid in differentiating between the 2 common Cryptococcus species causing disease (Cryptococcus neoformans and Cryptococcus gattii) and can be used for antifungal susceptibility testing, if necessary. CAD test should not be used as a screening procedure for the general population. Bloody lumbar puncture and/or contamination of the cerebrospinal fluid (CSF) specimen with serum, other yeast infections such as Trichosporon may lead to a positive Cryptococcus antigen result. CAD titers can be utilised to monitor therapy but titers acquired by different assays are not interchangeable; titers acquired by lateral flow assay may be higher than other antigen assays such as agglutination tests. Extremely high concentrations of cryptococcal antigen can result in negative CAD results. If high burden is suspected, sample may be diluted to resolve false negative. Please call the lab/medical director in such instances. \n","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1411,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2844,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1411,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7598,"DictMethodologyId":224,"TdTestInfoSpecificId":1411,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1411,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":148,"DictDaysPerformed":"Sun - Sat","DictReported":"6 weeks"},"TdSpecimenRequirements":[{"Id":28593,"SpecialInstructions":"Sterile technique should be used to collect specimen to decrease contamination issues. Larger volumes of specimen are preferred and concentrated to aid in recovery of fungal organisms. Grossly hemolysed sample may give a false positive result on CAD testing and as such will be rejected for the antigen test but fungal cultures will be set up. ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1411,"IsBeakerData":false},{"Id":28595,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1411,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":16300,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1411,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16301,"Description":"7 days (72 hours preferred for Cryptococcus Antigen test)","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1411,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":16302,"Description":"Indefinitely for CADs, Unacceptable for culture","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1411,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1411,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":2045,"PrimaryName":"AFB Susceptibility","IsRequired":false},{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3397,"PrimaryName":"Organism Identification, AFB","IsRequired":false},{"TdTestInfoCommonId":3400,"PrimaryName":"Organism Identification, Nocardia","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false},{"TdTestInfoCommonId":4587,"PrimaryName":"Mold Susceptibility One Drug","IsRequired":false}]},{"Id":2848,"LISCode":"GABA","PrimaryName":"Gabapentin","LISName":"Gabapentin","EMRName":"Gabapentin, serum or plasma","EMRCode":"SQGABA","LOINC":"9738-6","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9303,"Aka":"Gabarone","TdTestInfoCommonId":2848},{"Id":9304,"Aka":"Neurontin","TdTestInfoCommonId":2848}],"TdBillingCommons":[{"Id":19052,"CptCode":"80171","Quantity":1,"Tmid":"30103555","CclTechComponentPrice":104.00,"CclProfComponentPrice":null,"TestNameForCdm":"Gabapentin","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2848,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2848,"SpecialInfo":"Collect the specimen before the next dose (trough).  \nUnacceptable conditions: Whole blood, gel separator tubes.","ClinicalInfo":"Monitoring concentrations in serum or plasma to assess drug therapy and patient compliance.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1413,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2848,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1413,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9575,"DictMethodologyId":265,"TdTestInfoSpecificId":1413,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1413,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - Sat","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":36911,"SpecialInstructions":"Timing of specimen collection: Pre-dose (trough). Do not collect in a gel separator tube. Centrifuge and transfer the plasma/serum to a plastic CCL tube within 2 hours of collection and refrigerate. Transport and store at refrigerated temperature.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1413,"IsBeakerData":false},{"Id":36912,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1413,"IsBeakerData":false},{"Id":36913,"SpecialInstructions":"Timing of specimen collection: Pre-dose (trough). Do not collect in a gel separator tube. Centrifuge and transfer the plasma/serum to a plastic CCL tube within 2 hours of collection and refrigerate. 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Specimen must arrive at performing lab within 48 hours of collection. New York State approved.","ClinicalInfo":"Useful for diagnosis of galactokinase deficiency. Galactokinase (GALK) deficiency is the second most common form of galactosemia, affecting approximately 1/250,000 live births, with a higher frequency in the Romani population. Individuals with GALK deficiency have a milder clinical presentation than that seen in patients with classic galactosemia, galactose-1-phosphate uridyltransferase (GALT) deficiency. The major clinical manifestation is bilateral juvenile cataracts. GALK deficiency is treated with a lactose-restricted diet. Early treatment may prevent or reverse the formation of cataracts. In GALK deficiency, erythrocyte galactose-1-phosphate levels are generally normal and plasma galactose levels are generally elevated. The diagnosis is established by demonstrating deficient GALK enzyme activity in erythrocytes. Testing for GALK deficiency should be performed when there is a suspicion of galactosemia, either based upon the patient's clinical presentation or laboratory studies and GALT deficiency has been excluded. Specimens sent for GALT analysis may be used for GALK testing if the original specimen was received in the laboratory within 48 hours of draw. GALK deficiency is caused by mutations in the GALK1 gene. Gene analysis is available from some commercial laboratories. Cautions: It is important to notify the laboratory if the patient has been transfused prior to specimen collection. The results of testing performed in erythrocytes are invalid following a transfusion, including analysis of enzymes, biochemical phenotyping, or galactose-1-phosphate. \n\n\n \n\n\n\n\n\n\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1416,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2850,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1416,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7579,"DictMethodologyId":265,"TdTestInfoSpecificId":1416,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null},{"Id":7580,"DictMethodologyId":530,"TdTestInfoSpecificId":1416,"DictMethodology":{"Id":530,"Name":"Enzyme Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1416,"DictDaysPerformedId":24,"DictHoursPerformedId":null,"DictReportedId":78,"DictDaysPerformed":"Mon","DictReported":"9 - 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","LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":1425,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26627,"Description":"1 day","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1425,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26628,"Description":"90 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1425,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26629,"Description":"1 day","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1425,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1425,"TestCode":null,"IsReportable":false,"DictVendorId":71,"DictVendor":{"Id":71,"Name":"LabCorp","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4521,"LISCode":"HELMIN","PrimaryName":"Allergen, Helminthosporium halodes IgE","LISName":"ALGN Helminth halodes IgE","EMRName":"ALGN Helminth halodes IgE","EMRCode":"SQHELMIN","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12987,"Aka":"Setomelanomma rostrata","TdTestInfoCommonId":4521}],"TdBillingCommons":[{"Id":15981,"CptCode":"86003","Quantity":1,"Tmid":"30200030","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"ALLERGEN IGE QUANT/SEMI EA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4521,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4521,"SpecialInfo":"An extra 50uL will be required for each additional allergen ordered.","ClinicalInfo":"","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1426,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2011-12-12T00:00:00","CreatedById":393,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4521,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1426,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12623,"DictMethodologyId":166,"TdTestInfoSpecificId":1426,"DictMethodology":{"Id":166,"Name":"Fluorescent Enzyme Immunoassay (FEIA) by ImmunoCAP","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1426,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":49629,"SpecialInstructions":"An extra 50uL will be required for each additional allergen ordered. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1426,"IsBeakerData":false},{"Id":49630,"SpecialInstructions":"Submitting the minimum volume will not allow for repeat testing or addons. Required volume of 0.5mL is preferred when possible.","LogicalOperation":"Or","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1426,"IsBeakerData":false},{"Id":49631,"SpecialInstructions":null,"LogicalOperation":"Or","DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1426,"IsBeakerData":false},{"Id":49632,"SpecialInstructions":null,"LogicalOperation":"Or","DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1426,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28516,"Description":"1 day","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1426,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28517,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1426,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28518,"Description":"30 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1426,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1426,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2865,"LISCode":"GCCT","PrimaryName":"Gonorrhea/Chlamydia NAAT","LISName":"Gonorrhea/Chlamydia NAAT","EMRName":"Gonorrhea/Chlamydia NAAT","EMRCode":"SQGCCT","LOINC":"36902-5","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13637,"Aka":"GCCAMP","TdTestInfoCommonId":2865},{"Id":14049,"Aka":"CT","TdTestInfoCommonId":2865},{"Id":14050,"Aka":"CTAMP","TdTestInfoCommonId":2865},{"Id":14051,"Aka":"GC","TdTestInfoCommonId":2865},{"Id":14053,"Aka":"GCAMP","TdTestInfoCommonId":2865},{"Id":14056,"Aka":"UCT","TdTestInfoCommonId":2865},{"Id":14057,"Aka":"UGC","TdTestInfoCommonId":2865},{"Id":14058,"Aka":"UGCCT","TdTestInfoCommonId":2865},{"Id":14735,"Aka":"chlamydia trachomatis","TdTestInfoCommonId":2865},{"Id":14736,"Aka":"GCCT","TdTestInfoCommonId":2865},{"Id":14737,"Aka":"gonococcus","TdTestInfoCommonId":2865},{"Id":14738,"Aka":"neisseria","TdTestInfoCommonId":2865},{"Id":14739,"Aka":"neisseria gonorrhoeae","TdTestInfoCommonId":2865},{"Id":14740,"Aka":"SQGCCT","TdTestInfoCommonId":2865}],"TdBillingCommons":[{"Id":19588,"CptCode":"87494","Quantity":1,"Tmid":"30608925","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Amplified Probe, GC/CT","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2865,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2865,"SpecialInfo":"Microbiology Preanalytic Guidance: http://portals.ccf.org/plmi/Laboratory-Medicine/Microbiology-Specimen-Collection-Transport-Information.\n\nUp to two tests can be run on a single Aptima Multitest Swab specimen (ie. GCCT+TRVAMP) - if specimen sources have been correctly selected, the shared tests will print on the same label. Do not place more than one label on a single collection tube. \n\nCommon reasons for specimen rejection:\n1. Inappropriate collection device for source selected.\n2. Transport tubes containing a cleaning swab or more than 1 swab.\n3. Overfilled or underfilled urine transport tubes.\n4. Collection device expired prior to specimen collection.\n\nRelated alternative orders:\n1. MISCGC: in-house culture to recover GC for susceptibility testing (only suggested following positive NAAT if treatment failure is suspected).\n2. NGNAAO, CTNAAO, or CTNGAO: sendout GC, CT, or GC+CT NAAT for non-FDA approved sources including ocular, nasopharyngeal, and peritoneal.\n3. CTRACH: sendout CT culture for non-FDA approved sources including ocular, nasopharyngeal, and peritoneal.\n\n","ClinicalInfo":"Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (GC) infections are two of the most common sexually transmitted infections (STI) worldwide. CDC STI Treatment Guidelines include testing and screening recommendations for CT and GC and provide guidance on testing methodology and frequency, as well as specimen types for specific patient populations. The CDC recommends the use of nucleic acid amplification tests (NAATs) for the detection of CT and GC in patients with and without symptoms. \n\nThe Aptima Combo 2 assay is an FDA-cleared second generation NAAT that utilizes target capture, Transcription-Mediated Amplification (TMA), and Dual Kinetic Assay (DKA) technologies. The Aptima Combo 2 assay on the Panther system qualitatively detects CT and/or GC rRNA in clinician-collected endocervical, PreservCyt Solution liquid Pap specimens, vaginal, throat, rectal, and male urethral swab specimens; patient-collected vaginal swab specimens, and female and male urine specimens from symptomatic and asymptomatic individuals. The assay has been modified and additionally validated to accept rectal swabs self-collected by patients in a healthcare setting.\n\nIn 2019, novel C. trachomatis variants were discovered which contain point mutations affecting detection by the original version of the Aptima Combo 2 assay. Variant strains of chlamydia with mutations affecting diagnostic test performance have been reported previously and are a natural product of microbial evolution. The updated version of the Aptima Combo 2 assay provides detection coverage for the variant strains of C. trachomatis that emerged in 2019.","ClinicalReference":"Workowski KA, Bachmann LH, Chan PA, Johnston CM, Muzny CA, Park I, Reno H, Zenilman JM, Bolan GA. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187. doi: 10.15585/mmwr.rr7004a1. PMID: 34292926; PMCID: PMC8344968.\n","ClinicalLimitation":"1. The performance of the assay has not been evaluated in patients <14 years of age.\n2. The assay is not intended for the evaluation of suspected sexual abuse or for other medico-legal indications. For those patients for whom a false positive result may have adverse psycho-social impact, the CDC recommends retesting.\n3. Therapeutic failure or success cannot be determined with the assay since nucleic acid may persist following appropriate antimicrobial therapy.\n4. A negative result does not preclude a possible infection because results are dependent on adequate specimen collection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or target levels below the assay limit of detection.\n5. First catch female urine specimens are acceptable but may detect up to 10% fewer CT/GC infections when compared with vaginal and endocervical swab specimens.\n6. The effects of tampon use, douching, and specimen collection variables have not been assessed for their impact on assay detection.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1427,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2865,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1427,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13417,"DictMethodologyId":81,"TdTestInfoSpecificId":1427,"DictMethodology":{"Id":81,"Name":"Transcription-Mediated Amplification","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1427,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Sun","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":51397,"SpecialInstructions":"Endocervical Unisex (white tube blue swab): Remove excess mucus from cervical os and surrounding mucosa using the white cleaning swab, then DISCARD. Insert blue swab into the endocervical canal and gently rotate clockwise for 10-30 seconds. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":"Or","DictSpContainerId":104,"DictSpContainerName":"APTIMA Collection Unisex swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":147,"DictSpTypeName":"Endocervical","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":51398,"SpecialInstructions":"Male Urethral Unisex (white tube blue swab): The patient should not have urinated for at least 1 hr prior to sample collection. Insert the blue swab 2-4 cm into the urethra. Gently rotate the swab clockwise for 2-3 seconds in the urethra. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":"Or","DictSpContainerId":104,"DictSpContainerName":"APTIMA Collection Unisex swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":62,"DictSpTypeName":"Urethral","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":51399,"SpecialInstructions":"Vaginal Multitest (orange tube pink swab): A vaginal swab is the recommended specimen for female patients who are clinically suspected of having a chlamydial or gonococcal infection. Carefully insert the swab into the vagina about 2 inches past the introitus and gently rotate the swab for 10-30 seconds. Make sure the swab touches the vaginal walls so that moisture is absorbed by the swab. Vaginal swab specimens may be patient-collected in a clinical setting when a pelvic exam is not otherwise indicated (https://www.hologic.com/package-inserts/swab-collection-instructions-vaginal-main-english#4257225834-454981651). Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":"Or","DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":51400,"SpecialInstructions":"Rectal Multitest (orange tube pink swab): Carefully insert the swab into the rectum about 1-2 inches past the anal margin and gently rotate the swab for about 5-10 seconds. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":"Or","DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":73,"DictSpTypeName":"Rectal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":51401,"SpecialInstructions":"Throat Multitest (orange tube pink swab): Carefully insert swab into the throat ensuring contact with bilateral tonsils (if present) and the posterior pharyngeal wall, then withdraw the swab without touching the inside of the cheeks or tongue. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":"Or","DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":70,"DictSpTypeName":"Throat","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":51402,"SpecialInstructions":"PreservCyt Solution (ThinPrep) is an acceptable specimen  when added onto a ThinPrep Pap Test and no dedicated vaginal or endocervical swab specimens are available. It is not a recommended due to lower test sensitivity compared to other specimen types. For this reason, it is not available as a selectable specimen source/type during order entry, only as a laboratory add-on. In order to place an order on this specimen type, you must place a call to lab client services. \n\nIf consulted prior to specimen collection, lab client services should advise the provider to collect a separate dedicated Vaginal Multitest Swab for optimal test performance characteristics. If consulted after specimen collection, lab client services should assist the provider in placing an add on order with \"Fluid, Cervix\" as the specimen source, and have cytology perform the aliquot as below prior to cytology testing.\n\nPrior to cytology testing and within 30 days of collection, cytology will transfer a 1 mL aliquot into an APTIMA Specimen Transfer Tube. The specimen must have been stored at 2-30C.","LogicalOperation":null,"DictSpContainerId":108,"DictSpContainerName":"Cytyc PreservCyt solution (Thin Prep)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":148,"DictSpTypeName":"Cervical","DictSpVolumeId":102,"DictSpVolumeName":"Unspecified","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":677496,"SpecialInstructions":"First-catch urine is the optimal specimen for screening asymptomatic male patients. Urine may also be used for testing any symptomatic patient, but vaginal specimens are preferred when available due to greater test sensitivity. \n\nThe patient should not have urinated for at least 1 hour prior to specimen collection. The patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container. \n\nTransfer 2 mL of urine into the Aptima urine specimen transport tube using the disposable pipette provided within 24 hours of collection. Close the tube tightly. Work with one specimen at a time. \n\nThe correct volume of urine has been added when the fluid level is between the black fill lines (window) on the urine transport tube. Do not overfill or underfill the APTIMA Urine transport tube.","LogicalOperation":"Or","DictSpContainerId":107,"DictSpContainerName":"APTIMA Urine specimen collection kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":181,"DictSpTypeName":"Urine, first-catch","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1427,"IsBeakerData":false},{"Id":677499,"SpecialInstructions":"First-catch urine is the optimal specimen for screening asymptomatic male patients. Urine may also be used for testing any symptomatic patient, but vaginal specimens are preferred when available due to greater test sensitivity. \n\nThe patient should not have urinated for at least 1 hour prior to specimen collection. The patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container. ","LogicalOperation":"Or","DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":181,"DictSpTypeName":"Urine, first-catch","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1427,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29520,"Description":"15⁰C to 30⁰C.  \n\nSwab in APTIMA transport media: 60 days;  \nUrine in APTIMA transport media: 30 days;\nUrine unprocessed: 24 hours;\nThinPrep PreservCyt solution in APTIMA transport media: 14 days; \nThinPrep PreservCyt unprocessed: 30 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1427,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29521,"Description":"-20⁰C to -70⁰C\n\nSwab in APTIMA transport media: 12 months;  \nUrine in APTIMA transport media: 12 months;\nUrine unprocessed: Unacceptable;\nThinPrep PreservCyt solution in APTIMA transport media: 12 months; \nThinPrep PreservCyt unprocessed: Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1427,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29522,"Description":"2⁰C to 8⁰C\n\nSwab in APTIMA transport media: 60 days;  \nUrine in APTIMA transport media: 30 days;\nUrine unprocessed: 24 hours;\nThinPrep PreservCyt solution in APTIMA transport media: 30 days; \nThinPrep PreservCyt unprocessed: 30 days","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1427,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1427,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2868,"LISCode":"GENTPO","PrimaryName":"Gentamicin, Post Dose","LISName":"Gentamicin, Post Dos","EMRName":"Gentamicin Post Dose","EMRCode":"SQGENTPO","LOINC":"3663-2","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13109,"CptCode":"80170","Quantity":1,"Tmid":"30100310","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"GENTAMICIN ASSAY","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":2868,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":2868,"SpecialInfo":"Do not collect in a gel separator tube. \n\nThe aminoglycoside sisomicin cross-reacts with the QMS Gentamicin assay due to its structural similarity. Therefore, the results of this assay cannot be used to accurately quantify gentamicin serum or plasma levels in patients on sisomicin in combination with gentamicin.","ClinicalInfo":"Draw 30 minutes after completion of infusion","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1428,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2868,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1428,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10284,"DictMethodologyId":533,"TdTestInfoSpecificId":1428,"DictMethodology":{"Id":533,"Name":"Kinetic Interaction of Microparticles in a Solution","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1428,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":39765,"SpecialInstructions":"Do not collect in a gel separator tube. Centrifuge and transfer plasma/serum to a CCL tube and refrigerate. 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REQUIRED BY FEDERAL LAW: Requisition must be completely filled out with date of procedure, patient's name, date of birth or age, clinical history,  clinician, location of procedure, specimen submitted, initial of the nurse who assisted with the procedure and any requests for special procedures (i.e. FS).","ClinicalInfo":"Evaluation of cardiac transplant rejection  Interpretation by Pathologist.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1468,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2934,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1468,"IsStat":false,"Comments":null,"DictPerformingLabId":13,"DictPerformingLab":{"Id":13,"Name":"Anatomic Pathology (x46781)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":966,"DictMethodologyId":213,"TdTestInfoSpecificId":1468,"DictMethodology":{"Id":213,"Name":"Microscopy","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1468,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":77,"DictDaysPerformed":"Mon - Fri","DictReported":"1 day"},"TdSpecimenRequirements":[{"Id":4026,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":87,"DictSpTypeName":"Muscle, cardiac (fresh)","DictSpVolumeId":91,"DictSpVolumeName":"Several mm2 biopsies","TdTestInfoSpecificId":1468,"IsBeakerData":false},{"Id":4027,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":81,"DictSpTypeName":"Paraffin block","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":1468,"IsBeakerData":false}],"TdSpecimenStabilities":[],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1468,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":2947,"LISCode":"HPYLRI","PrimaryName":"Helicobacter pylori Ab, IgG","LISName":"Helico pylori Ab","EMRName":"Antibody Helicobacter pylori IgG","EMRCode":"SQHPYLRI","LOINC":"7902-0","RecommendedUse":"Helicobacter pylori IgG antibody test is used as an aid in diagnosis of recent or past infection with Helicobacter pylori. Other test methodologies such H. pylori stool antigen test or Urea Breath Test should be considered if current infection is clinically suspected. 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Bacterial contamination of samples may affect the test results.\nDo not heat inactivate serum. \nHeterophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays. \nPatients routinely exposed to animals or to animal serum products can be prone to this interference and anomalous values may be observed. \nThe assay has not been evaluated in a pediatric population.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1474,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2947,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1474,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12986,"DictMethodologyId":164,"TdTestInfoSpecificId":1474,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1474,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - 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Phenylketonurics: Contains Phenylalanine\nHypersensitivity: Patients who are hypersensitive to mannitol, citric acid, or Aspartame should avoid taking the drug solution as the drug solution contains these ingredients.\nRisk of Aspiration: Use with caution in patients with difficulty in swallowing or who may be at high risk for aspiration due to medical or physical conditions.\nPregnancy/Lactation: The safety of the BreathTek UBT kit during pregnancy and lactation is not established.\nIf particulate matter is visible in the reconstituted Pranactin-Citric solution after thorough mixing, the solution should not be used.\nFast at least 1 hour prior to administering the BreathTek UBT.\nPatient should not have taken antibiotics, proton pump inhibitors or bismuth preparations within 2 weeks prior to administrating the BreathTek UBT.\nThe effect of histamine 2-receptor antagonists may reduce urease activity on urea breath tests. They may be discontinued for 24-48 hours before the BreathTek UBT.\nDo not use any straw other than the straw provided in the kit.\nIf repeat testing is needed, BreathTek UBT can be administered the following day.\nThe UBT kits must be stored per package insert. Do not use past the stated expiration date. Additional kits can be obtained by contacting the Immunopathology lab at 216-444-9033.\n","ClinicalInfo":"A negative result does not rule out the possibility of H. pylori infection. If clinical signs are suggestive of H. pylori infection, retest with a new sample or an alternate method.\nDespite very high specificity, false positive results may occur due to other gastric organisms such as H. heilmanni as well as in patients with hypo- or achlorhydria. Despite very high sensitivity, false negative results may occur in patients who have received antibiotics, proton pump inhibitors, or bismuth preparations. Clinical correlation is required.                    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Approximately 85% of patients with hereditary hemochromatosis are homozygous for the C282Y mutation and approximately 4% are compound heterozygous for the C282Y and H63D mutations.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1479,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2005-11-15T00:00:00","CreatedById":359,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":2954,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1479,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service 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The HbA1c test should not be used to replace glucose testing in pediatric patients, pregnant women, or patients with Type 1 diabetes.  In cases of rapidly evolving Type 1 diabetes, the increase of HbA1c values might be delayed compared to the acute increase in glucose concentrations. In these conditions, diabetes mellitus must be diagnosed based on plasma glucose concentration and/or the typical clinical symptoms.  The HbA1c test should not be used to diagnose diabetes during pregnancy or to diagnose gestational diabetes. HbA1c reflects the average blood glucose levels over the preceding 3 months (the average life of a red blood cell), and therefore may be falsely low during pregnancy or any other condition associated with recent onset of hyperglycemia and/or decreased red cell survival.  The oral glucose tolerance test (OGTT) and/or fasting blood glucose test is performed instead for gestational diabetes diagnosis and maintenance.  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","LogicalOperation":"And","DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":97,"DictSpVolumeName":"100 mL","TdTestInfoSpecificId":1504,"IsBeakerData":false},{"Id":36214,"SpecialInstructions":"CSF","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1504,"IsBeakerData":false},{"Id":36215,"SpecialInstructions":"Urine","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1504,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20513,"Description":"48 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1504,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20514,"Description":"Indefinitely","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1504,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20515,"Description":"2 weeks","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1504,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1504,"TestCode":null,"IsReportable":false,"DictVendorId":2,"DictVendor":{"Id":2,"Name":"National Prion Disease Center","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":654,"Title":"National Prion Disease Test Request Form","FileName":"NationalPrionDiseaseTestRequestForm","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":4013,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":4118,"LISCode":"GASTST","PrimaryName":"Gastrin Secretin Stimulation","LISName":"Gastrin Secretin Stm","EMRName":"Gastrin Secretin Stimulation","EMRCode":"SQGASTST","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12479,"CptCode":"82938","Quantity":4,"Tmid":"30102215","CclTechComponentPrice":116.00,"CclProfComponentPrice":null,"TestNameForCdm":"%GASTST GASTRIN STIMX4","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4118,"IsBeakerData":false},{"Id":12480,"CptCode":"82941","Quantity":1,"Tmid":"30102225","CclTechComponentPrice":95.00,"CclProfComponentPrice":null,"TestNameForCdm":"%GASTST GASTRIN","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4118,"IsBeakerData":false}],"TdIncludes":[{"Id":17941,"TestName":"Gastrin at baseline","Rank":1,"TdTestInfoCommonId":4118},{"Id":17942,"TestName":"Gastrin at 4 timepoints post stimulation","Rank":2,"TdTestInfoCommonId":4118}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4118,"SpecialInfo":"Patients taking a Biotin dose of up to 5 mg/day should refrain from taking Biotin for 4 days prior to sample collection. Patients taking a Biotin dose > 5 mg/day to 10 mg/day should refrain from taking Biotin for 7 days prior to sample collection. Patients taking a Biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken.Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.","ClinicalInfo":"For diagnostic purposes, the results obtained should always be used in combination with the clinical exam, patient medical history, and other findings.","ClinicalReference":"","ClinicalLimitation":"Lipemic,icteric or grossly contaminated samples may give erroneous results.\nHemolyzed samples may indicate mistreatment of a specimen before receipt in the laboratory; hence the results should be interpreted with caution.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1523,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2007-07-10T00:00:00","CreatedById":389,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4118,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1523,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9796,"DictMethodologyId":164,"TdTestInfoSpecificId":1523,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1523,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":37814,"SpecialInstructions":"Collect separate samples for baseline and for each of the four timepoints post stimulation. Aliquot and freeze without delay.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1523,"IsBeakerData":false},{"Id":37815,"SpecialInstructions":"For each specimen collected.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1523,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21551,"Description":"30 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1523,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21552,"Description":"6 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1523,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1523,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4538,"LISCode":"NMEN","PrimaryName":"Neisseria meningitidis Tetravalent Antibodies, IgG (Vaccine Response)","LISName":"Neisseria meningitidis Tetravalent Antibodies, IgG (Vaccine Response)","EMRName":"Neisseria meningitidis Tetravalent Antibodies, IgG (Vaccine Response)","EMRCode":"SQNMEN","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9410,"Aka":"Neisseria meningitidis Tetravalent Antibodies","TdTestInfoCommonId":4538}],"TdBillingCommons":[{"Id":18803,"CptCode":"86741","Quantity":4,"Tmid":"30214805","CclTechComponentPrice":71.00,"CclProfComponentPrice":null,"TestNameForCdm":"N. 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This test is New York state approved.\n","ClinicalInfo":"This test is useful to assess immunocompetence following Neisseria meningitidis vaccination. To assess suspected immunodeficiency, use pre- and postvaccination serology. Do not use for diagnosis of infection or serotyping.\nResponder status is determined according to the ratio of the one month post-vaccination concentration to pre-vaccination concentration of IgG antibodies to N. meningitidis (Types A, C, Y, and W-135) as follows:\n1. If the one month post-vaccination concentration is less than 3.0 µg/mL, the patient is considered to be a non-responder.\n2. If the one-month post-vaccination concentration is greater than or equal to 3.0 µg/mL, a patient with a ratio of greater than or equal to 4 is a good responder, a ratio of 2-4 is a weak responder, and a ratio of less than 2 is considered a non-responder.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1524,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2012-01-09T00:00:00","CreatedById":445,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4538,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1524,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13610,"DictMethodologyId":14,"TdTestInfoSpecificId":1524,"DictMethodology":{"Id":14,"Name":"Quantitative Multiplex Bead Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1524,"DictDaysPerformedId":24,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Mon","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":37312,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube. 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Legionella species are found naturally in freshwater environments and can cause outbreaks when they grow in human-made water systems like indoor plumbing systems and cooling towers. The diseases associated with Legionella infection, known collectively as legionelloses, are generally caused by exposure to such contaminated water. The rapid and accurate detection of Legionella species in lower respiratory specimens is important for tailoring antimicrobial therapy and for epidemiologic investigation. Bacteriologic culture of these gram-negative bacilli requires specialized media, and is slow and relatively insensitive compared to molecular methods. Legionella urine antigen testing is a rapid and less-invasive method for diagnosis, but is only reliably positive in Legionella pneumophila serogroup 1 (sg1) infections. \n\nReal-time polymerase chain reaction (RT-PCR) is a fast and sensitive method to detect Legionella species in respiratory samples. This multiplex RT-PCR assay originally published by the Centers for Disease Control (CDC) simultaneously detects Legionella species, and differentiates between Legionella species (ssrA gene), L. pneumophila (mip gene), and L. pneumophila serogroup 1 (wzm gene).","ClinicalReference":"Benitez AJ, Winchell JM. Clinical application of a multiplex real-time PCR assay for simultaneous detection of Legionella species, Legionella pneumophila, and Legionella pneumophila serogroup 1. J Clin Microbiol. 2013 Jan;51(1):348-51. doi: 10.1128/JCM.02510-12. Epub 2012 Nov 7. Erratum in: J Clin Microbiol. 2014 Feb;52(2):709. PMID: 23135949.","ClinicalLimitation":"This assay is intended for use as a lab-developed test for the qualitative simultaneous detection and differentiation of Legionella spp., L. pneumophila and L. pneumophila sg1 from lower respiratory specimens. It is meant to be used as an aid in diagnosis of legionellosis, in conjunction with other clinical and laboratory information. Based on the methodology, the assay may be falsely negative in cases with very low bacterial burden, or caused by uncommon Legionella species. It may be falsely positive in cases of upper airway colonization/contamination, or transient/remnant presence of nucleic acid. Specimens positive for Legionella spp. by this assay will be reflexed to culture for attempted isolation of the organism, with results reported separately.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1525,"ActiveDate":"2010-03-23T00:00:00","CreatedOn":"2009-05-07T00:00:00","CreatedById":270,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4241,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1525,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7206,"DictMethodologyId":168,"TdTestInfoSpecificId":1525,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1525,"DictDaysPerformedId":17,"DictHoursPerformedId":null,"DictReportedId":167,"DictDaysPerformed":"6 days per week","DictReported":"3 days"},"TdSpecimenRequirements":[{"Id":27151,"SpecialInstructions":"Collect and submit the specimen in a sterile container (ie. 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If aliquoting is necessary, sterile tubes must be used.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":14,"DictSpTypeName":"Aspirate, tracheal","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1525,"IsBeakerData":false},{"Id":677411,"SpecialInstructions":"Collect and submit the specimen in a sterile container (ie. Oracle #1012787, Covidien #2200SA). 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Collect the anal rectal cytology by using water, moistened Dacron swab or a cytobrush.  The swab or brush should be inserted 5-6 cm into the anal canal.  Firm lateral pressure should be applied to the swab or brush as it is slowly withdrawn from the anal canal.  Care should be taken to ensure the transitional zone is sampled.  Vigorously rotate the swab or brush into Preservcyt solution.  HPV DNA, a molecular detection methodology can be performed on the anal rectal cytology sample submitted to the Cytology laboratory in CYTYC PreservCyt solution or from a separate HPV collection swab.  REQUIRED BY FEDERAL LAW: Specimen must be accompanied by a Cytology requisition or electronic equivalent, giving patient's name, age, medical record number, attending physician, clinical diagnosis including patient's pertinent medication, time, date and source of specimen submitted.  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Separate specimens must be submitted when multiple tests are ordered. Allow tube to sit for 15-20 minutes at room temperature to form clot. Centrifuge and separate serum from cells ASAP or within 2 hours of collection. 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Levels between 0.50 and 2.00 ng/mL should be interpreted in the clinical context of the patient, as a variety of non-infectious conditions such as burns, trauma, surgery, and severe cardiogenic shock can cause procalcitonin elevations.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1543,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2009-07-31T00:00:00","CreatedById":326,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4247,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1543,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12943,"DictMethodologyId":185,"TdTestInfoSpecificId":1543,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1543,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":51118,"SpecialInstructions":"aliquot specimen into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1543,"IsBeakerData":false},{"Id":51119,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1543,"IsBeakerData":false},{"Id":51120,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Steady-state concentrations are found 5-7 days after initiation or dose adjustment. Do not collect in a gel separator tube. Centrifuge and transfer serum/plasma to a CCL tube and refrigerate within 1 hour of collection.","ClinicalInfo":"Ranges are based on trough draw at steady-state concentration.\nTherapeutic: >0.9 µg/mL\nProphylactic: >0.9 µg/mL\nToxic: >5.9 µg/mL (Toxic values will not be called)","ClinicalReference":"","ClinicalLimitation":"Trough levels should generally not exceed 4.0 mcg/mL due to toxicity risk. However, the treating physician may target trough levels up to 6.0 mcg/mL in patients with severe infections without signs/symptoms of voriconazole toxicity. The treating physician must determine appropriate target levels/dosing based on the specific clinical situation.  The therapeutic, prophylactic, and toxic ranges were based on the 2016 Infectious Disease Society of America's (IDSA) Clinical Practice Guidelines for the Management of Aspergillosis and Candidiasis and consultation from Cleveland Clinic's Department of Infectious Disease. Reference ranges and high/low indicator flags are provided as general guidelines only.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1545,"ActiveDate":"2009-09-23T00:00:00","CreatedOn":"2009-09-22T00:00:00","CreatedById":383,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4258,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1545,"IsStat":false,"Comments":"Therapeutic: >0.9 µg/mL\nProphylactic: >0.9 µg/mL\nToxic: >5.9 µg/mL","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10728,"DictMethodologyId":265,"TdTestInfoSpecificId":1545,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1545,"DictDaysPerformedId":14,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"3 days per week","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":41325,"SpecialInstructions":"Do not use serum separator tubes.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1545,"IsBeakerData":false},{"Id":41326,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":1545,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23734,"Description":"After separation from cells: 15 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1545,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23735,"Description":"After separation from cells: 15 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1545,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23736,"Description":"After separation from cells: 60 days.","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1545,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1545,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4267,"LISCode":"BCL6FT","PrimaryName":"FISH for BCL6 (3q27) Tissue","LISName":"FISH for BCL6 (3q27) Tissue","EMRName":"FISH for BCL6 (3q27) Tissue","EMRCode":"SQBCL6FT","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14035,"Aka":"BCL6FT","TdTestInfoCommonId":4267}],"TdBillingCommons":[{"Id":16487,"CptCode":"88377","Quantity":1,"Tmid":"31001725","CclTechComponentPrice":557.00,"CclProfComponentPrice":null,"TestNameForCdm":"","SubComponent":"87647","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4267,"IsBeakerData":false}],"TdIncludes":[{"Id":25261,"TestName":"FISH for 3q27","Rank":1,"TdTestInfoCommonId":4267}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4267,"SpecialInfo":"","ClinicalInfo":"Interphase FISH analysis utilizing a dual color, break-apart probe for the BCL6 gene at 3q27.3. Rearrangements involving the BCL6 gene are observed in various B-cell lymphomas.  The translocation partner gene cannot be identified in this assay. If no cells are available for analysis, no analysis charges will be incurred.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1548,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2009-12-16T00:00:00","CreatedById":276,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4267,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1548,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13023,"DictMethodologyId":173,"TdTestInfoSpecificId":1548,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1548,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"5 days per week","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":51465,"SpecialInstructions":"One formalin-fixed, paraffin embedded block containing representative tissue OR unstained 4 μm tissue sections on electrostatically charged slides containing representative tumor. Tissue must be fixed in formalin NOT B5 or PREFER fixative\n","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":130,"DictSpTypeName":"Slide (s), unstained","DictSpVolumeId":160,"DictSpVolumeName":"2 slides","TdTestInfoSpecificId":1548,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29557,"Description":"Blocks and slides should be transported at ambient temperature.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1548,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1548,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4268,"LISCode":"ULEADQ","PrimaryName":"Lead, Urine 24 Hour Quantitative","LISName":"Lead, Urine 24 Hour Quantitative","EMRName":"Lead, Urine 24 Hour Quantitative","EMRCode":"SQULEADQ","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12543,"CptCode":"83655","Quantity":1,"Tmid":"30111140","CclTechComponentPrice":81.00,"CclProfComponentPrice":null,"TestNameForCdm":"LEAD, UR 24HR","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4268,"IsBeakerData":false}],"TdIncludes":[{"Id":25191,"TestName":"Hours Collected ","Rank":1,"TdTestInfoCommonId":4268},{"Id":25192,"TestName":"Total Volume","Rank":2,"TdTestInfoCommonId":4268},{"Id":25193,"TestName":"Creatinine, Urine - per volume","Rank":3,"TdTestInfoCommonId":4268},{"Id":25194,"TestName":"Creatinine, Urine - per 24h","Rank":4,"TdTestInfoCommonId":4268},{"Id":25195,"TestName":"Lead, Urine - per volume","Rank":5,"TdTestInfoCommonId":4268},{"Id":25196,"TestName":"Lead, Urine - per 24h","Rank":6,"TdTestInfoCommonId":4268},{"Id":25197,"TestName":"Lead, Urine - ratio to CRT","Rank":7,"TdTestInfoCommonId":4268}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4268,"SpecialInfo":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, nonessential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. High concentrations of iodine may interfere with testing. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected. Elevated results may be due to skin or collection-related contamination, including the use of collection containers that are not certified to be trace element-free. Confirmation with a second specimen collected in a certified trace-element free container is recommended if an elevated result is suspected to be due to contamination. This test is New York DOH approved.","ClinicalInfo":"This test may be useful in the assessment of chronic lead exposure or in monitoring chelation therapy. Quantification of urine excretion rates before or after chelation therapy has been used as an indicator of lead exposure. Urinary excretion of >125 mg of lead per 24 hours is usually associated with related evidence of lead toxicity.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1549,"ActiveDate":"2011-12-05T00:00:00","CreatedOn":"2009-12-17T00:00:00","CreatedById":274,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4268,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1549,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13401,"DictMethodologyId":178,"TdTestInfoSpecificId":1549,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1549,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":37960,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":7,"DictSpCollectionTemperatureName":"Refrigerate during collection.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":56,"DictSpTypeName":"Urine, 24-hour (well-mixed)","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":1549,"IsBeakerData":false},{"Id":37961,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1549,"IsBeakerData":false},{"Id":37962,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":6,"DictSpCollectionTemperatureName":"N/A","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":1549,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21652,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1549,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21653,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1549,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21654,"Description":"1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1549,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1549,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":455,"Title":"Heavy Metals Form","FileName":"HeavyMetalRequisitionDemographicForm","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":4268,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":4269,"LISCode":"PARPLS","PrimaryName":"Parvo B19  PCR","LISName":"Parvo B19  PCR","EMRName":"Parvovirus B19 PCR","EMRCode":"SQPARPLS","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":2613,"Aka":"Fifth Disease","TdTestInfoCommonId":4269}],"TdBillingCommons":[{"Id":2995,"CptCode":"87798","Quantity":1,"Tmid":"30601745","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"PARVO B19 PLASMA PCR","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4269,"IsBeakerData":false}],"TdIncludes":[{"Id":25885,"TestName":"Parvovirus B19 by Qualitative PCR","Rank":1,"TdTestInfoCommonId":4269}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4269,"SpecialInfo":"This test is New York state approved.","ClinicalInfo":"Qualitative nucleic acid amplification testing for parvovirus B19.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1550,"ActiveDate":"2009-12-22T00:00:00","CreatedOn":"2009-12-21T00:00:00","CreatedById":455,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4269,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1550,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13536,"DictMethodologyId":422,"TdTestInfoSpecificId":1550,"DictMethodology":{"Id":422,"Name":"Qualitative Polymerase Chain Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1550,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 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","ClinicalInfo":"For specimen validity interpretations, the following rules are applied: Diluted: Creatinine is greater than or equal to 2mg/dL but less than 20mg/dL and Specific Gravity is less than 1.003. Substituted: Creatinine is less than 2mg/dL and the Specific gravity is less than 1.003 or greater than or equal to 1.020. Adulterated: pH is less than 4 or greater than or equal to 11; Nitrite is greater than or equal to 500mg/L; Oxidant is greater than or equal to 200mg/L.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1552,"ActiveDate":"2010-01-21T00:00:00","CreatedOn":"2010-01-20T00:00:00","CreatedById":259,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4276,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1552,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13807,"DictMethodologyId":265,"TdTestInfoSpecificId":1552,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1552,"DictDaysPerformedId":17,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"6 days per week","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":18187,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":181,"DictSpContainerName":"Urine","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1552,"IsBeakerData":false},{"Id":18188,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1552,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":10100,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1552,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":10101,"Description":"14 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1552,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":10102,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1552,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1552,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4278,"LISCode":"MAGIGM","PrimaryName":"Myelin Associated Glycoprotein (MAG) Ab, IgM","LISName":"MAG AB, IGM","EMRName":"MAG Antibody, IGM ELISA","EMRCode":"SQMAGIGM","LOINC":"17314-6","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":8559,"Aka":"MAG IgM","TdTestInfoCommonId":4278},{"Id":8560,"Aka":"Myelin Associated Glycoprotein","TdTestInfoCommonId":4278}],"TdBillingCommons":[{"Id":11408,"CptCode":"83516","Quantity":1,"Tmid":"30108355","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"MAG ANTIBODY IGM","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4278,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4278,"SpecialInfo":"Hemolyzed, severely lipemic, contaminated or heat-inactivated specimens are unacceptable. Urine will be rejected. This test is New York DOH approved. ","ClinicalInfo":"This is a stand-alone test for autoimmune neuropathies. The test by itself is not diagnostic, and it should be used in conjunction with other clinical parameters to confirm disease. An elevated IgM antibody concentration > 999 Titer Units (TU) against myelin-associated glycoprotein (MAG) suggests active demyelination in peripheral neuropathy. A normal concentration (< 999 TU) generally rules out an anti-MAG antibody-associated peripheral neuropathy.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1553,"ActiveDate":"2010-03-11T00:00:00","CreatedOn":"2010-01-27T00:00:00","CreatedById":274,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4278,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1553,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8882,"DictMethodologyId":22,"TdTestInfoSpecificId":1553,"DictMethodology":{"Id":22,"Name":"Semi Quantitative Enzyme Linked Immunosorbent Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1553,"DictDaysPerformedId":66,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Tue, Thu, Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":34238,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1553,"IsBeakerData":false},{"Id":34239,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":5,"DictSpVolumeName":"0.1 mL","TdTestInfoSpecificId":1553,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19267,"Description":"After separation from cells: 2 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1553,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19268,"Description":"After separation from cells: 2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1553,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19269,"Description":"After separation from cells: 1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1553,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1553,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4280,"LISCode":"CDTRAP","PrimaryName":"Carbohydrate Deficient Transferrin, pediatric","LISName":"Carbohydrate Deficient Transferrin, pediatric","EMRName":"Carbohydrate Deficient Transferrin, pediatric","EMRCode":"SQCDTRAP","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8303,"Aka":"Carbohydrate Deficient Glycoprotein Syndrome","TdTestInfoCommonId":4280},{"Id":8304,"Aka":"CDGS","TdTestInfoCommonId":4280},{"Id":8305,"Aka":"Congenital Disorders of Glycosylation","TdTestInfoCommonId":4280}],"TdBillingCommons":[{"Id":10991,"CptCode":"82373","Quantity":1,"Tmid":"30109285","CclTechComponentPrice":237.00,"CclProfComponentPrice":null,"TestNameForCdm":"CARBOHYDR DEF TRANS PED","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4280,"IsBeakerData":false}],"TdIncludes":[{"Id":25713,"TestName":"Mono-oligo/Di-oligo Ratio","Rank":1,"TdTestInfoCommonId":4280},{"Id":25714,"TestName":"A-oligo/Di-oligo Ratio","Rank":2,"TdTestInfoCommonId":4280},{"Id":25715,"TestName":"Tri-sialo/Di-oligo Ratio","Rank":3,"TdTestInfoCommonId":4280},{"Id":25716,"TestName":"Apo CIII-1/Apo CIII-2 Ratio","Rank":4,"TdTestInfoCommonId":4280},{"Id":25717,"TestName":"Apo CIII-0/Apo CIII-2 Ratio","Rank":5,"TdTestInfoCommonId":4280},{"Id":25718,"TestName":"Interpretation","Rank":6,"TdTestInfoCommonId":4280}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4280,"SpecialInfo":"Patient's age and reason for referral are required. Must submit Biochemical Genetics Patient Information form with the specimen. Grossly hemolyzed specimens will be rejected.  This test is New York State approved.","ClinicalInfo":"This test is for congenital disorders of glycosylation. If looking for evaluation of alcohol abuse, please order Carbohydrate Deficient Transferrin (CDTRAN). Other conditions such as heredity fructose intolerance, galactosemia, and liver disease may result in increased levels of carbohydrate deficient transferrin.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1555,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2010-02-09T00:00:00","CreatedById":326,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4280,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1555,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8577,"DictMethodologyId":402,"TdTestInfoSpecificId":1555,"DictMethodology":{"Id":402,"Name":"Affinity Chromatography-Mass Spectrometry(MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1555,"DictDaysPerformedId":30,"DictHoursPerformedId":null,"DictReportedId":116,"DictDaysPerformed":"Mon, Thu","DictReported":"4 - 7 days"},"TdSpecimenRequirements":[{"Id":33010,"SpecialInstructions":"Must submit Biochemical Genetics Patient Information form with the specimen. Patient age is required. Centrifuge and transfer serum into standard plastic aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":5,"DictSpVolumeName":"0.1 mL","TdTestInfoSpecificId":1555,"IsBeakerData":false},{"Id":33011,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":135,"DictSpVolumeName":"0.05 mL","TdTestInfoSpecificId":1555,"IsBeakerData":false},{"Id":33012,"SpecialInstructions":"Must submit Biochemical Genetics Patient Information form with the specimen. Patient age is required. Centrifuge and transfer serum into standard plastic aliquot tube. ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":5,"DictSpVolumeName":"0.1 mL","TdTestInfoSpecificId":1555,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":18579,"Description":"45 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1555,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18580,"Description":"28 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1555,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18581,"Description":"7 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1555,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1555,"TestCode":null,"IsReportable":false,"DictVendorId":50,"DictVendor":{"Id":50,"Name":"Mayo Clinic Dpt of Lab Med & Pathology","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":372,"Title":"BIOCHEMICAL GENETICS PATIENT INFORMATION","FileName":"BiochemicalGeneticsPatientInfo","DictDocumentFormatId":1,"DictDocumentTypeId":4,"TdTestInfoCommonId":4280,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":4,"Name":"Patient Info Sheet","Description":null,"FolderName":"PatientInfoSheet","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":4281,"LISCode":"SGPG","PrimaryName":"SGPG Antibody, IgM","LISName":"SGPG Ab, IgM","EMRName":"SGPG Ab, IgM","EMRCode":"SQSGPG","LOINC":"31666-1","RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":2156,"Aka":"Sulfate-3-Glucuronyl Paragloboside Antibody, IgM","TdTestInfoCommonId":4281},{"Id":2157,"Aka":"SGPG","TdTestInfoCommonId":4281}],"TdBillingCommons":[{"Id":3017,"CptCode":"83516","Quantity":1,"Tmid":"30110125","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"SGPG ANTIBODY IGM","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4281,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4281,"SpecialInfo":"Centrifuge, aliquot and refrigerate ASAP.","ClinicalInfo":"The majority of SGPG IgM positive sera will show reactivity against MAG.  Patients that are SGPG IgM positive and MAG negative may have multi-focal motor neuropathy with conduction block.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1556,"ActiveDate":"2010-03-15T00:00:00","CreatedOn":"2010-02-11T00:00:00","CreatedById":383,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4281,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1556,"IsStat":false,"Comments":"This test along with the new  (MAG) Ab, IgM test will replace the MAG Dual Antigen autoantibody.","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":2243,"DictMethodologyId":170,"TdTestInfoSpecificId":1556,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1556,"DictDaysPerformedId":59,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Tue","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":9175,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":1556,"IsBeakerData":false},{"Id":9176,"SpecialInstructions":"Separate serum from cells ASAP.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1556,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":6157,"Description":"After separation from cells: 2 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1556,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":6158,"Description":"After separation from cells: 2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1556,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":6159,"Description":"After separation from cells: 1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1556,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1556,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4296,"LISCode":"URCAD","PrimaryName":"Cadmium, Urine","LISName":"Cadmium, Urine","EMRName":"Cadmium, Urine","EMRCode":"SQURCAD","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12545,"CptCode":"82300","Quantity":1,"Tmid":"30111160","CclTechComponentPrice":88.00,"CclProfComponentPrice":null,"TestNameForCdm":"CADMIUM, UR","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4296,"IsBeakerData":false}],"TdIncludes":[{"Id":18098,"TestName":"Creatinine, Urine per volume","Rank":3,"TdTestInfoCommonId":4296},{"Id":18099,"TestName":"Creatinine, Urine per 24 hour","Rank":4,"TdTestInfoCommonId":4296},{"Id":18100,"TestName":"Cadmium, Urine per volume","Rank":5,"TdTestInfoCommonId":4296},{"Id":18101,"TestName":"Cadmium, Urine per 24 hour","Rank":6,"TdTestInfoCommonId":4296},{"Id":18102,"TestName":"Cadmium, Urine ratio to CRT","Rank":7,"TdTestInfoCommonId":4296},{"Id":25204,"TestName":"Hours Collected","Rank":1,"TdTestInfoCommonId":4296},{"Id":25205,"TestName":"Total Volume","Rank":2,"TdTestInfoCommonId":4296}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4296,"SpecialInfo":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected. Elevated results may be due to skin or collection-related contamination, including the use of collection containers that are not certified to be trace element-free. Confirmation with a second specimen collected in a certified trace-element free container is recommended if an elevated result is suspected to be due to contamination.\nThis test is New York DOH approved. ","ClinicalInfo":"This test may be useful in the assessment of chronic exposure and determination of cadmium body burden. In chronic exposures, the kidneys are the primary target organ. Symptoms associated with cadmium toxicity vary based upon route of exposure and may include tubular proteinuria, fever, headache, dyspnea, chest pain, conjunctivitis, rhinitis, sore throat and cough. Ingestion of cadmium in high concentration may cause vomiting, diarrhea, salivation, cramps, and abdominal pain.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1561,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2010-04-16T00:00:00","CreatedById":412,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4296,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1561,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9841,"DictMethodologyId":178,"TdTestInfoSpecificId":1561,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1561,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":37970,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). 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Methylated species arise primarily from metabolism of inorganic species but may also come from dietary sources and are of moderate toxic potential. The organic species of arsenic are considered nontoxic and arise primarily from food. The sum of the inorganic, methylated, and organic species of arsenic may be lower than the total arsenic concentration due to the presence of unidentified organic species of arsenic.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1681,"ActiveDate":"2011-07-21T00:00:00","CreatedOn":"2011-07-21T00:00:00","CreatedById":481,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4477,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1681,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9839,"DictMethodologyId":167,"TdTestInfoSpecificId":1681,"DictMethodology":{"Id":167,"Name":"High Performance Liquid Chromatography (HPLC)","Description":null},"TdTestInfoSpecific":null},{"Id":13403,"DictMethodologyId":178,"TdTestInfoSpecificId":1681,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1681,"DictDaysPerformedId":63,"DictHoursPerformedId":null,"DictReportedId":224,"DictDaysPerformed":"Tue, Fri","DictReported":"2 - 11 days"},"TdSpecimenRequirements":[{"Id":37965,"SpecialInstructions":"HEAVY METALS FORM REQUIRED to meet State Health Department requirements. \nPatient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":7,"DictSpCollectionTemperatureName":"Refrigerate during collection.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":56,"DictSpTypeName":"Urine, 24-hour (well-mixed)","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":1681,"IsBeakerData":false},{"Id":37966,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1681,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21655,"Description":"2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1681,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21656,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1681,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21657,"Description":"2 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1681,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1681,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":456,"Title":"Heavy Metals Form","FileName":"HeavyMetalRequisitionDemographicForm","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":4477,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":4492,"LISCode":"IA2AB","PrimaryName":"Islet antigen-2 antibody","LISName":"IA 2 Antibody","EMRName":"Islet antigen-2 antibody","EMRCode":"SQIA2AB","LOINC":"","RecommendedUse":"Anti-insulinoma associated antigen 2 (IA-2) antibody test is used as an aid in diagnosis of type I diabetes mellitus, to predict the risk of progression to type I diabetes mellitus among susceptible individuals, and to predict the necessity of insulin therapy in adult-onset diabetes mellitus. Clinical correlation is required.  ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9784,"Aka":"Anti-IA2 antibodies","TdTestInfoCommonId":4492},{"Id":9785,"Aka":"IA-2 antibody ","TdTestInfoCommonId":4492},{"Id":9786,"Aka":"Insulinoma-associated antibody 2","TdTestInfoCommonId":4492},{"Id":9787,"Aka":"Islet antigen-2 antibody","TdTestInfoCommonId":4492},{"Id":9788,"Aka":"Islet cell antigen antibody ","TdTestInfoCommonId":4492},{"Id":9789,"Aka":"Tyrosine phosphatase-related islet antigen 2 antibody","TdTestInfoCommonId":4492}],"TdBillingCommons":[{"Id":12832,"CptCode":"86341","Quantity":1,"Tmid":"30201805","CclTechComponentPrice":141.00,"CclProfComponentPrice":null,"TestNameForCdm":"ISLET CELL ANTIBODY","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4492,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4492,"SpecialInfo":"The test is not to be used alone and is to be used in conjunction with other clinical and laboratory findings.","ClinicalInfo":"Anti-insulinoma associated antigen 2 (IA-2) antibody test is used as an aid in diagnosis of type I diabetes mellitus, to predict the risk of progression to type I diabetes mellitus among susceptible individuals, and to predict the necessity of insulin therapy in adult-onset diabetes mellitus. Clinical correlation is required.  ","ClinicalReference":"","ClinicalLimitation":"Plasma is unacceptable. Lipemic and grossly hemolyzed samples should not be tested. Visibly turbid samples will have interference with this assay.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1682,"ActiveDate":"2011-08-22T00:00:00","CreatedOn":"2011-08-18T00:00:00","CreatedById":233,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4492,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1682,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10065,"DictMethodologyId":170,"TdTestInfoSpecificId":1682,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1682,"DictDaysPerformedId":2,"DictHoursPerformedId":null,"DictReportedId":12,"DictDaysPerformed":"Wed","DictReported":"1 - 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Pre-immunization samples will be held and tested simultaneously with post-immunization samples. Plasma or other body fluids will be rejected. Contaminated, hemolyzed, or severely lipemic specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"A pre- and post-vaccination comparison is required to adequately assess the humoral immune response to Prevnar 7 (P7), Prevnar 13 (P13), and/or Pneumovax 23 (PNX) Streptococcus pneumoniae vaccines. Pre-vaccination samples should be collected prior to vaccine administration. Post-vaccination samples should be obtained at least 4 weeks after immunization. Testing of post-vaccination samples alone will provide only general immune status of the individual to various pneumococcal serotypes.\n\nIn the case of pure polysaccharide vaccine, indication of immune system competence is further delineated as an adequate response to at least 50 percent of the serotypes in the vaccine challenge for those 2-5 years of age and to at least 70 percent of the serotypes in the vaccine challenge for those 6-65 years of age. Individual immune response may vary based on age, past exposure, immunocompetence, and pneumococcal serotype.\n\nResponder Status                          Antibody Ratio\nNon-Responder . . . . . . . . . . . . . . Less than 2-fold\nWeak Responder . . . . . . . . . . . . . 2-fold to 4-fold\nGood Responder . . . . . . . . . . . . . Greater than 4-fold\n\nA response to 50-70 percent or more of the serotypes in the vaccine challenge is considered a normal humoral response1. Antibody concentration greater than 1.0 – 1.3 µg/mL is generally considered long-term protection2.\n\nReferences:\n1. Daly TM, Pickering JW, Zhang X, Prince HE, Hill HR. Multilaboratory assessment of threshold versus fold-change algorithms for minimizing analytical variability in multiplexed pneumococcal IgG measurements. Clin Vaccine Immunol. 2014;21(7):982-8.\n2. Daly TM, Hill HR. Use and Clinical Interpretation of Pneumococcal Antibody Measurements in the Evaluation of Humoral Immune Function. Clin Vaccine Immunol. 2015;22(2):148-152.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1683,"ActiveDate":"2011-09-29T00:00:00","CreatedOn":"2011-09-26T00:00:00","CreatedById":393,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4505,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1683,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13451,"DictMethodologyId":568,"TdTestInfoSpecificId":1683,"DictMethodology":{"Id":568,"Name":"Quantitative Multiplex Chemiluminescent Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1683,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":35573,"SpecialInstructions":"Post-immunization specimen should be drawn 30 days after immunization and must be received within 60 days of pre-immunization specimen. Label specimens clearly as 'Pre' or 'Post.' Separate serum from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube. 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Call the microbiology lab (216-444-5870) to obtain transport media (Brucella broth with glycerol). For optimal recovery of organisms, transport the specimen to the lab immediately. Culture will be incubated for 7 days before reporting as negative.  Fecal specimens are unacceptable.                                                                                                                                                                                 If culture is positive, identification will be performed at an additional charge. Identification CPT codes that may apply include: 87077, 87153. Antimicrobial susceptibilities are performed when indicated, and CPT code 87181 would apply. ","ClinicalInfo":"Helicobacter pylori is associated with peptic ulcer disease and gastric cancer. Noninvasive tests for diagnosing H. pylori infection include serology, urea breath test and stool antigen detection. 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Unacceptable conditions include specimen types other than serum, specimens left to clot at refrigerated temperature, specimens exposed to repeated freeze/thaw cycles, or specimens that are grossly hemolyzed, lipemic or icteric.","ClinicalInfo":"This test is useful as initial screening for suspected deficiency in the alternative complement pathway.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1719,"ActiveDate":"2012-05-03T00:00:00","CreatedOn":"2012-03-26T00:00:00","CreatedById":393,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4582,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1719,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13453,"DictMethodologyId":170,"TdTestInfoSpecificId":1719,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1719,"DictDaysPerformedId":56,"DictHoursPerformedId":null,"DictReportedId":115,"DictDaysPerformed":"Sun, Wed","DictReported":"8 - 15 days"},"TdSpecimenRequirements":[{"Id":36146,"SpecialInstructions":"CRITICAL FROZEN (-70°C). Locations without a -70°C freezer should not collect this test. Do not use gel separator tubes. Allow specimen to clot for 1 hour at room temperature. Centrifuge at 2-8 degrees C and separate serum from cells ASAP or within 2 hours of collection. Transfer into standard aliquot tube and freeze immediately in a -70°C freezer. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":17,"DictSpTransportTemperatureName":"Frozen, Critical","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1719,"IsBeakerData":false},{"Id":36147,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1719,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20468,"Description":"After separation from cells: 30 days at -70 degrees C (Avoid multiple freeze/thaw cycles)","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1719,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20469,"Description":"After separation from cells: Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1719,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20470,"Description":"After separation from cells: Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1719,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1719,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4584,"LISCode":"PANCST","PrimaryName":"Pancreastatin","LISName":"Pancreastatin","EMRName":"Pancreastatin","EMRCode":"SQPANCST","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":18889,"CptCode":"86316","Quantity":1,"Tmid":"30213125","CclTechComponentPrice":135.00,"CclProfComponentPrice":null,"TestNameForCdm":"Pancreastatin","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4584,"IsBeakerData":false}],"TdIncludes":[{"Id":26226,"TestName":"Pancreastatin, Serum\t","Rank":1,"TdTestInfoCommonId":4584}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4584,"SpecialInfo":"Patient must be fasting 10-12 hours and should avoid any medications that may influence insulin levels for 48 hours, if possible. Separate specimens must be submitted when multiple tests are ordered. CRITICAL FROZEN. Thawed specimens will be rejected. This test is New York DOH approved.","ClinicalInfo":"This test can be useful to diagnose and predict disease recurrence, potential outcome, and efficacy of therapy in neuroendocrine tumors (NETs). Pancreastatin plays a role in human intermediary metabolism and disease and qualitative hereditary alterations in the primary structure may give rise to individual differences in glucose disposition.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1720,"ActiveDate":"2012-04-19T00:00:00","CreatedOn":"2012-04-10T00:00:00","CreatedById":412,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4584,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1720,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13706,"DictMethodologyId":170,"TdTestInfoSpecificId":1720,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1720,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":211,"DictDaysPerformed":"Varies","DictReported":"8 - 11 days"},"TdSpecimenRequirements":[{"Id":48922,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1720,"IsBeakerData":false},{"Id":678889,"SpecialInstructions":"Patient must be fasting 10-12 hours and should avoid any medications that may influence insulin levels for 48 hours, if possible. Allow specimen to clot for 2 hours at room temperature. Separate serum from cells and transfer to standard aliquot tube and freeze. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":17,"DictSpTransportTemperatureName":"Frozen, Critical","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1720,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28147,"Description":"6 months","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1720,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28148,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1720,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28149,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1720,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1720,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4609,"LISCode":"CVZVM","PrimaryName":"Varicella Zoster IgM Ab, CSF","LISName":"VZV Ab CSF IgM","EMRName":"Varicella Zoster IgM Ab, CSF","EMRCode":"SQCVZVM","LOINC":"31695-0","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":8654,"Aka":"Chicken Pox, Shingles","TdTestInfoCommonId":4609},{"Id":8655,"Aka":"VZV Antibody IgM, CSF","TdTestInfoCommonId":4609}],"TdBillingCommons":[{"Id":11496,"CptCode":"86787","Quantity":1,"Tmid":"30201405","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"VARICELLA ZOSTER IGM","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4609,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4609,"SpecialInfo":"Specimen types other than CSF are unacceptable. Contaminated, heat-inactivated or hemolyzed specimens will be rejected.","ClinicalInfo":"The detection of antibodies to VZV in CSF may indicate central nervous system infection. However, consideration must be given to possible contamination by blood or transfer of serum antibodies across the blood-brain barrier. Interpretation: Negative: <=0.90 ISR; 0.91-1.09 ISR: Equivocal; 1.10 or greater ISR: Positive - Significant level of IgM antibody to VZV detected, which may indicate current or recent infection. However, low levels of IgM antibodies may occasionally persist for more than 12 months post-infection.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1721,"ActiveDate":"2005-01-01T00:00:00","CreatedOn":"2012-04-30T00:00:00","CreatedById":227,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4609,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1721,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8968,"DictMethodologyId":22,"TdTestInfoSpecificId":1721,"DictMethodology":{"Id":22,"Name":"Semi Quantitative Enzyme Linked Immunosorbent Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1721,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Mon - 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A completed 'NF1/SPRED1 Phenotypic Checklist must be included with the specimen.","ClinicalInfo":"Neurofibromatosis Type 1 (NF1) is a completely penetrant, autosomal dominant disorder with a frequency of 1/3500 births in all ethnic populations. NF1 is a progressive disorder, characterized by multiple café-au-lait spots, neurofibromas, and Lisch nodules, although additional features may develop. NF1 is notorious for its variable expression. 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Urine mercury levels may be useful in monitoring chelation therapy. The ACGIH Biological Exposure Index (BEI) for arsenic in urine is 35 µg/L measured at the end of the week. The ACGIH BEI is based on the sum of inorganic and methylated species. 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Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, nonessential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 to 72 hours. High concentrations of iodine may interfere with testing. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected. Elevated results may be due to skin or collection containers that are not certified to be trace element free. Confirmation with a second specimen collected in a trace element-free container is recommended if an elevated result is suspected due to contamination. This test is New York DOH approved.","ClinicalInfo":"This test may be useful in the assessment of acute and chronic exposure to arsenic, cadmium, mercury, and lead. Urine cadmium concentrations can be used to assess cadmium body burden. In chronic exposures, the kidneys are the primary target organ. Symptoms associated with cadmium toxicity vary based upon route of exposure and may include tubular proteinuria, fever, headache, dyspnea, chest pain, conjunctivitis, rhinitis, sore throat and cough. Ingestion of cadmium in high concentration may cause vomiting, diarrhea, salivation, cramps, and abdominal pain. Urinary mercury levels predominantly reflect acute or chronic elemental or inorganic mercury exposure. Urine concentrations in unexposed individuals are typically less than 10 µg/L. 24 hour urine concentrations of 30 to 100 µg/L may be associated with subclinical neuropsychiatric symptoms and tremor while concentrations greater than 100 µg/L can be associated with overt neuropsychiatric disturbances and tremors. Urine mercury concentrations may be useful in monitoring chelation therapy. The ACGIH Biological Exposure Index (BEI) for arsenic in urine is 35 µg/L measured at the end of the work week. The ACGIH BEI is based on the sum of inorganic and methylated species. For specimens with elevated total arsenic results, fractionation is automatically performed at additional cost to determine the proportions of inorganic, methylated and organic species. 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Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician) and avoid seafood for 48 hours. Avoid iodinated or gadolinium-based contrast media for at least 72 hours or 14 days for patients with impaired kidney function.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). 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The test may also be used in disease prognostication and for monitoring response to anti-fungal therapy. False positive and false negative results are not uncommon. Clinical and radiological correlation is required. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12792,"CptCode":"87305","Quantity":1,"Tmid":"30601710","CclTechComponentPrice":115.00,"CclProfComponentPrice":null,"TestNameForCdm":"ASPERGILLUS GALACT SERUM","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4671,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4671,"SpecialInfo":"Send specimen in original tube. Avoid exposure of specimen to atmosphere. Sample can not be shared with multiple tests. Add on testing not acceptable.","ClinicalInfo":"Regular screening (twice-weekly) of serum samples of high-risk patients is recommended to increase the sensitivity and early positivity of the test. This test is intended to be used as an aid in the diagnosis of Invasive Aspergillosis. Positive results obtained with this test should be considered in conjunction with other diagnostic procedures such as microbiological culture, histological examination of biopsy samples and radiographic evidence.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1734,"ActiveDate":"2012-10-18T00:00:00","CreatedOn":"2012-10-18T00:00:00","CreatedById":259,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4671,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1734,"IsStat":false,"Comments":"","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10029,"DictMethodologyId":161,"TdTestInfoSpecificId":1734,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1734,"DictDaysPerformedId":63,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Tue, Fri","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":38575,"SpecialInstructions":"Collect sample in a sterile container using aseptic technique. 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This test cannot be added on to other testing.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":16,"DictSpVolumeName":"1.5 mL","TdTestInfoSpecificId":1734,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22040,"Description":"14 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1734,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22041,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1734,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22042,"Description":"48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1734,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1734,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4672,"LISCode":"ASGALB","PrimaryName":"Aspergillus galactomannan BAL","LISName":"Aspergillus galactomannan BAL","EMRName":"Aspergillus galactomannan BAL","EMRCode":"SQASGALB","LOINC":"","RecommendedUse":"Aspergillus Galactomannan antigen assay is used as an aid in diagnosis of invasive aspergillosis in immunocompromised individuals especially in post-stem cell transplant, hematological malignancies on chemotherapy, and HIV-positive patients with very low CD4 T-cell counts. The test may also be used in disease prognostication and for monitoring response to anti-fungal therapy. False positive and false negative results are not uncommon. Clinical and radiological correlation is required. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12791,"CptCode":"87305","Quantity":1,"Tmid":"30601945","CclTechComponentPrice":115.00,"CclProfComponentPrice":null,"TestNameForCdm":"ASPER GALACTOMAN, BAL","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4672,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4672,"SpecialInfo":"If aliquoting is necessary, sterile aliquot tubes must be used. Avoid exposure of specimen to atmosphere. Add on testing not accepted due to exposure of specimen to atmosphere during initial testing procedure.","ClinicalInfo":"Regular screening (twice-weekly) of serum samples of high-risk patients is recommended to increase the sensitivity and early positivity of the test. This test is intended to be used as an aid in the diagnosis of Invasive Aspergillosis. Positive results obtained with this test should be considered in conjunction with other diagnostic procedures such as microbiological culture, histological examination of biopsy samples and radiographic evidence.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1735,"ActiveDate":"2012-10-18T00:00:00","CreatedOn":"2012-10-18T00:00:00","CreatedById":259,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4672,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1735,"IsStat":false,"Comments":"","DictPerformingLabId":10,"DictPerformingLab":{"Id":10,"Name":"Manual Lab (x42502)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10028,"DictMethodologyId":161,"TdTestInfoSpecificId":1735,"DictMethodology":{"Id":161,"Name":"Enzyme Immunoassay (EIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1735,"DictDaysPerformedId":63,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Tue, Fri","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":38571,"SpecialInstructions":"Collect sample in a sterile container using aseptic technique. If aliquoting is necessary, sterile aliquot tubes must be used. Sample cannot be shared with other testing. This test cannot be added on to other testing.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":150,"DictSpTypeName":"Bronch (BAL)","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1735,"IsBeakerData":false},{"Id":38572,"SpecialInstructions":"Collect sample in a sterile container using aseptic technique. If aliquoting is necessary, sterile aliquot tubes must be used. Sample cannot be shared with other testing. This test cannot be added on to other testing.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":16,"DictSpVolumeName":"1.5 mL","TdTestInfoSpecificId":1735,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22037,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1735,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22038,"Description":"14 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1735,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22039,"Description":"48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1735,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1735,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4673,"LISCode":"RASPBY","PrimaryName":"Allergen, Raspberry IgE","LISName":"ALGN Raspberry IgE","EMRName":"ALGN Raspberry IgE","EMRCode":"SQRASPBY","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13236,"Aka":"American Red Raspberry","TdTestInfoCommonId":4673},{"Id":13237,"Aka":"Black Raspberry","TdTestInfoCommonId":4673},{"Id":13238,"Aka":"Common Red Raspberry","TdTestInfoCommonId":4673},{"Id":13239,"Aka":"European Red Raspberry","TdTestInfoCommonId":4673},{"Id":13240,"Aka":"Red Raspberry","TdTestInfoCommonId":4673},{"Id":13241,"Aka":"Thimbleberry","TdTestInfoCommonId":4673},{"Id":13242,"Aka":"Wild Raspberry","TdTestInfoCommonId":4673}],"TdBillingCommons":[{"Id":16068,"CptCode":"86003","Quantity":1,"Tmid":"30200030","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"ALLERGEN IGE QUANT/SEMI EA","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4673,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4673,"SpecialInfo":"An extra 50uL will be required for each additional allergen ordered.","ClinicalInfo":"","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":1736,"ActiveDate":"2012-11-20T00:00:00","CreatedOn":"2012-10-22T00:00:00","CreatedById":412,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4673,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1736,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12709,"DictMethodologyId":166,"TdTestInfoSpecificId":1736,"DictMethodology":{"Id":166,"Name":"Fluorescent Enzyme Immunoassay (FEIA) by ImmunoCAP","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1736,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":50124,"SpecialInstructions":"An extra 50uL will be required for each additional allergen ordered. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":1736,"IsBeakerData":false},{"Id":50125,"SpecialInstructions":"Submitting the minimum volume will not allow for repeat testing or addons. Required volume of 0.5mL is preferred when possible.","LogicalOperation":"Or","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1736,"IsBeakerData":false},{"Id":50126,"SpecialInstructions":null,"LogicalOperation":"Or","DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Its antithrombotic mechanism is antithrombin-mediated selective inhibition of factor Xa after binding fondaparinux with antithrombin. However, fondaparinux does not inactivate thrombin and has no effect in platelet function or fibrinolysis. The Fondaparinux Activity assay allows the determination of the plasma levels of fondaparinux by measuring its acceleration of inhibition of activated factor X using a chromogenic substrate method using calibration curve calculated with a commercial Arixtra (fondaparanux) calibrator. This assay cannot be used to monitor patients receiving unfractionated or low molecular weight heparins. Fondaparinux has a half life of approximately 17-21 hours in healthy normal individuals, however, it can be prolonged in patients with renal impairment because fondaparinux is mainly eliminated in urine. While patients treated with fondaparinux are not typically monitored, there is clinical need for monitoring and therapeutic assessment in patients with bleeding or thrombotic complications.\n\nIn patients undergoing treatment with fondaparinux sodium injection 2.5 mg, once daily, the peak steady-state plasma concentration is, on average, 0.39 to 0.50 mg/L and is reached approximately 3 hours post-dose. In these patients, the minimum steady-state plasma concentration is 0.14 to 0.19 mg/L. In patients with symptomatic deep vein thrombosis and pulmonary embolism undergoing treatment with fondaparinux sodium injection 5 mg (body weight <50 kg), 7.5 mg (body weight 50 to 100 kg), and 10 mg (body weight >100 kg) once daily, the body-weight-adjusted doses provide similar mean steady-state peaks and minimum plasma concentrations across all body weight categories. The mean peak steady-state plasma concentration is in the range of 1.20 to 1.26 mg/L. 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List all antifungal agents patient is receiving. Separate orders are required for each specimen. Rejection criteria: Specimen that is too viscous to pipette; Tissue, biopsy, sputum, bronchial brush, tracheal aspirate, FNA, bone marrow aspirate, stool or samples in transport media, fixative or Isolator tubes","ClinicalInfo":"Cautions: Sodium hydroxide and sputolysin. 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Reflex algorithm: Each reflex test performed incurs additional charge. If positive (low/high), then the neuronal nuclear (ANNA) antibody and Purkinje cell (PCCA) antibody IgG are screened by IFA. If the IFA screen is positive at 1:10, then a specific titer (ANNA or PCCA) will be added. Grossly hemolyzed, heat-inactivated, contaminated, or lipemic specimens will be rejected.","ClinicalInfo":"This assay detects IgG antineuronal antibodies to Hu, Ri, Yo and Tr (DNER) antigens. Antineuronal antibodies serve as markers that aid in discriminating between a true paraneoplastic neurological disorder (PND) and other inflammatory disorders of the nervous system. Anti-Hu (antineuronal nuclear antibody, type I) is associated with small cell lung cancer. Anti-Ri (antineuronal nuclear antibody, type II) is associated with fallopian tube and breast cancer in adults and neuroblastoma in children. Anti-Yo (anti-Purkinje cell cytoplasmic antibody) is associated with ovarian and breast cancer. Anti-Tr(DNER) is associated with Hodgkin lymphoma. Presence of one or more of these antineuronal antibodies detected by both immunoblot (IB) and immunofluorescence (IFA) supports a clinical diagnosis of PND and should lead to a focused search for the underlying neoplasm. A positive IB result but negative IFA result is of questionable clinical significance. Thus, strong clinical correlation is recommended.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1879,"ActiveDate":"2013-05-20T00:00:00","CreatedOn":"2013-03-19T13:54:00","CreatedById":270,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4751,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1879,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11388,"DictMethodologyId":406,"TdTestInfoSpecificId":1879,"DictMethodology":{"Id":406,"Name":"Immunoblot (IB), Qualitative","Description":null},"TdTestInfoSpecific":null},{"Id":13867,"DictMethodologyId":34,"TdTestInfoSpecificId":1879,"DictMethodology":{"Id":34,"Name":"Semi-Quantitative Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1879,"DictDaysPerformedId":32,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Thu, Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":44161,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1879,"IsBeakerData":false},{"Id":44162,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":1879,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":25334,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1879,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25335,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1879,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25336,"Description":"After separation from cells: 1 month","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1879,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1879,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":7071,"PrimaryName":"PCCA/ANNA by IFA, Serum (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":6908,"PrimaryName":"Neuronal Nuclear Antibody (ANNA) IFA Titer, IgG, Serum (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":6911,"PrimaryName":"Purkinje Cell Antibody Titer IgG, Serum (Reflex only)","IsRequired":false}]},{"Id":4783,"LISCode":"OSMFER","PrimaryName":"Osmotic Fragility, Erythrocyte","LISName":"Osmotic Fragility Er","EMRName":"Osmotic Fragility Erythrocyte","EMRCode":"SQOSMFER","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":11413,"CptCode":"85555","Quantity":1,"Tmid":"30500615","CclTechComponentPrice":85.00,"CclProfComponentPrice":null,"TestNameForCdm":"OSMOTIC FRAG ERYTHRO","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4783,"IsBeakerData":false}],"TdIncludes":[{"Id":25613,"TestName":"Osmotic Fragility\t","Rank":1,"TdTestInfoCommonId":4783}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4783,"SpecialInfo":"Grossly hemolyzed specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Functional testing of red blood cell sensitivity to osmotic stress; do not use to distinguish between spherocytes in hereditary spherocytosis and acquired autoimmune hemolytic anemia. For patients with acute hemolysis, a normal red cell osmotic fragility test result cannot exclude an osmotic fragility abnormality since the osmotically labile cells may be hemolyzed and not present. Recommend testing during a state of prolonged homeostasis with stable hematocrit.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1881,"ActiveDate":"2013-05-02T00:00:00","CreatedOn":"2013-03-20T11:30:00","CreatedById":220,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4783,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1881,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8886,"DictMethodologyId":188,"TdTestInfoSpecificId":1881,"DictMethodology":{"Id":188,"Name":"Spectrophotometry (S)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1881,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Mon - Fri","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":34257,"SpecialInstructions":"Specimens should be refrigerated within 30 minutes after collection.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1881,"IsBeakerData":false},{"Id":34258,"SpecialInstructions":"Whole blood","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1881,"IsBeakerData":false},{"Id":34259,"SpecialInstructions":"Specimens should be refrigerated within 30 minutes after collection.","LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":1881,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19278,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1881,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19279,"Description":"72 hours","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1881,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19280,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1881,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1881,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4788,"LISCode":"CHRSER","PrimaryName":"Chromium, Serum","LISName":"Chromium, Serum","EMRName":"Chromium, Serum","EMRCode":"SQCHRSER","LOINC":"5622-6","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13799,"CptCode":"82495","Quantity":1,"Tmid":"30117385","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"CHSER","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4788,"IsBeakerData":false}],"TdIncludes":[{"Id":26767,"TestName":"Chromium, Serum","Rank":1,"TdTestInfoCommonId":4788}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4788,"SpecialInfo":"Patient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, and nonessential over-the-counter medications (upon the advice of their physician). Do not use utensils (i.e., syringes, needles, or pipettes) in the collection or transfer of the sample, pour directly into transport tube. Unacceptable conditions:  Serum that takes longer than two hours to aliquot or is collected or transported in containers other than specified will be rejected. This test is New York DOH approved.","ClinicalInfo":"Preferred test for evaluating metal ion release from metal-on-metal joint arthroplasty. May be useful in the assessment of deficiency or overload. For the assessment of hexavalent chromium exposure, chromium in blood or RBCs is preferred. Elevated results may be due to skin or collection-related contamination, including the use of a noncertified metal-free collection/transport tube. If contamination concerns exist due to elevated levels of serum chromium, confirmation with a second specimen collected in a certified metal-free tube is recommended. Whole blood is the preferred specimen type for evaluating chromium metal ion release from metal-on-metal joint arthroplasty. Whole blood chromium levels may be increased in asymptomatic patients with metal-on-metal prosthetics and should be considered in the context of the overall clinical scenario. The form of chromium greatly influences distribution. Trivalent chromium resides in the plasma and is usually not of clinical importance. Hexavalent chromium is considered highly toxic; however, chromium serum levels should not be used to assess toxic exposures to hexavalent chromium as it is predominately taken up and retained by red blood cells. Symptoms associated with chromium toxicity vary based on route of exposure and dose, and may include dermatitis, impairment of pulmonary function, gastroenteritis, hepatic necrosis, bleeding, and acute tubular necrosis.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1882,"ActiveDate":"2013-05-02T00:00:00","CreatedOn":"2013-03-20T15:02:00","CreatedById":274,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4788,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1882,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10872,"DictMethodologyId":178,"TdTestInfoSpecificId":1882,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1882,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":41843,"SpecialInstructions":"Patient should be encouraged to discontinue nutritional supplements, vitamins, minerals, and nonessential over-the-counter medications (upon the advice of their physician). Remove serum from cells ASAP or within 2 hours of collection and aliquot into a trace metal-free transport tube (ARUP #43116). Do not use utensils (i.e., syringes, needles, or pipettes) in the collection or transfer of the sample, pour directly into transport tube. 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Abstain from medications 72 hours prior to collection. This test is New York state approved.","ClinicalInfo":"This test is useful as the initial test for the diagnosis and monitoring of neuroblastoma. Vanillylmandelic acid (VMA) and homovanillic acid (HVA) results are expressed as a ratio to creatinine excretion (mg/g CRT). No reference interval is available for results reported in units of mg/L. Slight or moderate increases in catecholamine metabolites may be due to extreme anxiety, essential hypertension, intense physical exercise, or drug interactions. Significant increase of one or more catecholamine metabolites (several times the upper reference limit) is associated with an increased probability of a secreting neuroendocrine tumor. Moderately elevated HVA (homovanillic acid) and VMA (vanillylmandelic acid) can be caused by a variety of factors such as essential hypertension, intense anxiety, intense physical exercise, and numerous drug interactions (including some over-the-counter medications and herbal products). Medications that may interfere with catecholamines and their metabolites include amphetamines and amphetamine-like compounds, appetite suppressants, bromocriptine, buspirone, caffeine, chlorpromazine, clonidine, disulfiram, diuretics (in doses sufficient to deplete sodium), epinephrine, glucagon, guanethidine, histamine, hydrazine derivatives, imipramine, levodopa (L-dopa, Sinemet), lithium, MAO inhibitors, melatonin, methyldopa (Aldomet), morphine, nitroglycerin, nose drops, propafenone (Rythmol), radiographic agents, rauwolfia alkaloids (Reserpine), tricyclic antidepressants, and vasodilators. The effects of some drugs on catecholamine metabolite results may not be predicable.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1883,"ActiveDate":"2013-05-02T00:00:00","CreatedOn":"2013-03-20T10:50:00","CreatedById":270,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4775,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1883,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":5213,"DictMethodologyId":54,"TdTestInfoSpecificId":1883,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1883,"DictDaysPerformedId":53,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun, Tue - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":19581,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1883,"IsBeakerData":false},{"Id":679556,"SpecialInstructions":"Critical Refrigerated. 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If after 3 days cryoprecipitate is observed, then quantitative immunoglobulins (IgG, IgA, IgM) will be added at an additional cost. Fasting for a minimum of 8 hours is required. Do not use serum separator tubes. Collect in a pre-warmed (37C), no additive (Red) tube. Immediately after collection, place tube in heel warmer or 37°C (warm, not hot) water. Keep sample warm at 37C until clotting is complete (up to 1 hour). Grossly hemolyzed or lipemic specimens will be rejected. This test is New York state approved.","ClinicalInfo":"This test is useful in evaluation of patients with vasculitis, macroglobulinemia, or multiple myeloma in whom symptoms occur with exposure to cold.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1885,"ActiveDate":"2013-05-02T00:00:00","CreatedOn":"2013-03-22T17:03:00","CreatedById":259,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4802,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1885,"IsStat":false,"Comments":null,"DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":3775,"DictMethodologyId":431,"TdTestInfoSpecificId":1885,"DictMethodology":{"Id":431,"Name":"Qualitative Cold Precipitation","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1885,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":65,"DictDaysPerformed":"Sun - Sat","DictReported":"4 - 6 days"},"TdSpecimenRequirements":[{"Id":14392,"SpecialInstructions":"Fasting for a minimum of 8 hours is required. Do not use serum separator tubes. Collect in a pre-warmed (37C), no additive (Red) tube. Immediately after collection, place tube in heel warmer or 37°C (warm, not hot) water. Keep sample warm at 37C until clotting is complete (up to 1 hour). Separate serum from cells and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":1885,"IsBeakerData":false},{"Id":14393,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1885,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":7829,"Description":"After separation from cells: 1 week","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1885,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":7830,"Description":"After separation from cells: 1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1885,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":7831,"Description":"After separation from cells: Uncacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1885,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1885,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":4801,"PrimaryName":"Immunoglob IgG, IgM, IgA  Cryo","IsRequired":false}]},{"Id":4811,"LISCode":"MACPRO","PrimaryName":"Macroprolactin","LISName":"Macroprolactin","EMRName":"Macroprolactin","EMRCode":"SQMACPRO","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13482,"Aka":"Macroprolactin by PEG","TdTestInfoCommonId":4811},{"Id":13483,"Aka":"Macroprolactin by PEG","TdTestInfoCommonId":4811}],"TdBillingCommons":[{"Id":16208,"CptCode":"84146","Quantity":2,"Tmid":"30105920","CclTechComponentPrice":409.00,"CclProfComponentPrice":null,"TestNameForCdm":"*PROLACTIN ASSAY","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4811,"IsBeakerData":false}],"TdIncludes":[{"Id":26436,"TestName":"Prolactin","Rank":1,"TdTestInfoCommonId":4811},{"Id":26437,"TestName":"Monomeric Prolactin\t","Rank":2,"TdTestInfoCommonId":4811},{"Id":26438,"TestName":"Percent Macroprolactin\t","Rank":3,"TdTestInfoCommonId":4811}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4811,"SpecialInfo":"","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1887,"ActiveDate":"2013-05-02T00:00:00","CreatedOn":"2013-03-29T11:22:00","CreatedById":220,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4811,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1887,"IsStat":false,"Comments":"Restrict inside orders to endocrine providers and outpatients only.","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13784,"DictMethodologyId":185,"TdTestInfoSpecificId":1887,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1887,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":127,"DictDaysPerformed":"Varies","DictReported":"6 - 11 days"},"TdSpecimenRequirements":[{"Id":50643,"SpecialInstructions":"Patient must be awake for at least two hours before collection. Separate serum from cells ASAP or within 45 minutes of collection and transfer into standard aliquot tube. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1887,"IsBeakerData":false},{"Id":50644,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":1887,"IsBeakerData":false},{"Id":50645,"SpecialInstructions":"Patient must be awake for at least two hours before collection. Separate serum from cells ASAP or within 45 minutes of collection and transfer into standard aliquot tube. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":"Or","DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1887,"IsBeakerData":false},{"Id":50646,"SpecialInstructions":"Patient must be awake for at least two hours before collection. Separate plasma from cells ASAP or within 45 minutes of collection and transfer into standard aliquot tube. Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":"Or","DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":1887,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29066,"Description":"After separation from cells: 6 months","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1887,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29067,"Description":"After separation from cells: 14 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1887,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29068,"Description":"After separation from cells: 14 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1887,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1887,"TestCode":null,"IsReportable":false,"DictVendorId":71,"DictVendor":{"Id":71,"Name":"LabCorp","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4812,"LISCode":"ASPIGG","PrimaryName":"Aspergillus fumigatus Antibody IgG","LISName":"Aspergillus fumigatus Antibody IgG","EMRName":"Aspergillus fumigatus Antibody IgG","EMRCode":"SQASPIGG","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":18114,"CptCode":"86317","Quantity":1,"Tmid":"30213625","CclTechComponentPrice":106.00,"CclProfComponentPrice":null,"TestNameForCdm":"Aspergillus fumigatus Antibody IgG","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4812,"IsBeakerData":false}],"TdIncludes":[{"Id":26688,"TestName":"Aspergillus fumigatus Ab IgG","Rank":1,"TdTestInfoCommonId":4812}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4812,"SpecialInfo":"This test is New York DOH approved.","ClinicalInfo":"This test aids in the diagnosis of allergic bronchopulmonary aspergillosis (ABPA) and is not appropriate for diagnosing invasive aspergillosis. A positivity cutoff of 40 μg/mL was established based on a comparison study to precipitin assay results. Note that elevated specific IgG concentrations to Aspergillus fumigatus are not disease specific and could be found in healthy individuals. 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All other specimens have alternative test codes. \n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6106,"Aka":"Calcofluor Smear","TdTestInfoCommonId":4937},{"Id":6107,"Aka":"Dermatophyte Culture","TdTestInfoCommonId":4937},{"Id":6108,"Aka":"Fungal Culture Dermal","TdTestInfoCommonId":4937},{"Id":6109,"Aka":"Fungal Smear","TdTestInfoCommonId":4937},{"Id":6110,"Aka":"KOH Smear","TdTestInfoCommonId":4937},{"Id":6111,"Aka":"Mold Culture","TdTestInfoCommonId":4937},{"Id":6112,"Aka":"Yeast Culture","TdTestInfoCommonId":4937},{"Id":14445,"Aka":"Dermal","TdTestInfoCommonId":4937},{"Id":14446,"Aka":"Dermatophyte","TdTestInfoCommonId":4937},{"Id":14447,"Aka":"Fungal culture","TdTestInfoCommonId":4937},{"Id":14448,"Aka":"Fungal stain","TdTestInfoCommonId":4937},{"Id":14449,"Aka":"Fungus culture","TdTestInfoCommonId":4937},{"Id":14450,"Aka":"Mycology","TdTestInfoCommonId":4937},{"Id":14451,"Aka":"Ringworm","TdTestInfoCommonId":4937},{"Id":14452,"Aka":"Tinea","TdTestInfoCommonId":4937}],"TdBillingCommons":[{"Id":8721,"CptCode":"87101","Quantity":1,"Tmid":"30601935","CclTechComponentPrice":50.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation, Hair, Skin, Nail","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":8722,"CptCode":"87206","Quantity":1,"Tmid":"30600265","CclTechComponentPrice":35.00,"CclProfComponentPrice":null,"TestNameForCdm":"Smear, Fungal Fluorescent","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":18735,"CptCode":"87176","Quantity":1,"Tmid":"30600215","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Tissue Homogenization","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":18738,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":18739,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":18740,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4937,"IsBeakerData":false},{"Id":18746,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4937,"IsBeakerData":false}],"TdIncludes":[{"Id":25922,"TestName":"Specimens may include some pre-processing steps to aid in recovery of fungal organisms. ","Rank":1,"TdTestInfoCommonId":4937}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4937,"SpecialInfo":"Fungal smears are performed directly on specimen using a Calcofluor white stain that nonspecifically binds chitin in the cell wall of fungi. Fluorescent microscopy is utilized to detect and report as yeast and/or hyphae present. CPT code: 87206. Clinical specimens for dermal fungal cultures are processed and plated on selective fungal media to optimize recovery of fungal organisms. Cultures are incubated for 28 days; negative results are auto-updated daily. Any fungal organisms recovered will be isolated and identified by various methods.  Additional CPT codes may be applicable for recovery and identification of fungal organisms  87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing. Fungal susceptibility testing for yeast and filamentous mold recovered is ONLY performed by request when clinically relevant (CPT 87186). Yeast susceptibility testing is performed in-house by colorimetric microdilution broth. A standardized inoculation of test organism is incubated with appropriate dilutions of antifungal agents; minimum inhibitory concentration (MIC) are determined by inhibition of growth at the lowest antifungal concentration. MIC are determined and interpreted according to CLSI standards. Filamentous mold susceptibility testing is a send-out test and can be requested by contacting the lab. ","ClinicalInfo":"Aseptic technique should be utilized to minimize contamination and for optimal recovery of organisms. Specimen should be transported immediately to the microbiology laboratory in dry conditions at ambient temperatures. Refrigeration may impact recovery of dermatophytes. Isolation and identification of fungi from keratinized tissue such as hair, skin and nails are commonly due to dermatophytic fungi. Opportunistic superficial infections caused by other fungal organisms and yeasts resembling dermatophytoses will also be identified and reported. However, normally saprophytic or environmental fungi are often recovered from these sites. Clinical correlation with patient symptoms is necessary to determine significance of recovered organism. If specific fungi are suspected the \"rule out\" feature in Epic can be utilized. If fungal smears are needed order FCULSM; for fungal blood cultures HISTCL; for CSF order FUNCSF; for dermal samples of hair, skin and nail order  ACFSC or FHSNSM (with smear); for candidiasis on vaginal and oral samples order fungal screen FUNGSC.\nIf culture only (without smear) is desired, order ACFSC - Fungal Culture Hair, Skin, Nail.","ClinicalReference":"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. ","ClinicalLimitation":"Not all fungal organisms recovered in cultures may be significant; clinical correlation needed to determine significance.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1920,"ActiveDate":"2013-10-01T00:00:00","CreatedOn":"2013-09-10T10:37:00","CreatedById":220,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4937,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1920,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6770,"DictMethodologyId":224,"TdTestInfoSpecificId":1920,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null},{"Id":6771,"DictMethodologyId":260,"TdTestInfoSpecificId":1920,"DictMethodology":{"Id":260,"Name":"Stain","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1920,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":148,"DictDaysPerformed":"Sun - Sat","DictReported":"6 weeks"},"TdSpecimenRequirements":[{"Id":678368,"SpecialInstructions":"Hair root is essential for the recovery of fungal organisms so plucking or pulling hair with intact hair shaft is ideal. Cutting hair is not recommended. In cases of alopecia (hair loss), hair can be collected from the region by using a soft bristle toothbrush and rubbing in circular motions over the margins or patches. Collected specimens should be sent in a sterile container or dry paper envelope. Ensure that the specimen is secured within the container to prevent loss of specimen. Specimen should be transported dry in ambient temperatures for optimal recovery.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":40,"DictSpTypeName":"Hair","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":1920,"IsBeakerData":false},{"Id":678369,"SpecialInstructions":"The affected area should be cleaned with70% alcohol and allowed to dry. Skin should be scraped with a dull edged object or vigorously brushed in a circular motion with a toothbrush. Be careful to not draw blood. Leading edge of the skin lesion is the preferred sample for optimal recovery of fungal organisms. Ensure that the specimen is secured within the container to prevent loss of specimen. Specimen should be transported dry in ambient temperatures for optimal recovery.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":89,"DictSpTypeName":"Skin","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":1920,"IsBeakerData":false},{"Id":678370,"SpecialInstructions":"Nails should be cleaned with 70% alcohol and then clipped or scraped with a scalpel. Clip generous portion of the affected area and place in sterile container along with any material or debris from under the nail/nailbed. Ensure that the specimen is secured within the container to prevent loss of specimen. Specimen should be transported dry in ambient temperatures for optimal recovery.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":10,"DictSpTypeName":"Nails","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":1920,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":14413,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":1920,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14414,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":1920,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14415,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":1920,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":1920,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":2045,"PrimaryName":"AFB Susceptibility","IsRequired":false},{"TdTestInfoCommonId":4587,"PrimaryName":"Mold Susceptibility One Drug","IsRequired":false},{"TdTestInfoCommonId":3396,"PrimaryName":"Organism Identification, Aerobic","IsRequired":false},{"TdTestInfoCommonId":3397,"PrimaryName":"Organism Identification, AFB","IsRequired":false},{"TdTestInfoCommonId":3400,"PrimaryName":"Organism Identification, Nocardia","IsRequired":false},{"TdTestInfoCommonId":3402,"PrimaryName":"Organism MIC, Bacterial ","IsRequired":false}]},{"Id":4940,"LISCode":"ACFSC","PrimaryName":"Fungal culture - Dermal (hair, skin and nail)","LISName":"Fungal culture - Dermal (hair, skin and nail)","EMRName":"Fungal culture - Dermal (hair, skin and nail)","EMRCode":"SQACFSC","LOINC":"580-1","RecommendedUse":"Recovery and identification of dermatophyte fungal infections from hair, skin and nail specimens. For culture and smears on these sources order FHSNSM. All other specimens have alternative test codes. \n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6102,"Aka":"Dermatophyte Culture","TdTestInfoCommonId":4940},{"Id":6103,"Aka":"Fungal Culture Dermal","TdTestInfoCommonId":4940},{"Id":6104,"Aka":"Mold Culture","TdTestInfoCommonId":4940},{"Id":6105,"Aka":"Yeast Culture","TdTestInfoCommonId":4940},{"Id":14427,"Aka":"Ringworm","TdTestInfoCommonId":4940},{"Id":14428,"Aka":"Tinea","TdTestInfoCommonId":4940}],"TdBillingCommons":[{"Id":8720,"CptCode":"87101","Quantity":1,"Tmid":"30601935","CclTechComponentPrice":50.00,"CclProfComponentPrice":null,"TestNameForCdm":"Culture, Fungal Isolation, Hair, Skin, Nail","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":18708,"CptCode":"87176","Quantity":1,"Tmid":"30600215","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Tissue Homogenization","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":18711,"CptCode":"87106","Quantity":1,"Tmid":"30600085","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Yeast","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":18712,"CptCode":"87107","Quantity":1,"Tmid":"30600095","CclTechComponentPrice":67.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Mold","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":18713,"CptCode":"87153","Quantity":1,"Tmid":"30601285","CclTechComponentPrice":748.00,"CclProfComponentPrice":null,"TestNameForCdm":"Identification, Nucleic Acid Sequencing","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":18719,"CptCode":"87186","Quantity":1,"Tmid":"30608575","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Sensititre","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":19263,"CptCode":"87186","Quantity":1,"Tmid":"30608565","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Phoenix","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false},{"Id":19264,"CptCode":"87186","Quantity":1,"Tmid":"30608555","CclTechComponentPrice":56.00,"CclProfComponentPrice":null,"TestNameForCdm":"Susceptibility, Multi-antimicrobial Vitek","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":4940,"IsBeakerData":false}],"TdIncludes":[{"Id":25920,"TestName":"Specimens may include some pre-processing steps to aid in recovery of fungal organisms. ","Rank":1,"TdTestInfoCommonId":4940}],"TdLaboratoryCommon":{"TdTestInfoCommonId":4940,"SpecialInfo":"Fungal smears - direct detection of fungi from clinical specimens will NOT be performed. Please order FHSNSM if fungal smears are needed. Clinical specimens for dermal fungal cultures are processed and plated on selective fungal media to optimize recovery of fungal organisms. Cultures are incubated for 28 days; negative results are auto-updated daily. Any fungal organisms recovered will be isolated and identified by various methods.  Additional CPT codes may be applicable for recovery and identification of fungal organisms, 87106 - ID by MALDI-TOF Mass Spec for yeast, 87107 - ID by MALDI-TOF Mass Spec for Mold, 87153 - DNA sequencing. Fungal susceptibility testing for yeast and filamentous mold recovered is ONLY performed by request when clinically relevant (CPT 87186). Yeast susceptibility testing is performed in-house by colorimetric microdilution broth. A standardized inoculation of test organism is incubated with appropriate dilutions of antifungal agents; minimum inhibitory concentration (MIC) are determined by inhibition of growth at the lowest antifungal concentration. MIC are determined and interpreted according to CLSI standards. Filamentous mold susceptibility testing is a send-out test and can be requested by contacting the lab. ","ClinicalInfo":"Aseptic technique should be utilized to minimize contamination and for optimal recovery of organisms. Specimen should be transported immediately to the microbiology laboratory in dry conditions at ambient temperatures. Refrigeration may impact recovery of dermatophytes. Isolation and identification of fungi from keratinized tissue such as hair, skin and nails are commonly due to dermatophytic fungi. Opportunistic superficial infections caused by other fungal organisms and yeasts resembling dermatophytoses will also be identified and reported. However, normally saprophytic or environmental fungi are often recovered from these sites. Clinical correlation with patient symptoms is necessary to determine significance of recovered organism. If specific fungi are suspected the \"rule out\" feature in Epic can be utilised. If fungal smears are needed order FCULSM; for fungal blood cultures HISTCL; for CSF order FUNCSF; for dermal samples of hair, skin and nail order  ACFSC or FHSNSM (with smear); for candidiasis on vaginal and oral samples order fungal screen FUNGSC.\n\nFungal smear is not included. If desired, order Fungal Culture and Smear - Dermal (hair, skin and nail) (FHSNSM).","ClinicalReference":"Westblade et. al. Larone’s Medically Important Fungi, 7th edition, ASM press, Washington DC., 2024.  \nLeber et al., Clinical Microbiology Procedures Handbook, 5th edition, ASM press, Washington, DC.  2023. \nCarroll, et al.   Manual of Clinical Microbiology, 13th Edition, Volume 3, ASM Press, Washington, DC.  2024. ","ClinicalLimitation":"Not all fungal organisms recovered in cultures may be significant; clinical correlation needed to determine significance.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":1922,"ActiveDate":"2013-10-01T00:00:00","CreatedOn":"2013-09-24T09:44:00","CreatedById":220,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4940,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1922,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6769,"DictMethodologyId":224,"TdTestInfoSpecificId":1922,"DictMethodology":{"Id":224,"Name":"Culture","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1922,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":148,"DictDaysPerformed":"Sun - Sat","DictReported":"6 weeks"},"TdSpecimenRequirements":[{"Id":678351,"SpecialInstructions":"Hair root is essential for the recovery of fungal organisms so plucking or pulling hair with intact hair shaft is ideal. Cutting hair is not recommended. In cases of alopecia (hair loss), hair can be collected from the region by using a soft bristle toothbrush and rubbing in circular motions over the margins or patches. Collected specimens should be sent in a sterile container or dry paper envelope. Ensure that the specimen is secured within the container to prevent loss of specimen. Specimen should be transported dry in ambient temperatures for optimal recovery.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":40,"DictSpTypeName":"Hair","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":1922,"IsBeakerData":false},{"Id":678352,"SpecialInstructions":"The affected area should be cleaned with 70% alcohol and allowed to dry. Skin should be scraped with a dull edged object or vigorously brushed in a circular motion with a toothbrush. Be careful to not draw blood. Leading edge of the skin lesion is the preferred sample for optimal recovery of fungal organisms. Ensure that the specimen is secured within the container to prevent loss of specimen.  Specimen should be transported dry in ambient temperatures for optimal recovery.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":89,"DictSpTypeName":"Skin","DictSpVolumeId":52,"DictSpVolumeName":"Entire collection","TdTestInfoSpecificId":1922,"IsBeakerData":false},{"Id":678353,"SpecialInstructions":"Nails should be cleaned with 70% alcohol and then clipped or scraped with a scalpel. Clip generous portion of the affected area and place in sterile container along with any material or debris from under the nail/nailbed. Ensure that the specimen is secured within the container to prevent loss of specimen.  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This test is New York DOH approved.","ClinicalInfo":"This assay is intended for the qualitative determination of antibodies to steroid 21-hydroxylase in human serum. A positive result is indicative of primary adrenal insufficiency (Addison's disease). Results should be interpreted within the context of clinical symptoms, including functional adrenal testing. 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Congenital abnormalities are present in approximately 70% of FA patients and include: café au lait spots or hypopigmentation; short stature; radial ray defects; eye defects such as microphthalmia; malformations of the kidney, genitalia, heart, gastrointestinal tract, ears, and feet.  Currently, 21 genes have been identified that, when mutated, can cause FA or an FA-like phenotype.  \n\nThe first step in FA diagnosis is to perform a breakage analysis on peripheral blood.  However, some FA patients undergo a self-correction of cells in the hematopoietic lineage, resulting in a normal blood breakage study.  In such a case, breakage analysis of skin fibroblasts is necessary to detect the increased breakage and radial formation.   This phenomenon is known as somatic mosaicism.  Fibroblast breakage studies may also be preferable for patients with very low white blood cell counts.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1930,"ActiveDate":"2013-12-05T00:00:00","CreatedOn":"2013-10-17T16:50:00","CreatedById":269,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4956,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1930,"IsStat":false,"Comments":"Contact Knight Diagnostic Laboratories Client Services at (855) 535-1522 for additional information, if necessary.","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6334,"DictMethodologyId":465,"TdTestInfoSpecificId":1930,"DictMethodology":{"Id":465,"Name":"Stress test induced by mitomycin C (MMC) or diepoxybutane (DEB)","Description":null},"TdTestInfoSpecific":null},{"Id":13473,"DictMethodologyId":121,"TdTestInfoSpecificId":1930,"DictMethodology":{"Id":121,"Name":"Chromosome Analysis","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1930,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":211,"DictDaysPerformed":"Mon - Sat","DictReported":"8 - 11 days"},"TdSpecimenRequirements":[{"Id":23714,"SpecialInstructions":"Collect Monday through Friday only. 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Treatment with Carbamazepine in subjects positive for HLA-B*15:02 should be avoided. A negative result for HLA-B*15:02 does not rule out the possibility of such reactions. Therapy should be discontinued immediately and permanently should TEN or SJS develop.\n\n\nThe FDA recommends that individuals of Asian ancestry be genotyped for the presence of the HLA-B*15:02 allele prior to receiving:\n\n-Carbamazepine, a drug used to treat epilepsy, manic/bipolar disorders, and neuropathic pain\n-Phenytoin and its soluble precursor fosphenytoin, drugs used to control seizures\n\nSome studies have also suggested a connection between HLA-B*15:02 positivity and adverse reactions to lamotrigine used for treating epilepsy and bipolar disorder. \n\n","ClinicalReference":"Positive/Negative","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":1933,"ActiveDate":"2013-11-07T00:00:00","CreatedOn":"2013-10-28T09:47:00","CreatedById":255,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":4961,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":1933,"IsStat":false,"Comments":"","DictPerformingLabId":14,"DictPerformingLab":{"Id":14,"Name":"Allogen Lab (x46583)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8448,"DictMethodologyId":168,"TdTestInfoSpecificId":1933,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null},{"Id":8449,"DictMethodologyId":494,"TdTestInfoSpecificId":1933,"DictMethodology":{"Id":494,"Name":"Polymerase Chain reaction(PCR)/Sequence Specific Oligo Probes(SSO)","Description":null},"TdTestInfoSpecific":null},{"Id":8450,"DictMethodologyId":479,"TdTestInfoSpecificId":1933,"DictMethodology":{"Id":479,"Name":"Sequence based typing, PCR","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":1933,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":169,"DictDaysPerformed":"Mon - 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","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2000,"IsBeakerData":false},{"Id":51159,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2000,"IsBeakerData":false},{"Id":51160,"SpecialInstructions":"Send to Cleveland Clinic Laboratories ASAP on the day of collection. ","LogicalOperation":null,"DictSpContainerId":28,"DictSpContainerName":"Sodium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2000,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29412,"Description":"72 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2000,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29413,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2000,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29414,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2000,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2000,"TestCode":null,"IsReportable":false,"DictVendorId":97,"DictVendor":{"Id":97,"Name":"Quest SJC","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5081,"LISCode":"NARCAB","PrimaryName":"Narcolepsy HLA-DQ Genotyping (HLA-DQB1*06:02)","LISName":"Narcolepsy HLA-DQ Genotyping (HLA-DQB1*06:02)","EMRName":"Narcolepsy HLA-DQ Genotyping (HLA-DQB1*06:02)","EMRCode":"SQNARCAB","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":5,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12626,"Aka":"HLA-DQB1*06:02 ","TdTestInfoCommonId":5081}],"TdBillingCommons":[{"Id":18614,"CptCode":"81382","Quantity":1,"Tmid":"31004785","CclTechComponentPrice":278.00,"CclProfComponentPrice":null,"TestNameForCdm":"Narcolepsy Genotyping (HLADQB1* 06:02)","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5081,"IsBeakerData":false}],"TdIncludes":[{"Id":25732,"TestName":"HLA-DQB1, Allele 1","Rank":1,"TdTestInfoCommonId":5081},{"Id":25733,"TestName":"HLA-DQB1, Allele 2","Rank":2,"TdTestInfoCommonId":5081},{"Id":25734,"TestName":"Narcolepsy HLA Interpretation","Rank":3,"TdTestInfoCommonId":5081}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5081,"SpecialInfo":"Counseling and informed consent are recommended for genetic testing. Clotted or grossly hemolyzed specimens will be rejected. This test is New York DOH approved.","ClinicalInfo":"May help rule out narcolepsy when clinical history and sleep studies are inconclusive. Background Information: Characteristics: Narcolepsy is a sleep disorder associated with invalidating excessive daytime sleepiness and cataplexy. Disturbed nighttime sleep, sleep paralysis, and hypnagogic hallucinations (occurring in the period between sleep and wakefulness) are common. Incidence: Narcolepsy affects approximately 1 in 2,000 individuals. Inheritance: Multifactorial.\nCause: The HLA-DQB1*06:02 allele is strongly associated with narcolepsy, but by itself is not causative. Recent studies indicate HLA-DRB1*15 is not associated with narcolepsy. Mutations Tested: HLA-DQB1*06:02 allele. Clinical Sensitivity: 85-95% depending on ethnicity. Greater than 98% of affected Caucasians with cataplexy have the HLA-DQB1*06:02 allele. Clinical Specificity: < 1%; 15-25% of unaffected Caucasians have the HLA-DQB1*06:02 allele. Methodology: PCR with melting curve analysis. Analytical Sensitivity and Specificity: 99%","ClinicalReference":"","ClinicalLimitation":"Rare diagnostic errors may occur due to primer site mutations. Other genetic and nongenetic factors that influence narcolepsy disease are not evaluated. In cases where an HLA allele cannot be resolved unambiguously, the allele assignment will be reported as the most common, based on allele frequencies from the common, intermediate, and well-documented alleles catalogue version 3.0.0 (Hurley CK et al, 2020).","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2002,"ActiveDate":"2015-01-19T00:00:00","CreatedOn":"2014-09-09T13:23:00","CreatedById":261,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5081,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2002,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12471,"DictMethodologyId":168,"TdTestInfoSpecificId":2002,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null},{"Id":13509,"DictMethodologyId":500,"TdTestInfoSpecificId":2002,"DictMethodology":{"Id":500,"Name":"Massive Parallel Sequencing","Description":null},"TdTestInfoSpecific":null},{"Id":13510,"DictMethodologyId":296,"TdTestInfoSpecificId":2002,"DictMethodology":{"Id":296,"Name":"Sequence Specific Oligonucleotide Probe (SSOP)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2002,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":78,"DictDaysPerformed":"Mon - 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There are 3 pathways to complement activation: 1) The classic pathway, 2) the alternative (or properdin) pathway, and 3) the lectin activation (mannan-binding protein: MBP) pathway.  The classic pathway of the complement system is composed of a series of proteins that are activated in response to the presence of immune complexes. The activation process results in the generation of peptides that are chemotactic for neutrophils and that bind to immune complexes and complement receptors. The end result of the complement activation cascade is the formation of the lytic membrane attack complex (MAC).\nPatients with deficiencies of the late complement proteins (C5, C6, C7, C8, and C9) are unable to form the MAC and may have increased susceptibility to neisserial infections.  More than 30 cases of C5 deficiency have been reported.  Most of these patients have neisserial infections.\nComplement levels can be detected by antigen assays that quantitate the amount of the protein (C5AG/ C5 Complement, Antigen, Serum). For most of the complement proteins, a small number of cases have been described in which the protein is present but is nonfunctional. These rare cases require a functional assay to detect the deficiency.\n","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2004,"ActiveDate":"2015-01-20T00:00:00","CreatedOn":"2014-09-11T09:36:00","CreatedById":220,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5094,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2004,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13939,"DictMethodologyId":246,"TdTestInfoSpecificId":2004,"DictMethodology":{"Id":246,"Name":"Turbidimetry (TURB)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2004,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Mon - Fri","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":13920,"SpecialInstructions":"Fasting preferred. Place tube on wet ice immediately after collection and allow specimen to clot. Separate serum from cells and transfer to standard aliquot tube. Freeze immediately.\n","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":8,"DictSpCollectionTemperatureName":"Place specimen on ice after draw.","DictSpTransportTemperatureId":17,"DictSpTransportTemperatureName":"Frozen, Critical","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2004,"IsBeakerData":false},{"Id":13921,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2004,"IsBeakerData":false},{"Id":679412,"SpecialInstructions":"Fasting preferred. Place tube on wet ice immediately after collection and allow specimen to clot. Separate serum from cells and transfer to standard aliquot tube. Freeze immediately.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":8,"DictSpCollectionTemperatureName":"Place specimen on ice after draw.","DictSpTransportTemperatureId":17,"DictSpTransportTemperatureName":"Frozen, Critical","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2004,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":7491,"Description":"14 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2004,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":8685,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2004,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":8686,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2004,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2004,"TestCode":null,"IsReportable":false,"DictVendorId":50,"DictVendor":{"Id":50,"Name":"Mayo Clinic Dpt of Lab Med & Pathology","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5103,"LISCode":"FPIGG","PrimaryName":"Allergy Food Panel IgG","LISName":"Allergy Food Pnl IgG","EMRName":"Allergy Food Pnl IgG","EMRCode":"SQFPIGG","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8679,"Aka":"Allergens, Food, Extended Panel IgG","TdTestInfoCommonId":5103}],"TdBillingCommons":[{"Id":11522,"CptCode":"86001","Quantity":19,"Tmid":"30212495","CclTechComponentPrice":342.00,"CclProfComponentPrice":null,"TestNameForCdm":"ALGN FOOD PANEL IGG X19","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5103,"IsBeakerData":false}],"TdIncludes":[{"Id":16438,"TestName":"Wheat IgG","Rank":1,"TdTestInfoCommonId":5103},{"Id":16439,"TestName":"Potato IgG","Rank":2,"TdTestInfoCommonId":5103},{"Id":16440,"TestName":"Rye IgG","Rank":3,"TdTestInfoCommonId":5103},{"Id":16441,"TestName":"Soybean IgG","Rank":4,"TdTestInfoCommonId":5103},{"Id":16442,"TestName":"Tomato IgG","Rank":5,"TdTestInfoCommonId":5103},{"Id":16443,"TestName":"Orange IgG","Rank":6,"TdTestInfoCommonId":5103},{"Id":16444,"TestName":"Peanut IgG","Rank":7,"TdTestInfoCommonId":5103},{"Id":16445,"TestName":"Pork IgG","Rank":8,"TdTestInfoCommonId":5103},{"Id":16446,"TestName":"Lettuce IgG","Rank":9,"TdTestInfoCommonId":5103},{"Id":16447,"TestName":"Malt IgG","Rank":10,"TdTestInfoCommonId":5103},{"Id":16448,"TestName":"Casein IgG","Rank":11,"TdTestInfoCommonId":5103},{"Id":16449,"TestName":"Oat IgG","Rank":12,"TdTestInfoCommonId":5103},{"Id":16450,"TestName":"Chicken meat IgG","Rank":13,"TdTestInfoCommonId":5103},{"Id":16451,"TestName":"Cacao (Chocolate) IgG","Rank":14,"TdTestInfoCommonId":5103},{"Id":16452,"TestName":"Corn IgG","Rank":15,"TdTestInfoCommonId":5103},{"Id":16453,"TestName":"Egg white IgG","Rank":16,"TdTestInfoCommonId":5103},{"Id":16454,"TestName":"Yeast (bakers/brewers) IgG","Rank":17,"TdTestInfoCommonId":5103},{"Id":16455,"TestName":"Barley (food) IgG","Rank":18,"TdTestInfoCommonId":5103},{"Id":16456,"TestName":"Beef IgG","Rank":19,"TdTestInfoCommonId":5103}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5103,"SpecialInfo":"Hemolyzed, icteric, or lipemic specimens are not acceptable. Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible. ","ClinicalInfo":"Values < 2.00 mcg/mL represent absent or undetectable levels of allergen-specific IgG antibody. The units of measure mcg/mL and mgA/L are interchangeable. 1 mg/L = 1000 mcg/1000 mL \n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2011,"ActiveDate":"2014-09-11T00:00:00","CreatedOn":"2014-07-15T10:31:00","CreatedById":198,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5103,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2011,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8994,"DictMethodologyId":413,"TdTestInfoSpecificId":2011,"DictMethodology":{"Id":413,"Name":"Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2011,"DictDaysPerformedId":46,"DictHoursPerformedId":null,"DictReportedId":94,"DictDaysPerformed":"Sun","DictReported":"2 - 9 days"},"TdSpecimenRequirements":[{"Id":34709,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2011,"IsBeakerData":false},{"Id":34710,"SpecialInstructions":"Per allergen","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":138,"DictSpVolumeName":"0.25 mL","TdTestInfoSpecificId":2011,"IsBeakerData":false},{"Id":679688,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2011,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19554,"Description":"After separation from cells: 1 year","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2011,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19555,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2011,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19556,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2011,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2011,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":4951,"LISCode":"TITAN","PrimaryName":"Titanium, Serum or Plasma","LISName":"Titanium, Serum or Plasma","EMRName":"Titanium, Serum or Plasma","EMRCode":"SQTITAN","LOINC":"8244-6","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13450,"CptCode":"83018","Quantity":1,"Tmid":"30109505","CclTechComponentPrice":142.00,"CclProfComponentPrice":null,"TestNameForCdm":"TITANIUM SER/PLAS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":4951,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":4951,"SpecialInfo":"Separator tubes are unacceptable. 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The presence of histamine releasing factors (including but not limited to IgE and Fc epsilon R1 alpha-specific autoantibodies) in the patient serum can be indirectly determined by evaluating basophil/mast cell activation status using histamine release assays, autologous serum-skin test, and flow cytometric measurement of the basophil and mast-cell specific marker CD203c. 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Separate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2048,"IsBeakerData":false},{"Id":33436,"SpecialInstructions":"Separate plasma from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube. 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Required volume of 0.5mL is preferred when possible.","LogicalOperation":"Or","DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2050,"IsBeakerData":false},{"Id":49839,"SpecialInstructions":null,"LogicalOperation":"Or","DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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Category: Environmental/Occupational toxin. Avoid exposure to gadolinium or iodine-based contrast media for 96 hours prior to sample collection. Do not use disinfectants containing iodine, such as Betadine®, during venipuncture. Sodium fluoride/potassium oxalate (gray) tubes and EDTA (lavender) tubes will be rejected. This test is New York State approved.","ClinicalInfo":"The general range of normal levels is usually between 1.4 and 8.8 mg/L (2.5th - 97.5th percentiles). Background\nconcentrations are diet dependent. Workers exposed to\nmethyl bromide with blood bromide concentrations\ngreater than 12 mg/L have shown 3.5 times higher\nrisk of electroencephalogram disturbances than compared\nto those with normal levels. Reporting limit: 0.5 mg/L","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2051,"ActiveDate":"2015-01-19T00:00:00","CreatedOn":"2014-08-19T09:08:00","CreatedById":291,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5055,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2051,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9148,"DictMethodologyId":266,"TdTestInfoSpecificId":2051,"DictMethodology":{"Id":266,"Name":"ICP/Mass Spectrometry","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2051,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":155,"DictDaysPerformed":"Mon - Sun","DictReported":"8 days"},"TdSpecimenRequirements":[{"Id":35309,"SpecialInstructions":"Do not use disinfectants containing iodine, such as Betadine®, during venipuncture.","LogicalOperation":null,"DictSpContainerId":37,"DictSpContainerName":"EDTA (Royal blue)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2051,"IsBeakerData":false},{"Id":35310,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":12,"DictSpVolumeName":"0.7 mL","TdTestInfoSpecificId":2051,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19946,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2051,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19947,"Description":"12 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2051,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19948,"Description":"30 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2051,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2051,"TestCode":null,"IsReportable":false,"DictVendorId":76,"DictVendor":{"Id":76,"Name":"National Med Serv Inc","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5068,"LISCode":"MYGAMP","PrimaryName":"Mycoplasma genitalium NAAT","LISName":"Mycoplasma genitalium NAAT","EMRName":"Mycoplasma genitalium NAAT","EMRCode":"SQMYGAMP","LOINC":"88226-6 urine; 69935-5 non urine","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14071,"Aka":"MYGPCR","TdTestInfoCommonId":5068},{"Id":14757,"Aka":"m genitalium","TdTestInfoCommonId":5068},{"Id":14758,"Aka":"m. gen","TdTestInfoCommonId":5068},{"Id":14759,"Aka":"m. genitalium","TdTestInfoCommonId":5068},{"Id":14760,"Aka":"mgen","TdTestInfoCommonId":5068},{"Id":14761,"Aka":"MYGAMP","TdTestInfoCommonId":5068},{"Id":14762,"Aka":"SQMYGAMP","TdTestInfoCommonId":5068}],"TdBillingCommons":[{"Id":13605,"CptCode":"87563","Quantity":1,"Tmid":"30607705","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Amplified Probe, Mycoplasma genitalium","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5068,"IsBeakerData":true}],"TdIncludes":[{"Id":24800,"TestName":"Mycoplasma genitalium Result","Rank":1,"TdTestInfoCommonId":5068}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5068,"SpecialInfo":"Microbiology Preanalytic Guidance: http://portals.ccf.org/plmi/Laboratory-Medicine/Microbiology-Specimen-Collection-Transport-Information.\n\nUp to two tests can be run on a single Aptima Multitest Swab specimen (ie. GCCT+MYGAMP) - if specimen sources have been correctly selected, the shared tests will print on the same label. Do not place more than one label on a single collection tube. \n\nCommon reasons for specimen rejection:\n1. Inappropriate collection device for source selected.\n2. Transport tubes containing a cleaning swab or more than 1 swab.\n3. Overfilled or underfilled urine transport tubes.\n4. Collection device expired prior to specimen collection.\n\nRelated alternative orders:\n1. URMPCR: sendout PCR test for Ureaplasma parvum, Ureaplasma urealyticum, Mycoplasma hominis, and Mycoplasma genitalium from urogenital sites. Not recommended due to inconsistent data and unclear role for urogenital Ureaplasma and M. hominis testing. The majority of Ureaplasma infections are not associated with overt urethritis or cervicitis symptoms.\n2. MYPLAS: in-house culture for Ureaplasma urealyticum and Mycoplasma hominis from urogenital sites. Not recommended due to inconsistent data and unclear role for urogenital Ureaplasma and M. hominis testing. Will not recover M. genitalium. \n3. All other available mycoplasma and ureaplasma orders are for testing from non-urogenital sites.\n","ClinicalInfo":"Mycoplasma genitalium  is a sexually-transmitted gram-negative bacterium that lives on and in the epithelial cells of the urinary and genital tracts. M. genitalium can cause acute and chronic nongonoccal urethritis (NGU), cervicitis, and pelvic inflammatory disease. In lower risk populations, M. genitalium prevalence of approximately 1-3% has been reported in both men and women. In higher risk populations, prevalence of 10- 41% in men and 7.3-14% in women has been reported. The prevalence of M. genitalium in higher risk populations often exceeds that of Neisseria gonorrhoeae and is similar to the prevalence of Chlamydia trachomatis. M. genitalium infections largely go unrecognized, and infected individuals are either asymptomatic or have symptoms similar to those associated with other bacterial infections of the urogenital tract. \n\nBecause M. genitalium is fastidious and difficult to culture, nucleic acid amplification testing (NAAT) is the diagnostic test of choice. The CDC recommends male patients with recurrent NGU should be tested for M. genitalium using an FDA-cleared NAAT. Female patients with recurrent cervicitis should be tested for M. genitalium, and testing should be considered for those with pelvic inflammatory disease. Screening of asymptomatic M. genitalium infection or extragenital testing for M. genitalium is not recommended.\n\nThe Aptima Mycoplasma genitalium assay is an FDA-approved in vitro NAAT that utilizes target capture, transcription-mediated amplification (TMA), and hybridization protection assay (HPA) technologies to detect 16s rRNA of M. genitalium. It is intended for use as an aid in the diagnosis of M. genitalium urogenital infections from clinician-collected and self-collected vaginal swabs (in a clinical setting), clinician-collected endocervical swabs, female and male urine, clinician-collected male urethral swabs, and self-collected penile meatal swabs (in a clinical setting).\n","ClinicalReference":"Workowski KA, Bachmann LH, Chan PA, Johnston CM, Muzny CA, Park I, Reno H, Zenilman JM, Bolan GA. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187. doi: 10.15585/mmwr.rr7004a1. PMID: 34292926; PMCID: PMC8344968.\n","ClinicalLimitation":"1. The performance of the assay has not been evaluated in individuals  <15 years of age.\n2. Therapeutic failure or success cannot be determined with the assay since nucleic acid may persist following appropriate antimicrobial therapy.\n3. A negative result does not preclude a possible infection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or target levels below the assay limit of detection (LoD).\n4. The effects of tampon use, douching, and specimen collection variables have not been evaluated for their impact on assay detection.\n5. For females patients, a vaginal swab is the preferred specimen type due to higher clinical sensitivity for detecting M. genitalium than other specimen types; however, female urine or clinician collected endocervical swabs may be used as alternative specimens when vaginal swab specimens are not available. If female urine or clinician-collected endocervical swab specimens test negative, testing with a vaginal swab may be indicated.\n5. Assay interference may occur at high concentrations of mucus in the specimen. Competitive interference may preclude detection of M. genitalium in low quantities if M. pneumoniae is present in high quantities.\n","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2052,"ActiveDate":"2015-01-01T00:00:00","CreatedOn":"2014-08-26T11:48:00","CreatedById":269,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5068,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2052,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13185,"DictMethodologyId":81,"TdTestInfoSpecificId":2052,"DictMethodology":{"Id":81,"Name":"Transcription-Mediated Amplification","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2052,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Sun","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":676796,"SpecialInstructions":"Male Urethral Unisex (white tube blue swab): The patient should not have urinated for at least 1 hr prior to sample collection. Insert the blue swab 2-4 cm into the urethra. Gently rotate the swab clockwise for 2-3 seconds in the urethra. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":104,"DictSpContainerName":"APTIMA Collection Unisex swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":62,"DictSpTypeName":"Urethral","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2052,"IsBeakerData":false},{"Id":676801,"SpecialInstructions":"Endocervical Unisex (white tube blue swab): Remove excess mucus from cervical os and surrounding mucosa using the white cleaning swab, then DISCARD. Insert blue swab into the endocervical canal and gently rotate clockwise for 10-30 seconds. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.\n","LogicalOperation":null,"DictSpContainerId":104,"DictSpContainerName":"APTIMA Collection Unisex swab","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":147,"DictSpTypeName":"Endocervical","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2052,"IsBeakerData":false},{"Id":676803,"SpecialInstructions":"For female patients, vaginal specimens are preferred due to superior test performance characteristics. The patient should not have urinated for at least 1 hour prior to specimen collection. The patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container. Transfer 2 mL of urine into the Aptima urine specimen transport tube using the disposable pipette provided within 24 hours of collection. Close the tube tightly. Work with one specimen at a time. The correct volume of urine has been added when the fluid level is between the black fill lines (window) on the urine transport tube. Do not overfill or underfill the APTIMA Urine transport tube.","LogicalOperation":null,"DictSpContainerId":107,"DictSpContainerName":"APTIMA Urine specimen collection kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":181,"DictSpTypeName":"Urine, first-catch","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2052,"IsBeakerData":false},{"Id":676807,"SpecialInstructions":"Vaginal Multitest (orange tube pink swab): A vaginal swab is the recommended specimen for female patients due to superior test performance characteristics. Carefully insert the swab into the vagina about 2 inches past the introitus and gently rotate the swab for 10-30 seconds. Make sure the swab touches the vaginal walls so that moisture is absorbed by the swab. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2052,"IsBeakerData":false},{"Id":677505,"SpecialInstructions":"Penile Meatal (orange tube pink swab):  Roll the swab on the tip of the penis, outside the opening of the penis (hole through which urine is passed). It is not necessary to put the swab inside the opening of the penis. Make sure to roll the swab all the way around the opening of the penis to get the best sample. Ensure the swab does not touch any other area of the skin. Place swab into Aptima transport tube. 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Adulterated: pH is less than 4 or greater than or equal to 11; Nitrite is greater than or equal to 500mg/L; Oxidant is greater than or equal to 200mg/L.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2056,"ActiveDate":"2014-10-27T00:00:00","CreatedOn":"2014-08-29T10:47:00","CreatedById":7,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5155,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2056,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10313,"DictMethodologyId":265,"TdTestInfoSpecificId":2056,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2056,"DictDaysPerformedId":17,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"6 days per week","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":39864,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":181,"DictSpContainerName":"Urine","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2056,"IsBeakerData":false},{"Id":39865,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2056,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22830,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2056,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22831,"Description":"14 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2056,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22832,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2056,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2056,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5157,"LISCode":"HEPGEN","PrimaryName":"Hepatitis C Virus (HCV) Genotyping by RT-PCR, Plasma/Serum","LISName":"Hepatitis C Virus (HCV) Genotyping by RT-PCR, Plasma/Serum","EMRName":"Hepatitis C Virus (HCV) Genotyping by RT-PCR, Plasma/Serum","EMRCode":"SQHEPGEN","LOINC":"32286-7","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":7,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14086,"Aka":"HCV genotype","TdTestInfoCommonId":5157},{"Id":14087,"Aka":"Hep C Genotype","TdTestInfoCommonId":5157},{"Id":14088,"Aka":"Hepatitis C Genotype","TdTestInfoCommonId":5157},{"Id":14089,"Aka":"Abbott HCV Genotype II","TdTestInfoCommonId":5157},{"Id":14769,"Aka":"HEPGEN","TdTestInfoCommonId":5157},{"Id":14770,"Aka":"SQHEPGEN","TdTestInfoCommonId":5157}],"TdBillingCommons":[{"Id":15213,"CptCode":"87902","Quantity":1,"Tmid":"30600735","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Genotype, Hepatitis C Virus","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5157,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5157,"SpecialInfo":"This Hepatitis C virus (HCV) genotyping assay should only be ordered on patients with a diagnosis of HCV infection with detectable viral load. Genotyping may be unsuccessful in specimens with viral load <500 IU/mL. A negative result does not exclude HCV infection. \n\t\t\t\t\t\nIf a genotype is unable to be determined using this assay and the viral load is >500 IU/mL, the specimen may be sent out to a reference laboratory for genotyping by an alternative method (ARUP Hepatitis C Virus Genotype by Sequencing: https://ltd.aruplab.com/Tests/Pub/0055593).","ClinicalInfo":"The Hepatitis C virus (HCV), a significant cause of blood-borne hepatitis, is an enveloped virus containing a single-stranded positive sense RNA genome of approximately 9,500 nucleotides. It has been identified as the major etiological agent for post-transfusion non-A and non-B hepatitis worldwide. Based on genetic similarity, HCV has been classified into six major genotypes (1-6) and numerous subtypes (1a, 1b, etc.). Genotypes 1a, 1b, 2, and 3 are the most common HCV genotypes in the United States. \n\nHCV genotype testing may be considered for those in whom it may alter treatment recommendations. With the advent of pangenotypic HCV treatment regimens, HCV genotyping is no longer required prior to treatment initiation for all individuals. In those with evidence of cirrhosis and/or past unsuccessful HCV treatment, treatment regimens may differ by genotype and thus pretreatment genotyping is recommended. For noncirrhotic treatment-naive patients, although genotyping may impact the preferred treatment approach, it is not required if a pangenotypic regimen is used. HCV genotyping may also be ordered to obtain insurance pre-authorization for medications.\n\nThe Abbott RealTime HCV Genotype II is an FDA-cleared in vitro reverse transcription-polymerase chain reaction (RT-PCR) assay used for the qualitative identification of hepatitis C virus (HCV) genotypes 1, 1a, 1b, and 2-5 in plasma or serum from individuals chronically infected with HCV. The Abbott RealTime HCV Genotype II is intended for use as an aid in the management of HCV-infected individuals and in guiding the selection of therapeutic treatment indicated for the above listed genotypes. The assay is intended for use on patients who are chronically infected with HCV, are being considered for antiviral treatment, and are positive for HCV RNA. The Abbott RealTime HCV Genotype II assay is not for screening blood, plasma, serum or tissue donors for HCV.","ClinicalReference":"1. AASLD-IDSA. HCV testing and linkage to care. Recommendations for testing, managing, and treating hepatitis C. http://www.hcvguidelines.org/full-report/hcv-testing-and-linkage-care. [Last Accessed: 4/28/2023].\n2. US Food and Drug Administration. Abbott RealTime HCV Genotype II: Summary of Safety and Effectiveness Data. Approved June 20, 2013. https://www.accessdata.fda.gov/cdrh_docs/pdf12/P120012b.pdf. [Last Accessed: 4/28/2023].","ClinicalLimitation":"1. Multiple genotype assay results may be caused by a mixed genotype infection, recombination of HCV genotypes, or assay probe cross-reactivity.\n2. The Abbott RealTime HCV Genotype II assay is capable of detecting both genotypes in a genotype mixture when the concentrations of both genotypes are near equal; however, the assay may not detect the lower concentration genotype.\n3. Performance has not been established with the Abbott RealTime HCV Genotype II assay for HCV genotype 6 specimens. HCV genotype 6 specimens may generate a HCV genotype 1 result with the Abbott RealTime HCV Genotype II assay based on probe cross-reactivity of the HCV genotype 1 probe.\n4. A specimen with a result of “Unable to Genotype” cannot be presumed to be negative for HCV RNA.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2058,"ActiveDate":"2014-11-04T00:00:00","CreatedOn":"2014-10-09T15:07:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5157,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2058,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12069,"DictMethodologyId":219,"TdTestInfoSpecificId":2058,"DictMethodology":{"Id":219,"Name":"Reverse Transcription/Polymerase Chain Reaction (RT/PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2058,"DictDaysPerformedId":13,"DictHoursPerformedId":null,"DictReportedId":68,"DictDaysPerformed":"2 days per week","DictReported":"3 - 6 days"},"TdSpecimenRequirements":[{"Id":47499,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Separate plasma by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 6 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample can only be shared with AHCV1B, HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2058,"IsBeakerData":false},{"Id":47500,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2058,"IsBeakerData":false},{"Id":47501,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 6 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2058,"IsBeakerData":false},{"Id":47502,"SpecialInstructions":"Collect serum according to standard protocol. Separate serum by centrifugation (at 1,100 RCF for a minimum of 10 minutes) within 6 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HCQPCR or HBVDNU.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2058,"IsBeakerData":false},{"Id":47503,"SpecialInstructions":"Collect serum according to standard protocol. Centrifuge (at 1,100 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 6 hours of collection. Serum must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with AHCV1B, HCQPCR, or HBVDNU.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2058,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27166,"Description":"3 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2058,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27167,"Description":"60 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2058,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27168,"Description":"24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2058,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2058,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5167,"LISCode":"UBARBC","PrimaryName":"Barbiturates Confirmation, Urine","LISName":"Barbiturates Conf Ur","EMRName":"Barbiturates Confirmation Urine","EMRCode":"SQUBARBC","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":16210,"CptCode":"G0480","Quantity":1,"Tmid":"30100810","CclTechComponentPrice":70.00,"CclProfComponentPrice":null,"TestNameForCdm":"BARBITURATES","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5167,"IsBeakerData":true}],"TdIncludes":[{"Id":24326,"TestName":"Pentobarbital","Rank":2,"TdTestInfoCommonId":5167},{"Id":24327,"TestName":"Phenobarbital","Rank":3,"TdTestInfoCommonId":5167},{"Id":24328,"TestName":"Butalbital","Rank":1,"TdTestInfoCommonId":5167}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5167,"SpecialInfo":"","ClinicalInfo":"Cutoff concentrations for all analytes: 50 ng/mL. For medical purposes only, not for forensic use. The absence of expected drug(s) and/or drug metabolite(s) may indicate noncompliance, inappropriate timing of specimen collection relative to drug administration, poor drug absorption, diluted/adulterated urine, or limitations of testing. The concentration value must be greater than or equal to the cutoff to be reported as positive.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2061,"ActiveDate":"2014-11-13T00:00:00","CreatedOn":"2014-08-20T09:56:00","CreatedById":198,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5167,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2061,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12819,"DictMethodologyId":76,"TdTestInfoSpecificId":2061,"DictMethodology":{"Id":76,"Name":"Quantitative Liquid Chromatography - Tandem Mass Spectrometry","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2061,"DictDaysPerformedId":66,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Tue, Thu, Sat","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":50655,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":16,"DictSpVolumeName":"1.5 mL","TdTestInfoSpecificId":2061,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29072,"Description":"1 month","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2061,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29073,"Description":"3 years","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2061,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29074,"Description":"1 week","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2061,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2061,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5171,"LISCode":"HIV12M","PrimaryName":"HIV-1/2 Ab Confirmatory","LISName":"HIV-1/2 Ab Confirm","EMRName":"HIV-1/2 Ab Confirmatory","EMRCode":"SQHIV12M","LOINC":"69668-2","RecommendedUse":"As a confirmatory test ONLY in reflex to positive HIV screen test. ","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12175,"Aka":"Acquired Immune Deficiency Syndrome (AIDS)","TdTestInfoCommonId":5171},{"Id":12176,"Aka":"HIT Types 1 and 2 Antibodies","TdTestInfoCommonId":5171},{"Id":12177,"Aka":"HIV Antibody Differentiation","TdTestInfoCommonId":5171},{"Id":12178,"Aka":"Human Immunodeficiency Virus (HIV)","TdTestInfoCommonId":5171}],"TdBillingCommons":[{"Id":14988,"CptCode":"86689","Quantity":1,"Tmid":"30200545","CclTechComponentPrice":185.00,"CclProfComponentPrice":null,"TestNameForCdm":"HIV12 AB","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5171,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5171,"SpecialInfo":"Testing should not be performed on pediatric patients under the age of 2 years.","ClinicalInfo":"A positive assay result  interpretation confirms the presence of specific antibodies to HIV-1 and/or HIV-2 in the sample. HIV and AIDS-related conditions are clinical syndromes caused by HIV-1 and HIV-2 and their diagnoses can only be established clinically.","ClinicalReference":"","ClinicalLimitation":"False negative results may occur in individuals infected with HIV-1 and/or HIV-2 who are receiving highly active antiretroviral therapy.\nA negative or indeterminate result does not preclude the possibility of exposure to HIV or infection with HIV. An antibody response to a recent exposure may take several months to reach detectable levels. It is recommended that testing be repeated on a specimen freshly drawn after 2-4 weeks.\nA person who has antibodies to HIV-1 or HIV-2 is presumed to be infected with the virus; however, a person who has participated in in an HIV vaccine study may develop antibodies to the vaccine and may or may not be infected with HIV. It is recommended that testing be repeated on a freshly drawn sample after 2-4 weeks.\nAn indeterminate interpretation does not exclude the possibility of early seroconversion of the test subject or a cross-reaction with other retroviruses. The homology between HIV-1 and HIV-2 viruses can lead to cross reactivity between anti-HIV-1 and anti-HIV-2 antibodies. It is recommended that testing be repeated on a specimen freshly drawn after 2-4 weeks.\nSamples that met the HIV-1 positive criteria may, in some rare case, show cross reactivity on one of the HIV-2 envelope bands. In most of the cases, this profile that confirms an HIV-1 infection does not exclude the rare possibilty of a secondary HIV-2 seroconversion (co-infection).\nSamples which meet the HIV-2 positive criteria can show cross reactivity on one or more HIV-1 bands. In most cases, an HIV-1 indeterminate profile associated with an HIV-2 positive profile is a true HIV-2 only infection. 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Label specimens plainly as 'acute' or 'convalescent.' Hemolyzed, contaminated, or severely lipemic specimens will be rejected. This test is New York DOH approved.","ClinicalInfo":"A low positive result suggests past exposure or infection, while a high positive result may indicate recent or current infection, but is inconclusive for diagnosis. Seroconversion between acute and convalescent sera is considered strong evidence of recent infection. the best evidence for infection is a significant change on two appropriately timed specimens where both tests are done in the same laboratory at the same time, The presence of IgM antibodies suggests recent infection. 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Affected individuals have less than 1 percent of normal ADA catalytic activity in red cell hemolysates. ADA deficiency is the cause of 20-30 percent of SCID cases. If the patient has been recently transfused, ADA deficiency may be masked; interpret results with caution. Heterozygotes cannot be identified by this test. If clinical suspicion remains, consider testing to determine the ADA genotype: Severe Combined Immunodeficiency (SCID) Panel, Sequencing and Deletion/Duplication, 19 Genes (ARUP test code 2010219).","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2125,"ActiveDate":"2015-05-11T00:00:00","CreatedOn":"2015-04-06T07:41:00","CreatedById":183,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5228,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2125,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6108,"DictMethodologyId":33,"TdTestInfoSpecificId":2125,"DictMethodology":{"Id":33,"Name":"Kinetic Spectrophotometry (KS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2125,"DictDaysPerformedId":54,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Sun, Tue, Thu","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":22977,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2125,"IsBeakerData":false},{"Id":22978,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":34,"DictSpContainerName":"Sodium or Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2125,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":12926,"Description":"15 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2125,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":12927,"Description":"15 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2125,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":12928,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2125,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2125,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5260,"LISCode":"CMVQNT","PrimaryName":"Cytomegalovirus (CMV) DNA, Quantitative PCR, Plasma","LISName":"Cytomegalovirus (CMV) DNA, Quantitative PCR, Plasma","EMRName":"Cytomegalovirus (CMV) DNA, Quantitative PCR, Plasma","EMRCode":"SQCMVQNT","LOINC":"30247-1 ","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13645,"Aka":"CMV DNA","TdTestInfoCommonId":5260},{"Id":14553,"Aka":"CMVQNT","TdTestInfoCommonId":5260},{"Id":14554,"Aka":"SQCMVQNT","TdTestInfoCommonId":5260},{"Id":14555,"Aka":"viral load","TdTestInfoCommonId":5260},{"Id":14556,"Aka":"CMVDNA","TdTestInfoCommonId":5260}],"TdBillingCommons":[{"Id":16457,"CptCode":"87497","Quantity":1,"Tmid":"30600475","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Quantification, Cytomegalovirus","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5260,"IsBeakerData":false}],"TdIncludes":[{"Id":26291,"TestName":"CMV DNA","Rank":1,"TdTestInfoCommonId":5260},{"Id":26292,"TestName":"CMV DNA (IU/mL)","Rank":2,"TdTestInfoCommonId":5260},{"Id":26293,"TestName":"CMV DNA (log IU/mL)","Rank":3,"TdTestInfoCommonId":5260}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5260,"SpecialInfo":"CMVQNT should only be utilized for EDTA plasma. For saliva and urine, utilize CMVQL. For amniotic fluid, utilize CMVAMF. For all other specimen types (CSF, BAL, fluids, tissue, bone marrow), utilize CMVCSF.","ClinicalInfo":"Cytomegalovirus (CMV) is a common viral pathogen that can cause severe disease in immunocompromised patients, and lead to a range of presentations in congenitally-exposed infants. cobas CMV is an FDA-approved in vitro nucleic acid amplification test for the quantitation of cytomegalovirus (CMV) DNA in human EDTA plasma, and is intended for use as an aid in the management of CMV in solid organ transplant patients and in hematopoietic stem cell transplant patients. In patients receiving anti-CMV therapy, serial DNA measurements can be used to assess viral response to treatment. The results from cobas CMV must be interpreted within the context of all relevant clinical and laboratory findings. This test is not intended for use as a screening test for blood or blood products. The assay is a quantitative PCR assay that targets highly-conserved regions of the CMV DNA polymerase (UL54) gene, and is reported out in international units (IU/mL). The linear range of the assay is 34.5 to 10,000,000 IU/mL (1.54 - 7.00 log IU/mL). The lower limit of detection of the assay is 34.5 IU/mL.","ClinicalReference":"1. Kotton CN, Kumar D, Caliendo AM, Huprikar S, Chou S, Danziger-Isakov L, Humar A; The Transplantation Society International CMV Consensus Group. The Third International Consensus Guidelines on the Management of Cytomegalovirus in Solid-organ Transplantation. Transplantation. 2018 Jun;102(6):900-931. doi: 10.1097/TP.0000000000002191. PMID: 29596116.\n2. U.S. Food and Drug Administration (FDA). Premarket Approval Summary of Safety and Effectiveness Data P160041. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/pdf16/P160041B.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Mutations within the highly-conserved regions of the CMV DNA polymerase (UL54) gene covered by cobas CMV may affect primers and/or probe binding resulting in the under-quantitation of virus or failure to detect the presence of virus. The cobas CMV mitigates this risk through the use of redundant amplification primers. Negative test results do not preclude CMV infection or tissue-invasive CMV disease, and test results should therefore not be the sole basis for patient management decisions. Due to potential variability from measurements with different CMV assays, it is recommended that the same device (or assay) be used for the measurement of CMV viral load when managing CMV infection in individual patients. Current guidelines based on the precision of PCR tests suggest that the changes in serial viral load measurements should be at least 3-fold (0.5 log10) to represent biologically important changes.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2128,"ActiveDate":"2015-06-30T00:00:00","CreatedOn":"2015-04-13T11:30:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5260,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2128,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13014,"DictMethodologyId":482,"TdTestInfoSpecificId":2128,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2128,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":51422,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. 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Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.\n","LogicalOperation":null,"DictSpContainerId":32,"DictSpContainerName":"EDTA PPT (White)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2128,"IsBeakerData":false},{"Id":51423,"SpecialInstructions":"Minimum volume for testing is 1.0 mL of plasma. 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Sample cannot be shared with a test performed outside of Molecular Microbiology. Sample can only be shared with HSVPCR, VZVPCR, CMVQNT, HCQPCR, HIVRNA, HBVDNU, EBVQNT, or BKQUAN.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":20,"DictSpTransportTemperatureName":"Centrifuge, aliquot and refrigerate ASAP.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2128,"IsBeakerData":false},{"Id":678980,"SpecialInstructions":"Collect EDTA plasma according to standard protocol. Centrifuge (at 1,300 RCF for a minimum of 10 minutes) and aliquot into a sterile secondary tube within 24 hours of collection. Plasma must be aliquoted first if sample is to be frozen. Sample cannot be shared with a test performed outside of Molecular Microbiology. 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When TPMT activity is low, it is predicted that proportionately more 6-mercaptopurine can be converted into the cytotoxic 6-thioguanine nucleotides that accumulate in the bone marrow causing excessive toxicity. The activity of TPMT is measured by the nanomoles of 6-methylmercaptopurine (inactive metabolite) produced per 1 mL of packed red blood cells, (U/mL). TPMT phenotype testing does not replace the need for clinical monitoring of patients treated with thiopurine drugs. Genotype for TPMT cannot be inferred from TPMT activity (phenotype). Phenotype testing should not be requested for patients currently treated with thiopurine drugs. Current TPMT phenotype may not reflect future TPMT phenotype, particularly in patients who received blood transfusion within 30-60 days of testing. TPMT enzyme activity can be inhibited by several drugs such as: naproxen (Aleve), ibuprofen (Advil, Motrin), ketoprofen (Orudis), furosemide (Lasix), sulfasalazine (Azulfidine), mesalamine (Asacol), olsalazine (Dipentum), mefenamic acid (Ponstel), thiazide diuretics, and benzoic acid inhibitors. TPMT inhibitors may contribute to falsely low results; patients should abstain from these drugs for at least 48 hours prior to TPMT testing. Falsely low results may also occur as a result of inappropriate specimen handling and hemolysis.\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2171,"ActiveDate":"2015-10-22T00:00:00","CreatedOn":"2015-10-16T09:34:00","CreatedById":183,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5297,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2171,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8178,"DictMethodologyId":182,"TdTestInfoSpecificId":2171,"DictMethodology":{"Id":182,"Name":"Enzymatic","Description":null},"TdTestInfoSpecific":null},{"Id":8179,"DictMethodologyId":265,"TdTestInfoSpecificId":2171,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2171,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":65,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"4 - 6 days"},"TdSpecimenRequirements":[{"Id":31360,"SpecialInstructions":"Collect 2 separate EDTA tubes. 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Substituted: Creatinine is less than 2mg/dL and the Specific gravity is less than 1.003 or greater than or equal to 1.020. Adulterated: pH is less than 4 or greater than or equal to 11; Nitrite is greater than or equal to 500mg/L; Oxidant is greater than or equal to 200mg/L.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2174,"ActiveDate":"2014-12-30T00:00:00","CreatedOn":"2014-10-28T10:58:00","CreatedById":7,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5187,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2174,"IsStat":false,"Comments":"","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13808,"DictMethodologyId":265,"TdTestInfoSpecificId":2174,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2174,"DictDaysPerformedId":17,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"6 days per week","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":39860,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":181,"DictSpContainerName":"Urine","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2174,"IsBeakerData":false},{"Id":39861,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2174,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22827,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2174,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22828,"Description":"14 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2174,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22829,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2174,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2174,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5195,"LISCode":"MSHA","PrimaryName":"Melanocyte Stimulation Hormone, Alpha (a-MSH)","LISName":"Melanocyte Stimulation Hormone, Alpha (a-MSH)","EMRName":"Melanocyte Stimulation Hormone, Alpha (a-MSH)","EMRCode":"SQMSHA","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9610,"Aka":"Alpha-Melanocyte-Stimulating Hormone","TdTestInfoCommonId":5195},{"Id":9611,"Aka":"a-MSH","TdTestInfoCommonId":5195}],"TdBillingCommons":[{"Id":12638,"CptCode":"83519","Quantity":1,"Tmid":"30105865","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"MELANOCYTE STIM HORMONE ALP","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5195,"IsBeakerData":false}],"TdIncludes":[{"Id":26611,"TestName":"Melanocyte Stimulating Hormone, Alpha\t","Rank":1,"TdTestInfoCommonId":5195}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5195,"SpecialInfo":"Morning fasting specimen is preferred. 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Please refer any requests from outside laboratories to Client Services at 800-628-6816 or 216-444-5755. Specialized blood collection tubes are required. Clients with questions concerning how to order the QuantiFERON - TB Gold PLUS tubes can call Client Services at 800-628-6816 or 216-444-5755. Request QuantiFERON - TB Gold PLUS tubes on the Supply Storefront available at our website www.clevelandcliniclabs.com. Blood collection tubes should be at room temperature 17 - 25 °C (62.6 - 77 °F) at the time of blood collection. For each patient, collect 1 mL of blood by venipuncture directly into each of the QFT - Plus Blood Collection Tubes. This procedure should be performed by a trained phlebotomist. As 1 mL tubes draw blood relatively slowly, keep the tube on the needle for 2 - 3 seconds once the tube appears to have completed filling. This will ensure that the correct volume is drawn. The black mark on the side of the tubes indicates the validated range of 0.8 - 1.2 mL. If the level of blood in any tube is outside of the indicator mark, a new blood sample should be obtained. Under or over - filling of the tubes outside of the 0.8 - 1.2 mL range may lead to erroneous results. If a “butterfly needle” is being used to collect blood, a “purge” tube should be used to ensure that the tubing is filled with blood prior to the QFT - Plus Blood Collection Tubes being used. DO NOT COLLECT USING A LINE DRAW. QFT - Plus Blood Collection Tubes can be used up to an altitude of 2650 feet (810 meters) above sea level. HA QFT - Plus Blood Collection Tubes should be used at altitudes between 3350 and 6150 feet (1020 and 1875 meters). If using QFT - Plus Blood Collection Tubes outside these altitude ranges between 2650 and 3350 feet (810 and 1020 meters) or above 6150 feet (1875 meters), or if low blood draw volume occurs, users can collect blood with a syringe and immediately transfer 1 mL to each of the 4 tubes. For safety reasons, this is best performed by removing the syringe needle, ensuring appropriate safety procedures, removing the caps from the 4 QFT - Plus Blood Collection Tubes and adding 1 mL of blood to each (to the black mark on the side of the tube label which indicates the validated range of 0.8 - 1.2 mL). Replace the caps securely and mix as described below. Ensure each tube (Nil, TB1, TB2 and Mitogen) is identifiable by its label or other means once the cap is removed by the performing laboratory. Immediately after filling the tubes, shake them 10 times just firmly enough to make sure the entire inner surface of the tube is coated with blood. This will dissolve antigens on the tube walls. Over vigorous shaking may cause gel disruption and could lead to aberrant results. The tubes must be kept at room temperature and sent ASAP. DO NOT CENTRIFUGE. Tubes must reach Cleveland Clinic Laboratories at the Main Campus within 12 hours of collection. ","ClinicalInfo":"Screening test for Tuberculosis (TB)","ClinicalReference":"","ClinicalLimitation":"Inaccurate or indeterminate results may occur if adherence to collection instructions are not followed.\nGrossly hemolyzed samples, lipemic samples, and samples containing particulate matter or exhibiting obvious microbial contamination will be rejected.\nBacterial contamination or heat inactivation of samples may affect the results.\nHeterophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays. Patients routinely exposed to animals or to animal serum products can be prone to this interference and anomalous values may be observed.\nThe performance characteristics have not been evaluated for individuals younger than 18 years, pregnant women, individuals with impaired or altered immune function or other clinical conditions (HIV infection, transplant recipients, hematological disorders, malignancies, diabetes, chronic renal failure).\n","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2216,"ActiveDate":"2018-09-12T00:00:00","CreatedOn":"2018-06-06T15:53:00","CreatedById":144,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5666,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2216,"IsStat":false,"Comments":"Note the requirements for External Clients.","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13157,"DictMethodologyId":164,"TdTestInfoSpecificId":2216,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2216,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":71,"DictDaysPerformed":"Mon - Sun","DictReported":"2 - 3 days"},"TdSpecimenRequirements":[{"Id":37738,"SpecialInstructions":"Four special tubes (QuantiFERON Gold PLUS tubes only) must be drawn: Grey cap with white ring (Nil control); Green cap with white ring (TB1 Ag); Yellow cap with white ring (TB2 Ag); Purple cap with white ring (Mitogen Control). Tubes must be kept at ambient temperature until received in the testing laboratory. DO NOT CENTRIFUGE. See Special information section. Samples collected on Saturday or Sunday must be received at Cleveland Clinic Laboratories by 11:00 p.m. See Special Information section.","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":99,"DictSpTypeName":"See note","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":2216,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21491,"Description":"Refer To Special Information","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2216,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21492,"Description":" Unacceptable  ","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2216,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21493,"Description":" Unacceptable  ","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2216,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2216,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5667,"LISCode":"INTPGP","PrimaryName":" Mycobacterium tuberculosis by QuantiFERON TB Gold Plus, Incubated  ","LISName":"TB by QuantiFERON","EMRName":"Blood TB Screen, Incubated","EMRCode":"SQINTPGP","LOINC":"","RecommendedUse":"Mycobacterium tuberculosis by QuantiFERON TB Gold Plus test is a cellular assay that is used as an aid in diagnosis of latent tuberculosis (TB) infection (LTBI). The test is not suitable for active TB work up. Clinical and epidemiological correlation is required.  ","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12421,"CptCode":"86480","Quantity":1,"Tmid":"30200365","CclTechComponentPrice":113.00,"CclProfComponentPrice":null,"TestNameForCdm":"TB GOLD PLUS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5667,"IsBeakerData":true}],"TdIncludes":[{"Id":17866,"TestName":"TB Result","Rank":1,"TdTestInfoCommonId":5667},{"Id":17867,"TestName":"TB1 Antigen minus Nil Result","Rank":3,"TdTestInfoCommonId":5667},{"Id":17868,"TestName":"TB2 Antigen minus Nil Result","Rank":4,"TdTestInfoCommonId":5667},{"Id":17869,"TestName":"Mitogen minus Nil Result","Rank":5,"TdTestInfoCommonId":5667},{"Id":17870,"TestName":"TB Interpretation","Rank":6,"TdTestInfoCommonId":5667},{"Id":17871,"TestName":"Nil Result","Rank":2,"TdTestInfoCommonId":5667}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5667,"SpecialInfo":"External clients must be pre-approved to collect and submit specimens. Please refer any requests from outside laboratories to Client Services at 800-628-6816 or 216-444-5755. Specialized blood collection tubes are required. Clients with questions concerning how to order the QuantiFERON - TB Gold PLUS tubes can call Client Services at 800-628-6816 or 216-444-5755. Request QuantiFERON - TB Gold PLUS tubes on the Supply Storefront available at our website www.clevelandcliniclabs.com. Blood collection tubes should be at room temperature 17 - 25 °C (62.6 - 77 °F) at the time of blood collection. For each patient, collect 1 mL of blood by venipuncture directly into each of the QFT - Plus Blood Collection Tubes. This procedure should be performed by a trained phlebotomist. As 1 mL tubes draw blood relatively slowly, keep the tube on the needle for 2 - 3 seconds once the tube appears to have completed filling. The black mark on the side of the tubes indicates the validated range of 0.8 - 1.2 mL. If the level of blood in any tube is outside of the indicator mark, a new blood sample should be obtained. Under or over - filling of the tubes outside of the 0.8 - 1.2 mL range may lead to erroneous results. If a “butterfly needle” is being used to collect blood, a “purge” tube should be used to ensure that the tubing is filled with blood prior to the QFT - Plus Blood Collection Tubes being used. DO NOT COLLECT USING A LINE DRAW. QFT - Plus Blood Collection Tubes can be used up to an altitude of 2650 feet (810 meters) above sea level. Refer to the manufacturer’s instructions for use if outside this altitude. Immediately after filling the tubes, shake them 10 times just firmly enough to make sure the entire inner surface of the tube is coated with blood. This will dissolve antigens on the tube walls. Over vigorous shaking may cause gel disruption and could lead to aberrant results. Following labeling, filling and shaking, the tubes must be transferred to a 37°C ± 1 °C  incubator as soon as possible, and within 16 hours of collection. Prior to incubation, maintain tubes at room temperature (22 °C ± 5 °C [71.6 °F ± 9 °F]). If QFT - Plus Blood Collection Tubes are not incubated at 37 °C directly after blood collection and shaking, invert the tubes to mix 10 times prior to incubation at 37 °C. Incubate the QFT - Plus Blood Collection Tubes UPRIGHT at 37 °C ± 1 °C for 16 to 24 hours. The incubator does not require CO2 or humidification. After incubation of the blood collection tubes at 37 °C ± 1 °C, tubes may be held between 4 - 27 °C for up to 3 days prior to centrifugation. After incubation of the tubes at 37 °C ± 1 °C, harvesting of the plasma is facilitated by centrifuging tubes for 15 minutes at 2000 to 3000 RCF (g). The gel plug will separate the cells from the plasma. If this does not occur, the tubes should be re-centrifuged. Samples can be stored in centrifuged QFT - Plus Blood Collection Tubes for up to 28 days at 2 - 8 °C.","ClinicalInfo":"Screening test for Tuberculosis (TB)","ClinicalReference":"","ClinicalLimitation":"Inaccurate or indeterminate results may occur if adherence to collection instructions are not followed.\nGrossly hemolyzed samples, lipemic samples, and samples containing particulate matter or exhibiting obvious microbial contamination will be rejected.\nBacterial contamination or heat inactivation of samples may affect the results.\nHeterophilic antibodies in human serum can react with reagent immunoglobulins, interfering with in vitro immunoassays. Patients routinely exposed to animals or to animal serum products can be prone to this interference and anomalous values may be observed.\nThe performance characteristics have not been evaluated for individuals younger than 18 years, pregnant women, individuals with impaired or altered immune function or other clinical conditions (HIV infection, transplant recipients, hematological disorders, malignancies, diabetes, chronic renal failure).","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2217,"ActiveDate":"2018-09-12T00:00:00","CreatedOn":"2018-06-06T16:30:00","CreatedById":144,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5667,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2217,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13154,"DictMethodologyId":164,"TdTestInfoSpecificId":2217,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2217,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":71,"DictDaysPerformed":"Mon - Sun","DictReported":"2 - 3 days"},"TdSpecimenRequirements":[{"Id":37606,"SpecialInstructions":"Note: External clients must be pre-approved by testing laboratory manager to collect and submit specimens (800-628-6816 or 216-444-5755). Four special Qiagen collection tubes must be drawn. Do not collect using a line draw. Tubes must be incubated and processed per the protocol in Special Information section.","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":53,"DictSpVolumeName":"Other","TdTestInfoSpecificId":2217,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21404,"Description":"Refer to Special Information.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2217,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21405,"Description":"28 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2217,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21406,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2217,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2217,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5616,"LISCode":"SUSANA","PrimaryName":"Antimicrobial Susceptibility - Anaerobic Organism","LISName":"Antimicrobial Susceptibility - Anaerobic Organism","EMRName":"Antimicrobial Susceptibility - Anaerobic Organism","EMRCode":"SQSUSANA","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":2,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":11814,"CptCode":"varies","Quantity":1,"Tmid":"99999998","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"USING WILD CODE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5616,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5616,"SpecialInfo":"Note: Specimen source and isolate identification are required. Aerobic conditions are unacceptable. Also, mixed cultures or non-viable organisms are not acceptable. The following agents are available for testing: ampicillin/sulbactam, amoxicillin/clavulanic acid, cefoxitin, clindamycin, doxycycline, ertapenem, imipenem, meropenem, metronidazole, moxifloxicin, penicillin G, piperacillin/tazobactam, tigecycline, and vancomycin. Selective reporting by organism and source. Antibiotics other than those listed are available as an individual MIC by request only. There will be an additional charge for all organisms not submitted in pure culture. Species identification MUST be provided or the lab will perform the ID at an additional cost. ","ClinicalInfo":"Useful for determining in vitro susceptibility to antimicrobial agents for anaerobic bacterial organisms. Anaerobic susceptibility testing is appropriate in the case of serious infections involving blood, bone, joint, tissue, or brain abscess.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2219,"ActiveDate":"2018-04-19T00:00:00","CreatedOn":"2018-03-09T13:08:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5616,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2219,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9242,"DictMethodologyId":152,"TdTestInfoSpecificId":2219,"DictMethodology":{"Id":152,"Name":"Broth Dilution","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2219,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":103,"DictDaysPerformed":"Sun - Sat","DictReported":"6 - 9 days"},"TdSpecimenRequirements":[{"Id":680278,"SpecialInstructions":"Collect actively growing isolate in pure culture. Transport sealed container with pure culture on agar slant in anaerobic transport pouch or on a swab in anaerobic transport media, and place each specimen in an individually sealed bag. Note: Specimen source and isolate identification are required.","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":21,"DictSpTypeName":"Isolate of organism","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":2219,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20176,"Description":"72 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2219,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20177,"Description":"Unacceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2219,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20178,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2219,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2219,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5660,"LISCode":"ABS19","PrimaryName":"CD19 Count","LISName":"CD19 Absolute Count","EMRName":"CD19 Absolute Count","EMRCode":"SQABS19","LOINC":"8116-6, 8117-4, 26464-8","RecommendedUse":"","DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":3,"DictIntendedFor":null,"TdAlias":[{"Id":13480,"Aka":"CD19","TdTestInfoCommonId":5660}],"TdBillingCommons":[{"Id":16203,"CptCode":"86355","Quantity":1,"Tmid":"30200235","CclTechComponentPrice":142.00,"CclProfComponentPrice":null,"TestNameForCdm":"%IMMDEF B CELL TOTAL CNT","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5660,"IsBeakerData":false},{"Id":17760,"CptCode":"85048","Quantity":1,"Tmid":"30500090","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"LEUKO (WBC) COUNT AUTO","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5660,"IsBeakerData":true}],"TdIncludes":[{"Id":24321,"TestName":"CD19%","Rank":1,"TdTestInfoCommonId":5660},{"Id":24322,"TestName":"CD19 absolute number","Rank":2,"TdTestInfoCommonId":5660}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5660,"SpecialInfo":"4ml Lavender (EDTA).  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It is not meant for enumeration of T-cells or NK cells.","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":2224,"ActiveDate":"2018-08-23T00:00:00","CreatedOn":"2018-05-25T14:14:00","CreatedById":2,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5660,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2224,"IsStat":false,"Comments":"","DictPerformingLabId":2,"DictPerformingLab":{"Id":2,"Name":"Flow Cytometry (x40042)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2224,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Mon - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":50633,"SpecialInstructions":"Draw one 2 ml EDTA tube.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2224,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29059,"Description":"Maintain at room temperature when transporting to laboratory. \nSpecimen stability is < 72 hours old. 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This test is New York DOH approved.","ClinicalInfo":"Used to confirm and quantify the presence of hepatitis D virus. The quantitative range of this assay is 2.0 - 6.7 log IU/mL (92 - 4,600,000 IU/mL). A negative result (< 2.0 log IU/mL or < 92 IU/mL) does not rule out the presence of PCR inhibitors in the patient specimen or HDV RNA concentrations below the level of detection of the test. Inhibition may also lead to underestimation of viral quantitation. The limit of quantification for this test is 2.0 log IU/mL (92 IU/mL). If the test did NOT detect the virus, the result will be reported as \"Not Detected < 2.0 log IU/mL (< 92 IU/mL).\" If the test DETECTED the presence of the virus but was not able to accurately quantify the number of copies, the result will be reported as \"Detected, < 2.0 log IU/mL (< 92 IU/mL).\" ","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2270,"ActiveDate":"2018-10-11T00:00:00","CreatedOn":"2018-06-21T13:31:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5680,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2270,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9131,"DictMethodologyId":482,"TdTestInfoSpecificId":2270,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2270,"DictDaysPerformedId":30,"DictHoursPerformedId":null,"DictReportedId":68,"DictDaysPerformed":"Mon, Thu","DictReported":"3 - 6 days"},"TdSpecimenRequirements":[{"Id":35231,"SpecialInstructions":"Specimen source required. Separate serum from cells and transfer into sterile aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2270,"IsBeakerData":false},{"Id":35232,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2270,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19895,"Description":"30 days","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2270,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19896,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2270,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19897,"Description":"24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2270,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2270,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5741,"LISCode":"2C19CY","PrimaryName":"CYP2C19 (Cytochrome P450 2C19)","LISName":"CYP450 2C19,12 Var","EMRName":"CYP450 2C19 - 12 Variants","EMRCode":"SQ2C19CY","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12650,"Aka":"P450 2C19 Genotype","TdTestInfoCommonId":5741}],"TdBillingCommons":[{"Id":15831,"CptCode":"81225","Quantity":1,"Tmid":"31002905","CclTechComponentPrice":355.00,"CclProfComponentPrice":null,"TestNameForCdm":"CYTOCHROME P450 2C19","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5741,"IsBeakerData":false}],"TdIncludes":[{"Id":23190,"TestName":"Interpretation","Rank":3,"TdTestInfoCommonId":5741},{"Id":24756,"TestName":"CYP2C19 Genotype","Rank":1,"TdTestInfoCommonId":5741},{"Id":24757,"TestName":"CYP2C19 Phenotype","Rank":2,"TdTestInfoCommonId":5741},{"Id":25651,"TestName":"EER CYP2C19","Rank":4,"TdTestInfoCommonId":5741}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5741,"SpecialInfo":"Plasma, serum and frozen specimens in glass collection tubes will be rejected. Specimens collected in sodium heparin or lithium heparin are unacceptable. Whole blood is the preferred specimen. Saliva samples that yield inadequate DNA quality and/or quantity will be reported as inconclusive if test performance does not meet laboratory-determined criteria for reporting. This test is New York DOH approved.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2272,"ActiveDate":"2019-05-20T00:00:00","CreatedOn":"2019-04-07T09:08:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5741,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2272,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12490,"DictMethodologyId":271,"TdTestInfoSpecificId":2272,"DictMethodology":{"Id":271,"Name":"Fluorescence Monitoring","Description":null},"TdTestInfoSpecific":null},{"Id":12491,"DictMethodologyId":168,"TdTestInfoSpecificId":2272,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2272,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":127,"DictDaysPerformed":"Varies","DictReported":"6 - 11 days"},"TdSpecimenRequirements":[{"Id":48915,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2272,"IsBeakerData":false},{"Id":48916,"SpecialInstructions":"Whole blood","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2272,"IsBeakerData":false},{"Id":48917,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":33,"DictSpContainerName":"ACD A or B (Yellow)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2272,"IsBeakerData":false},{"Id":48918,"SpecialInstructions":"Collect using Saliva Collection Device by DNA Genotek (OCD-100, ARUP supply #49295)","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":61,"DictSpTypeName":"Saliva","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":2272,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28144,"Description":"Whole blood: 1 week; Saliva: Unacceptable","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2272,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28145,"Description":"Whole blood: 72 hours; Saliva: 2 weeks","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2272,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28146,"Description":"Whole blood: 1 month; Saliva: Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2272,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2272,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5742,"LISCode":"CHAETG","PrimaryName":"Allergen, Fungi and Molds, Chaetomium globosum IgE","LISName":"ALGN C. globosum IgE","EMRName":"ALGN, Chaetomium globosum IgE","EMRCode":"SQCHAETG","LOINC":"7200-9","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12572,"CptCode":"86003","Quantity":1,"Tmid":"30212835","CclTechComponentPrice":35.00,"CclProfComponentPrice":null,"TestNameForCdm":"ALGN CHAETOMIUM GLOB IGE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5742,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5742,"SpecialInfo":"Hemolyzed, icteric, or lipemic specimens will be rejected. This test is New York DOH approved.","ClinicalInfo":"Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":2273,"ActiveDate":"2019-05-21T00:00:00","CreatedOn":"2019-03-25T10:21:00","CreatedById":198,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5742,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2273,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9871,"DictMethodologyId":413,"TdTestInfoSpecificId":2273,"DictMethodology":{"Id":413,"Name":"Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2273,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":38080,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2273,"IsBeakerData":false},{"Id":38081,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":138,"DictSpVolumeName":"0.25 mL","TdTestInfoSpecificId":2273,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21730,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2273,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21731,"Description":"1 year","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2273,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21732,"Description":"48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2273,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2273,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5743,"LISCode":"2D6GTP","PrimaryName":"CYP2D6 (Cytochrome P450 2D6)","LISName":"CYP450 2D6 Geno","EMRName":"CYP450 2D6 Genotype","EMRCode":"SQ2D6GTP","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12611,"Aka":"2D6","TdTestInfoCommonId":5743},{"Id":12612,"Aka":"P450 2D6 Genotype","TdTestInfoCommonId":5743}],"TdBillingCommons":[{"Id":15785,"CptCode":"81226","Quantity":1,"Tmid":"31002915","CclTechComponentPrice":515.00,"CclProfComponentPrice":null,"TestNameForCdm":"CYTOCHROME P450 2D6","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5743,"IsBeakerData":false},{"Id":18232,"CptCode":"if reflexed, add 81479","Quantity":1,"Tmid":"31004565","CclTechComponentPrice":550.00,"CclProfComponentPrice":null,"TestNameForCdm":"CYP2D6 UNLISTED MOLEC PATH","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5743,"IsBeakerData":false}],"TdIncludes":[{"Id":23123,"TestName":"Interpretation","Rank":4,"TdTestInfoCommonId":5743},{"Id":24758,"TestName":"CYP2D6 Genotype","Rank":2,"TdTestInfoCommonId":5743},{"Id":24759,"TestName":"CYP2D6 Phenotype","Rank":3,"TdTestInfoCommonId":5743},{"Id":24971,"TestName":"2D6GENO Specimen","Rank":1,"TdTestInfoCommonId":5743},{"Id":25680,"TestName":"EER CYP2D6","Rank":5,"TdTestInfoCommonId":5743}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5743,"SpecialInfo":"Plasma, serum and frozen specimens in glass collection tubes will be rejected. Specimens collected in sodium heparin or lithium heparin are unacceptable. Whole blood is the preferred specimen type. Saliva samples that yield inadequate DNA quality and/or quantity will be reported as inconclusive if test performance does not meet laboratory-determined criteria for reporting. Saliva is only validated for the OpenArray and CNV portions of testing and not the long-range PCR/duplication testing. Long-range PCR/duplication testing will not be performed for saliva samples. If long-range PCR/duplication testing is performed, additional charges will apply and TAT will be extended by five to seven days. Approximately less than 5% of samples require 2D6 copy number determination. This test is New York DOH approved.","ClinicalInfo":"Background: Characteristics: The cytochrome P450 (CYP) isozyme 2D6 is involved in the metabolism of many drugs. Variants in the gene that codes for CYP2D6 may influence pharmacokinetics of CYP2D6 substrates, and may predict or explain non-standard dose requirement, therapeutic failure or adverse reactions. Inheritance: Autosomal co-dominant. Cause: CYP2D6 gene variants and copy number affect enzyme function. Variants tested: Negative: No variants detected is predictive of the *1 functional allele. *2 (rs16947, c.2850C>T; rs1135840, c.4180G>C), *2A (rs1080985, c.-1584C>G; rs16947, c.2850C>T; rs1135840, c.4180G>C), *3 (rs35743686, c.2549delA), *4 (rs1065852, c.100C>T; rs3892097, c.1846G>A; rs1135840, c.4180G>C), *5 (gene deletion), *6 (rs5030655, c.1707delT; rs1135840, c.4180G>C), *7 (rs5030867, c.2935A>C), *8 (rs5030865, c.1758G>T; rs16947, c.2850C>T; rs1135840, c.4180G>C), *9 (rs5030656, c.2615_2617delAAGA), *10 (rs1065852, c.100C>T; rs1135840, c.4180G>C), *11 (rs1080985, c.-1584C>G; rs201377835, c.883G>C; rs16947, c.2850C>T; rs1135840, c.4180G>C), *12 (rs5030862, c.124G>A; rs16947, c.2850C>T; rs1135840, c.4180G>C), *13 (a CYP2D7-derived exon 1 conversion), *14 (rs5030865, c.1758G>A; rs16947, c.2850C>T; rs1135840, c.4180G>C), *15 (rs774671100, c.137_138insT), *17 (rs28371706, c.1023C>T; rs16947, c.2850C>T; rs1135840, c.4180G>C), *29 (rs16947, c.2850C>T; rs59421388, c.3183G>A; rs1135840, c.4180G>C), *35 (rs769258, c.31G>A; rs16947, c.2850C>T; rs1135840, c.4180G>C), *36 (a CYP2D6*10 carrying a CYP2D7-derived exon 9 conversion), *36-*10 ( a CYP2D6*36 and a CYP2D6*10 in tandem, *41 (rs16947, c.2850C>T; rs28371725, c.2988G>A; rs1135840, c.4180G>C), *45 (rs28371710, c.1716G>A; rs16947, c.2850C>T; rs1135840, c.4180G>C), *46 (rs28371696, c.77G>A; rs28371710, c.1716G>A; rs16947, c.2850C>T; rs1135840, c.4180G>C), *49 (rs1065852, c.100C>T; rs1135822, c.1611T>A; rs1135840, c.4180G>C), *53 (rs1135822, c.1611T>A), *69 (rs1065852, c.100C>T; rs16947, c.2850C>T; rs28371725, c.2988G>A; rs1135840, c.4180G>C), *114 (rs1065852, c.100C>T; rs5030865, c.1758G>A; rs16947, c.2850C>T; rs1135840, c.4180G>CDUP: complete gene duplications) Clinical Sensitivity: Drug-dependent. Methodology: Polymerase chain reaction (PCR) and fluorescence monitoring. Sequencing is only performed if needed to characterize a duplicated CYP2D6 gene. Analytical Sensitivity and Specificity: Greater than 99%","ClinicalReference":"","ClinicalLimitation":"Only the targeted CYP2D6 variants will be detected by this panel, and assumptions about phase and content are made to assign alleles. Publicly available sources such as the www.pharmvar.org or www.pharmgkb.org provide guidance on phenotype predictions and allele frequencies. A combination of the *5 (gene deletion) and a gene duplication cannot be specifically identified. This combination is not expected to adversely affect the phenotype prediction. Diagnostic errors can occur due to rare sequence variations. Risk of therapeutic failure or adverse reactions with CYP2D6 substrates may be affected by genetic and non-genetic factors that are not detected by this test. This result does not replace the need for therapeutic drug or clinical monitoring.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2274,"ActiveDate":"2019-05-20T00:00:00","CreatedOn":"2019-04-07T10:00:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5743,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2274,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12447,"DictMethodologyId":271,"TdTestInfoSpecificId":2274,"DictMethodology":{"Id":271,"Name":"Fluorescence Monitoring","Description":null},"TdTestInfoSpecific":null},{"Id":12448,"DictMethodologyId":168,"TdTestInfoSpecificId":2274,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null},{"Id":13159,"DictMethodologyId":82,"TdTestInfoSpecificId":2274,"DictMethodology":{"Id":82,"Name":"Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2274,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":127,"DictDaysPerformed":"Varies","DictReported":"6 - 11 days"},"TdSpecimenRequirements":[{"Id":48774,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2274,"IsBeakerData":false},{"Id":48775,"SpecialInstructions":"Whole blood","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2274,"IsBeakerData":false},{"Id":48776,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":33,"DictSpContainerName":"ACD A or B (Yellow)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2274,"IsBeakerData":false},{"Id":48777,"SpecialInstructions":"Collect using Saliva Collection Device by DNA Genotek (OCD-100, ARUP Supply #49295)","LogicalOperation":null,"DictSpContainerId":1,"DictSpContainerName":"See note","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":61,"DictSpTypeName":"Saliva","DictSpVolumeId":54,"DictSpVolumeName":"N/A","TdTestInfoSpecificId":2274,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28058,"Description":"Whole blood: 1 week; 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Pertussis occurs most commonly in children but also occurs in adolescents and adults and outbreaks have been documented in fully vaccinated populations due to waning immunity (immunity has been shown to decrease 5-10 years after vaccination). Early (catarrhal) pertussis disease is non-specific, and classic signs of pertussis (paroxysmal coughing, inspiratory ‘whoop’, post-tussive emesis, as well as apnea or cyanosis in infants) do not arise until approximately two weeks after the initial onset of symptoms. Bordetella parapertussis (BPP) is known to cause a milder pertussis-like disease. For diagnosis of pertussis, NAAT performed on a nasopharyngeal swab collected within 2-3 weeks of symptom onset is the most sensitive method.\n\nThe Simplexa Bordetella Direct Assay is an in vitro diagnostic test for the qualitative detection and differentiation of Bp and BPP nucleic acids from nasopharyngeal specimens from patients with signs and symptoms of Bordetella infection of the respiratory tract. The assay uses real-time PCR to target the IS481 and IS1001 sequence of BP and BPP genomes respectively. Both targets can exhibit cross reactivity with other members of the Bordetella genus.","ClinicalReference":"Chow SK, Arbefeville S, Boyanton BL Jr, Dault EM, Dunn J, Ferrieri P, Greene W, Pence MA, Otiso J, Richter S, Schutzbank TE. Multicenter Performance Evaluation of the Simplexa Bordetella Direct Kit in Nasopharyngeal Swab Specimens. J Clin Microbiol. 2020 Dec 17;59(1):e01041-20. doi: 10.1128/JCM.01041-20. PMID: 33055187","ClinicalLimitation":"The IS481 insertional element can also be present in B. holmesii and B. bronchiseptica. Specimens collected from patients with respiratory infection caused by B. pertussis, B. holmesii or B. bronchiseptica may yield positive test results in IS481 assays. B. holmesii infection may cause clinical illness similar to B. pertussis, and mixed outbreaks involving both B. pertussis and B. holmesii infection have been reported. Additional testing should be performed if necessary to differentiate B. holmesii and B. pertussis. B. bronchiseptica is a rare cause of infection in humans. When clinical factors suggest that B. pertussis may not be the cause of respiratory infection, other clinically appropriate investigation(s) should be carried out in accordance with published guidelines.\n\nEnvironmental contamination of an exam room from a prior patient or a recent pertussis vaccination administration may result in false-positive test results. As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. 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Rotate the swabs against the inside of the nostril for 3 seconds. Apply slight pressure with a finger on the outside of the nose to ensure good contact between the swabs and inside of the nose. Using the same swabs, repeat for the other nostril. Place the swabs into the transport tube (swabs should stay attached to the red cap). Make sure the red cap is tightly on the transport tube. \n","ClinicalInfo":"This test detects Staphylococcus aureus (SA) and methicillin-resistant Staphylococcus aureus (MRSA) from nasal swabs to determine if the patient carries S. aureus in their normal microbiome. This test is only for nares specimens. Specimens other than nares require culture (SANSAL). ","ClinicalReference":"","ClinicalLimitation":"The Staphylococcus aureus PCR test is a screening test for nasal carriage.  A negative result does not preclude MRSA/SA colonization.  \n\nResults from the Xpert SA Nasal Complete assay should be interpreted in conjunction with other laboratory and clinical data available to the clinician, and should be used as an adjunct to nosocomial infection control efforts to identify patients needing enhanced precautions. Results should not be used to guide or monitor treatment for MRSA or SA infections.  \nErroneous test results might occur from improper specimen collection, failure to follow the recommended sample collection, handling and storage procedures, technical error, sample mix-up, or because the number of organisms in the specimen is too low to be detected by the test. Careful compliance with the instructions in this insert is necessary to avoid erroneous results.  \nA positive test result does not necessarily indicate the presence of viable organisms. It is however, presumptive for the presence of MRSA or SA.  \nThe Xpert SA Nasal Complete assay positive result does not necessarily indicate intervention eradication failure since nonviable DNA may persist. A negative result following a previously positive test result may or may not indicate eradication success.  \nThe performance characteristics were not established for patients ≤ 21 years of age. \nBecause the detection of MRSA and SA is dependent on the number of organisms present in the sample, reliable results are dependent on proper specimen collection, handling, and storage. \nMutations or polymorphisms in primer or probe binding regions may affect detection of new or unknown MRSA variants resulting in a false negative result.  \nIn samples containing both MRSA and SA, the Xpert SA Nasal Complete assay may not detect the MRSA organisms. The pivotal clinical study included one sample with documented MRSA/SA mixed infection; the Xpert SA Nasal Complete assay successfully identified the sample as MRSA positive/SA positive.  \nIn a mixed culture, the analytical LoD of MRSA is variable when extremely high concentrations of SA are present. Competition from SA was observed at a MRSA:SA ratio of 1:1×106 in 7 of 8 SCCmec types tested. For SCCmec type VIII, competition from SA was observed at a MRSA:SA ratio of 1:1×103.  \nInhibition of the SA Nasal Complete assay resulting in Invalid test results has been observed in the presence of inhaled nasal steroids Flonase and Nasonex in SA negative samples at concentrations greater than 5% v/v, and 10% v/v, respectively. \nInhibition of the SA Nasal Complete assay resulting in false negative test results has been observed in the presence of inhaled nasal steroids Flonase and Nasonex in MRSA positive samples at concentrations greater than 1% (v/v) and 5% (v/v), respectively.  \nThe Xpert SA Nasal Complete assay may generate a false positive MRSA result when testing a mixed infection nasal specimen containing both methicillin-resistant coagulase-negative Staphylococcus and empty cassette SA.  \nThe Xpert SA Nasal Complete assay may generate false negative MRSA results when testing borderline oxacillin resistant S. aureus (BORSA). The mechanism of oxacillin resistance in BORSA strains is due to an increased production of ß-lactamases, not the mecA gene. BORSA with oxacillin MICs of 4 – 8 µg/mL are considered borderline resistant but would be reported as MRSA negative by the Xpert SA Nasal Complete assay. BORSA strains are rare in the United States.The Xpert SA Nasal Complete assay may generate false negative MRSA results when testing modified S. aureus (MOD-SA). The mechanism of oxacillin resistance in MOD-SA strains is due to changes in affinity of penicillin binding proteins for oxacillin, not the mecA gene. MOD-SA with oxacillin MICs of 4 – 8 µg/mL are considered borderline resistant but, would be reported as MRSA negative by the Xpert SA Nasal Complete assay. 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Medical Director is drafting comment and it will be shared with assigned analyst.  ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":12197,"Aka":"HAVAB-G","TdTestInfoCommonId":5958}],"TdBillingCommons":[{"Id":15022,"CptCode":"86708","Quantity":1,"Tmid":"30211730","CclTechComponentPrice":48.00,"CclProfComponentPrice":null,"TestNameForCdm":"","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5958,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5958,"SpecialInfo":"","ClinicalInfo":"The test is used to determine the immune status to Hepatitis A Virus (HAV) as a result of vaccination or past infection. Should recent infection be suspected, this test needs to be ordered along with HAV IgM test. ","ClinicalReference":"","ClinicalLimitation":"Serum is the only acceptable sample type. Performance has not been established for the use of cadaveric specimens or other body fluids. Do not use specimens with the following conditions: heat-inactivated, grossly hemolyzed or obvious microbial contamination. This assay has not been FDA cleared or approved for the screening of blood or plasma donors. This assay cannot be used for the diagnosis of acute HAV infection. Specimens from individuals with anti-E. coli, anti-CMV, or hemodialysis patients may cross-react with this assay. \n","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2371,"ActiveDate":"2020-11-24T00:00:00","CreatedOn":"2020-10-07T09:14:00","CreatedById":5,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5958,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2371,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11910,"DictMethodologyId":396,"TdTestInfoSpecificId":2371,"DictMethodology":{"Id":396,"Name":"Chemiluminescent Microparticle Immunoassay (CMIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2371,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":46771,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2371,"IsBeakerData":false},{"Id":46772,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2371,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26735,"Description":"4 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2371,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26736,"Description":"8 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2371,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":26737,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2371,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2371,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5963,"LISCode":"CVFLRS","PrimaryName":"COVID & Influenza A/B & RSV PCR, Routine","LISName":"COVID & Influenza A/B & RSV PCR, Routine","EMRName":"COVID & Influenza A/B & RSV PCR, Routine","EMRCode":"SQCVFLRS","LOINC":"95941-1","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14106,"Aka":"COV2","TdTestInfoCommonId":5963},{"Id":14107,"Aka":"COVID","TdTestInfoCommonId":5963},{"Id":14108,"Aka":"Flu","TdTestInfoCommonId":5963},{"Id":14109,"Aka":"Influenza","TdTestInfoCommonId":5963},{"Id":14111,"Aka":"Respiratory syncytial virus","TdTestInfoCommonId":5963},{"Id":14113,"Aka":"RSV","TdTestInfoCommonId":5963},{"Id":14114,"Aka":"SARS","TdTestInfoCommonId":5963},{"Id":14507,"Aka":"CVFLRS","TdTestInfoCommonId":5963},{"Id":14508,"Aka":"Respiratory","TdTestInfoCommonId":5963},{"Id":14509,"Aka":"SQCVFLRS","TdTestInfoCommonId":5963}],"TdBillingCommons":[{"Id":18581,"CptCode":"87637","Quantity":1,"Tmid":"30608405","CclTechComponentPrice":257.00,"CclProfComponentPrice":null,"TestNameForCdm":"Amplification, Routine, COVID & Influenza A/B & RSV","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5963,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5963,"SpecialInfo":"For Cleveland Clinic providers, note that this test can only be ordered from an ambulatory setting, unless it is for a lower respiratory specimen. Inpatient/ED providers should order the expedited version of this test (SQEXCFR) on upper respiratory specimens.","ClinicalInfo":"Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2 (agent of COVID-19), influenza A (Flu A), influenza B (Flu B), and respiratory syncytial virus (RSV) can be similar. These viruses are responsible for significant morbidity and mortality, especially in young, immunocompromised, and elderly patients. Accurate and timely diagnosis and differentiation between these viruses can help guide appropriate antiviral therapy, decrease inappropriate use of antibiotics, and assist in infection prevention/control efforts.\n\nThe FDA-cleared Panther Fusion SARS-CoV-2/Flu A/B/RSV assay is a fully automated multiplexed reverse-transcription real-time polymerase chain reaction (RT-PCR) test intended to aid in the differential diagnosis of SARS-CoV-2, Flu A, Flu B, and RSV infections in humans. It is not intended to detect influenza C virus infections. SARS-CoV-2, Flu A, Flu B, and RSV are generally detectable in nasopharyngeal (NP) and nasal swabs during the acute phase of infection. The assay has been modified and validated to additionally accept lower respiratory specimens (bronchoalveolar lavage, tracheal aspirate, sputum), and swabs in alternative transport media such as liquid Amies (eSwab) and saline. Nasal swabs demonstrate modestly decreased analytical sensitivity compared to NP swabs in some studies, but can be useful in cases where a patient is unable or unwilling to have an NP swab collected. Some individuals can have disease isolated to the lower respiratory tract; consider submitting these specimen types in patients with evidence of lower respiratory disease.","ClinicalReference":"1. U.S. Centers for Disease Control (CDC). Testing Guidance for Clinicians When SARS-CoV-2 and Influenza Viruses are Co-circulating. Accessed September 1, 2023. https://www.cdc.gov/flu/professionals/diagnosis/testing-guidance-for-clinicians.htm.\n2. U.S. Centers for Disease Control (CDC). Respiratory Syncytial Virus Infection (RSV): For Healthcare Providers. Accessed September 1, 2023. https://www.cdc.gov/rsv/clinical/index.html.\n3. U.S. Food and Drug Administration (FDA). 510(k) Substantial Equivalence Determination Decision Summary K222736. Accessed September 1, 2023. https://www.accessdata.fda.gov/cdrh_docs/reviews/K222736.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows.\n\nIn co-infections, there may be competitive interference causing loss of analytical sensitivity for one or more targets. Recent administration of intranasal vaccines (ie. FluMist) may lead to false positive results. As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2372,"ActiveDate":"2020-12-01T00:00:00","CreatedOn":"2020-11-17T12:17:00","CreatedById":278,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5963,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2372,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13707,"DictMethodologyId":219,"TdTestInfoSpecificId":2372,"DictMethodology":{"Id":219,"Name":"Reverse Transcription/Polymerase Chain Reaction (RT/PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2372,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":77,"DictDaysPerformed":"Sun - Sat","DictReported":"1 day"},"TdSpecimenRequirements":[{"Id":677881,"SpecialInstructions":"1. Tilt patient's head back 70 degrees. 2. Gently and slowly insert a mini-tipped flocked swab with a flexible shaft (ie. Oracle 1172111) through the nostril parallel to the palate (not upwards) until resistance is encountered or the distance is equivalent to that from the ear to the nostril of the patient, indicating contact with the nasopharynx. 3. Gently rub and roll the swab. 4. Leave swab in place for several seconds to absorb secretions. 5. Slowly remove swab while rotating it. Specimens can be collected from both sides using the same swab, but it is not necessary to collect specimens from both sides if the swab is saturated with fluid from the first collection. If a deviated septum or blockage create difficulty in obtaining the specimen from one nostril, use the same swab to obtain the specimen from the other nostril. 6. Place swab, tip first, into the transport tube provided. Break the swab shaft at the score line, discard the top portion of the stem, and close the cap.","LogicalOperation":null,"DictSpContainerId":165,"DictSpContainerName":"Universal Transport Media (UTM)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":34,"DictSpTypeName":"Nasopharyngeal swab","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":677886,"SpecialInstructions":"Sterile saline may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":82,"DictSpContainerName":"Saline","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":677887,"SpecialInstructions":"E-swabs in liquid amies may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":130,"DictSpContainerName":"E Swab","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":677888,"SpecialInstructions":"Viral transport media (including VTM, M4RT, M5, or M6) may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":113,"DictSpContainerName":"Viral Transport Media","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":678891,"SpecialInstructions":"1. Insert the entire collection tip of the regular-tip flocked swab with a rigid shaft (ie. Orcale 1063581) 1/2-3/4 of an inch or 1-1.5 cm inside the nostril. 2. Firmly sample the nasal wall by rotating the swab in a circular path against the nasal wall at least 4 times. 3. Take approximately 15 seconds to collect the specimen. Be sure to collect any nasal drainage that may be present on the swab. 4. Repeat in the other nostril using the same swab. 5. Place swab, tip first, into the transport tube provided. Break the swab shaft at the score line, discard the top portion of the stem, and close the cap.","LogicalOperation":null,"DictSpContainerId":165,"DictSpContainerName":"Universal Transport Media (UTM)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":69,"DictSpTypeName":"Nasal","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":678892,"SpecialInstructions":"Collect 2-3 mL into a sterile, leak-proof, screw-cap collection cup or sterile dry container (ie. Oracle 1619591). If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":150,"DictSpTypeName":"Bronch (BAL)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":678893,"SpecialInstructions":"Before collecting a sputum, have the patient rinse their mouth with water and discard the rinse fluid. Ask the patient to breathe deeply for three or four breaths, then hold their breath and expectorate deep cough sputum directly into a sterile, leak-proof, screw-cap collection cup or sterile dry container (ie. Oracle 1619591). Induced sputum is also acceptable. If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":59,"DictSpTypeName":"Sputum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false},{"Id":678894,"SpecialInstructions":"Collect 2-3 mL into a sterile, leak-proof, screw-cap collection cup or sterile dry container (ie. Oracle 1619591). If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":14,"DictSpTypeName":"Aspirate, tracheal","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2372,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27007,"Description":"96 hours","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2372,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27008,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2372,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30818,"Description":"24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2372,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2372,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5972,"LISCode":"CHRNPT","PrimaryName":"Chromosome Analysis, Neoplastic Tissue","LISName":"Chromosome NeoTissue","EMRName":"Chromosome Analysis Neoplastic Tissue","EMRCode":"SQCHRNPT","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":15251,"CptCode":"88239","Quantity":1,"Tmid":"31103135","CclTechComponentPrice":464.00,"CclProfComponentPrice":null,"TestNameForCdm":"CHROMO NEOPLS TIS CULTURE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5972,"IsBeakerData":false},{"Id":15252,"CptCode":"88264","Quantity":1,"Tmid":"31103145","CclTechComponentPrice":400.00,"CclProfComponentPrice":null,"TestNameForCdm":"CHRNPT CHROM ANLY 20-25","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5972,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5972,"SpecialInfo":"","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2375,"ActiveDate":"2021-03-29T00:00:00","CreatedOn":"2020-02-26T13:43:00","CreatedById":387,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5972,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2375,"IsStat":false,"Comments":"","DictPerformingLabId":28,"DictPerformingLab":{"Id":28,"Name":"Cytogenetics (x42489)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2375,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":124,"DictDaysPerformed":"Sun - Sat","DictReported":"21 days"},"TdSpecimenRequirements":[{"Id":47650,"SpecialInstructions":"Tissue should be cut with sterile instruments and placed in sterile container which holds sterile saline.  If delay in transport is anticipated sterile transport media (such as RPMI 1640) should be obtained from the Cytogenomics Laboratory.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":53,"DictSpTypeName":"Tissue","DictSpVolumeId":113,"DictSpVolumeName":"2 cubic cm","TdTestInfoSpecificId":2375,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27271,"Description":"Preferred","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2375,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27272,"Description":"Not preferred.  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Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":2399,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27724,"Description":"2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2399,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27725,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2399,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27726,"Description":"1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2399,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2399,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6052,"LISCode":"HIVNGS","PrimaryName":"HIV 1 Drug Resistance by Next Generation Sequencing","LISName":"HIV 1 Drug Resistance by NGS","EMRName":"HIV 1 Drug Resistance by NGS","EMRCode":"SQHIVNGS","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":16228,"CptCode":"87900","Quantity":1,"Tmid":"30608075","CclTechComponentPrice":319.00,"CclProfComponentPrice":null,"TestNameForCdm":"HIVNGS PHENOTYPE INFECT AGENT DRUG","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6052,"IsBeakerData":true},{"Id":16229,"CptCode":"87906","Quantity":1,"Tmid":"30608095","CclTechComponentPrice":314.00,"CclProfComponentPrice":null,"TestNameForCdm":"HIVNGS GENOTYPE DNA/RNA HIV","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6052,"IsBeakerData":true},{"Id":16230,"CptCode":"87901","Quantity":1,"Tmid":"30608085","CclTechComponentPrice":627.00,"CclProfComponentPrice":null,"TestNameForCdm":"HIVNGS GENOTYPE DNA HIV REVERSE T","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6052,"IsBeakerData":true}],"TdIncludes":[{"Id":25990,"TestName":"HIV-1 Drug Resistance by NGS\t","Rank":1,"TdTestInfoCommonId":6052},{"Id":25991,"TestName":"EER HIV-1 Drug Resistance by NGS\t","Rank":2,"TdTestInfoCommonId":6052}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6052,"SpecialInfo":"Please submit most recent viral load and test date, if available. Serum and heparinized specimens are unacceptable. This test is New York State approved.","ClinicalInfo":"This assay predicts HIV-1 resistance to protease inhibitors, nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors and integrase inhibitors. The protease gene, integrase gene and the reverse transcriptase gene of the viral genome are sequenced using Next Generation Sequencing. Drug resistance is assigned using the Stanford hivdb database. This test should be used in conjunction with clinical presentation and other laboratory markers. A patient's response to therapy depends on multiple factors, including patient adherence, percentage of resistant virus population, dosing, and drug pharmacology issues.","ClinicalReference":"","ClinicalLimitation":"This test detects populations down to 10 percent of the total population which may account for resistance interpretation differences between methods. Some insertions or deletions may be difficult to detect using this software. This test may be unsuccessful if the plasma HIV-1 RNA viral load is less than 500 copies per mL of plasma.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2401,"ActiveDate":"2021-08-16T00:00:00","CreatedOn":"2021-07-07T15:45:00","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6052,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2401,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12835,"DictMethodologyId":500,"TdTestInfoSpecificId":2401,"DictMethodology":{"Id":500,"Name":"Massive Parallel Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2401,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":237,"DictDaysPerformed":"Sun - Sat","DictReported":"5 - 11 days"},"TdSpecimenRequirements":[{"Id":50718,"SpecialInstructions":"Separate plasma from cells within 24 hours and transfer plasma to a standard aliquot tube. Please submit most recent viral load and test date, if available.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2401,"IsBeakerData":false},{"Id":50719,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":18,"DictSpVolumeName":"2.5 mL","TdTestInfoSpecificId":2401,"IsBeakerData":false},{"Id":679540,"SpecialInstructions":"Separate plasma from cells within 24 hours and transfer plasma to a standard aliquot tube. Please submit most recent viral load and test date, if available.","LogicalOperation":null,"DictSpContainerId":244,"DictSpContainerName":"White PPT EDTA","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2401,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29114,"Description":"After separation from cells: 3 months","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2401,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29115,"Description":"After separation from cells: 72 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2401,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29116,"Description":"After separation from cells: 24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2401,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2401,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6062,"LISCode":"TTAUTO","PrimaryName":"ALLOGEN AutoAntibody","LISName":"ALLOGEN AutoAntibody","EMRName":"ALLOGEN AutoAntibody","EMRCode":"LAB1507","LOINC":"","RecommendedUse":"Non-HLA Antibody kit is designed to detect IgG antibodies to non-HLA proteins. ","DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":16277,"CptCode":"83516","Quantity":1,"Tmid":"30121215","CclTechComponentPrice":875.00,"CclProfComponentPrice":null,"TestNameForCdm":"","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6062,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6062,"SpecialInfo":"(3)x6mL Red Top tubes.  Transport WHOLE BLOOD at AMBIENT temperature.  DO NOT CENTRIFUGE.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2405,"ActiveDate":"2021-09-30T00:00:00","CreatedOn":"2021-02-03T11:43:00","CreatedById":103,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6062,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2405,"IsStat":false,"Comments":"","DictPerformingLabId":14,"DictPerformingLab":{"Id":14,"Name":"Allogen Lab (x46583)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12864,"DictMethodologyId":445,"TdTestInfoSpecificId":2405,"DictMethodology":{"Id":445,"Name":"Multiplex Bead Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2405,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":136,"DictDaysPerformed":"Mon - Fri","DictReported":"15 days"},"TdSpecimenRequirements":[{"Id":50819,"SpecialInstructions":"(3)x6mL Red Top tubes. DO NOT CENTRIFUGE OR SEPARATE. ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":106,"DictSpVolumeName":"18 mL","TdTestInfoSpecificId":2405,"IsBeakerData":false}],"TdSpecimenStabilities":[],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2405,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6063,"LISCode":"BDGLUC","PrimaryName":"(1,3) B-D Glucan","LISName":"(1,3) B-D Glucan","EMRName":"(1,3) B-D Glucan","EMRCode":"SQBDGLUC","LOINC":"42176-8","RecommendedUse":"The assay is used as aid in diagnosing certain systemic fungal infections such as Candidemia, and in prognostication and monitoring response to anti-fungal therapy in hospitalized patients. ","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13510,"Aka":"Beta-D Glucan","TdTestInfoCommonId":6063},{"Id":13511,"Aka":"Fungitell","TdTestInfoCommonId":6063},{"Id":13512,"Aka":"Glucan","TdTestInfoCommonId":6063}],"TdBillingCommons":[{"Id":16279,"CptCode":"87449","Quantity":1,"Tmid":"30200905","CclTechComponentPrice":100.00,"CclProfComponentPrice":null,"TestNameForCdm":"AG DETECT NOS IA MULT","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6063,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6063,"SpecialInfo":"Certain fungi, such as the genus Cryptococcus which produces very low levels of (1,3)-ß-D-glucan, may not result in serum (1,3)-ß-D-glucan sufficiently elevated so as to be detected by the assay. Infections with fungi of the order Mucorales such as Absidia, Mucor and Rhizopus which are not known to produce (1,3)-ß-D-glucan, are also observed to yield low serum (1,3)-ß-D-glucan titers. In addition, the yeast phase of Blastomyces dermatitidis produces little (1,3)-ß-D-glucan and may not be detected by the assay.","ClinicalInfo":"Some individuals have elevated levels of (1,3)-ß-D-glucan that fall into the indeterminate zone. In such cases, additional surveillance testing is recommended. The frequency of patient testing will depend upon the relative risk of fungal infection.","ClinicalReference":"","ClinicalLimitation":"Samples obtained by heel or finger stick methods are unacceptable as the alcohol-soaked gauze used to prepare the site (and, potentially, the skin surface-pooling of blood) has been shown to contaminate the specimens.\n**The following sample conditions can interfere with an accurate result: hemolysis, turbidity caused by lipemia, visual bilirubin, turbid serum, and elevated levels of Immunoglobulin G.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2406,"ActiveDate":"2021-09-30T00:00:00","CreatedOn":"2021-06-02T11:39:00","CreatedById":5,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6063,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2406,"IsStat":false,"Comments":"For CCF patients, this test is limited to hospitalized patients and may not be sampled more than twice per week.","DictPerformingLabId":15,"DictPerformingLab":{"Id":15,"Name":"Immunopathology Lab (x49033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12866,"DictMethodologyId":273,"TdTestInfoSpecificId":2406,"DictMethodology":{"Id":273,"Name":"Colorimetric, Kinetic","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2406,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":50826,"SpecialInstructions":"Sample should be collected in a sterile container using aseptic technique. If aliquoting is necessary, sterile aliquot tubes must be used. The sample should be transported to the laboratory as soon as possible or within 2 hours of collection. The sample should be centrifuged to separate the serum from the cells and then immediately placed into refrigerated storage pending delivery to the testing laboratory. Heel and fingerstick collections are unacceptable. This test cannot be added on to other testing. Sample cannot be shared with other testing.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2406,"IsBeakerData":false},{"Id":50827,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":138,"DictSpVolumeName":"0.25 mL","TdTestInfoSpecificId":2406,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29197,"Description":"unacceptable","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2406,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29198,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2406,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29199,"Description":"1 year","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2406,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2406,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6064,"LISCode":"BVAMP","PrimaryName":"Bacterial Vaginosis NAAT","LISName":"Bacterial Vaginosis NAAT","EMRName":"Bacterial Vaginosis NAAT","EMRCode":"SQBVAMP","LOINC":"74635-4","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14744,"Aka":"BV","TdTestInfoCommonId":6064},{"Id":14745,"Aka":"BVAMP","TdTestInfoCommonId":6064},{"Id":14746,"Aka":"SQBVAMP","TdTestInfoCommonId":6064},{"Id":14747,"Aka":"vaginitis","TdTestInfoCommonId":6064},{"Id":14748,"Aka":"vaginosis","TdTestInfoCommonId":6064}],"TdBillingCommons":[{"Id":16653,"CptCode":"81513","Quantity":1,"Tmid":"30608155","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Amplification, Bacterial Vaginosis","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6064,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6064,"SpecialInfo":"Microbiology Preanalytic Guidance: http://portals.ccf.org/plmi/Laboratory-Medicine/Microbiology-Specimen-Collection-Transport-Information.\n\nThe specimen must be a vaginal swab collected and transported using the Aptima Multitest Swab Specimen Collection Kit. Up to two tests can be run on a single Aptima Multitest Swab specimen (ie. TRVAMP+BVAMP or CVTV+BVAMP) - if specimen sources have been correctly selected, the shared tests will print on the same label. Do not place more than one label on a single collection tube. \n\nSpecimens collected from a non-vaginal source, with an inappropriate or expired collection device, or containing >1 swab may be rejected.\n","ClinicalInfo":"Vaginitis syndrome is characterized by a spectrum of conditions including vaginal and vulvar irritation, odor, discharge and pruritus. Causes of vaginitis include mechanical and chemical factors (feminine hygiene products, contraceptive materials, etc.) as well as infectious agents. Up to 90% of infectious vaginitis cases are caused by bacterial vaginosis (BV), vulvovaginal candidiasis (candida vaginitis, CV) and trichomoniasis (Trichomonas vaginalis, TV). BV has been diagnosed in 22-50% of symptomatic patients, CV in 17-39%, and TV in 4-35%. \n\nBV is characterized by a change in the vaginal microbiota dominated by Lactobacillus species to a polymicrobial anaerobe-dominated microbiota that includes Gardnerella vaginalis, Atopobium vaginae, Prevotella, Bacteroides, Peptostreptococcus, Mobiluncus, Sneathia (Leptotrichia), Mycoplasma, and BV associated bacteria. \n\nThe Aptima BV assay is an FDA-cleared in vitro NAAT that utilizes real time transcription-mediated amplification (TMA) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae. The assay uses an algorithm to report a qualitative result for BV based on detection of target organisms, and does not report results for individual organisms. The assay is intended to aid in the diagnosis of BV on the automated Panther system using clinician-collected and patient-collected vaginal swab specimens from patients with a clinical presentation consistent with vaginitis and/or vaginosis.\n","ClinicalReference":"Workowski KA, Bachmann LH, Chan PA, Johnston CM, Muzny CA, Park I, Reno H, Zenilman JM, Bolan GA. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187. doi: 10.15585/mmwr.rr7004a1. PMID: 34292926; PMCID: PMC8344968.\n","ClinicalLimitation":"1. The performance of the assay has not been evaluated in patients <14 years of age.\n2. Therapeutic failure or success cannot be determined with the assay since nucleic acid may persist following appropriate antimicrobial therapy.\n3. A negative result does not preclude a possible infection because results are dependent on adequate specimen collection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or other factors.\n4. The effects of tampon use and other specimen collection variables have not been assessed for their impact on assay detection.\n5. Interference with the Aptima BV assay was observed in the presence of the following substances: Mucus (1.5% V/V), Vaginal Moisturizing Gel (0.5% W/V) and Tioconazole (5% W/V).\n6. Additional microorganisms not detected by the Aptima BV assay such as Prevotella species and Mobiluncus species, Ureaplasma, Mycoplasma, and numerous fastidious or uncultivated anaerobes have also been found in women with BV, but are less associated with BV due to their relatively low prevalence, sensitivity, and/or specificity.\n7. Cross-reactivity was observed with the Aptima BV assay in the presence of Lactobacillus acidophilus.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2407,"ActiveDate":"2021-10-07T00:00:00","CreatedOn":"2021-07-09T14:03:00","CreatedById":89,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6064,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2407,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13006,"DictMethodologyId":81,"TdTestInfoSpecificId":2407,"DictMethodology":{"Id":81,"Name":"Transcription-Mediated Amplification","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2407,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Sun","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":51923,"SpecialInstructions":"Vaginal Multitest (orange tube pink swab): A vaginal swab is the only acceptable specimen. Carefully insert the swab into the vagina about 2 inches past the introitus and gently rotate the swab for 10-30 seconds. Make sure the swab touches the vaginal walls so that moisture is absorbed by the swab. Vaginal swab specimens may be patient-collected in a clinical setting when a pelvic exam is not otherwise indicated (https://www.hologic.com/package-inserts/swab-collection-instructions-vaginal-main-english#4257225834-454981651). Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2407,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29511,"Description":"15⁰C to 30⁰C, 30 days.\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2407,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29512,"Description":"2⁰C to 8⁰C, 30 days.\n","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2407,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29513,"Description":"-20⁰C to -70⁰C, 90 days.\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2407,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2407,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6065,"LISCode":"CVTV","PrimaryName":"Candida/Trichomonas NAAT","LISName":"Candida/Trichomonas NAAT","EMRName":"Candida/Trichomonas NAAT","EMRCode":"SQCVTV","LOINC":"62461-9, 62460-1, 94421-5","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14749,"Aka":"candida glabrata","TdTestInfoCommonId":6065},{"Id":14750,"Aka":"candidiasis","TdTestInfoCommonId":6065},{"Id":14751,"Aka":"CV","TdTestInfoCommonId":6065},{"Id":14752,"Aka":"CVTV","TdTestInfoCommonId":6065},{"Id":14753,"Aka":"SQCVTV","TdTestInfoCommonId":6065},{"Id":14754,"Aka":"vaginitis","TdTestInfoCommonId":6065},{"Id":14755,"Aka":"vulvovaginitis","TdTestInfoCommonId":6065},{"Id":14756,"Aka":"yeast","TdTestInfoCommonId":6065}],"TdBillingCommons":[{"Id":16449,"CptCode":"87481","Quantity":1,"Tmid":"30608105","CclTechComponentPrice":98.00,"CclProfComponentPrice":null,"TestNameForCdm":"CANDIDA DNA AMP PROBE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6065,"IsBeakerData":true},{"Id":16450,"CptCode":"87661","Quantity":1,"Tmid":"30600875","CclTechComponentPrice":98.00,"CclProfComponentPrice":null,"TestNameForCdm":"TRICHOMONAS VAG AMP","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6065,"IsBeakerData":true}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6065,"SpecialInfo":"Microbiology Preanalytic Guidance: http://portals.ccf.org/plmi/Laboratory-Medicine/Microbiology-Specimen-Collection-Transport-Information.\n\nThe specimen must be a vaginal swab collected and transported using the Aptima Multitest Swab Specimen Collection Kit. Up to two tests can be run on a single Aptima Multitest Swab specimen (ie. GCCT+CVTV or CVTV+BVAMP) - if specimen sources have been correctly selected, the shared tests will print on the same label. Do not place more than one label on a single collection tube. \n\nSpecimens collected from a non-vaginal source, with an inappropriate or expired collection device, or containing >1 swab may be rejected.\n\nRelated alternative orders:\n1. TRVAMP: in-house Trichomonas vaginalis standalone NAAT (use when complicated vulvovaginal candidiasis is not on the differential).\n2. FUNGSC: in-house Yeast Screen (culture). Note that the Aptima Multitest Swab Specimen cannot be used to add-on FUNGSC. Please refer to FUNGSC test directory entry for specimen collection requirements and details.","ClinicalInfo":"Vaginitis syndrome is characterized by a spectrum of conditions including vaginal and vulvar irritation, odor, discharge and pruritus. Causes of vaginitis include mechanical and chemical factors (feminine hygiene products, contraceptive materials, etc.) as well as infectious agents. Up to 90% of infectious vaginitis cases are caused by bacterial vaginosis (BV), vulvovaginal candidiasis (candida vaginitis, CV) and trichomoniasis (Trichomonas vaginalis, TV). BV has been diagnosed in 22-50% of symptomatic patients, CV in 17-39%, and TV in 4-35%. \n\nThe Aptima CV/TV assay is an FDA-cleared in vitro nucleic acid amplification test (NAAT) for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis. The assay utilizes real time transcription-mediated amplification (TMA) to detect and qualitatively report results for the following organisms: Candida species group (C. albicans, C. tropicalis, C. parapsilosis, C. dubliniensis), Candida glabrata, and Trichomonas vaginalis.\n\nThe assay differentiates between Candida glabrata and the Candida species group (C. spp) by targeting the RNA component of RNAse P ribonucleoprotein; the assay does not differentiate among C. spp. For Trichomonas vaginalis, the assay targets ribosomal RNA (rRNA) and differentiates the result from results for Candida glabrata and C. spp. The assay is intended to aid in the diagnosis of vulvovaginal candidiasis and trichomoniasis on the automated Panther system using clinician-collected and patient-collected vaginal swab specimens from patients with a clinical presentation consistent with vaginitis or vulvovaginitis.\n\nTrichomonas only testing by NAAT is available as a stand-alone test (order code TRVAMP) when complicated vulvovaginal candidiasis is not on the differential. Yeast screen is available as a stand-alone test (order code FUNGSC) and is the test of choice when trying to recover a yeast isolate for potential susceptibility testing. FUNGSC cannot be added onto the Aptima Multitest Swab Specimen – please refer to FUNGSC test directory entry for specimen collection requirements and details.","ClinicalReference":"Workowski KA, Bachmann LH, Chan PA, Johnston CM, Muzny CA, Park I, Reno H, Zenilman JM, Bolan GA. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187. doi: 10.15585/mmwr.rr7004a1. PMID: 34292926; PMCID: PMC8344968.\n","ClinicalLimitation":"1. The performance of the assay has not been evaluated in patients <14 years of age.\n2. Therapeutic failure or success cannot be determined with the assay since nucleic acid may persist following appropriate antimicrobial therapy.\n3. A negative result does not preclude a possible infection because results are dependent on adequate specimen collection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or target levels below the assay limit of detection.\n4. The effects of tampon use, douching, and specimen collection variables have not been assessed for their impact on assay detection.\n5. Interference with the Aptima CV/TV assay was observed in the presence of the following substances: Tioconazole 6.5% Ointment (3% W/V, all analytes), Vaginal Moisturizing Gel (1% W/V, C spp; 5% W/V, C. glabrata; 3% W/V, TV), and Glacial Acetic Acid (5% V/V, C spp only).\n6. Competitive interference may preclude detection of C. glabrata in low quantities if T. vaginalis is present in high quantities.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2408,"ActiveDate":"2021-10-07T00:00:00","CreatedOn":"2021-07-12T08:42:00","CreatedById":89,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6065,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2408,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13007,"DictMethodologyId":81,"TdTestInfoSpecificId":2408,"DictMethodology":{"Id":81,"Name":"Transcription-Mediated Amplification","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2408,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Sun","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":51380,"SpecialInstructions":"Vaginal Multitest (orange tube pink swab): A vaginal swab is the only acceptable specimen. Carefully insert the swab into the vagina about 2 inches past the introitus and gently rotate the swab for 10-30 seconds. Make sure the swab touches the vaginal walls so that moisture is absorbed by the swab. Vaginal swab specimens may be patient-collected in a clinical setting when a pelvic exam is not otherwise indicated (https://www.hologic.com/package-inserts/swab-collection-instructions-vaginal-main-english#4257225834-454981651). Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":38,"DictSpVolumeName":"Swab","TdTestInfoSpecificId":2408,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29514,"Description":"15⁰C to 30⁰C, 30 days.\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2408,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29515,"Description":"2⁰C to 8⁰C, 30 days.\n","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2408,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29516,"Description":"-20⁰C to -70⁰C, 90 days.\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2408,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2408,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5309,"LISCode":"A1APHE","PrimaryName":"Alpha-1-Antitrypsin Phenotype by Electrophoresis","LISName":"Alpha1 Antitry Pheno","EMRName":"Alpha 1 Antitrypsin Phenotype","EMRCode":"SQA1APHE","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":12225,"CptCode":"82103","Quantity":1,"Tmid":"30104825","CclTechComponentPrice":35.00,"CclProfComponentPrice":null,"TestNameForCdm":"%A1APHE A1A TOTAL","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5309,"IsBeakerData":false},{"Id":12226,"CptCode":"82104","Quantity":1,"Tmid":"30104505","CclTechComponentPrice":38.00,"CclProfComponentPrice":null,"TestNameForCdm":"%A1APHE A1A PHENOTYPE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5309,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5309,"SpecialInfo":"Grossly hemolyzed specimens will be rejected. This test is New York DOH approved. ","ClinicalInfo":"Use to determine specific AAT protein variant(s) in individual with decreased concentration of AAT (< 90 mg/dL). Interpret with caution if the patient has been transfused within the previous 21 days. ","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":2416,"ActiveDate":"2015-12-07T00:00:00","CreatedOn":"2015-09-08T09:23:00","CreatedById":208,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5309,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2416,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9581,"DictMethodologyId":243,"TdTestInfoSpecificId":2416,"DictMethodology":{"Id":243,"Name":"Immunoturbidometric Assay","Description":null},"TdTestInfoSpecific":null},{"Id":9582,"DictMethodologyId":72,"TdTestInfoSpecificId":2416,"DictMethodology":{"Id":72,"Name":"Isoelectric Focusing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2416,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"Sun - Sat","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":36937,"SpecialInstructions":"Transfer 1 mL serum to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2416,"IsBeakerData":false},{"Id":36938,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2416,"IsBeakerData":false},{"Id":36939,"SpecialInstructions":"Transfer 1 mL serum to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2416,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":20989,"Description":"After separation from cells: 1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2416,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20990,"Description":"After separation from cells: 3 months","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2416,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":20991,"Description":"After separation from cells: 3 months (Avoid repeated freeze/thaw cycles) ","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2416,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2416,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5329,"LISCode":"BMHSNP","PrimaryName":"Bone marrow Cancer Chromosome Microarray","LISName":"Cancer Chromosome ","EMRName":"BM Cancer Chromosome Microarray","EMRCode":"SQBMHSNP","LOINC":"","RecommendedUse":"To detect copy number changes and loss of heterzygosity (LOH)/copy neutral LOH in hematological malignancies at diagnosis, prognostication or disease progression for clinically relevant chromosomal abmormalities.","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":10378,"Aka":"Bone marrow heme array","TdTestInfoCommonId":5329},{"Id":10379,"Aka":"Bone marrow SNP array","TdTestInfoCommonId":5329},{"Id":10380,"Aka":"Cancer Array","TdTestInfoCommonId":5329},{"Id":10381,"Aka":"Cancer SNP Array","TdTestInfoCommonId":5329},{"Id":10382,"Aka":"Chromosomal SNP arrays for bone marrow","TdTestInfoCommonId":5329},{"Id":10383,"Aka":"Hematologic SNP Array","TdTestInfoCommonId":5329}],"TdBillingCommons":[{"Id":13606,"CptCode":"81277","Quantity":1,"Tmid":"31003185","CclTechComponentPrice":1660.00,"CclProfComponentPrice":null,"TestNameForCdm":"BMHSNP CYTO NEOPL MICROAR","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5329,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5329,"SpecialInfo":"Notes: Collect specimen Monday - Friday only. If aliquoting is necessary, sterile aliquot tubes must be used.","ClinicalInfo":"","ClinicalReference":"Refer to report","ClinicalLimitation":"Refer to report","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2417,"ActiveDate":"2016-02-22T00:00:00","CreatedOn":"2015-11-06T13:58:00","CreatedById":382,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5329,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2417,"IsStat":false,"Comments":"","DictPerformingLabId":28,"DictPerformingLab":{"Id":28,"Name":"Cytogenetics (x42489)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10707,"DictMethodologyId":108,"TdTestInfoSpecificId":2417,"DictMethodology":{"Id":108,"Name":"Microarray","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2417,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":105,"DictDaysPerformed":"Mon - Fri","DictReported":"14 days"},"TdSpecimenRequirements":[{"Id":41258,"SpecialInstructions":"Notes: Collect specimen Monday - Friday only.\r\nIf aliquoting is necessary, sterile aliquot tubes must be used.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2417,"IsBeakerData":false},{"Id":41259,"SpecialInstructions":"EDTA is preferred container type. Collect specimen Monday-Friday only. If aliquoting is necessary, sterile aliquot tubes must be used.","LogicalOperation":null,"DictSpContainerId":28,"DictSpContainerName":"Sodium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":146,"DictSpVolumeName":"5 - 7 mL","TdTestInfoSpecificId":2417,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":23691,"Description":"48 hours\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2417,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23692,"Description":"Not preferred","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2417,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":23693,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2417,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2417,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5381,"LISCode":"RBCB3","PrimaryName":"RBC Band 3 Protein Reduction in Hereditary Spherocytosis","LISName":"RBC Band 3 Protein Reduction in Hereditary Spherocytosis","EMRName":"RBC Band 3 Protein Reduction in Hereditary Spherocytosis","EMRCode":"SQRBCB3","LOINC":"","RecommendedUse":"ARUP Quarterly Hotline update to special information.","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":5294,"Aka":"Hereditary Spherocytosis, EMA, Band 3, Osmotic Fragility","TdTestInfoCommonId":5381}],"TdBillingCommons":[{"Id":7682,"CptCode":"88184","Quantity":1,"Tmid":"31101415","CclTechComponentPrice":106.00,"CclProfComponentPrice":null,"TestNameForCdm":"RBCB3 PROTEIN RED","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5381,"IsBeakerData":false}],"TdIncludes":[{"Id":26219,"TestName":"RBC Band 3 Protein Reduction in HS\t","Rank":1,"TdTestInfoCommonId":5381}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5381,"SpecialInfo":"Specimens must be analyzed within 7 days of collection. Clotted or grossly hemolyzed specimens will be rejected. Ambient samples greater than 3 days, refrigerated sample greater than 7 days, and bone marrow will be rejected. This test is New York state approved.","ClinicalInfo":"Use to confirm diagnosis of hereditary spherocytosis when hemolytic anemia and spherocytes are present.\n\nThis test can be used to confirm the suspected diagnosis of Hereditary Spherocytosis (HS). HS is a common inherited hemolytic anemia characterized by the presence of spherical erythrocytes (spherocytes). HS can be diagnosed based on family history and clinical features, along with clinical laboratory tests including peripheral smear examination, osmotic fragility (OF), ektacytometry or flow cytometry. Band 3 is the most abundant transmembrane protein found in the human RBC. Eosin-5-maleimide (EMA) dye binds to band 3 on intact RBCs and a reduction of fluorescence intensity is seen in hereditary spherocytosis. This test by flow cytometry has been reported to have a sensitivity of 93 percent for diagnosis of HS. Congenital Dyserythropoietic Anemia Type II, Southeast Asian Ovalocytosis and Hereditary Pyropoikilocytosis are rare disorders that may have a positive result in this test.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2421,"ActiveDate":"2016-05-02T00:00:00","CreatedOn":"2016-02-09T13:41:00","CreatedById":198,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5381,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2421,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service 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FISH analysis with the AML1 and ETO probes is valuable in cases of AML M2 because of its ability to reveal masked or variant, t(8;21) (q22;q22) translocations.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":1,"DictTestCategorization":{"Id":1,"Code":"ASR","Name":"Analyte Specific Reagent"}},"TdTestInfoSpecifics":[{"Id":2432,"ActiveDate":"2021-03-29T00:00:00","CreatedOn":"2019-04-10T09:14:00","CreatedById":110,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6034,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2432,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12310,"DictMethodologyId":173,"TdTestInfoSpecificId":2432,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2432,"DictDaysPerformedId":15,"DictHoursPerformedId":null,"DictReportedId":110,"DictDaysPerformed":"4 days per week","DictReported":"5 - 7 days"},"TdSpecimenRequirements":[{"Id":48307,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":114,"DictSpVolumeName":"2 - 3 mL","TdTestInfoSpecificId":2432,"IsBeakerData":false},{"Id":48308,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":28,"DictSpContainerName":"Sodium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":145,"DictSpTypeName":"Bone marrow","DictSpVolumeId":114,"DictSpVolumeName":"2 - 3 mL","TdTestInfoSpecificId":2432,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27742,"Description":"48 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2432,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27743,"Description":"Acceptable","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2432,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27744,"Description":"Not acceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2432,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2432,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6050,"LISCode":"T1418","PrimaryName":"FISH for IGH/BCL2 Tissue","LISName":"FISH for IGH/BCL2 Tissue","EMRName":"FISH for IGH/BCL2 Tissue","EMRCode":"","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":13659,"Aka":"FISH for t(14;18)","TdTestInfoCommonId":6050}],"TdBillingCommons":[{"Id":16524,"CptCode":"88377","Quantity":2,"Tmid":"31004225","CclTechComponentPrice":786.00,"CclProfComponentPrice":95.00,"TestNameForCdm":"FISH FOR IGH/BCL2 TIS X2","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6050,"IsBeakerData":false}],"TdIncludes":[{"Id":25609,"TestName":"LSI 14q32.33","Rank":1,"TdTestInfoCommonId":6050},{"Id":25610,"TestName":"LSI 18q21.33","Rank":2,"TdTestInfoCommonId":6050}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6050,"SpecialInfo":"","ClinicalInfo":"Interphase FISH analysis utilizing a dual color, dual fusion probe set specific to the IGH gene at 14q32.33 and the BCL2 gene at 18q21.33. This is useful in identifying the t(14;18) translocation present in follicular lymphoma and diffuse large B-cell lymphoma.  If no cells are available for analysis, no analysis charges will be incurred.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2440,"ActiveDate":"2021-05-18T00:00:00","CreatedOn":"2021-03-19T12:59:00","CreatedById":387,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6050,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2440,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13036,"DictMethodologyId":173,"TdTestInfoSpecificId":2440,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2440,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"5 days per week","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":51521,"SpecialInstructions":"4 μm tissue sections on electrostatically charged slides containing representative tissue.  Tissue must be formalin fixed.  Samples must not be fixed in B5 or Prefer fixative.","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":130,"DictSpTypeName":"Slide (s), unstained","DictSpVolumeId":160,"DictSpVolumeName":"2 slides","TdTestInfoSpecificId":2440,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29586,"Description":"Blocks and slides should be transported at ambient temperature.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2440,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2440,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6051,"LISCode":"T1114","PrimaryName":"FISH for IGH/CCND1 Tissue","LISName":"FISH for IGH/CCND1 Tissue","EMRName":"FISH for IGH/CCND1 Tissue","EMRCode":"","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":14226,"Aka":"FISH for t(11;14)","TdTestInfoCommonId":6051}],"TdBillingCommons":[{"Id":16523,"CptCode":"88377","Quantity":2,"Tmid":"31004235","CclTechComponentPrice":786.00,"CclProfComponentPrice":95.00,"TestNameForCdm":"FISH FOR IGH/CCND1 TIS X2","SubComponent":"T11141","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6051,"IsBeakerData":false}],"TdIncludes":[{"Id":25605,"TestName":"LSI 11q13.3","Rank":1,"TdTestInfoCommonId":6051},{"Id":25606,"TestName":"LSI 14q32.33","Rank":2,"TdTestInfoCommonId":6051}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6051,"SpecialInfo":"","ClinicalInfo":"Interphase FISH analysis utilizing a dual color, dual fusion probe set specific to the CCND1 gene at 11q13.3 and the IGH gene at 14q32.33. This is useful in distinguishing patients with the t(11;14) translocation. If no cells are available for analysis, no analysis charges will be incurred.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2441,"ActiveDate":"2021-05-18T00:00:00","CreatedOn":"2021-03-19T13:36:00","CreatedById":387,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6051,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2441,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13035,"DictMethodologyId":173,"TdTestInfoSpecificId":2441,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2441,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"5 days per week","DictReported":"3 - 5 days"},"TdSpecimenRequirements":[{"Id":51515,"SpecialInstructions":"4 μm tissue sections on electrostatically charged slides containing representative tumor.  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","ClinicalInfo":"TPMT genotyping test is used for identifying patients at risk for myelosuppression with the standard dosage of thiopurine drugs, and for adjusting the drug dosage or to select alternate drug therapy.\nReference Range for the test is TPMT*1/TPMT*1. No variants detected is an indication of homozygous wild type (two *1 functional alleles), which is associated with normal TPMT enzyme activity. \nPatients with two functional *1 alleles are predicted to have normal (high or extensive) TPMT enzyme activity. Patients with one functional allele (*1) and one nonfunctional allele (*2, *3A, *3B, or *3C) are predicted to have intermediate TPMT enzyme activity. These patients are at risk for severe myelosuppression or drug toxicity, and may require only a lower than standard dosage of thiopurine drugs. Patients with two nonfunctional allele (*2, *3A, *3B, or *3C) are predicted to have deficient (no or low) TPMT enzyme activity. These patients are at a greater risk (almost 100%) of experiencing myelosuppression, who may require even a reduced dosage of thiopurine drugs than patients with one nonfunctional allele and should be considered for an alternate drug therapy.\n\n","ClinicalReference":"Relling MV et al. Clinical Pharmacogenetics Implementation Consortium Guidelines for Thiopurine Methyltransferase Genotype and Thiopurine Dosing. Clin Pharmacol Ther. 2013 update. 93:324-325.\n ","ClinicalLimitation":"The TPMT genotyping assay detects only TPMT*2, TPMT*3A, TPMT*3B, and TPMT*3C variants. This assay does not interrogate other TPMT variants and therefore their genotype-phenotype associations to thiopurine drugs are not indicated. This genotyping test will not distinguish *1/*3A heterozygous from the rare *3B/*3C genotype, which can only be identified with a test for TPMT enzyme activity.   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The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis. ","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2487,"ActiveDate":"2017-12-20T00:00:00","CreatedOn":"2017-11-08T10:14:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5563,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2487,"IsStat":false,"Comments":"","DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12579,"DictMethodologyId":413,"TdTestInfoSpecificId":2487,"DictMethodology":{"Id":413,"Name":"Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2487,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"Sun - Sat","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":49371,"SpecialInstructions":"An extra 50ul will be required for each additional allergen ordered.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":13,"DictSpVolumeName":"0.8 mL","TdTestInfoSpecificId":2487,"IsBeakerData":false},{"Id":49372,"SpecialInstructions":"Submitting the minimum volume will not allow for repeat testing or addons. Required volume of 0.8mL is preferred","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2487,"IsBeakerData":false},{"Id":49373,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":13,"DictSpVolumeName":"0.8 mL","TdTestInfoSpecificId":2487,"IsBeakerData":false},{"Id":49374,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":24,"DictSpContainerName":"Lithium heparin (Green)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":13,"DictSpVolumeName":"0.8 mL","TdTestInfoSpecificId":2487,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28384,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2487,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28385,"Description":"30 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2487,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28386,"Description":"1 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2487,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2487,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5564,"LISCode":"FANCSF","PrimaryName":"Fungal Antibodies with Reflex to Blastomyces dermatitidis Antibodies by Immunodiffusion, CSF","LISName":"FUNGAL ABs, CSF","EMRName":"Fungal Abs with Reflex, CSF","EMRCode":"SQFANCSF","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":11233,"Aka":"FUNGAL ABs with Reflex,CS","TdTestInfoCommonId":5564},{"Id":14034,"Aka":"FUNGAL ABs with Rflx, CSF","TdTestInfoCommonId":5564}],"TdBillingCommons":[{"Id":14434,"CptCode":"86612","Quantity":1,"Tmid":"30201065","CclTechComponentPrice":24.00,"CclProfComponentPrice":null,"TestNameForCdm":"%FABCSF BLASTOMYCES","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5564,"IsBeakerData":false},{"Id":14435,"CptCode":"86606","Quantity":1,"Tmid":"30201045","CclTechComponentPrice":22.00,"CclProfComponentPrice":null,"TestNameForCdm":"ASPERGILLUS QUAL OR SEMI","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5564,"IsBeakerData":false},{"Id":14436,"CptCode":"86635","Quantity":1,"Tmid":"30201115","CclTechComponentPrice":22.00,"CclProfComponentPrice":null,"TestNameForCdm":"%FABCSF COCCIDI IGG/M ABS","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5564,"IsBeakerData":false},{"Id":14437,"CptCode":"86698","Quantity":2,"Tmid":"30210850","CclTechComponentPrice":22.00,"CclProfComponentPrice":null,"TestNameForCdm":"HISTOPLASMA","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5564,"IsBeakerData":false}],"TdIncludes":[{"Id":24889,"TestName":"Coccidioides Ab by CF, CSF","Rank":1,"TdTestInfoCommonId":5564},{"Id":24890,"TestName":"Histoplasma M, CSF (CF)","Rank":2,"TdTestInfoCommonId":5564},{"Id":24891,"TestName":"Histoplasma Y, CSF (CF) ","Rank":3,"TdTestInfoCommonId":5564},{"Id":24892,"TestName":"Aspergillus Antibody, CSF (CF)","Rank":4,"TdTestInfoCommonId":5564},{"Id":24893,"TestName":"Blastomyces Antibodies EIA, CSF","Rank":5,"TdTestInfoCommonId":5564}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5564,"SpecialInfo":"If Blastomyces antibodies are equivocal or positive by immunoassay then Blastomyces dermatitidis Antibodies by Immunodiffusion, CSF will be added at an additional charge. Body fluids other than cerebrospinal fluid (CSF) are not acceptable. Contaminated, hemolyzed, xanthochromic, or severely lipemic specimens are unacceptable.","ClinicalInfo":"This test detects antibodies to Aspergillus, Coccidioides, and Histoplasma by complement fixation and Blastomyces by immunoassay. Negative fungal serology does not rule out the possibility of current infection.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2494,"ActiveDate":"2018-01-03T00:00:00","CreatedOn":"2017-12-21T10:54:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5564,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2494,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11392,"DictMethodologyId":223,"TdTestInfoSpecificId":2494,"DictMethodology":{"Id":223,"Name":"Immunodiffusion (ID)","Description":null},"TdTestInfoSpecific":null},{"Id":11393,"DictMethodologyId":22,"TdTestInfoSpecificId":2494,"DictMethodology":{"Id":22,"Name":"Semi Quantitative Enzyme Linked Immunosorbent Assay","Description":null},"TdTestInfoSpecific":null},{"Id":11394,"DictMethodologyId":421,"TdTestInfoSpecificId":2494,"DictMethodology":{"Id":421,"Name":"Semi-Quantitative Complement Fixation","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2494,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":70,"DictDaysPerformed":"Sun - 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Specimens positive for organisms of public health concern may be reflexed to culture and/or sendout testing at a public health lab as indicated in the result comments.\n\nThe Infectious Diseases Society of America recommends stool pathogen testing in individuals with diarrhea accompanied by fever, bloody or mucoid stools, severe abdominal cramping or tenderness, or signs of sepsis; in an outbreak setting; and in immunocompromised hosts with diarrhea. Identification of the infectious etiology of diarrheal illness can help guide appropriate therapy, prevent unnecessary or harmful antibiotic exposure, and facilitate further workup. Repeat testing within 14 days of the same episode of diarrhea, or for test of cure, is not recommended.\n\nImmunocompromised individuals with persistent diarrhea may benefit from additional testing (ie. SQSTLPCR: Expanded Stool Gastrointestinal Panel by PCR, SQOVAP: Stool Ova/Parasite Exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora Exam, SQMICSPO: Microsporidia Exam, and gastrointestinal biopsy, among others). Individuals with travel history outside the United States with persistent diarrhea lasting >14 days may benefit from additional parasitic testing (ie. SQOVAP: Stool Ova/Parasite exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora exam). Individuals with onset of diarrhea after more than 3 days of hospital admission or with prior antibiotic exposure history may benefit from testing for C. difficile (SQCDPCR).","ClinicalReference":"1. Shane AL, Mody RK, Crump JA, Tarr PI, Steiner TS, Kotloff K, Langley JM, Wanke C, Warren CA, Cheng AC, Cantey J, Pickering LK. 2017 Infectious Diseases Society of America Clinical Practice Guidelines for the Diagnosis and Management of Infectious Diarrhea. Clin Infect Dis. 2017 Nov 29;65(12):e45-e80. doi: 10.1093/cid/cix669. PMID: 29053792.\n2. Harrington SM, Buchan BW, Doern C, Fader R, Ferraro MJ, Pillai DR, Rychert J, Doyle L, Lainesse A, Karchmer T, Mortensen JE. Multicenter evaluation of the BD max enteric bacterial panel PCR assay for rapid detection of Salmonella spp., Shigella spp., Campylobacter spp. (C. jejuni and C. coli), and Shiga toxin 1 and 2 genes. J Clin Microbiol. 2015 May;53(5):1639-47. doi: 10.1128/JCM.03480-14. Epub 2015 Mar 4. PMID: 25740779.\n3. Collins JP, Shah HJ, Weller DL, Ray LC, Smith K, McGuire S, Trevejo RT, Jervis RH, Vugia DJ, Rissman T, Garman KN, Lathrop S, LaClair B, Boyle MM, Harris S, Kufel JZ, Tauxe RV, Bruce BB, Rose EB, Griffin PM, Payne DC. Preliminary Incidence and Trends of Infections Caused by Pathogens Transmitted Commonly Through Food - Foodborne Diseases Active Surveillance Network, 10 U.S. Sites, 2016-2021. MMWR Morb Mortal Wkly Rep. 2022 Oct 7;71(40):1260-1264. doi: 10.15585/mmwr.mm7140a2. PMID: 36201372.\n","ClinicalLimitation":"The BD Max Enteric Bacterial Panel results are meant to be used in conjunction with clinical presentation, laboratory findings, and epidemiological information. Results of this test should not be used as the sole basis for diagnosis, treatment, or other patient management decisions. Positive results do not rule out co-infection with other organisms that are not detected by this test, and may not be the sole or definitive cause of patient illness. Some targets on this panel have potential for false positives due to non-specific cross reactivity. Negative results in the setting of clinical illness compatible with gastroenteritis may be due to infection by pathogens that are not detected by this test or non-infectious causes such as ulcerative colitis, irritable bowel syndrome, or Crohn’s disease.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2496,"ActiveDate":"2018-01-09T00:00:00","CreatedOn":"2017-10-10T12:05:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5567,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2496,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7941,"DictMethodologyId":422,"TdTestInfoSpecificId":2496,"DictMethodology":{"Id":422,"Name":"Qualitative Polymerase Chain Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2496,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":678268,"SpecialInstructions":"The stool must be passed into a clean, dry, wide mouthed container and not contaminated by urine or water. A bed pan is an ideal initial collection container provided it has been thoroughly cleaned and the patient is cautioned against contaminating the specimen with urine. A plastic bag placed over the toilet seat is also acceptable. Select bloody, slimy, or watery portions of the stool using the collection spoon provided in the cap of the container. Place enough stool (~1g) in the Cary-Blair transport vial (Oracle #1124361, or #1570140 as part of STUL kit) to bring the liquid level up to the “fill to here” line. Mash and mix the stool with the spoon along the sides of the container. Tighten the cap and shake the vial until the mixture appears homogeneous.\n","LogicalOperation":null,"DictSpContainerId":97,"DictSpContainerName":"Cary-Blair kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":52,"DictSpTypeName":"Stool","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2496,"IsBeakerData":false},{"Id":678269,"SpecialInstructions":"The stool must be passed into a clean, dry, wide mouthed container and not contaminated by urine or water. A bed pan is an ideal initial collection container provided it has been thoroughly cleaned and the patient is cautioned against contaminating the specimen with urine. A plastic bag placed over the toilet seat is also acceptable. Select bloody, slimy, or watery portions of the stool using the collection spoon provided in the cap of the container. 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Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":67,"DictSpContainerName":"Clean container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2505,"IsBeakerData":false},{"Id":48502,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":12,"DictSpVolumeName":"0.7 mL","TdTestInfoSpecificId":2505,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27875,"Description":"11 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2505,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27876,"Description":"1 week","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2505,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27877,"Description":"2 weeks","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2505,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2505,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5584,"LISCode":"AQPCSF","PrimaryName":"Aquaporin-4 Receptor Antibody, IgG by CBA-IFA, CSF with Reflex to Titer","LISName":"AQP4 IgG by CBA-IFA, CSF","EMRName":"AQP4 IgG by CBA-IFA, CSF","EMRCode":"SQAQPCSF","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13727,"Aka":"Neuromyelitis Optica (NMO), CSF","TdTestInfoCommonId":5584}],"TdBillingCommons":[{"Id":16580,"CptCode":"86052","Quantity":1,"Tmid":"30205165","CclTechComponentPrice":325.00,"CclProfComponentPrice":null,"TestNameForCdm":"AQPCSF AQ-4 AB EA","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5584,"IsBeakerData":false}],"TdIncludes":[{"Id":25517,"TestName":"Neuromyelitis Optica/AQP4-IgG, CSF\t","Rank":1,"TdTestInfoCommonId":5584}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5584,"SpecialInfo":"If AQP4 antibody IgG is positive, then an AQP4 antibody IgG titer is reported. 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This test is New York DOH approved. ","ClinicalInfo":"This test is primarily used to verify compliance, optimize therapy, and identify elevated metabolite concentrations that\nmay result in toxicity after initiation of thiopurine drug therapy for the treatment of inflammatory bowel disease.\nRecommended time points for monitoring include: 4 weeks after starting treatment to verify patient compliance and\nlook for early risk of toxicity; 12 to 16 weeks after starting therapy when 6-thioguanine nucleotides have reached\nsteady-state; and annually. It may also be ordered in patients who do not respond to therapy as expected or as\nneeded for dose changes, flare-ups, signs of toxicity, or suspicion of noncompliance. The test will measure\n6-methylmercaptopurine (6-MMP) and 6-thioguanine nucleotides (6-TGN) in erythrocytes. Target 6-thioguanine (6-TGN) concentrations are 235 to 450 pmol/8x10(8) RBC with lower levels suggesting suboptimal dosing and higher levels associated with increased risk of myelotoxicity and leukopenia. High 6-methylmercaptopurine (6-MMP) levels (greater than 5700 pmol/8x10[8] RBC) suggest an increased risk for hepatotoxicity and potentially \"thiopurine hypermethylation.\"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2507,"ActiveDate":"2018-03-06T00:00:00","CreatedOn":"2017-12-07T11:54:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5585,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2507,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12889,"DictMethodologyId":265,"TdTestInfoSpecificId":2507,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2507,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Mon - Sat","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":50919,"SpecialInstructions":"Separate specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2507,"IsBeakerData":false},{"Id":50920,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":16,"DictSpVolumeName":"1.5 mL","TdTestInfoSpecificId":2507,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29261,"Description":"8 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2507,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29262,"Description":"24 hours","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2507,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29263,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2507,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2507,"TestCode":null,"IsReportable":false,"DictVendorId":50,"DictVendor":{"Id":50,"Name":"Mayo Clinic Dpt of Lab Med & Pathology","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5587,"LISCode":"UIODNE","PrimaryName":"Iodine, Urine","LISName":"Iodine, Urine","EMRName":"Iodine, Urine","EMRCode":"SQUIODNE","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13814,"CptCode":"83018","Quantity":1,"Tmid":"30106415","CclTechComponentPrice":75.00,"CclProfComponentPrice":null,"TestNameForCdm":"IODINE TOTAL URINE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5587,"IsBeakerData":false}],"TdIncludes":[{"Id":25184,"TestName":"Hours Collected","Rank":1,"TdTestInfoCommonId":5587},{"Id":25185,"TestName":"Total Volume","Rank":2,"TdTestInfoCommonId":5587},{"Id":25186,"TestName":"Creatinine, Urine - per volume","Rank":3,"TdTestInfoCommonId":5587},{"Id":25187,"TestName":"Creatinine, Urine - per 24h","Rank":4,"TdTestInfoCommonId":5587},{"Id":25188,"TestName":"Iodine, Urine - per volume","Rank":5,"TdTestInfoCommonId":5587},{"Id":25189,"TestName":"Iodine, Urine - per 24h","Rank":6,"TdTestInfoCommonId":5587},{"Id":26885,"TestName":"Iodine, Urine - ratio to CRT","Rank":7,"TdTestInfoCommonId":5587}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5587,"SpecialInfo":"Patient Prep: Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). High concentrations of iodine may interfere with testing. Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.\nUrine transported in a non-trace element-free tube or contaminated with iodine, gadolinium, blood, fecal material or acid preservative will be rejected. Elevated results may be due to skin or collection-related contamination, including the use of collection containers that are not certified to be trace element-free. Confirmation with a second specimen collected in a certified trace-element free container is recommended if an elevated result is suspected to be due to contamination. This test is New York DOH approved. ","ClinicalInfo":"This test is useful for the assessment of iodine nutritional status. This test reports total iodine from all iodine-containing species present in the specimen but does not determine the chemical form (species) of the iodine present. Values > 1000 µg/L may indicate dietary excess, but more frequently suggest recent drug or contrast media exposure.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2508,"ActiveDate":"2018-03-08T00:00:00","CreatedOn":"2017-11-30T12:37:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5587,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2508,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13400,"DictMethodologyId":178,"TdTestInfoSpecificId":2508,"DictMethodology":{"Id":178,"Name":"Inductively Coupled Plasma / Mass Spectrometry (ICP-MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2508,"DictDaysPerformedId":66,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Tue, Thu, Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":41899,"SpecialInstructions":"Patient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":56,"DictSpTypeName":"Urine, 24-hour (well-mixed)","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":2508,"IsBeakerData":false},{"Id":41900,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2508,"IsBeakerData":false},{"Id":41901,"SpecialInstructions":"Patient Prep: High concentrations of iodine may interfere with testing. Diet, medication, and nutritional supplements may introduce interfering substances. Patients should be encouraged to discontinue nutritional supplements, vitamins, minerals, non-essential over-the-counter medications (upon the advice of their physician). Avoid iodine-containing medications or contrast agents for at least 1 month. Avoid gadolinium-based contrast media for at least 48 hours.\nCollection: Collect in a plastic container, mix well and aliquot into a trace metal free transport tube (ARUP #43116). Record total volume and collection time interval on specimen.","LogicalOperation":null,"DictSpContainerId":45,"DictSpContainerName":"Plastic container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":27,"DictSpVolumeName":"8 mL","TdTestInfoSpecificId":2508,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":24133,"Description":"2 months","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2508,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24134,"Description":"2 months","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2508,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":24135,"Description":"2 months","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2508,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2508,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5588,"LISCode":"PANPOL","PrimaryName":"Pancreatic Polypeptide by Quantitative Radioimmunoassay","LISName":"PANCREATC POLYPEPTID","EMRName":"Pancreatic Polypeptide","EMRCode":"SQPANPOL","LOINC":"2721-9","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[{"Id":8130,"Aka":"Human Pancreatic Polypeptide","TdTestInfoCommonId":5588}],"TdBillingCommons":[{"Id":10663,"CptCode":"83519","Quantity":1,"Tmid":"30105965","CclTechComponentPrice":232.00,"CclProfComponentPrice":null,"TestNameForCdm":"PANCREATIC POLYPEP","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5588,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5588,"SpecialInfo":"Patient Prep: :Patient should be fasting for 10 hours prior to specimen collection. Plasma is not acceptable. Severely hemolyzed or lipemic specimens are unacceptable. This test is New York DOH approved. ","ClinicalInfo":"Aids in the diagnosis and monitoring of pancreatic neuroendocrine tumors.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2509,"ActiveDate":"2018-03-13T00:00:00","CreatedOn":"2017-11-29T13:31:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5588,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2509,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8343,"DictMethodologyId":470,"TdTestInfoSpecificId":2509,"DictMethodology":{"Id":470,"Name":"Quantitative Radioimmunoassay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2509,"DictDaysPerformedId":2,"DictHoursPerformedId":null,"DictReportedId":91,"DictDaysPerformed":"Wed","DictReported":"4 - 12 days"},"TdSpecimenRequirements":[{"Id":32020,"SpecialInstructions":"Patient should be fasting for 10 hours prior to specimen collection. Allow specimen to sit in collection tube for 15-20 minutes at room temperature for proper clot formation. Centrifuge and separate serum from cells ASAP or within 2 hours of collection. Transfer serum to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2509,"IsBeakerData":false},{"Id":32021,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2509,"IsBeakerData":false},{"Id":32022,"SpecialInstructions":"Patient should be fasting for 10 hours prior to specimen collection. Allow specimen to sit in collection tube for 15-20 minutes at room temperature for proper clot formation. Centrifuge and separate serum from cells ASAP or within 2 hours of collection. Transfer serum to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2509,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":18138,"Description":"After separation from cells: 2 months ","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2509,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18139,"Description":"After separation from cells: 24 hours","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2509,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":18140,"Description":"After separation from cells: 24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2509,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2509,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5592,"LISCode":"APOL1S","PrimaryName":"APOL1 Sequencing","LISName":"APOL1 Sequencing","EMRName":"APOL1 SEQUENCING","EMRCode":"SQAPOL1S","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":10813,"CptCode":"81479","Quantity":1,"Tmid":"30118265","CclTechComponentPrice":355.00,"CclProfComponentPrice":null,"TestNameForCdm":"APOL1 SEQUENCING","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5592,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5592,"SpecialInfo":"Prior to any genetic testing we recommend genetic counseling. MUST submit Molecular Genetics test requisition form with specimen. Ethnicity MUST be included. Include detailed information including ethnicity, clinical history and family history. Package and ship specimen to remain cold, but not frozen. Ship via overnight express (FedEx).  ","ClinicalInfo":"Compared to individuals without recent African ancestry, African Americans have high rates of kidney disease. Two independent polymorphisms in the APOL1 gene have been shown to be likely associated with the following forms of kidney disease: focal segmental glomerulosclerosis (FSGS) and hypertension-attributed end-stage kidney disease (H-ESKD). The first polymorphism, termed G1, is a two-locus APOL1 polymorphic allele consisting of c.1024A>G; p.Ser342Gly (rs73885319) and c.1152T>G; p.Ile384Met (rs60910145); the second polymorphism, termed G2, is a 6-base pair deletion c.1164_1169delTTATAA (rs71785313). Individuals carrying two risk alleles (G1/G2) have an odds ratio of 7.3 of developing renal disease as compared to individuals carrying neither G1 or G2, while individuals carrying only one risk allele (G1 or G2) have an odds ratio of just 1.26 as compared to individuals carrying neither G1 or G2. A recessive model of inheritance best explains this finding. These APOL1 risk polymorphisms for kidney disease occur in more than 30% of African-American chromosomes while virtually absent in non-African chromosomes. Natural selection provides a plausible explanation as either of the resulting variant proteins provides heightened Trypanosoma lytic activity for heterozygotes with little increased risk for kidney disease. Reasons for Referral: Determination of c.1024A>G, c.1152T>G, and c.1164_1169delTTATAA status: \nPrior to donation of a kidney, as a limited diagnostic tool, for determination of carrier status. Methodology: Targeted gene sequencing of APOL1 exon 6 in which c.1024A>G, c.1152T>G, and c.1164_1169delTTATAA are embedded. References: 1. S.B. Satko, et al. Kidney Int. suppl 67, (s94), S46 (2005). 2. G. Genovese, et al. Science 329: 841-845 (2010). 3.D. Cohen, et al. Transplantation 92:722-725 (2011).\n\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2510,"ActiveDate":"2018-03-20T00:00:00","CreatedOn":"2018-01-18T14:36:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5592,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2510,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8432,"DictMethodologyId":82,"TdTestInfoSpecificId":2510,"DictMethodology":{"Id":82,"Name":"Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2510,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":79,"DictDaysPerformed":"Varies","DictReported":"8 - 16 days"},"TdSpecimenRequirements":[{"Id":32460,"SpecialInstructions":"Must submit the Molecular Genetics test requisition form with the specimen. Please include detailed clinical information including ethnicity, clinical history, and family history. Send specimen with cold pack.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2510,"IsBeakerData":false},{"Id":32461,"SpecialInstructions":"Absolute minimum with a normal WBC count.  Preferred volumes are 5 mL for adult and child, 2 - 3 mL for infant.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":2510,"IsBeakerData":false},{"Id":32462,"SpecialInstructions":"10 ug extracted DNA (from whole blood ONLY) at minimum of 100 ng/uL. Must submit the Molecular Genetics test requisition form with the specimen. Please include detailed clinical information including ethnicity, clinical history, and family history. ","LogicalOperation":null,"DictSpContainerId":33,"DictSpContainerName":"ACD A or B (Yellow)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":165,"DictSpTypeName":"Extracted DNA","DictSpVolumeId":68,"DictSpVolumeName":"10 ug","TdTestInfoSpecificId":2510,"IsBeakerData":false},{"Id":32463,"SpecialInstructions":"10 ug extracted DNA (from whole blood ONLY) at minimum of 100 ng/uL. Must submit the Molecular Genetics test requisition form with the specimen. Please include detailed clinical information including ethnicity, clinical history, and family history. ","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":165,"DictSpTypeName":"Extracted DNA","DictSpVolumeId":68,"DictSpVolumeName":"10 ug","TdTestInfoSpecificId":2510,"IsBeakerData":false},{"Id":32464,"SpecialInstructions":"Must submit the Molecular Genetics test requisition form with the specimen. Please include detailed clinical information including ethnicity, clinical history, and family history. Send specimen with cold pack.","LogicalOperation":null,"DictSpContainerId":33,"DictSpContainerName":"ACD A or B (Yellow)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":2510,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":18242,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2510,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2510,"TestCode":null,"IsReportable":false,"DictVendorId":122,"DictVendor":{"Id":122,"Name":"Knight Diagnostic Laboratories","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":652,"Title":"Molecular Genetics Test Requisition","FileName":"MolecularGeneticsTestRequisition","DictDocumentFormatId":1,"DictDocumentTypeId":5,"TdTestInfoCommonId":5592,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":5,"Name":"Requisition","Description":null,"FolderName":"Requisition","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5307,"LISCode":"PHI","PrimaryName":"Prostate Health Index","LISName":"Prostate Health Indx","EMRName":"Prostate Health Index","EMRCode":"SQPHI","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9527,"Aka":"PHI","TdTestInfoCommonId":5307},{"Id":9528,"Aka":"Prostate Health Index, Serum","TdTestInfoCommonId":5307}],"TdBillingCommons":[{"Id":12478,"CptCode":"84153","Quantity":1,"Tmid":"30122685","CclTechComponentPrice":37.00,"CclProfComponentPrice":null,"TestNameForCdm":"PHI PROST SPEC AG TOT","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5307,"IsBeakerData":false}],"TdIncludes":[{"Id":17940,"TestName":"Total PSA","Rank":1,"TdTestInfoCommonId":5307}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5307,"SpecialInfo":"If reflex testing is performed, additional charges apply. If Total PSA is between 4.0 and 10.0 ng/mL, free PSA and p2PSA will be performed. Patients should not be collected within six weeks after prostatic biopsy or immediately after digital rectal examination (DRE), prostatic massage, or transrectal ultrasound (TRUS). Separate specimens must be submitted when multiple tests are ordered. ","ClinicalInfo":"This Beckman Coulter Access Hybritech PSA assay is indicated for the measurement of serum PSA in conjunction with digital rectal examination (DRE) as an aid in the detection of prostate cancer in men aged 50 years or older. Low Beckman Coulter PHI scores are associated with a lower probability of prostate cancer on biopsy, and higher scores are associated with an increased probability of prostate cancer on biopsy. The choice of an appropriate Beckman Coulter PHI score to be used in guiding clinical decision-making may vary for each patient and may depend in part on other clinically important factors or on family history of disease. Values obtained with different assays should not be used interchangeably in serial testing. It is recommended that only one assay method be used consistently to monitor each patient's course of therapy.  It should be noted that a PSA range of 4 to 10 ng/mL using Hybritech calibration corresponds to a PSA range of 3.1 to 7.8 ng/mL using WHO calibration. 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Each of these complexes consists of between 4 and 46 subunits encoded by both nuclear and mitochondrial DNA. Mitochondrial diseases are caused by defects in any of the relevant metabolic pathways and have an estimated prevalence of 1:8,500. Mitochondrial diseases are varied, including mitochondrial DNA deletion syndromes such as Kearns-Sayre syndrome (KSS), mitochondrial depletion syndromes such as those caused by mutations in TK2 and SUCLA2 or POLG and C10orf2, and mitochondrial point mutation syndromes such as mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), as well as others. The clinical features of mitochondrial diseases vary widely, but they can include lactic acidosis, myopathy, ophthalmoplegia, ptosis, cardiomyopathy, sensorineural hearing loss, optic atrophy, pigmentary retinopathy, diabetes mellitus, encephalomyopathy, seizures, and stroke-like episodes. A diagnostic workup for a mitochondrial disorder may demonstrate elevations of the lactate-to-pyruvate ratio (LAA / Lactate, Plasma and PYR / Pyruvic Acid, Blood) and an elevated growth differentiation factor 15 (GDF15) level. GDF15 is a protein of the transforming growth factor beta superfamily. GDF15 is overexpressed in muscle and serum in patients with various types of mitochondrial diseases, including those with mitochondrial deletion, depletion, and point mutation syndromes. Therefore, increased levels of GDF15 can indicate the need for further investigations including molecular studies and muscle biopsy to confirm the presence of a possible neuromuscular mitochondrial disease. This is a screening test for neuromuscular mitochondrial disease. Results can be elevated for other reasons including in individuals with cancer, cardiovascular disease, diabetes, and pregnancy. Results are normally elevated in children younger than 3 months of age due to the high levels found in the placenta during pregnancy. This assay is not suitable for carrier detection. References: 1. DiMauro S and Schon EA: Mechanisms of Disease: Mitochondrial Respiratory-Chain Diseases. N Engl J Med 2003;348:2656-2668 2. Kalko SG, Paco S, Jou C, et al: Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC Genomics 2014;15:91 3. Sugulle M, Dechend R, Herse F et al: Circulating and placental growth-differentiation factor 15 in preeclampsia and in pregnancy complicated by diabetes mellitus. 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HSV infections in humans can cause lesions at a variety of cutaneous and mucocutaneous sites. These lesions can be a result of the primary infection by the virus or they can result from a reactivation of the latent virus, causing recurrent episodes of the disease. Primary VZV infection results in chickenpox (varicella), which may rarely result in complications including encephalitis or pneumonia. Even when clinical symptoms of chickenpox have resolved, VZV remains dormant in the nervous system of the infected person (virus latency). In approximately 10 to 20% of cases, VZV reactivates later in life producing shingles.\n\nThis lab-developed multiplex real-time PCR assay simultaneously qualitatively detects and differentiates HSV-1, HSV-2, and VZV DNA targets. Viral nucleic acid is extracted from clinical samples using the EZ2 Connect (Qiagen). Viral DNA is amplified and detected using the RealStar alpha Herpesvirus PCR kit 1.0 (Altona) using species-specific primers and fluorescently labeled hydrolysis probes on a RotorGene Q (Qiagen) thermocycler. \n\nThis specific procedure code (SQHSVVZV) can be used to order this test on mucocutaneous lesion swabs. Utilize SQHSPCRC for HSV testing on CSF; SQHSVNEO for HSV testing on neonatal surface swabs; SQHSVPCR for HSV testing on all other non-lesional specimen types; and SQVZVPCR for VZV testing on all other non-lesional specimen types.","ClinicalReference":"1. Yip CCY, Sridhar S, Leung KH, Cheng AKW, Chan KH, Chan JFW, Cheng VCC, Yuen KY. Evaluation of RealStar® Alpha Herpesvirus PCR Kit for Detection of HSV-1, HSV-2, and VZV in Clinical Specimens. Biomed Res Int. 2019 Oct 9;2019:5715180. doi: 10.1155/2019/5715180. PMID: 31687393.\n2. Nikolic D, Kohn D, Yen-Lieberman B, Procop GW. Detection of Herpes Simplex Virus and Varicella-Zoster Virus by Traditional and Multiplex Molecular Methods. Am J Clin Pathol. 2019 Jan 1;151(1):122-126. doi: 10.1093/ajcp/aqy111. PMID: 30239569.","ClinicalLimitation":"As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. 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GCCT+TRVAMP) - if specimen sources have been correctly selected, the shared tests will print on the same label. Do not place more than one label on a single collection tube. \n\nCommon reasons for specimen rejection:\n1. Inappropriate collection device for source selected.\n2. Transport tubes containing a cleaning swab or more than 1 swab.\n3. Overfilled or underfilled urine transport tubes.\n4. Collection device expired prior to specimen collection.","ClinicalInfo":"Trichomonas vaginalis is a protozoan parasite that is a common cause of vaginitis and the most common nonviral sexually transmitted infection worldwide. The majority of persons who have trichomoniasis (70%–85%) either have minimal or no genital symptoms, and untreated infections might last from months to years, and have been associated with reproductive morbidity. Symptomatic patients can present with vaginitis, vaginal discharge, cervicitis, urethritis, and/or other genitourinary symptoms. The CDC recommends diagnostic testing for T. vaginalis in patients seeking care for vaginal discharge, as well as considering asymptomatic screening in certain high risk groups. T. vaginalis can be diagnosed via wet mount, culture, rapid antigen testing, and nucleic acid amplification testing (NAAT), with the latter having the highest sensitivity.\n\nThe Aptima Trichomonas vaginalis Assay is an in vitro FDA-cleared qualitative nucleic acid amplification test (NAAT) for the detection of ribosomal RNA (rRNA) from Trichomonas vaginalis to aid in the diagnosis of trichomoniasis using the Panther System. The assay uses target capture, transcription-mediated amplification (TMA), and hybridization protection assay (HPA) technologies. The assay may be used to test the following specimens from symptomatic or asymptomatic individuals: clinician-collected endocervical swabs, clinician-collected and patient-collected vaginal swabs (in a clinical setting), female and male urine, and specimens collected in PreservCyt Solution.","ClinicalReference":"Workowski KA, Bachmann LH, Chan PA, Johnston CM, Muzny CA, Park I, Reno H, Zenilman JM, Bolan GA. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recomm Rep. 2021 Jul 23;70(4):1-187. doi: 10.15585/mmwr.rr7004a1. PMID: 34292926; PMCID: PMC8344968.\n","ClinicalLimitation":"1. The performance of the assay has not been evaluated in patients <14 years of age.\n2. Therapeutic failure or success cannot be determined with the assay since nucleic acid may persist following appropriate antimicrobial therapy.\n3. A negative result does not preclude a possible infection because results are dependent on adequate specimen collection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or target levels below the assay limit of detection.\n4. The effects of tampon use, douching, and specimen collection variables have not been assessed for their impact on assay detection.\n5. Competitive interference may preclude detection of T. vaginalis in low quantities if Trichomonas tenax or Pentatrichomonas hominis are present in high quantities (commensals of the oral cavity and large intestine respectively).","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2546,"ActiveDate":"2016-10-04T00:00:00","CreatedOn":"2016-07-05T15:48:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5426,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2546,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13418,"DictMethodologyId":81,"TdTestInfoSpecificId":2546,"DictMethodology":{"Id":81,"Name":"Transcription-Mediated Amplification","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2546,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"Mon - Sun","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":24349,"SpecialInstructions":"Endocervical Unisex (white tube blue swab): Remove excess mucus from cervical os and surrounding mucosa using the white cleaning swab, then DISCARD. Insert blue swab into the endocervical canal and gently rotate clockwise for 10-30 seconds. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":104,"DictSpContainerName":"APTIMA Collection Unisex swab","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":147,"DictSpTypeName":"Endocervical","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2546,"IsBeakerData":false},{"Id":24353,"SpecialInstructions":"The patient should not have urinated for at least 1 hour prior to specimen collection. The patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container.\n\nTransfer 2 mL of urine into the Aptima urine specimen transport tube using the disposable pipette provided within 24 hours of collection. Close the tube tightly. Work with one specimen at a time.\n\nThe correct volume of urine has been added when the fluid level is between the black fill lines (window) on the urine transport tube. Do not overfill or underfill the APTIMA Urine transport tube.","LogicalOperation":null,"DictSpContainerId":107,"DictSpContainerName":"APTIMA Urine specimen collection kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":181,"DictSpTypeName":"Urine, first-catch","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2546,"IsBeakerData":false},{"Id":24355,"SpecialInstructions":"Vaginal Multitest (orange tube pink swab): A vaginal swab is the recommended specimen for female patients due to this being a specimen type ideal for sharing with other testing. Carefully insert the swab into the vagina about 2 inches past the introitus and gently rotate the swab for 10-30 seconds. Make sure the swab touches the vaginal walls so that moisture is absorbed by the swab. Place swab into Aptima transport tube. Snap off swab at the score line, and close the tube tightly.","LogicalOperation":null,"DictSpContainerId":256,"DictSpContainerName":"Aptima Multitest Collection Kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2546,"IsBeakerData":false},{"Id":24357,"SpecialInstructions":"PreservCyt Solution (ThinPrep) is an acceptable specimen when added onto a ThinPrep Pap Test and no dedicated vaginal or endocervical swab specimens are available. It is not a recommended due to lower test sensitivity for gonorrhea and chlamydia detection (often ordered on the same swab) compared to other specimen types. Due to this reason, it is not available as a selectable specimen source/type during order entry, only as a laboratory add-on. In order to place an order on this specimen type, you must place a call to lab client services. \n\nIf consulted prior to specimen collection, lab client services should advise the provider to collect a separate dedicated Vaginal Multitest Swab for optimal test performance characteristics. If consulted after specimen collection, lab client services should assist the provider in placing an add on order with \"Fluid, Cervix\" as the specimen source, and have cytology perform the aliquot as below prior to cytology testing. \n\nPrior to cytology testing and within 30 days of collection, cytology will transfer a 1 mL aliquot into an APTIMA Specimen Transfer Tube. The specimen must have been stored at 2-30C.","LogicalOperation":null,"DictSpContainerId":108,"DictSpContainerName":"Cytyc PreservCyt solution (Thin Prep)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":148,"DictSpTypeName":"Cervical","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2546,"IsBeakerData":false},{"Id":677502,"SpecialInstructions":"The patient should not have urinated for at least 1 hour prior to specimen collection. The patient should collect first portion of random voided urine (first part of stream) into a sterile, plastic, preservative-free container.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":181,"DictSpTypeName":"Urine, first-catch","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2546,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":13795,"Description":"15⁰C to 30⁰C. \n\nSwab in Aptima transport media: 60 days; \nUrine in Aptima transport media: 30 days; \nUrine unprocessed: 24 hours; \nThinPrep PreservCyt solution in Aptima transport media: 14 days; \nThinPrep PreservCyt unprocessed: 30 days\n","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2546,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":13797,"Description":"2⁰C to 8⁰C.\n\nSwab in Aptima transport media: 60 days; \nUrine in Aptima transport media: 30 days; \nUrine unprocessed: 24 hours; \nThinPrep PreservCyt solution in Aptima transport media: 30 days; \nThinPrep PreservCyt unprocessed: 30 days\n","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2546,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30985,"Description":"-20⁰C to -70⁰C. \n\nSwab in Aptima transport media: 24 months; \nUrine in Aptima transport media: 12 months; \nUrine unprocessed: unacceptable; \nThinPrep PreservCyt solution in Aptima transport media: 12 months; \nThinPrep PreservCyt unprocessed: unacceptable\n","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2546,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2546,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5430,"LISCode":"URCAT2","PrimaryName":"Catecholamines Fractionated by LC-MS/MS, 24- hour Urine, Free","LISName":"Catecholamines Fractionated by LC-MS/MS, 24- hour Urine, Free","EMRName":"Catecholamines Fractionated by LC-MS/MS, 24- hour Urine, Free","EMRCode":"SQURCAT2","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":11244,"Aka":"Adrenaline","TdTestInfoCommonId":5430},{"Id":11247,"Aka":"Fractionation, Catecholamines","TdTestInfoCommonId":5430},{"Id":11248,"Aka":"Free Catecholamine Fractionation","TdTestInfoCommonId":5430},{"Id":11249,"Aka":"Noradrenaline","TdTestInfoCommonId":5430},{"Id":15155,"Aka":"Catecholamines, 24-hour urine","TdTestInfoCommonId":5430},{"Id":15156,"Aka":"Dopamine","TdTestInfoCommonId":5430},{"Id":15157,"Aka":"Epinephrine","TdTestInfoCommonId":5430},{"Id":15158,"Aka":"Norepinephrine","TdTestInfoCommonId":5430}],"TdBillingCommons":[{"Id":14492,"CptCode":"82384","Quantity":1,"Tmid":"30109295","CclTechComponentPrice":43.00,"CclProfComponentPrice":null,"TestNameForCdm":"CATECHOLAMINE FRACT UR","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5430,"IsBeakerData":false}],"TdIncludes":[{"Id":25668,"TestName":"Creatinine, Urine - per volume","Rank":1,"TdTestInfoCommonId":5430},{"Id":25669,"TestName":"Creatinine, Urine - per 24h","Rank":2,"TdTestInfoCommonId":5430},{"Id":25670,"TestName":"Epinephrine, Urine - per 24h","Rank":3,"TdTestInfoCommonId":5430},{"Id":25671,"TestName":"Epinephrine, Urine - ratio to CRT","Rank":4,"TdTestInfoCommonId":5430},{"Id":25672,"TestName":"Epinephrine, Urine - per volume","Rank":5,"TdTestInfoCommonId":5430},{"Id":25673,"TestName":"Norepinephrine, Urine - per 24h","Rank":6,"TdTestInfoCommonId":5430},{"Id":25674,"TestName":"Norepinephrine, Urine - ratio to CRT","Rank":7,"TdTestInfoCommonId":5430},{"Id":25675,"TestName":"Norepinephrine, Urine - per volume","Rank":8,"TdTestInfoCommonId":5430},{"Id":25676,"TestName":"Dopamine, Urine - per 24h","Rank":9,"TdTestInfoCommonId":5430},{"Id":25677,"TestName":"Dopamine, Urine - ratio to CRT","Rank":10,"TdTestInfoCommonId":5430},{"Id":25678,"TestName":"Dopamine, Urine - per volume","Rank":11,"TdTestInfoCommonId":5430},{"Id":25679,"TestName":"Catecholamines, Urine Interpretation","Rank":12,"TdTestInfoCommonId":5430}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5430,"SpecialInfo":"Drugs and medications may affect results and should be discontinued for at least 72 hours prior to specimen collection, if possible. Catecholamines are not stable above pH 7. The pH of such specimens must be adjusted by the addition of 6M HCl acid or sulfamic acid prior to transport. A pH less than 2 can cause assay interference. Record total volume and collection time interval on transport tube and test request form. \nSpecimen preservation Option 1: Transfer a 4 mL aliquot (Min: 2.5 mL) to an ARUP Standard Transport Tube. Adjust pH to 2.0-4.0 with 6M HCl. \nSpecimen Preservation Option 2: Transfer a 4 mL aliquot (Min: 2.5 mL) to an ARUP Standard Transport Tube containing 20 mg sulfamic acid (ARUP Supply #48098), available by contacting Client Services at 800.628.6816 or 216.444.5755 (Min: 2.5 mL). Room temperature specimens, specimens preserved with boric acid or acetic acid, or specimens with pH > 7 will be rejected. This test is New York DOH approved.","ClinicalInfo":"This test is useful to evaluate clinical symptoms of excess catecholamine secretion. Not recommended for evaluation of paraganglioma or pheochromocytoma. The optimal specimen for this testing is a 24-hour urine collection. 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Record total volume and collection time interval on sample and test request form.","LogicalOperation":null,"DictSpContainerId":213,"DictSpContainerName":"24 HR Urine Container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":7,"DictSpCollectionTemperatureName":"Refrigerate during collection.","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":56,"DictSpTypeName":"Urine, 24-hour (well-mixed)","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2547,"IsBeakerData":false},{"Id":44287,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":18,"DictSpVolumeName":"2.5 mL","TdTestInfoSpecificId":2547,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":25400,"Description":"1 week (unpreserved); 1 month (preserved)","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2547,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25401,"Description":"Unacceptable (unpreserved); 6 months (preserved)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2547,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":25402,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2547,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2547,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5437,"LISCode":"METOP","PrimaryName":"Metoprolol, Serum/Plasma","LISName":"Metoprolol, Serum/Plasma","EMRName":"Metoprolol, Serum/Plasma","EMRCode":"SQMETOP","LOINC":"3815-8","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8794,"Aka":"Lopressor","TdTestInfoCommonId":5437}],"TdBillingCommons":[{"Id":11707,"CptCode":"80375/G0480","Quantity":1,"Tmid":"30113405","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"METOPROLOL, SER/PL","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5437,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5437,"SpecialInfo":"Polymer gel separation tubes (SST or PST) will be rejected.  This test is New York State approved.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2551,"ActiveDate":"2016-11-16T00:00:00","CreatedOn":"2016-10-04T08:31:00","CreatedById":198,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5437,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2551,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9145,"DictMethodologyId":54,"TdTestInfoSpecificId":2551,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2551,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":158,"DictDaysPerformed":"Mon - Sun","DictReported":"7 days"},"TdSpecimenRequirements":[{"Id":35297,"SpecialInstructions":"Do not use serum separator tubes. Promptly centrifuge and separate serum into a plastic screw capped vial.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2551,"IsBeakerData":false},{"Id":35298,"SpecialInstructions":"Promptly centrifuge and separate plasma into a plastic screw capped vial.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2551,"IsBeakerData":false},{"Id":35299,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":9,"DictSpVolumeName":"0.4 mL","TdTestInfoSpecificId":2551,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19937,"Description":"30 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2551,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19938,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2551,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19939,"Description":"14 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2551,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2551,"TestCode":null,"IsReportable":false,"DictVendorId":76,"DictVendor":{"Id":76,"Name":"National Med Serv Inc","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5438,"LISCode":"TORSE","PrimaryName":"Torsemide, Serum/Plasma","LISName":"Torsemide, Serum/Plasma","EMRName":"Torsemide, Serum/Plasma","EMRCode":"SQTORSE","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":8796,"Aka":"Demadex","TdTestInfoCommonId":5438},{"Id":8797,"Aka":"Torasemide","TdTestInfoCommonId":5438}],"TdBillingCommons":[{"Id":11709,"CptCode":"80375","Quantity":1,"Tmid":"30113415","CclTechComponentPrice":115.00,"CclProfComponentPrice":null,"TestNameForCdm":"TORSEMIDE, SER/PL","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5438,"IsBeakerData":false},{"Id":18052,"CptCode":"G0480","Quantity":1,"Tmid":"30113415","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"TORSEMIDE, SER/PL","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5438,"IsBeakerData":true}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5438,"SpecialInfo":"Polymer gel separation tubes (SST or PST) will be rejected. 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Promptly centrifuge and separate serum into a plastic screw capped vial.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2552,"IsBeakerData":false},{"Id":35307,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":9,"DictSpVolumeName":"0.4 mL","TdTestInfoSpecificId":2552,"IsBeakerData":false},{"Id":35308,"SpecialInstructions":"Promptly centrifuge and separate plasma into a plastic screw capped vial.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2552,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":19943,"Description":"1 month","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2552,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19944,"Description":"24 months","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2552,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":19945,"Description":"1 month","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2552,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2552,"TestCode":null,"IsReportable":false,"DictVendorId":76,"DictVendor":{"Id":76,"Name":"National Med Serv Inc","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5441,"LISCode":"RENIND","PrimaryName":"Direct Renin","LISName":"Direct Renin","EMRName":"Direct Renin Plasma","EMRCode":"SQRENIND","LOINC":"2915-7","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":16423,"CptCode":"84244","Quantity":1,"Tmid":"30101685","CclTechComponentPrice":66.00,"CclProfComponentPrice":null,"TestNameForCdm":"RENIN PLASMA","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5441,"IsBeakerData":true}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5441,"SpecialInfo":"Fasting specimens are recommended but not required. Record the time of day and patient's posture during blood collection (supine or upright). DO NOT pre-chill collection tubes, store tubes on ice or refrigerate; cryoactivation of prorenin occurs when samples are refrigerated. Biotin levels of up to 100mg/day have not shown interference with this assay. Patients taking >100 mg/day to 300 mg/day should refrain from taking Biotin for 1 hour prior to sample collection. Patients taking a Biotin dose >300 mg/day should consult with their physician or the laboratory prior to having a sample taken. Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.","ClinicalInfo":"Diagnosis of disorders of the renin-angiotensin-aldosterone system (RAAS).  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Patients taking a biotin dose of 5 to 10 mg/day should refrain from taking biotin for 8 hours prior to sample collection. Patients taking a biotin dose > 10 mg/day should consult with their physician or the laboratory prior to having a sample taken. Clinicians should consider biotin interference as a source of error, when clinically suspicious of the laboratory result.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"These calculations have only been validated for adult males.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2554,"ActiveDate":"2016-12-01T00:00:00","CreatedOn":"2016-05-09T14:21:00","CreatedById":208,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5442,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2554,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10814,"DictMethodologyId":261,"TdTestInfoSpecificId":2554,"DictMethodology":{"Id":261,"Name":"Bromocresol Green","Description":null},"TdTestInfoSpecific":null},{"Id":10815,"DictMethodologyId":185,"TdTestInfoSpecificId":2554,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2554,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":41631,"SpecialInstructions":"Submit in original tube or aliquot specimen into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":26,"DictSpContainerName":"Lithium heparin PST (Lt. 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This assay should not be used for blood donor screening or associated re-entry protocols, or for screening Human Cell and Cellular Tissue-Based Products (HCT/Ps). This test is New York State approved. Assay is performed using the Hemagen Chagas kit.","ClinicalInfo":"Aid in the diagnosis of non-acute (chronic phase) Chagas disease (T. cruzi). According to the CDC, at least two different serologic tests should be used to make the laboratory diagnosis of chronic Chagas Disease, as no single serologic test is sufficiently sensitive and specific. If results between the two assays are discrepant, repeat testing or testing by a third method may be helpful.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2555,"ActiveDate":"2016-12-07T00:00:00","CreatedOn":"2016-10-25T16:15:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5443,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2555,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8050,"DictMethodologyId":22,"TdTestInfoSpecificId":2555,"DictMethodology":{"Id":22,"Name":"Semi Quantitative Enzyme Linked Immunosorbent Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2555,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":16,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 7 days"},"TdSpecimenRequirements":[{"Id":30948,"SpecialInstructions":"Separate serum from cells ASAP or within 2 hours of collection and transfer serum to standard aliquot tube. 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Please mark specimens plainly as \"acute\" or \"convalescent.\"","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2555,"IsBeakerData":false},{"Id":30949,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2555,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":17447,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2555,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":17448,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2555,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":17449,"Description":"After separation from cells: 1 year","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2555,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2555,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5456,"LISCode":"MLH1PH","PrimaryName":"MLH1 Promoter Hypermethylation","LISName":"MLH1 Promoter Hypermethylation","EMRName":"","EMRCode":"SQMLH1PH","LOINC":"","RecommendedUse":"","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":10451,"Aka":"MLH1PH","TdTestInfoCommonId":5456}],"TdBillingCommons":[{"Id":13680,"CptCode":"81288","Quantity":1,"Tmid":"30114035","CclTechComponentPrice":562.00,"CclProfComponentPrice":null,"TestNameForCdm":"MLH1 PROMOTER HYPERMETH","SubComponent":"MLH1PRHM","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5456,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5456,"SpecialInfo":"Submit tissue specimen with anatomic pathology request form, and indicate MLH1 Promoter Hypermethylation on the form. 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Heat-treated or contaminated specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2594,"ActiveDate":"2019-01-29T00:00:00","CreatedOn":"2018-10-26T12:39:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5721,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2594,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":11848,"DictMethodologyId":406,"TdTestInfoSpecificId":2594,"DictMethodology":{"Id":406,"Name":"Immunoblot (IB), Qualitative","Description":null},"TdTestInfoSpecific":null},{"Id":11849,"DictMethodologyId":238,"TdTestInfoSpecificId":2594,"DictMethodology":{"Id":238,"Name":"Immunoprecipitation","Description":null},"TdTestInfoSpecific":null},{"Id":11850,"DictMethodologyId":376,"TdTestInfoSpecificId":2594,"DictMethodology":{"Id":376,"Name":"Semi-Quantitative Multiplex Bead Assay","Description":null},"TdTestInfoSpecific":null},{"Id":13827,"DictMethodologyId":34,"TdTestInfoSpecificId":2594,"DictMethodology":{"Id":34,"Name":"Semi-Quantitative Indirect Fluorescent Antibody","Description":null},"TdTestInfoSpecific":null},{"Id":13865,"DictMethodologyId":582,"TdTestInfoSpecificId":2594,"DictMethodology":{"Id":582,"Name":"Qualitative Particle-Based Multianalyte Technology (PMAT)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2594,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":267,"DictDaysPerformed":"Sun - Sat","DictReported":"8 - 19 days"},"TdSpecimenRequirements":[{"Id":46497,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume.\nSeparate serum from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2594,"IsBeakerData":false},{"Id":46498,"SpecialInstructions":"","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2594,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":26564,"Description":"2 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pneumoniae","Rank":20,"TdTestInfoCommonId":5727},{"Id":25575,"TestName":"SARS-CoV-2","Rank":6,"TdTestInfoCommonId":5727},{"Id":25576,"TestName":"Human Rhinovirus/Enterovirus","Rank":8,"TdTestInfoCommonId":5727},{"Id":25577,"TestName":"Influenza A virus","Rank":9,"TdTestInfoCommonId":5727},{"Id":25578,"TestName":"Influenza A virus A/H1","Rank":10,"TdTestInfoCommonId":5727},{"Id":25579,"TestName":"Influenza A virus A/H3","Rank":11,"TdTestInfoCommonId":5727},{"Id":25580,"TestName":"Influenza A virus A/H1-2009","Rank":12,"TdTestInfoCommonId":5727},{"Id":25581,"TestName":"Influenza B virus","Rank":13,"TdTestInfoCommonId":5727},{"Id":25582,"TestName":"Respiratory syncytial virus","Rank":18,"TdTestInfoCommonId":5727},{"Id":25585,"TestName":"Chlamydia pneumoniae","Rank":19,"TdTestInfoCommonId":5727},{"Id":26737,"TestName":"Influenza A (no subtype)","Rank":21,"TdTestInfoCommonId":5727}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5727,"SpecialInfo":"This test order is intentionally restricted to only lower respiratory specimens. Patients who may benefit include immunocompromised patients and those who are critically ill. The test is very expensive, and if not covered by insurance, the patient will incur a substantial charge. Recommend discussing risks and benefits with the patient, and considering seeking insurance preauthorization.","ClinicalInfo":"Respiratory pathogens cause acute local and systemic disease, with the most severe cases occurring in children, the elderly, and immunocompromised individuals. Due to the similarity of diseases caused by many viruses and bacteria, diagnosis based on clinical symptoms alone is difficult. Identification of potential causative agents provides data to aid providers in determining appropriate patient treatment or triage, and public health response for disease containment.\n\nThe BioFire Respiratory Panel 2.1 (RP2.1) is a multiplexed nucleic acid test that qualitatively detects and identifies nucleic acids from the following viral and bacterial targets from respiratory specimens: SARS-CoV-2 (Agent of COVID-19); Influenza A and subtypes H1, H1N1 2009, H3; Influenza B; Respiratory syncytial virus (RSV); Human metapneumovirus (hMPV); Human rhinovirus/enterovirus; Adenovirus; Parainfluenza 1-4; Coronaviruses 229E, OC43, NL63, HKU1; Chlamydia pneumoniae; and Mycoplasma pneumoniae. B. pertussis and parapertussis targets are not reported for lower respiratory specimens. These respiratory pathogens are assayed in a single pouch through array-based localization and endpoint melting curve data analysis.\n\nThe assay is FDA-cleared for nasopharyngeal swab testing, and has been modified and validated as a lab-developed test for lower respiratory specimens including bronchoalveolar lavage, sputum, and tracheal aspirate. ","ClinicalReference":"1. Berry GJ, Zhen W, Smith E, Manji R, Silbert S, Lima A, Harington A, McKinley K, Kensinger B, Neff C, Lu D. Multicenter Evaluation of the BioFire Respiratory Panel 2.1 (RP2.1) for Detection of SARS-CoV-2 in Nasopharyngeal Swab Samples. J Clin Microbiol. 2022 May 18;60(5):e0006622. doi: 10.1128/jcm.00066-22. Epub 2022 Apr 7. PMID: 35387475.\n2. Leber AL, Everhart K, Daly JA, Hopper A, Harrington A, Schreckenberger P, McKinley K, Jones M, Holmberg K, Kensinger B. Multicenter Evaluation of BioFire FilmArray Respiratory Panel 2 for Detection of Viruses and Bacteria in Nasopharyngeal Swab Samples. J Clin Microbiol. 2018 May 25;56(6):e01945-17. doi: 10.1128/JCM.01945-17. PMID: 29593057.\n3. U.S. Food and Drug Administration (FDA). Evaluation of Automatic Class III Designation for Biofire Respiratory Panel 2.1 Decision Summary DEN200031. Accessed May 28, 2024. https://www.accessdata.fda.gov/cdrh_docs/reviews/DEN200031.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Recent administration of intranasal vaccines (ie. FluMist) may lead to false positive results. As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. Some patients may experience financial toxicity with this expanded multiplex panel, as it is variably reimbursed by insurance.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2595,"ActiveDate":"2019-02-26T00:00:00","CreatedOn":"2018-10-03T13:57:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5727,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2595,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13710,"DictMethodologyId":219,"TdTestInfoSpecificId":2595,"DictMethodology":{"Id":219,"Name":"Reverse Transcription/Polymerase Chain Reaction (RT/PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2595,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":71,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 3 days"},"TdSpecimenRequirements":[{"Id":37074,"SpecialInstructions":"Collect 2-3 mL into a sterile, leak-proof, screw-cap collection cup or sterile dry container (i.e. Oracle 1619591). If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":150,"DictSpTypeName":"Bronch (BAL)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2595,"IsBeakerData":false},{"Id":37075,"SpecialInstructions":"Before collecting a sputum, have the patient rinse their mouth with water and discard the rinse fluid. Ask the patient to breathe deeply for three or four breaths, then hold their breath and expectorate deep cough sputum directly into a sterile, leak-proof, screw-cap collection cup or sterile dry container (i.e. Oracle 1619591). Induced sputum is also acceptable. If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":116,"DictSpTypeName":"Sputum, induced","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2595,"IsBeakerData":false},{"Id":678907,"SpecialInstructions":"Collect 2-3 mL into a sterile, leak-proof, screw-cap collection cup or sterile dry container (i.e. Oracle 1619591). If aliquotting is necessary, sterile aliquot tubes must be used. Do not dilute with transport media.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":14,"DictSpTypeName":"Aspirate, tracheal","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2595,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":21077,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2595,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":21078,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2595,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30413,"Description":"24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2595,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2595,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5794,"LISCode":"ZKAPCR","PrimaryName":"Zika Virus by PCR, Blood","LISName":"Zika Virus, PCR Bld","EMRName":"Zika Virus by PCR, Blood","EMRCode":"SQZKAPCR","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13210,"CptCode":"87662","Quantity":1,"Tmid":"30607255","CclTechComponentPrice":169.00,"CclProfComponentPrice":null,"TestNameForCdm":"Zika Virus by PCR, Blood","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5794,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5794,"SpecialInfo":"Testing should only be performed on individuals meeting Centers for Disease Control and Prevention (CDC) clinical criteria for Zika virus (e.g., clinical signs and symptoms associated with Zika virus infection) and/or CDC epidemiological criteria for Zika virus (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). A positive RT-PCR result confirms Zika virus infection, and no additional testing is indicated. When test results are negative, the serum should be tested as outlined in the current CDC-issued algorithm (http://www.cdc.gov/zika/laboratories/lab-guidance.html). The Zika Virus by PCR test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA). This test has not been FDA cleared or approved. Specimen source is required. Urine is unacceptable; refer to Zika Virus by PCR, Urine (UZKPCR). This test is New York DOH approved.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2597,"ActiveDate":"2019-08-19T00:00:00","CreatedOn":"2019-05-01T08:56:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5794,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2597,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10366,"DictMethodologyId":422,"TdTestInfoSpecificId":2597,"DictMethodology":{"Id":422,"Name":"Qualitative Polymerase Chain Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2597,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":40055,"SpecialInstructions":"Separate serum from cells and transfer to a sterile aliquot tube. Specimen source is required. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2597,"IsBeakerData":false},{"Id":40056,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2597,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22954,"Description":"6 weeks ","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2597,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22955,"Description":"5 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2597,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22956,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2597,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2597,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5795,"LISCode":"UZKPCR","PrimaryName":"Zika Virus by PCR, Urine","LISName":"Zika Virus, PCR Ur","EMRName":"Zika Virus by PCR, Urine","EMRCode":"SQUZKPCR","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":2,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13211,"CptCode":"87662","Quantity":1,"Tmid":"30607265","CclTechComponentPrice":169.00,"CclProfComponentPrice":null,"TestNameForCdm":"Zika Virus by PCR, Urine","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5795,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5795,"SpecialInfo":"Testing should only be performed on individuals meeting Centers for Disease Control and Prevention (CDC) clinical criteria for Zika virus (e.g., clinical signs and symptoms associated with Zika virus infection) and/or CDC epidemiological criteria for Zika virus (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). Health care providers are strongly encouraged to collect serum specimens alongside other specimen types to provide additional opportunities for diagnosing Zika. A positive RT-PCR result confirms Zika virus infection, and no additional testing is indicated. When test results are negative for urine,  serum should be tested as outlined in the current CDC-issued algorithm (http://www.cdc.gov/zika/laboratories/lab-guidance.html). The Zika Virus by PCR test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA). This test has not been FDA cleared or approved.\nSpecimen source is required. Serum is unacceptable; refer to Zika Virus by PCR, Blood (ZKAPCR). This test is New York DOH approved.","ClinicalInfo":"","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2598,"ActiveDate":"2019-08-19T00:00:00","CreatedOn":"2019-05-01T10:42:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5795,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2598,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10367,"DictMethodologyId":422,"TdTestInfoSpecificId":2598,"DictMethodology":{"Id":422,"Name":"Qualitative Polymerase Chain Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2598,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":85,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"2 - 5 days"},"TdSpecimenRequirements":[{"Id":40059,"SpecialInstructions":"Specimen source is required.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2598,"IsBeakerData":false},{"Id":40060,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2598,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22957,"Description":"6 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2598,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22958,"Description":"5 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2598,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22959,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2598,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2598,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5796,"LISCode":"ZKAIGM","PrimaryName":"Zika Virus IgM Antibody Capture (MAC), by ELISA","LISName":"Zika Virus IgM","EMRName":"Zika Virus IgM","EMRCode":"SQZKAIGM","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":13212,"CptCode":"86794 ","Quantity":1,"Tmid":"30204785","CclTechComponentPrice":109.00,"CclProfComponentPrice":null,"TestNameForCdm":"ZIKA VIRUS IGM","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5796,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5796,"SpecialInfo":"Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Label specimens plainly as 'acute' or 'convalescent,' and submit Patient History for Zika Virus testing form with the specimen. Contaminated, heat-inactivated, hemolyzed, lipemic, or turbid specimens are unacceptable. This test is New York DOH approved.","ClinicalInfo":"Use for patients whose symptoms began, or whose documented exposure occurred, ≥14 days prior to testing. Use as follow-up for patients with negative serum and urine results from molecular testing performed <14 days after symptom onset.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2599,"ActiveDate":"2019-08-19T00:00:00","CreatedOn":"2019-05-01T14:47:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5796,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2599,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":10368,"DictMethodologyId":22,"TdTestInfoSpecificId":2599,"DictMethodology":{"Id":22,"Name":"Semi Quantitative Enzyme Linked Immunosorbent Assay","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2599,"DictDaysPerformedId":29,"DictHoursPerformedId":null,"DictReportedId":16,"DictDaysPerformed":"Mon, Fri","DictReported":"2 - 7 days"},"TdSpecimenRequirements":[{"Id":40063,"SpecialInstructions":"Separate from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube. Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Label specimen plainly as 'acute' or 'convalescent.' It is recommended that the Patient History for Zika Virus Testing form is submitted with the specimen. ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":2599,"IsBeakerData":false},{"Id":40064,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2599,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":22960,"Description":"After separation from cells: 2 weeks","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2599,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22961,"Description":"After separation from cells: 1 year (Avoid repeated freeze/thaw cycles) ","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2599,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":22962,"Description":"After separation from cells: 48 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2599,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2599,"TestCode":null,"IsReportable":false,"DictVendorId":4,"DictVendor":{"Id":4,"Name":"ARUP","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":634,"Title":"Zika Virus IgM Antibody Testing","FileName":"ZikaVirusIGMAntibodyTesting","DictDocumentFormatId":1,"DictDocumentTypeId":4,"TdTestInfoCommonId":5796,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":4,"Name":"Patient Info Sheet","Description":null,"FolderName":"PatientInfoSheet","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5805,"LISCode":"AIDYSA","PrimaryName":"Autoimmune Dysautonomia Evaluation, Serum","LISName":"Autoimmune Dysautono","EMRName":"Autoimmune Dysautonomia Evaluation","EMRCode":"SQAIDYSA","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":15772,"CptCode":"83519","Quantity":1,"Tmid":"30119825","CclTechComponentPrice":99.00,"CclProfComponentPrice":null,"TestNameForCdm":"AIDYSA RIA NONAB","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5805,"IsBeakerData":false},{"Id":15773,"CptCode":"86255","Quantity":7,"Tmid":"30213015","CclTechComponentPrice":65.00,"CclProfComponentPrice":null,"TestNameForCdm":"AIDYSA FLUOR AB SCRN","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5805,"IsBeakerData":false}],"TdIncludes":[{"Id":23092,"TestName":"AChR Ganglionic Neuronal Ab","Rank":2,"TdTestInfoCommonId":5805},{"Id":23093,"TestName":"ANNA-1","Rank":3,"TdTestInfoCommonId":5805},{"Id":23095,"TestName":"Dysautonomia, Interpretation","Rank":1,"TdTestInfoCommonId":5805},{"Id":23096,"TestName":"CASPR2-IgG CBA,","Rank":6,"TdTestInfoCommonId":5805},{"Id":23097,"TestName":"CRMP-5-IgG","Rank":5,"TdTestInfoCommonId":5805},{"Id":23098,"TestName":"LGI1-IgG CBA","Rank":8,"TdTestInfoCommonId":5805},{"Id":23099,"TestName":"Purkinje Cell Cytoplasmic Ab Type 2","Rank":9,"TdTestInfoCommonId":5805},{"Id":25093,"TestName":"AP3B2 IFA, S","Rank":4,"TdTestInfoCommonId":5805},{"Id":25986,"TestName":"DPPX Ab CBA, S","Rank":7,"TdTestInfoCommonId":5805}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5805,"SpecialInfo":"Reflex Algorithm: Each reflex test performed incurs additional charge. \nIf the indirect immunofluorescence assay (IFA) patterns suggest collapsin response-mediator protein (CRMP)-5-IgG, then CRMP-5-IgG IFA titer and CRMP-5-IgG Western blot will be performed. If the IFA pattern suggests antineuronal nuclear antibody type 1 (ANNA-1), then ANNA-1 immunoblot, ANNA-1 IFA titer, and ANNA-2 immunoblot will be performed. If the IFA pattern suggests adaptor protein 3 beta 2 (AP3B2) antibody, then AP3B2 cell-binding assay (CBA) and AP3B2 IFA titer will be performed at an additional charge. If DPPX antibody CBA is positive, then DPPX IFA titer will be performed. If the IFA pattern suggests Purkinje cytoplasmic antibody type 2 (PCA-2), then PCA-2 titer is performed.\nNeuron-restricted patterns of IgG staining that do not fulfill criteria for ANNA-1, CRMP-5-IgG, or PCA-2 may be reported as \"unclassified anti-neuronal IgG.\" Complex patterns that include nonneuronal elements may be reported as \"uninterpretable.\" \nInclude ordering provider name, number, address, and email. Include relevant clinical information. \nPatient Prep: For optimal antibody detection, collection of specimen before initiation of immunosuppressant medication is recommended. This test should not be requested in patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed, or canceled if radioactivity remains. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Grossly hemolyzed, grossly lipemic, or grossly icteric specimens will be rejected.","ClinicalInfo":"Investigation of idiopathic dysautonomic symptoms. In patients with idiopathic dysautonomia, directing a focused search for cancer. Investigation of autonomic symptoms that appear in the course or wake of cancer therapy and are not explainable by recurrent cancer or metastasis; detection of autoantibodies in this profile helps differentiate autoimmune dysautonomia from the effects of chemotherapy. Caution:  Negative results do not exclude autoimmune dysautonomia or cancer. Note: CRMP-5 titers < 1:240 are detectable by recombinant CRMP-5 Western blot analysis, which can be done upon request on stored serum (held 4 weeks). This supplemental testing is recommended in cases of chorea, vision loss, cranial neuropathy, and myelopathy.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2602,"ActiveDate":"2019-09-05T00:00:00","CreatedOn":"2019-07-23T08:50:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5805,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2602,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12436,"DictMethodologyId":487,"TdTestInfoSpecificId":2602,"DictMethodology":{"Id":487,"Name":"Cell Binding Assay (CBA)","Description":null},"TdTestInfoSpecific":null},{"Id":12438,"DictMethodologyId":162,"TdTestInfoSpecificId":2602,"DictMethodology":{"Id":162,"Name":"Radioimmunoassay (RIA)","Description":null},"TdTestInfoSpecific":null},{"Id":13331,"DictMethodologyId":118,"TdTestInfoSpecificId":2602,"DictMethodology":{"Id":118,"Name":"Immunofluorescence","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2602,"DictDaysPerformedId":104,"DictHoursPerformedId":null,"DictReportedId":211,"DictDaysPerformed":"Mon - Sun","DictReported":"8 - 11 days"},"TdSpecimenRequirements":[{"Id":48742,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Specimen collection is recommended before initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2602,"IsBeakerData":false},{"Id":48743,"SpecialInstructions":"Serum","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":18,"DictSpVolumeName":"2.5 mL","TdTestInfoSpecificId":2602,"IsBeakerData":false},{"Id":48744,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Specimen collection is recommended before initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). 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This test is New York DOH approved.","ClinicalInfo":"This is the preferred panel for diagnosing possible tick-borne disease (i.e., Anaplasmosis or Ehrlichiosis) during the acute phase of the disease. A negative result does not rule out the presence of PCR inhibitors in the patient specimen or test-specific nucleic acid in concentrations below the level of detection by this test.","ClinicalReference":"","ClinicalLimitation":"This test detects and speciates Anaplasma phagocytophilum; Ehrlichia chaffeensis; E. ewingii/E. canis; E. muris-like. The nucleic acid detected from E. ewingii and E. canis cannot be differentiated by this test. A result of 'Detected' for E. ewingii/canis indicates the presence of either of these two organisms in the specimen. 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A diagnostic cutoff for the 1 hr time point is not established, and should be clinically determined.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2648,"ActiveDate":"2017-03-21T00:00:00","CreatedOn":"2016-12-13T11:56:00","CreatedById":30,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5479,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2648,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7357,"DictMethodologyId":255,"TdTestInfoSpecificId":2648,"DictMethodology":{"Id":255,"Name":"Glucose Hexokinase","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2648,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":27731,"SpecialInstructions":"Aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":23,"DictSpContainerName":"Potassium oxalate/sodium fluoride (Gray)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2648,"IsBeakerData":false},{"Id":27732,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2648,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":15747,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2648,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15748,"Description":"After removed from cells: 72 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2648,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15749,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2648,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2648,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":338,"Title":"Oral Glucose Tolerance","FileName":"OralGlucoseToleranceTesting1224","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":5479,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5480,"LISCode":"GTNG5","PrimaryName":"75 gram, fasting, 5-hour, non-gestational glucose tolerance","LISName":"75g 5hr nongest OGTT","EMRName":"GLUC TOL, 5-HR NON-GEST, 75 GM, FASTING","EMRCode":"SQGTNG5","LOINC":"","RecommendedUse":"","DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":9450,"CptCode":"82951","Quantity":1,"Tmid":"30101820","CclTechComponentPrice":49.00,"CclProfComponentPrice":null,"TestNameForCdm":"GLUC NON GEST TOLERANCE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5480,"IsBeakerData":false},{"Id":9451,"CptCode":"82952","Quantity":3,"Tmid":"30101830","CclTechComponentPrice":11.00,"CclProfComponentPrice":null,"TestNameForCdm":"GTT EA ADD SPEC BEYOND 3","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5480,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5480,"SpecialInfo":"Patient should be fasting at least 8 hours prior to the test. Collect a fasting specimen, then administer 75 grams of Dextrose within 5 minutes. Collect specimens at 1,2,3,4 and 5 hours post glucose load. Indicate collection time on each specimen.\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n","ClinicalInfo":"Evaluation of disorders of glucose metabolism.\n\nAmerican Diabetes Association guidelines state a diabetes mellitus diagnosis is preliminarily made when the fasting plasma glucose meets or exceeds 126 mg/dL and/or the 2 hr glucose tolerance meets or exceeds 200 mg/dL. In the absence of unequivocal hyperglycemia, results should be confirmed with repeat testing. Patients are at increased risk for diabetes mellitus (prediabetes) when the fasting glucose is 100 to 125 mg/dL or the 2 hr glucose tolerance result is 140 to 199 mg/dL. Diagnostic cutoffs for the other time points are not established, and should be clinically determined.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2649,"ActiveDate":"2017-03-21T00:00:00","CreatedOn":"2016-12-20T04:04:00","CreatedById":30,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5480,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2649,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2649,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":27727,"SpecialInstructions":"Aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":23,"DictSpContainerName":"Potassium oxalate/sodium fluoride (Gray)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2649,"IsBeakerData":false},{"Id":27728,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2649,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":15744,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2649,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15745,"Description":"After removed from cells: 72 hours\n","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2649,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15746,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2649,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2649,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":337,"Title":"Oral Glucose Tolerance","FileName":"OralGlucoseToleranceTesting1224","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":5480,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5477,"LISCode":"ISACON","PrimaryName":"Isavuconazole","LISName":"Isavuconazole","EMRName":"Isavuconazole","EMRCode":"SQISACON","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":8791,"CptCode":"80299","Quantity":1,"Tmid":"30104215","CclTechComponentPrice":88.00,"CclProfComponentPrice":null,"TestNameForCdm":"ISAVUCONAZOLE","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5477,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5477,"SpecialInfo":"Collect immediately prior to next dose. Steady-state concentrations are found 3-5 days after initiation of loading dose or 14 days without loading dose. Do not collect in a gel separator tube. Centrifuge and transfer serum/plasma to a CCL tube and refrigerate within 1 hour of collection.","ClinicalInfo":"Therapeutic, prophylactic, and toxic ranges are not well established.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2650,"ActiveDate":"2017-03-07T00:00:00","CreatedOn":"2016-12-12T13:21:00","CreatedById":6,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5477,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2650,"IsStat":false,"Comments":"Therapeutic, prophylactic, and toxic ranges are not well established.","DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":6828,"DictMethodologyId":54,"TdTestInfoSpecificId":2650,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2650,"DictDaysPerformedId":14,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"3 days per week","DictReported":"1 - 4 days"},"TdSpecimenRequirements":[{"Id":25692,"SpecialInstructions":"Do not use serum separator tubes.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":2650,"IsBeakerData":false},{"Id":25693,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":2650,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":14548,"Description":"After separation from cells: 15 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2650,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14549,"Description":"After separation from cells: 15 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2650,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":14550,"Description":"After separation from cells: 60 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2650,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2650,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5429,"LISCode":"HPVHRT","PrimaryName":"High Risk Human Papilloma Virus (HPV), PCR for Detection and Genotyping","LISName":"High Risk Human Papilloma Virus (HPV), PCR for Detection and Genotyping","EMRName":"High Risk Human Papilloma Virus (HPV), PCR for Detection and Genotyping","EMRCode":"SQHPVHRT","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6686,"Aka":"High-Risk HPV","TdTestInfoCommonId":5429},{"Id":14347,"Aka":"HPV 16","TdTestInfoCommonId":5429},{"Id":14348,"Aka":"HPV 18","TdTestInfoCommonId":5429},{"Id":14349,"Aka":"HPVHRR","TdTestInfoCommonId":5429},{"Id":14350,"Aka":"HPVHRT","TdTestInfoCommonId":5429},{"Id":14351,"Aka":"hrHPV","TdTestInfoCommonId":5429},{"Id":14352,"Aka":"SQHPVHRT","TdTestInfoCommonId":5429}],"TdBillingCommons":[{"Id":9583,"CptCode":"87626","Quantity":1,"Tmid":"30608715","CclTechComponentPrice":455.00,"CclProfComponentPrice":null,"TestNameForCdm":"Amplification, HPV, high-risk type and high-risk pooled","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5429,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5429,"SpecialInfo":"In order to facilitate accurate and complete interpretation of cervical screening results, hrHPV test results associated with a cytology report will be held until the cytology report is finalized.","ClinicalInfo":"Persistent infection with human papillomavirus (HPV) is the principal cause of cervical cancer and its precursor cervical intraepithelial neoplasia (CIN). The presence of HPV has been implicated in greater than 99% of cervical cancers worldwide. HPV is a small, non-enveloped, double-stranded DNA virus, with a genome of approximately 8000 nucleotides. There are more than 118 different types of HPV and approximately 40 different HPVs that can infect the human anogenital mucosa. However, only a subset of approximately 14 of these types are considered high-risk for the development of cervical cancer and its precursor lesions.\n\nThe cobas HPV test performed on the Roche cobas 4800 platform is multiplexed qualitative real-time PCR assay that detects and differentiates between high-risk HPV (hrHPV) types 16, 18, and other (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68). The assay targets a ~200 nucleotide portion of the polymorphic L1 region of the HPV genome, while type-specific probes labeled with different fluorophores differentiates between hrHPV types 16, 18, and other. The test does not detect low-risk HPV types. The assay is FDA-approved for cervical cancer screening in the following situations: reflex testing from ASCUS cervical cytology test results for patients 21 years and older, co-testing with cervical cytology for patients 30 years and older, and first-line primary cervical cancer screening for patients 25 years and older. This lab only accepts specimens collected in ThinPrep PreservCyt solution.\n\nThis assay has been additionally modified and validated as a lab-developed test to accept fine-needle aspirate (FNA) specimens in ThinPrep PreservCyt solution from patient suspected to have or diagnosed with squamous cell carcinoma of the head and neck. Determination of tumor hrHPV-status in patients suspected to have oropharyngeal squamous cell carcinoma (OPSCC) is critical to staging, prognostication, and therapeutic decision-making. While p16 immunohistochemistry (IHC) is a surrogate marker that can be used to predict hrHPV status, it may be either impossible to perform or unreliable on FNA specimens with scant material. Additionally, p16 IHC can be nonspecifically positive in SCCs from other sites. Accurate classification and staging of a tumor is enhanced when more than one biomarker is utilized (i.e. p16 IHC alongside hrHPV-specific testing) to assess for hrHPV status. ","ClinicalReference":"1. Fontham ETH, Wolf AMD, Church TR, Etzioni R, Flowers CR, Herzig A, Guerra CE, Oeffinger KC, Shih YT, Walter LC, Kim JJ, Andrews KS, DeSantis CE, Fedewa SA, Manassaram-Baptiste D, Saslow D, Wender RC, Smith RA. Cervical cancer screening for individuals at average risk: 2020 guideline update from the American Cancer Society. CA Cancer J Clin. 2020 Sep;70(5):321-346. doi: 10.3322/caac.21628. Epub 2020 Jul 30. PMID: 32729638.\n2. Perkins RB, Guido RS, Castle PE, Chelmow D, Einstein MH, Garcia F, Huh WK, Kim JJ, Moscicki AB, Nayar R, Saraiya M, Sawaya GF, Wentzensen N, Schiffman M; 2019 ASCCP Risk-Based Management Consensus Guidelines Committee. 2019 ASCCP Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors. J Low Genit Tract Dis. 2020 Apr;24(2):102-131. doi: 10.1097/LGT.0000000000000525. Erratum in: J Low Genit Tract Dis. 2020 Oct;24(4):427. PMID: 32243307\n3. American College of Obstetricians and Gynecologists. Updated guidelines for management of cervical cancer screening abnormalities. Practice Advisory. Washington, DC: American College of Obstetricians and Gynecologists; 2020. Available at: https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/10/updated-guidelines-for-management-of-cervical-cancer-screening-abnormalities. Retrieved April 12, 2021.\n4. Maghami E, Ismaila N, Alvarez A, Chernock R, Duvvuri U, Geiger J, Gross N, Haughey B, Paul D, Rodriguez C, Sher D, Stambuk HE, Waldron J, Witek M, Caudell J. Diagnosis and Management of Squamous Cell Carcinoma of Unknown Primary in the Head and Neck: ASCO Guideline. J Clin Oncol. 2020 Aug 1;38(22):2570-2596. doi: 10.1200/JCO.20.00275. Epub 2020 Apr 23. PMID: 32324430. \n5. Baldassarri R, Aronberg R, Levi AW, Yarbrough WG, Kowalski D, Chhieng D. Detection and genotype of high-risk human papillomavirus in fine-needle aspirates of patients with metastatic squamous cell carcinoma is helpful in determining tumor origin. Am J Clin Pathol. 2015 May;143(5):694-700. doi: 10.1309/AJCPCZA4PSZCFHQ4. PMID: 25873503.\n","ClinicalLimitation":"Detection of high-risk HPV is dependent on the number of copies present in the specimen and may be affected by specimen collection methods, patient factors, stage of infection and the presence of interfering substances. Though rare, mutations within the highly conserved regions of the genomic DNA of Human papillomavirus covered by the cobas HPV Test’s primers and/or probes may result in failure to detect the presence of the viral DNA. \n\nFor FNA specimens from patients suspected of head and neck squamous cell carcinoma, hrHPV PCR results should be evaluated in the context of clinical history and cytology/pathology results (i.e. tumor type and location, p16 immunohistochemical stain, and hrHPV in-situ hybridization studies if available). Assay analytical sensitivity may be diminished with suboptimal collection or specimen pre-processing. Visibly bloody specimens and those contaminated with excessive ultrasound gel may cause assay inhibition leading to false-negative or indeterminate results. If results are incongruent with history, recommend submitting a dedicated specimen for re-testing or request an alternate method for hrHPV detection.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2655,"ActiveDate":"2016-10-11T00:00:00","CreatedOn":"2016-07-11T09:15:00","CreatedById":94,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5429,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2655,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13549,"DictMethodologyId":393,"TdTestInfoSpecificId":2655,"DictMethodology":{"Id":393,"Name":"Qualitative Real-Time PCR","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2655,"DictDaysPerformedId":26,"DictHoursPerformedId":null,"DictReportedId":110,"DictDaysPerformed":"Mon - Sat","DictReported":"5 - 7 days"},"TdSpecimenRequirements":[{"Id":28027,"SpecialInstructions":"Cervical specimens should be collected in ThinPrep PreservCyt solution using an endocervical brush/spatula. Follow the manufacturer's instructions for collecting cervical specimens. High Risk HPV testing can be performed on a sterile aliquot of the specimen made prior to Cytology processing. Residual specimen after Cytology processing is only acceptable if the ThinPrep processor used is a T2000 or T3000 instrument, or a molecular microbiology lab-validated processor. Specimens treated with glacial acetic acid are not acceptable for hrHPV testing.","LogicalOperation":null,"DictSpContainerId":189,"DictSpContainerName":"PreservCyt","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":6,"DictSpCollectionTemperatureName":"N/A","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":148,"DictSpTypeName":"Cervical","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2655,"IsBeakerData":false},{"Id":678262,"SpecialInstructions":"High Risk HPV testing of fine needle aspirate (FNA) specimens is only indicated for patients suspected of HPV-positive Head and Neck Squamous Cell Carcinoma (HNSCC). Fine needle aspirate (FNA) specimens may be collected directly into ThinPrep PreservCyt solution for maximal analytic sensitivity. Residual FNA specimen resuspended in PreservCyt solution after Cytology processing (including after initial collection into intermediary media such as ThinPrep CytoLyt solution or Roswell Park Memorial Institute [RPMI] medium) is also acceptable if the ThinPrep processor used is a T2000 or T3000 instrument, or a molecular microbiology lab-validated processor.","LogicalOperation":null,"DictSpContainerId":189,"DictSpContainerName":"PreservCyt","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":6,"DictSpCollectionTemperatureName":"N/A","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":92,"DictSpTypeName":"Aspirate, fine needle","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2655,"IsBeakerData":false},{"Id":678263,"SpecialInstructions":"Vaginal specimens may be collected for patients without an intact cervix. The specimen should be collected from the vaginal apex in ThinPrep PreservCyt solution using an endocervical brush/spatula. High Risk HPV testing can be performed on a sterile aliquot of the specimen made prior to Cytology processing. Residual specimen after Cytology processing is only acceptable if the ThinPrep processor used is a T2000 or T3000 instrument, or a molecular microbiology lab-validated processor. Specimens treated with glacial acetic acid are not acceptable for hrHPV testing.","LogicalOperation":null,"DictSpContainerId":189,"DictSpContainerName":"PreservCyt","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":6,"DictSpCollectionTemperatureName":"N/A","DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":63,"DictSpTypeName":"Vaginal","DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":2655,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":15941,"Description":"6 months in PreservCyt","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2655,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15942,"Description":"6 months in PreservCyt","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2655,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2655,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5439,"LISCode":"OMEGAC","PrimaryName":"OmegaCheck","LISName":"OmegaCheck","EMRName":"OmegaCheck","EMRCode":"SQOMEGAC","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":9450,"Aka":"Omega 3 and 6 Fatty Acids","TdTestInfoCommonId":5439}],"TdBillingCommons":[{"Id":12373,"CptCode":"82542","Quantity":1,"Tmid":"30113495","CclTechComponentPrice":157.00,"CclProfComponentPrice":null,"TestNameForCdm":"OMEGACHECK","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5439,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5439,"SpecialInfo":"Fasting: Preferred, but not required. Causes for rejection: Specimens other than EDTA whole blood; improper labeling; samples not stored properly; samples older than stability limits; lipemic samples.","ClinicalInfo":"OmegaCheck™ may be performed on individuals with hypercholesterolemia, hypertriglyceridemia, hypertension, and/or those at high metabolic or cardiovascular risk. Relative Risk: Low Risk OmegaCheck™ (% by weight): > or =5.5; Moderate Risk OmegaCheck™  (% by weight): 3.8 - 5.4; High Risk OmegaCheck™  (% by weight): < or = 3.7 \n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2656,"ActiveDate":"2016-11-21T00:00:00","CreatedOn":"2016-10-07T16:13:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5439,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2656,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":9710,"DictMethodologyId":265,"TdTestInfoSpecificId":2656,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2656,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":210,"DictDaysPerformed":"Mon - Fri","DictReported":"5 - 8 days"},"TdSpecimenRequirements":[{"Id":37460,"SpecialInstructions":"Gently invert tube 8-10 times immediately after draw. DO NOT SHAKE. Do not centrifuge. Store EDTA whole blood at 2°C to 8°C after collection and ship the same day. 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Collect a fasting specimen, then administer 100 gm of Dextrose within 5 minutes. Collect specimens at 1, 2 and 3 hours post glucose load. Indicate collection time on each specimen.\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n","ClinicalInfo":"Confirmation of Gestational Diabetes Mellitus\n\nAmerican Congress of Obstetricians and Gynecologists (Carpenter/Coustan) guidelines state gestational diabetes mellitus is present when 2 or more of the plasma glucose concentrations meet or exceed the following levels: fasting: 95 mg/dL; 1 hr: 180 mg/dL; 2 hr: 155 mg/dL; and 3 hr: 140 mg/dL.","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2659,"ActiveDate":"2017-03-21T00:00:00","CreatedOn":"2016-12-12T12:06:00","CreatedById":30,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5482,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2659,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7356,"DictMethodologyId":255,"TdTestInfoSpecificId":2659,"DictMethodology":{"Id":255,"Name":"Glucose Hexokinase","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2659,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":27723,"SpecialInstructions":"Aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":23,"DictSpContainerName":"Potassium oxalate/sodium fluoride (Gray)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2659,"IsBeakerData":false},{"Id":27724,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2659,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":15741,"Description":" 24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2659,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15742,"Description":"After removed from cells: 72 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2659,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15743,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2659,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2659,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":336,"Title":"Oral Glucose Tolerance","FileName":"OralGlucoseToleranceTesting1224","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":5482,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5483,"LISCode":"GLTGST","PrimaryName":"50 gram, non-fasting, 1-hour, gestational glucose screen","LISName":"50g, 1hr gest. 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Collect 1 hour post administration.\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n","ClinicalInfo":"Screening for Gestational Diabetes Mellitus\n\nAmerican Congress of Obstetricians and Gynecologists  (Carpenter/Coustan) guidelines state a gestational diabetes mellitus positive screen is made, in women not previously diagnosed with overt diabetes, when the 1 hr plasma glucose level is equal to or above 140 mg/dL. The Cleveland Clinic Ob/Gyn and Women’s Health Institute recommends a 135 mg/dL cut-off. \t\t","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2660,"ActiveDate":"2017-03-21T00:00:00","CreatedOn":"2016-12-13T05:55:00","CreatedById":30,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5483,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2660,"IsStat":false,"Comments":"","DictPerformingLabId":6,"DictPerformingLab":{"Id":6,"Name":"Auto Lab (x45476)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":7355,"DictMethodologyId":255,"TdTestInfoSpecificId":2660,"DictMethodology":{"Id":255,"Name":"Glucose Hexokinase","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2660,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"Sun - Sat","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":27719,"SpecialInstructions":"Aliquot into CCL aliquot tube","LogicalOperation":null,"DictSpContainerId":23,"DictSpContainerName":"Potassium oxalate/sodium fluoride (Gray)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":9,"DictSpTransportTemperatureName":"Centrifuge and refrigerate.","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":2660,"IsBeakerData":false},{"Id":27720,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":8,"DictSpVolumeName":"0.3 mL","TdTestInfoSpecificId":2660,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":15738,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2660,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15739,"Description":"After removed from cells: 72 hours","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2660,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":15740,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2660,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2660,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[{"Id":335,"Title":"Oral Glucose Tolerance ","FileName":"OralGlucoseToleranceTesting1224","DictDocumentFormatId":1,"DictDocumentTypeId":1,"TdTestInfoCommonId":5483,"DictDocumentFormat":{"Id":1,"Code":"PDF","Description":"Portable Document Format","SupportDocuments":[],"TdSupportDocuments":[]},"DictDocumentType":{"Id":1,"Name":"Technical Brief","Description":null,"FolderName":"TechnicalBrief","SupportDocuments":[],"TdSupportDocuments":[]},"SupportDocuments":null}],"TdReflexedTests":[]},{"Id":5490,"LISCode":"HPYLAG","PrimaryName":"Helicobacter pylori Antigen by EIA,  Stool","LISName":"Helicobacter pylori Antigen by EIA, Stool","EMRName":"Helicobacter pylori Antigen by EIA, Stool","EMRCode":"SQHPYLAG","LOINC":"17780-8","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":6210,"Aka":"Campylobacter pylori","TdTestInfoCommonId":5490},{"Id":6211,"Aka":"H pylori Antigen, fecal","TdTestInfoCommonId":5490},{"Id":6212,"Aka":"H. pylori","TdTestInfoCommonId":5490},{"Id":14280,"Aka":"Stool kit","TdTestInfoCommonId":5490},{"Id":14281,"Aka":"Stool test","TdTestInfoCommonId":5490},{"Id":14282,"Aka":"STUL kit","TdTestInfoCommonId":5490}],"TdBillingCommons":[{"Id":8855,"CptCode":"87338","Quantity":1,"Tmid":"30600840","CclTechComponentPrice":94.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, H. pylori","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5490,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":5490,"SpecialInfo":"Avoid ingestion of antimicrobials, proton pump inhibitors and bismuth within 14 days of specimen collection.  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Both solid and liquid stools can be tested.  Transport promptly to Microbiology.  Refrigerated transport is preferred.  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This panel does not contain Clostridium difficile, which must be ordered separately (SQCDPCR) if clinically appropriate. This panel contains the following targets: Campylobacter species (C. jejuni/C. coli/C. upsaliensis), Plesiomonas shigelloides, Salmonella species, Vibrio species (V. parahaemolyticus/V. vulnificus/ V. cholerae), Vibrio cholerae, Yersinia enterocolitica, Enteroaggregative E.coli (EAEC), Enteropathogenic E.coli (EPEC), Enterotoxigenic E.coli (ETEC), Shiga-like toxin producing E.coli (STEC), E.coli O157, Shigella/Enteroinvasive E.coli (EIEC), Adenovirus F 40/41, Astrovirus, Norovirus GI/GII, Rotavirus A, Sapovirus (Genogroups I, II, IV, V), Cryptosporidium, Cyclospora cayetanensis, Entamoeba histolytica, and Giardia lamblia. Specimens positive for organisms of public health concern may be reflexed to culture and/or sendout testing at a public health lab as indicated in the result comments. \n\nThe Infectious Diseases Society of America recommends stool pathogen testing in individuals with diarrhea accompanied by fever, bloody or mucoid stools, severe abdominal cramping or tenderness, or signs of sepsis; in an outbreak setting; and in immunocompromised hosts with diarrhea. Identification of the infectious etiology of diarrheal illness can help guide appropriate therapy, prevent unnecessary or harmful antibiotic exposure, and facilitate further workup. Repeat testing within 14 days of the same episode of diarrhea, or for test of cure, is not recommended.\n\nConsider a more limited PCR panel for the most common enteric bacterial pathogens only (SQSTLPCR) for patients who are not immunocompromised or severely-ill. Immunocompromised individuals with persistent diarrhea may benefit from additional testing (ie. SQOVAP: Stool Ova/Parasite Exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora Exam, SQMICSPO: Microsporidia Exam, and gastrointestinal biopsy, among others). Individuals with travel history outside the United States with persistent diarrhea lasting >14 days may benefit from additional parasitic testing (ie. SQOVAP: Stool Ova/Parasite exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora exam). Individuals with onset of diarrhea after more than 3 days of hospital admission or with prior antibiotic exposure history may benefit from testing for C. difficile (SQCDPCR).","ClinicalReference":"1. Shane AL, Mody RK, Crump JA, Tarr PI, Steiner TS, Kotloff K, Langley JM, Wanke C, Warren CA, Cheng AC, Cantey J, Pickering LK. 2017 Infectious Diseases Society of America Clinical Practice Guidelines for the Diagnosis and Management of Infectious Diarrhea. Clin Infect Dis. 2017 Nov 29;65(12):e45-e80. doi: 10.1093/cid/cix669. PMID: 29053792.\n2. Buss SN, Leber A, Chapin K, Fey PD, Bankowski MJ, Jones MK, Rogatcheva M, Kanack KJ, Bourzac KM. Multicenter evaluation of the BioFire FilmArray gastrointestinal panel for etiologic diagnosis of infectious gastroenteritis. J Clin Microbiol. 2015 Mar;53(3):915-25. doi: 10.1128/JCM.02674-14. Epub 2015 Jan 14. PMID: 25588652.\n3. Collins JP, Shah HJ, Weller DL, Ray LC, Smith K, McGuire S, Trevejo RT, Jervis RH, Vugia DJ, Rissman T, Garman KN, Lathrop S, LaClair B, Boyle MM, Harris S, Kufel JZ, Tauxe RV, Bruce BB, Rose EB, Griffin PM, Payne DC. Preliminary Incidence and Trends of Infections Caused by Pathogens Transmitted Commonly Through Food - Foodborne Diseases Active Surveillance Network, 10 U.S. Sites, 2016-2021. MMWR Morb Mortal Wkly Rep. 2022 Oct 7;71(40):1260-1264. doi: 10.15585/mmwr.mm7140a2. PMID: 36201372.","ClinicalLimitation":"The Biofire FilmArray Gastrointestinal (GI) Panel is indicated as an aid in the diagnosis of specific agents of gastrointestinal illness and results are meant to be used in conjunction with other clinical, laboratory, and epidemiological data. Positive results do not rule out coinfection with organisms not included in the panel. The agent detected may not be the definite cause of the disease. Some targets on this panel have potential for false positives due to contaminated transport media, or non-specific cross reactivity. Some have been associated with asymptomatic colonization/infection. Negative results in the setting of clinical illness compatible with gastroenteritis may be due to infection by pathogens that are not detected by this test or non-infectious causes such as ulcerative colitis, irritable bowel syndrome, or Crohn’s disease. 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This test is New York DOH approved.","ClinicalInfo":"Note: Reference ranges for 17-Hydroxyprogesterone following stimulation are not well defined and are dependent on the stimulation method utilized.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2709,"ActiveDate":"2018-04-05T00:00:00","CreatedOn":"2018-01-16T15:48:00","CreatedById":457,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5603,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2709,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":8467,"DictMethodologyId":54,"TdTestInfoSpecificId":2709,"DictMethodology":{"Id":54,"Name":"High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC/MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2709,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":13,"DictDaysPerformed":"Sun - Sat","DictReported":"2 - 6 days"},"TdSpecimenRequirements":[{"Id":32585,"SpecialInstructions":"THIS TEST REQUIRES TWO SPECIMEN TUBES. 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This test is New York DOH approved. ","ClinicalInfo":"Order before initiating treatment with NS5A inhibitors. Do not order prior to molecular confirmation of positive hepatitis C virus (HCV) screen and confirmation of genotype 1a or 1b. This assay detects resistance-associated variants in NS5A codons 20-101 for HCV genotypes 1a and 1b. Variants in viral sub-populations below 20% of total may not be detected. For more information, please refer to drug package inserts for the applicable direct-acting antiviral drug and current HCV treatment guidelines (e.g., AASLD/IDSA guidelines or EASL HCV treatment recommendations).\n","ClinicalReference":"","ClinicalLimitation":"This test may be unsuccessful if the HCV RNA viral load is < log 3.4 or 2500 IU/mL and/or if the HCV RNA genotype is not 1a or 1b. 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NOTE: Testing of fetal specimens or specimens from patients under the age of 18 years is not offered. Plasma, serum and frozen specimens in glass collection tubes will be rejected. This test is New York DOH approved.","ClinicalInfo":"Supports a clinical diagnosis of Alzheimer disease (AD) in symptomatic individuals. Use for AD risk assessment only. Background Information: Characteristics: Alzheimer disease (AD), the most common cause of dementia, is characterized by progressive cognitive decline including memory, problem-solving skills, multi-step tasks, planning, and changes in personality. A clinical diagnosis of probable AD can be made based on clinical signs and neuroimaging, and the diagnosis is confirmed postmortem based on neuropathologic findings. The e4 allele of the APOE gene has been widely demonstrated to be associated with increased risk of AD. In individuals with a clinical diagnosis of AD, the presence of the e4 allele increases the likelihood that the diagnosis is correct, but is not diagnostic alone. APOE genotyping is not recommended for predicting AD risk in asymptomatic individuals. Prevalence of APOE e4: Heterozygosity and homozygosity for the e4 allele is present in approximately 25% and 1-2% of the general population, respectively. Inheritance of APOE e4: Semi-dominant. Penetrance of APOE e4: Incomplete and influenced by age, gender, ethnicity, family history and environmental factors. The e4 allele is neither necessary nor sufficient for diagnosing AD; therefore, not all individuals with AD have the e4 allele and not all individuals with the e4 allele will develop AD. Cause: Multi-factorial. Variants Tested: Two single nucleotide polymorphisms in the APOE gene at codons 130 (rs429358) and 176 (rs7412). The e3 allele (Cysteine at 130 and Arginine at 176) is the most common in the general population. The e4 allele (Arginine at 130 and 176) is associated with increased AD risk. The e2 allele (Cysteine at codons 130 and 176) may be associated with a lower risk for AD but homozygosity has been associated with increased risk for type III hyperlipoproteinemia. Clinical Sensitivity: Approximately 30-60% of individuals diagnosed with AD carry at least one e4 allele. The e4/e4 genotype is found in approximately 13% of the AD population and 20% of the familial AD population. Methodology: Polymerase chain reaction (PCR) and fluorescence monitoring using hybridization probes. Analytical Sensitivity and Specificity: 99%\n\n\n\n\n\n\n\n\n ","ClinicalReference":"","ClinicalLimitation":"Only the APOE alleles e2, e3 and e4 will be detected; rare alleles are not detected by this test. 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If no cells are available for analysis, no analysis charges will be incurred.\n","ClinicalReference":"","ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":2805,"ActiveDate":"2020-10-06T00:00:00","CreatedOn":"2020-07-07T15:20:00","CreatedById":387,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5932,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2805,"IsStat":false,"Comments":"","DictPerformingLabId":16,"DictPerformingLab":{"Id":16,"Name":"FISH (x42130)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13486,"DictMethodologyId":173,"TdTestInfoSpecificId":2805,"DictMethodology":{"Id":173,"Name":"Fluorescent In-Situ Hybridization (FISH)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2805,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":7,"DictDaysPerformed":"5 days per week","DictReported":"3 - 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Refer to order code SQRPPCR for testing on lower respiratory specimens. Patients who may benefit from this test include immunocompromised patients, those with severe underlying respiratory comorbidities, and those in whom testing may help avoid hospital admission. The test is very expensive, and if not covered by insurance, the patient will incur a substantial charge.","ClinicalInfo":"Respiratory pathogens cause acute local and systemic disease, with the most severe cases occurring in children, the elderly, and immunocompromised individuals. Due to the similarity of diseases caused by many viruses and bacteria, diagnosis based on clinical symptoms alone is difficult. Identification of potential causative agents provides data to aid providers in determining appropriate patient treatment or triage, and public health response for disease containment.\n\nThe BioFire Respiratory Panel 2.1 (RP2.1) is a multiplexed nucleic acid test that qualitatively detects and identifies nucleic acids from the following viral and bacterial targets from respiratory specimens: SARS-CoV-2 (Agent of COVID-19); Influenza A and subtypes H1, H1N1 2009, H3; Influenza B; Respiratory syncytial virus (RSV); Human metapneumovirus (hMPV); Human rhinovirus/enterovirus; Adenovirus; Parainfluenza 1-4; Coronaviruses 229E, OC43, NL63, HKU1; Chlamydia pneumoniae; Mycoplasma pneumoniae; and Bordetella pertussis and parapertussis. These respiratory pathogens are assayed in a single pouch through array-based localization and endpoint melting curve data analysis.","ClinicalReference":"1. Berry GJ, Zhen W, Smith E, Manji R, Silbert S, Lima A, Harington A, McKinley K, Kensinger B, Neff C, Lu D. Multicenter Evaluation of the BioFire Respiratory Panel 2.1 (RP2.1) for Detection of SARS-CoV-2 in Nasopharyngeal Swab Samples. J Clin Microbiol. 2022 May 18;60(5):e0006622. doi: 10.1128/jcm.00066-22. Epub 2022 Apr 7. PMID: 35387475.\n2. Leber AL, Everhart K, Daly JA, Hopper A, Harrington A, Schreckenberger P, McKinley K, Jones M, Holmberg K, Kensinger B. Multicenter Evaluation of BioFire FilmArray Respiratory Panel 2 for Detection of Viruses and Bacteria in Nasopharyngeal Swab Samples. J Clin Microbiol. 2018 May 25;56(6):e01945-17. doi: 10.1128/JCM.01945-17. PMID: 29593057.\n3. U.S. Food and Drug Administration (FDA). Evaluation of Automatic Class III Designation for Biofire Respiratory Panel 2.1 Decision Summary DEN200031. Accessed May 28, 2024. https://www.accessdata.fda.gov/cdrh_docs/reviews/DEN200031.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. This assay has lower sensitivity than others for detecting Bordetella pertussis. If pertussis infection is suspected, a dedicated B.pertussis molecular test should be ordered. Cross reactivity has been reported between B. bronchiseptica/parapertussis with B. pertussis, and between B. pertussis and Human rhinovirus/enterovirus. Recent administration of intranasal vaccines (ie. FluMist) may lead to false positive results. As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. Some patients may experience financial toxicity with this expanded multiplex panel, as it is variably reimbursed by insurance.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":2812,"ActiveDate":"2021-02-25T00:00:00","CreatedOn":"2021-01-26T16:35:00","CreatedById":90,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5965,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2812,"IsStat":false,"Comments":"","DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13709,"DictMethodologyId":219,"TdTestInfoSpecificId":2812,"DictMethodology":{"Id":219,"Name":"Reverse Transcription/Polymerase Chain Reaction (RT/PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2812,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":84,"DictDaysPerformed":"7 days a week","DictReported":"2 hours"},"TdSpecimenRequirements":[{"Id":47475,"SpecialInstructions":"1. 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Break the swab shaft at the score line, discard the top portion of the stem, and close the cap.","LogicalOperation":null,"DictSpContainerId":165,"DictSpContainerName":"Universal Transport Media (UTM)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":34,"DictSpTypeName":"Nasopharyngeal swab","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2812,"IsBeakerData":false},{"Id":678903,"SpecialInstructions":"Viral transport media (including VTM, M4RT, M5, or M6) may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":113,"DictSpContainerName":"Viral Transport Media","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":34,"DictSpTypeName":"Nasopharyngeal swab","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":2812,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":27154,"Description":"4 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2812,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27155,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2812,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":27156,"Description":"3 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2812,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2812,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":5970,"LISCode":"MYNGSM","PrimaryName":"Myeloid Panel NGS Bone Marrow","LISName":"Myeloid Panel NGS BM","EMRName":"Myeloid NGS Panel Bone Marrow","EMRCode":"SQMYNGSM","LOINC":"","RecommendedUse":"Used in the evaluation of bone marrow for known or suspected chronic myeloid neoplasms, including but not limited to myeloproliferative neoplasms, myelodysplastic syndromes, and overlap myelodysplastic/myeloproliferative neoplasms. 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Do not expose to formalin or other fixatives. Do not freeze. Place specimen in a sterile container containing RPMI, Hank's solution or sterile saline. Keep at room temperature; may refrigerate if specimen must be held overnight. 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If the IFA patterns suggest amphiphysin antibody, then amphiphysin IFA titer and amphiphysin immunoblot will be performed. If the IFA pattern suggests antiglial nuclear antibody (AGNA)-1, then AGNA-1 IFA titer and AGNA-1 immunoblot will be performed. If the IFA pattern suggests antineuronal nuclear antibody type 1 (ANNA-1), then ANNA-1 IFA titer, ANNA-1 immunoblot, and ANNA-2 immunoblot will be performed. If the IFA pattern suggests ANNA-2 antibody, then ANNA-2 IFA titer, ANNA-2 immunoblot, and ANNA-1 immunoblot will be performed. If the IFA pattern suggests Purkinje cytoplasmic antibody type 1 (PCA-1), then PCA-1 IFA titer and PCA-1 immunoblot will be performed. If IFA pattern suggests PCA-Tr antibody, then PCA-Tr IFA titer and PCA-Tr immunoblot will be performed. If IgLON5 cell-binding assay (CBA) is positive, then IgLON5 IFA titer will be performed. If AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) receptor antibody CBA is positive, then AMPA-receptor antibody IFA titer assay will be performed. If gamma-aminobutyric acid B (GABA-B) receptor antibody is positive, then GABA-B-receptor antibody IFA titer assay will be performed. If the IFA pattern suggests glial fibrillary acidic protein (GFAP) antibody, then GFAP IFA titer and GFAP CBA will be performed. If N-methyl-D-aspartate (NMDA) receptor antibody CBA is positive, then NMDA-receptor antibody IFA titer assay will be performed. If DPPX antibody CBA is positive, then DPPX IFA titer will be performed. If the IFA pattern suggests metabotropic glutamate receptor 1 (mGluR1) antibody, then mGluR1 antibody CBA and mGluR1 IFA titer will be performed. If the IFA pattern suggests neuronal intermediate filament (NIF) antibody, then alpha internexin CBA, NIF heavy chain CBA, NIF light chain CBA, and NIF IFA titer will be performed. If the indirect immunofluorescence (IFA) pattern suggests phosphodiesterase 10A (PDE10A) IgG, then the PDE10A antibody IFA titer will be performed. If the indirect immunofluorescence (IFA) pattern suggests tripartite motif-containing protein 46 (TRIM46) IgG, then the TRIM46 antibody cell-binding assay (CBA) and TRIM46 antibody IFA titer will be performed.\nNeuron-restricted patterns of IgG staining that do not fulfill criteria for ANNA-1, ANNA-2, CRMP-5-IgG, PCA-1, PCA-2, or PCA-Tr may be reported as \"unclassified anti-neuronal IgG.\" Complex patterns that include nonneuronal elements may be reported as \"uninterpretable.\" For optimal antibody detection, specimen collection is recommended prior to initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes because of potential assay interference. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed, or canceled if radioactivity remains. Patient should have no general anesthetic or muscle-relaxant drugs in the previous 24 hours. Grossly hemolyzed, lipemic or icteric specimens will be rejected.","ClinicalInfo":"This test is useful for evaluating new onset encephalopathy (noninfectious or metabolic) comprising confusional states, psychosis, delirium, memory loss, hallucinations, movement disorders, sensory or motor complaints, seizures, dyssomnias, ataxias, nausea, vomiting, inappropriate antidiuresis, coma, dysautonomias, or hypoventilation in serum specimens. Diagnosis of autoimmune encephalopathy should be suspected on the basis of clinical course, coexisting autoimmune disorder (eg, thyroiditis, diabetes), serological evidence of autoimmunity, spinal fluid evidence of intrathecal inflammation, neuroimaging or electroencephalographic abnormalities, and favorable response to trial of immunotherapy. Detection of one or more neural autoantibodies aids the diagnosis of autoimmune encephalopathy and may guide a search for cancer. Importantly, autoimmune encephalopathies are reversible. Misdiagnosis as a progressive (currently irreversible) neurodegenerative condition is not uncommon and has devastating consequences for the patient. Clinicians must consider the possibility of an autoimmune etiology in the differential diagnoses of encephalopathy. Neurological accompaniments of neural autoantibodies are generally not syndromic, but diverse and multifocal. ","ClinicalReference":"","ClinicalLimitation":"Specimens from pediatric patients are no longer accepted for the Autoimmune Encephalopathy Evaluation. The Autoimmune Pediatric CNS Disorders may be ordered as APCNSS for serum and APCNSC for CSF, or specific antibodies may be ordered directly: GAD65 Antibody, CSF (GADCSF); MOG IgG, Serum (MOGFAC).","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":2815,"ActiveDate":"2021-03-23T00:00:00","CreatedOn":"2020-12-09T14:38:00","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":5983,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":2815,"IsStat":false,"Comments":"Patients 18 years and or older.","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":12439,"DictMethodologyId":487,"TdTestInfoSpecificId":2815,"DictMethodology":{"Id":487,"Name":"Cell Binding Assay (CBA)","Description":null},"TdTestInfoSpecific":null},{"Id":12441,"DictMethodologyId":162,"TdTestInfoSpecificId":2815,"DictMethodology":{"Id":162,"Name":"Radioimmunoassay (RIA)","Description":null},"TdTestInfoSpecific":null},{"Id":13330,"DictMethodologyId":118,"TdTestInfoSpecificId":2815,"DictMethodology":{"Id":118,"Name":"Immunofluorescence","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":2815,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":135,"DictDaysPerformed":"Sun - Sat","DictReported":"11 - 14 days"},"TdSpecimenRequirements":[{"Id":48747,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Specimen collection is recommended before initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). ","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2815,"IsBeakerData":false},{"Id":48748,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":18,"DictSpVolumeName":"2.5 mL","TdTestInfoSpecificId":2815,"IsBeakerData":false},{"Id":48749,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. Patient should have no general anesthetic or muscle-relaxant medications in the previous 24 hours. Specimen collection is recommended before initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). ","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":2815,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":28043,"Description":"28 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":2815,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28044,"Description":"28 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":2815,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":28045,"Description":"72 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":2815,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":2815,"TestCode":null,"IsReportable":false,"DictVendorId":50,"DictVendor":{"Id":50,"Name":"Mayo Clinic Dpt of Lab Med & Pathology","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":5866,"PrimaryName":"AGNA-1 Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5867,"PrimaryName":"Amphiphysin Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5868,"PrimaryName":"ANNA-1 Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5869,"PrimaryName":"ANNA-2 Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":2600,"PrimaryName":"CRMP-5 Western Blot (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5811,"PrimaryName":"DPPX Ab IFA Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6767,"PrimaryName":"Purkinje Cell Cytoplasmic Antibody Type Tr (PCA-Tr) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6768,"PrimaryName":"Septin-7 Antibody, Cell-Binding Assay, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6769,"PrimaryName":"Septin-7 Antibody, Tissue Immunofluorescence Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6758,"PrimaryName":"Antineuronal Nuclear Antibody-Type 1 (ANNA-1) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6762,"PrimaryName":"Collapsin Response-Mediator Protein-5 (CRMP-5) Neuronal IgG Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6763,"PrimaryName":"Neurochondrin Antibody, Cell-Binding Assay, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6764,"PrimaryName":"Neurochondrin Antibody, Tissue Immunofluorescence Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6765,"PrimaryName":"Purkinje Cell Cytoplasmic Antibody Type 1 (PCA-1) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6766,"PrimaryName":"Purkinje Cell Cytoplasmic Antibody Type 2 (PCA-2) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5981,"PrimaryName":"NIF IFA Titer, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5982,"PrimaryName":"NIF Light Chain CBA, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":6761,"PrimaryName":"Amphiphysin Antibody Titer Assay, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6757,"PrimaryName":"Anti-Glial/Neuronal Nuclear Antibody-Type 1 (AGNA-1) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6759,"PrimaryName":"Antineuronal Nuclear Antibody Type 2 (ANNA-2) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":6760,"PrimaryName":"Antineuronal Nuclear Antibody Type 3 (ANNA-3) Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5138,"PrimaryName":"AMPA-Receptor Antibody, IFA Titer (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5975,"PrimaryName":"Alpha Internexin CBA, S (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5976,"PrimaryName":"GFAP CBA, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5977,"PrimaryName":"GFAP IFA Titer, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5979,"PrimaryName":"IgLON5 IFA Titer, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5980,"PrimaryName":"NIF Heavy Chain CBA, S (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5139,"PrimaryName":"GABA-B-Receptor Antibody, IFA Titer","IsRequired":false},{"TdTestInfoCommonId":5802,"PrimaryName":"mGluR1 Ab CBA, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5804,"PrimaryName":"mGluR1 Ab IFA Titer, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5137,"PrimaryName":"NMDA-Receptor Antibody IFA Titer (Reflex only)","IsRequired":false},{"TdTestInfoCommonId":5870,"PrimaryName":"PCA-1 Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5871,"PrimaryName":"PCA-Tr Immunoblot, Serum (Reflex Only)","IsRequired":false}]},{"Id":5984,"LISCode":"ENCCSF","PrimaryName":"Autoimmune Encephalopathy Evaluation, CSF","LISName":"Autoim Encephal CSF","EMRName":"Autoimmune Encephalopathy Evaluation, CSF","EMRCode":"SQENCCSF","LOINC":"","RecommendedUse":"","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":15272,"CptCode":"86255","Quantity":23,"Tmid":"30213515","CclTechComponentPrice":40.00,"CclProfComponentPrice":null,"TestNameForCdm":"ENCCSF Fluorescent AB x21","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5984,"IsBeakerData":false},{"Id":15273,"CptCode":"86341","Quantity":1,"Tmid":"30213525","CclTechComponentPrice":71.00,"CclProfComponentPrice":null,"TestNameForCdm":"ENCCSF Islet cell AB","SubComponent":"","Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":5984,"IsBeakerData":false}],"TdIncludes":[{"Id":22735,"TestName":"Encephalopathy Interpretation, CSF","Rank":1,"TdTestInfoCommonId":5984},{"Id":22736,"TestName":"AMPA-R Ab CBA, CSF","Rank":2,"TdTestInfoCommonId":5984},{"Id":22737,"TestName":"Amphiphysin Ab, CSF","Rank":3,"TdTestInfoCommonId":5984},{"Id":22738,"TestName":"Anti-Glial Nuclear Ab, Type 1","Rank":4,"TdTestInfoCommonId":5984},{"Id":22739,"TestName":"Anti-Neuronal Nuclear Ab, Type 1","Rank":5,"TdTestInfoCommonId":5984},{"Id":22740,"TestName":"Anti-Neuronal Nuclear Ab, Type 2","Rank":6,"TdTestInfoCommonId":5984},{"Id":22741,"TestName":"Anti-Neuronal Nuclear Ab, Type 3","Rank":7,"TdTestInfoCommonId":5984},{"Id":22742,"TestName":"CASPR2-IgG CBA, CSF","Rank":8,"TdTestInfoCommonId":5984},{"Id":22743,"TestName":"CRMP-5-IgG, CSF","Rank":9,"TdTestInfoCommonId":5984},{"Id":22745,"TestName":"GABA-B-R Ab CBA, CSF","Rank":11,"TdTestInfoCommonId":5984},{"Id":22746,"TestName":"GAD65 Ab Assay, CSF","Rank":12,"TdTestInfoCommonId":5984},{"Id":22747,"TestName":"GFAP IFA, CSF","Rank":13,"TdTestInfoCommonId":5984},{"Id":22749,"TestName":"LGI1-IgG CBA, CSF","Rank":15,"TdTestInfoCommonId":5984},{"Id":22750,"TestName":"mGluR1 Ab IFA, CSF","Rank":16,"TdTestInfoCommonId":5984},{"Id":22751,"TestName":"NIF IFA, CSF","Rank":18,"TdTestInfoCommonId":5984},{"Id":22752,"TestName":"NMDA-R Ab CBA, CSF","Rank":19,"TdTestInfoCommonId":5984},{"Id":22753,"TestName":"Purkinje Cell Cytoplasmc Ab Type Tr","Rank":20,"TdTestInfoCommonId":5984},{"Id":22754,"TestName":"Purkinje Cell Cytoplasmic Ab Type 1","Rank":21,"TdTestInfoCommonId":5984},{"Id":22755,"TestName":"Purkinje Cell Cytoplasmic Ab Type 2","Rank":22,"TdTestInfoCommonId":5984},{"Id":25089,"TestName":"Neurochondrin IFA, CSF","Rank":17,"TdTestInfoCommonId":5984},{"Id":25090,"TestName":"Septin-7 IFA, CSF","Rank":24,"TdTestInfoCommonId":5984},{"Id":26001,"TestName":"DPPX Ab CBA, CSF","Rank":10,"TdTestInfoCommonId":5984},{"Id":26002,"TestName":"IgLON5 CBA, CSF","Rank":14,"TdTestInfoCommonId":5984},{"Id":26003,"TestName":"PDE10A Ab IFA, CSF","Rank":23,"TdTestInfoCommonId":5984},{"Id":26004,"TestName":"TRIM46 Ab IFA, CSF","Rank":25,"TdTestInfoCommonId":5984}],"TdLaboratoryCommon":{"TdTestInfoCommonId":5984,"SpecialInfo":"Reflex Algorithm: Each reflex test performed incurs additional charge.\nIf the immunofluorescence (IFA) patterns suggest collapsin response-mediator protein-5-IgG (CRMP-5-IgG), then CRMP-5-IgG IFA titer and CRMP-5-IgG Western blot will be performed. If the IFA patterns suggest amphiphysin antibody, then amphiphysin IFA titer and amphiphysin immunoblot will be performed. If the IFA pattern suggests antiglial nuclear antibody (AGNA-1), then AGNA-1 IFA titer and AGNA-1 immunoblot will be performed. If the IFA pattern suggests antineuronal nuclear antibody type 1 (ANNA-1), then ANNA-1 IFA titer, ANNA-1 immunoblot, and ANNA-2 immunoblot will be performed. If the IFA pattern suggests ANNA-2 antibody, then ANNA-2 IFA titer, ANNA-1 immunoblot, and ANNA-2 immunoblot will be performed. If the IFA pattern suggests Purkinje cytoplasmic antibody type 1 (PCA-1), then PCA-1 IFA titer and PCA-1 immunoblot will be performed. If the IFA pattern suggests PCA-2 antibody, then PCA-2 IFA titer will be performed. If the IFA pattern suggests PCA-Tr antibody, then PCA-Tr IFA titer and PCA-Tr immunoblot will be performed. If IgLON5 cell-binding assay (CBA) is positive, then IgLON5 IFA titer will be performed. If AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid) receptor antibody CBA is positive, then AMPA-receptor antibody IFA titer assay will be performed. If gamma-aminobutyric acid B (GABA-B) receptor antibody CBA is positive, then GABA-B-receptor antibody IFA titer assay will be performed. If the IFA pattern suggests glial fibrillary acidic protein (GFAP) antibody, then GFAP IFA titer and GFAP CBA will be performed. If N-methyl-D-aspartate (NMDA) receptor antibody CBA is positive, then NMDA-receptor antibody IFA titer assay will be performed. If DPPX antibody CBA is positive, then DPPX IFA titer will be performed. If the IFA pattern suggests metabotropic glutamate receptor 1 (mGluR1) antibody, then mGluR1 antibody CBA and mGluR1 IFA titer will be performed. If the IFA pattern suggests neuronal intermediate filament (NIF) antibody, then alpha internexin CBA, NIF heavy chain CBA, NIF light chain CBA, and NIF IFA titer will be performed. If the IFA pattern suggests neurochondrin antibody, then neurochondrin antibody CBA and neurochondrin IFA titer will be performed. If the IFA pattern suggests septin-7 antibody, then septin-7 antibody CBA and septin-7 IFA titer will be performed. If the indirect immunofluorescence (IFA) pattern suggests phosphodiesterase 10A (PDE10A) IgG, then the PDE10A antibody IFA titer will be performed. If the indirect immunofluorescence (IFA) pattern suggests tripartite motif-containing protein 46 (TRIM46) IgG, then TRIM46 antibody cell-binding assay (CBA) and IFA titer will be performed.\nNeuron-restricted patterns of IgG staining that do not fulfill criteria for ANNA-1, ANNA-2, ANNA-3, CRMP-5-IgG, PCA-1, PCA-2, or PCA-Tr may be reported as \"unclassified anti-neuronal IgG.\" Complex patterns that include nonneuronal elements may be reported as \"uninterpretable.\" Relevant clinical information, ordering provider name, phone number, mailing address, and e-mail address are required. Grossly hemolyzed, lipemic or icteric specimens will be rejected.","ClinicalInfo":"Aids in evaluating new onset encephalopathy (noninfectious or metabolic) comprising confusional states, psychosis, delirium, memory loss, hallucinations, movement disorders, sensory or motor complaints, seizures, dyssomnias, ataxias, nausea, vomiting, inappropriate antidiuresis, coma, dysautonomias, or hypoventilation in spinal fluid specimens. A diagnosis of autoimmune encephalopathy should be suspected on the basis of clinical course, coexisting autoimmune disorder (eg, thyroiditis, diabetes), serological evidence of autoimmunity, spinal fluid evidence of intrathecal inflammation, neuroimaging or electroencephalographic abnormalities, and favorable response to trial of immunotherapy. Detection of one or more neural autoantibodies aids the diagnosis of autoimmune encephalopathy and may guide a search for cancer. Importantly, autoimmune encephalopathies are reversible. Misdiagnosis as a progressive (currently irreversible) neurodegenerative condition is not uncommon and has devastating consequences for the patient. Clinicians must consider the possibility of an autoimmune etiology in the differential diagnoses of encephalopathy.","ClinicalReference":"","ClinicalLimitation":"Specimens from pediatric patients are no longer accepted for the Autoimmune Encephalopathy Evaluation. 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DNA","Rank":4,"TdTestInfoCommonId":6377},{"Id":26816,"TestName":"Streptococcus agalactiae DNA","Rank":5,"TdTestInfoCommonId":6377},{"Id":26817,"TestName":"Streptococcus pneumoniae DNA","Rank":6,"TdTestInfoCommonId":6377},{"Id":26818,"TestName":"Cryptococcus neoformans/gattii DNA","Rank":7,"TdTestInfoCommonId":6377},{"Id":26819,"TestName":"Enterovirus RNA","Rank":8,"TdTestInfoCommonId":6377},{"Id":26820,"TestName":"Human parechovirus RNA","Rank":9,"TdTestInfoCommonId":6377},{"Id":26821,"TestName":"Herpes simplex virus 1 (HSV-1) DNA","Rank":10,"TdTestInfoCommonId":6377},{"Id":26822,"TestName":"Herpes simplex virus 2 (HSV-2) DNA","Rank":11,"TdTestInfoCommonId":6377},{"Id":26823,"TestName":"Varicella zoster virus (VZV) DNA","Rank":12,"TdTestInfoCommonId":6377},{"Id":26824,"TestName":"Cytomegalovirus (CMV) DNA","Rank":13,"TdTestInfoCommonId":6377},{"Id":26825,"TestName":"Human herpesvirus 6 (HHV-6) DNA","Rank":14,"TdTestInfoCommonId":6377}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6377,"SpecialInfo":null,"ClinicalInfo":"The Biofire FilmArray Meningitis/Encephalitis (ME) Panel is an FDA-approved qualitative multiplexed nucleic acid-based in vitro diagnostic test capable of simultaneous detection and identification of multiple bacterial, viral, and yeast nucleic acids directly from CSF specimens obtained via lumbar puncture from individuals with signs and/or symptoms of meningitis and/or encephalitis. The following organisms are included on the panel: E. coli (K1 strains only), Haemophilus influenzae, Listeria monocytogenes, Neisseria meningitidis (encapsulated strains only), Streptococcus agalactiae (group B Streptococcus), Streptococcus pneumoniae, cytomegalovirus (CMV), human herpesvirus 6 (HHV-6), human parechoviruses (HPeV), varicella zoster virus (VZV), enteroviruses (EV), herpes simplex viruses 1 and 2 (HSV-1, HSV-2), and Cryptococcus neoformans/gattii.\n\nThe assay is designed to target the most common causes of community-onset meningitis/encephalitis, and has the highest yield when use is restricted to patients with CSF pleocytosis. Severely immunocompromised patients and neonates may also benefit from testing in the absence of pleocytosis. This panel does not cover the most common pathogens in post-surgical or shunt infection, and should not be used in these settings. This assay should always be accompanied by cultures when bacterial meningitis is suspected. If there is suspicion of cryptococcal meningitis, antigen (CrAg) testing should be ordered separately due to its superior sensitivity. See clinical limitations section for additional assay limitations.","ClinicalReference":"1. Leber AL, Everhart K, Balada-Llasat JM, Cullison J, Daly J, Holt S, Lephart P, Salimnia H, Schreckenberger PC, DesJarlais S, Reed SL, Chapin KC, LeBlanc L, Johnson JK, Soliven NL, Carroll KC, Miller JA, Dien Bard J, Mestas J, Bankowski M, Enomoto T, Hemmert AC, Bourzac KM. Multicenter Evaluation of BioFire FilmArray Meningitis/Encephalitis Panel for Detection of Bacteria, Viruses, and Yeast in Cerebrospinal Fluid Specimens. J Clin Microbiol. 2016 Sep;54(9):2251-61. doi: 10.1128/JCM.00730-16. Epub 2016 Jun 22. PMID: 27335149.\n2. Trujillo-Gómez J, Tsokani S, Arango-Ferreira C, Atehortúa-Muñoz S, Jimenez-Villegas MJ, Serrano-Tabares C, Veroniki AA, Florez ID. Biofire FilmArray Meningitis/Encephalitis panel for the aetiological diagnosis of central nervous system infections: A systematic review and diagnostic test accuracy meta-analysis. EClinicalMedicine. 2022 Feb 14;44:101275. doi: 10.1016/j.eclinm.2022.101275. PMID: 35198914.\n3. Broadhurst MJ, Dujari S, Budvytiene I, Pinsky BA, Gold CA, Banaei N. Utilization, Yield, and Accuracy of the FilmArray Meningitis/Encephalitis Panel with Diagnostic Stewardship and Testing Algorithm. J Clin Microbiol. 2020 Aug 24;58(9):e00311-20. doi: 10.1128/JCM.00311-20. PMID: 32493787.\n4. U.S. Food and Drug Administration (FDA). Evaluation of Automatic Class III Designation for FilmArray Meningitis/Encephalitis (ME) Panel DEN150013. Accessed Aug 8, 2025. https://www.accessdata.fda.gov/cdrh_docs/reviews/DEN150013.pdf.\n\n\n","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. \n\nThis test is not intended for use with CSF collected from indwelling medical devices (e.g., CSF shunts). \nOnly E. coli strains possessing the K1 capsular antigen will be detected by the BIOFIRE ME Panel. All other E. coli strains/serotypes will not be detected. \n\nOnly encapsulated strains of N. meningitidis will be detected by the BIOFIRE ME Panel. Unencapsulated N. meningitidis will not be detected. \n\nPatients with a suspicion of cryptococcal meningitis and a negative cryptococcal PCR result, such as by the BIOFIRE ME Panel, should be tested for cryptococcal antigen (CrAg). \n\nViral shedding into the CSF often occurs in cases of zoster (shingles; caused by reactivation of VZV). Detection of VZV in CSF may not indicate the cause of CNS disease in these cases. \n\nHerpesviruses (CMV, HHV-6, HSV-1, HSV-2, and VZV) can exist in latent forms that may be reactivated during infection by other pathogens, including agents not detected by the BIOFIRE ME Panel that may cause meningitis/encephalitis (e.g., Mycobacterium tuberculosis or HIV). HHV-6 can be chromosomally integrated into somatic cells (ciHHV-6) and into the germ cell line (iciHHV-6) allowing for persistent and sporadic reactivation in confirmed carriers or someone related to a confirmed carrier. When detected by the BIOFIRE ME Panel, herpesvirus results should be considered as the likely cause of meningitis/encephalitis only in appropriate clinical context and following expert consultation.\n\nIn meta-analyses, this panel has been shown to be less analytically sensitive than targeted HSV-1/2 PCR testing. Standalone HSV-1/2 PCR testing should be considered for patients with a high pre-test probability of HSV encephalitis even if this panel is negative.\n\nAs with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. \n\nSome patients may experience financial toxicity with this expanded multiplex panel, as it is variably reimbursed by insurance.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":3786,"ActiveDate":"2021-09-28T08:58:00","CreatedOn":"2021-09-28T08:58:00","CreatedById":312,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6377,"IsBeakerData":true,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":3786,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13929,"DictMethodologyId":168,"TdTestInfoSpecificId":3786,"DictMethodology":{"Id":168,"Name":"Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":3786,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":67,"DictDaysPerformed":"7 days a week","DictReported":"8 hours"},"TdSpecimenRequirements":[{"Id":679814,"SpecialInstructions":"Collect lumbar puncture CSF using standard protocol. Note that CSF collected from indwelling medical devices such as shunts are not accepted because the assay does not cover the pathogens most likely to cause shunt or post-surgical infections. CSF from any tube of collection (Tubes 1-4) may be used for this assay. Make a dedicated aliquot into a sterile tube using sterile technique in a biosafety cabinet. Residual specimen from non-Microbiology laboratories is NOT acceptable.","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":146,"DictSpTypeName":"Cerebrospinal fluid (CSF)","DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":3786,"IsBeakerData":false},{"Id":679815,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":7,"DictSpVolumeName":"0.2 mL","TdTestInfoSpecificId":3786,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29966,"Description":"24 hours","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":3786,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29967,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":3786,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":3786,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6656,"LISCode":"VGPIBM","PrimaryName":"VWF GPIbM Activity","LISName":"VWF GPIbM Activity","EMRName":"VWF GPIbM Activity","EMRCode":"SQVGPIBM","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":18647,"CptCode":"85245","Quantity":1,"Tmid":"30500535","CclTechComponentPrice":188.00,"CclProfComponentPrice":null,"TestNameForCdm":"CLOT FACTOR VIII VW RISTOCTN","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6656,"IsBeakerData":false}],"TdIncludes":[{"Id":24742,"TestName":"VWF GPIbM Activity","Rank":1,"TdTestInfoCommonId":6656}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6656,"SpecialInfo":"","ClinicalInfo":"","ClinicalReference":null,"ClinicalLimitation":"","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":13518,"ActiveDate":"2022-04-12T04:00:00","CreatedOn":"2022-01-25T05:47:08.7333333","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6656,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13518,"IsStat":false,"Comments":null,"DictPerformingLabId":19,"DictPerformingLab":{"Id":19,"Name":"Manual Lab (x42519)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13138,"DictMethodologyId":170,"TdTestInfoSpecificId":13518,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13518,"DictDaysPerformedId":107,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Varies, Mon - Fri","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":676625,"SpecialInstructions":"Centrifuge samples; Aliquot plasma into a separate tube and label with Epic Beaker labels. Specimens should be frozen (-20C or colder)","LogicalOperation":null,"DictSpContainerId":27,"DictSpContainerName":"Sodium citrate (Lt. 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Not intended for use in initial evaluation of known or suspected acute leukemias (recommended test is Acute Leukemia NGS panel), chronic myeloid neoplasms (recommended test is Chronic Myeloid NGS panel or \"Myeloid NGS panel\"), eosinophilia related neoplasms (recommended test is FISH for Myeloproliferative Neoplasms Panel) or chronic myeloid leukemia (recommended test is BCR-ABL Qualitative Multiplex RT-PCR). This test may be useful in evaluation for these conditions as a follow-up when the initial recommended tests are inconclusive, clinically incongruent or cannot be performed. May also be performed by the laboratory for Acute Lymphocytic Leukemias (ALLs) with insufficient specimen for combined DNA and RNA NGS testing.\n","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":3,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":13791,"Aka":"HemeFusion","TdTestInfoCommonId":6659}],"TdBillingCommons":[{"Id":18118,"CptCode":"81455","Quantity":1,"Tmid":"31004385","CclTechComponentPrice":1512.00,"CclProfComponentPrice":null,"TestNameForCdm":"HFPNGS HN FUSION NGS PNL BLD","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6659,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6659,"SpecialInfo":"ABL1, ABL2, AFDN (MLLT4), ALK, BCL11B, BCL2, BCL3, BCL6, BCR, BIRC3, BLNK, CBFB, CBL, CCND1, CCND2, CCND3, CD274, CD28, CDK6, CDKN2A, CEBPA, CEBPD, CEBPE, CEBPG, CHD1, CHIC2, CIITA, CREBBP, CRLF2, CSF1R, CTLA4, DEK, DGKH, DUSP22, EBF1, EIF4A1, EPOR, ERG, ETV6, FGFR1, FLT3, FOXP1, GLIS2, HLF, ID4, IKZF1, IKZF2, IKZF3, IL2RB, IRF4, IRF8, ITK, JAK2, KAT6A, KLF2, LMO1, LMO2, LYN, MALT1, MECOM, KMT2A, MEF2D, MLF1, MLLT10, MRTFA (MKL1), MUC1, MYC, MYH11, NF1, NFKB2, NOTCH1, NTRK3, NUP214, NUP98, NUTM1, P2RY8, PAG1, PAX5, PBX1, PDCD1, PDCD1LG2, PDGFRA, PDGFRB, PICALM, PML, PRDM16, PTK2B, RARA, RBM15, ROS1, RUNX1, RUNX1T1, SEMA6A, SETD2, STIL, SYK, TAL1, TCF3, TFG, TLX1, TLX3, TP63, TSLP, TYK2, VAV1, ZCCHC7, ZNF384. 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Content is identical to the fusion component genes in the Acute Leukemia NGS panel.","ClinicalReference":null,"ClinicalLimitation":"","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13521,"ActiveDate":"2022-05-26T04:00:00","CreatedOn":"2022-02-04T11:31:14.4566667","CreatedById":14,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6659,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13521,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13141,"DictMethodologyId":461,"TdTestInfoSpecificId":13521,"DictMethodology":{"Id":461,"Name":"Next Gen Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13521,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":73,"DictDaysPerformed":"Mon - Fri","DictReported":"10 days"},"TdSpecimenRequirements":[{"Id":676646,"SpecialInstructions":"Aliquots are not accepted. 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Not intended for use in initial evaluation of known or suspected acute leukemias (recommended test is Acute Leukemia NGS panel), chronic myeloid neoplasms (recommended test is Chronic Myeloid NGS panel or \"Myeloid NGS panel\"), eosinophilia related neoplasms (recommended test is FISH for Myeloproliferative Neoplasms Panel) or chronic myeloid leukemia (recommended test is BCR-ABL Qualitative Multiplex RT-PCR). This test may be useful in evaluation for these conditions as a follow-up when the initial recommended tests are inconclusive, clinically incongruent or cannot be performed. May also be performed by the laboratory for Acute Lymphocytic Leukemias (ALLs) with insufficient specimen for combined DNA and RNA NGS testing.","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":3,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":13792,"Aka":"HemeFusion","TdTestInfoCommonId":6660}],"TdBillingCommons":[{"Id":18119,"CptCode":"81455","Quantity":1,"Tmid":"31004395","CclTechComponentPrice":1512.00,"CclProfComponentPrice":null,"TestNameForCdm":"HFMNGS HN FUSION NGS PNL BM ","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6660,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6660,"SpecialInfo":"ABL1, ABL2, AFDN (MLLT4), ALK, BCL11B, BCL2, BCL3, BCL6, BCR, BIRC3, BLNK, CBFB, CBL, CCND1, CCND2, CCND3, CD274, CD28, CDK6, CDKN2A, CEBPA, CEBPD, CEBPE, CEBPG, CHD1, CHIC2, CIITA, CREBBP, CRLF2, CSF1R, CTLA4, DEK, DGKH, DUSP22, EBF1, EIF4A1, EPOR, ERG, ETV6, FGFR1, FLT3, FOXP1, GLIS2, HLF, ID4, IKZF1, IKZF2, IKZF3, IL2RB, IRF4, IRF8, ITK, JAK2, KAT6A, KLF2, KMT2A, LMO1, LMO2, LYN, MALT1, MECOM, MEF2D, MLF1, MLLT10, MRTFA (MKL1), MUC1, MYC, MYH11, NF1, NFKB2, NOTCH1, NTRK3, NUP214, NUP98, NUTM1, P2RY8, PAG1, PAX5, PBX1, PDCD1, PDCD1LG2, PDGFRA,\nPDGFRB, PICALM, PML, PRDM16, PTK2B, RARA, RBM15, ROS1, RUNX1, RUNX1T1, SEMA6A, SETD2, STIL, SYK, TAL1, TCF3, TFG, TLX1, TLX3, TP63, TSLP, TYK2, VAV1, ZCCHC7, ZNF384. 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Aliquots are not accepted. 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Not intended for use in initial evaluation of known or suspected acute leukemias (recommended test is Acute Leukemia NGS panel), chronic myeloid neoplasms (recommended test is Chronic Myeloid NGS panel or \"Myeloid NGS panel\"), eosinophilia related neoplasms (recommended test is FISH for Myeloproliferative Neoplasms Panel) or chronic myeloid leukemia (recommended test is BCR-ABL Qualitative Multiplex RT-PCR). This test may be useful in evaluation for these conditions as a follow-up when the initial recommended tests are inconclusive, clinically incongruent or cannot be performed. 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Content is identical to the fusion component genes in the Acute Leukemia NGS panel.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13523,"ActiveDate":"2022-05-26T04:00:00","CreatedOn":"2022-02-04T15:59:25.7733333","CreatedById":14,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6661,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13523,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13143,"DictMethodologyId":461,"TdTestInfoSpecificId":13523,"DictMethodology":{"Id":461,"Name":"Next Gen Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13523,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":73,"DictDaysPerformed":"Mon - Fri","DictReported":"10 days"},"TdSpecimenRequirements":[{"Id":676652,"SpecialInstructions":"Need 10 charged, unbaked, unstained slides plus 1 H&E slide. Specimens that undergo heavy metal fixation or are decalcified with strong acids (i.e., formic acid) are not acceptable for molecular testing. Non-decalcified specimens or samples that undergo EDTA decalcification are acceptable. 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Aids in the diagnosis, classification, prognosis and/or therapeutic options for these neoplasms; includes evaluation of FLT3 internal tandem duplication, which is resulted separately.","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":3,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":14017,"Aka":"CEBPA","TdTestInfoCommonId":6662},{"Id":14018,"Aka":"HDPNGS","TdTestInfoCommonId":6662},{"Id":14019,"Aka":"Hematologic Neoplasm Dual NGS, Blood","TdTestInfoCommonId":6662},{"Id":14020,"Aka":"NPM1","TdTestInfoCommonId":6662}],"TdBillingCommons":[{"Id":18121,"CptCode":"81455","Quantity":1,"Tmid":"31004415","CclTechComponentPrice":3000.00,"CclProfComponentPrice":null,"TestNameForCdm":"HDPNGS ACUTE LEUK NGS PNL BLD","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6662,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6662,"SpecialInfo":"RNA_genes: ABL1, ABL2, AFDN (MLLT4), ALK, BCL11B, BCL2, BCL3, BCL6, BCR, BIRC3, BLNK, CBFB, CBL, CCND1, CCND2, CCND3, CD274, CD28, CDK6, CDKN2A, CEBPA, CEBPD, CEBPE, CEBPG, CHD1, CHIC2, CIITA, CREBBP, CRLF2, CSF1R, CTLA4, DEK, DGKH, DUSP22, EBF1, EIF4A1, EPOR, ERG, ETV6, FGFR1, FLT3, FOXP1, GLIS2, HLF, ID4, IKZF1, IKZF2, IKZF3, IL2RB, IRF4, IRF8, ITK, JAK2, KAT6A, KLF2, KMT2A, LMO1, LMO2, LYN, MALT1, MECOM, MEF2D, MLF1, MLLT10, MRTFA (MKL1), MUC1, MYC, MYH11, NF1, NFKB2, NOTCH1, NTRK3, NUP214, NUP98, NUTM1, P2RY8, PAG1, PAX5, PBX1, PDCD1, PDCD1LG2, PDGFRA,\nPDGFRB, PICALM, PML, PRDM16, PTK2B, RARA, RBM15, ROS1, RUNX1, RUNX1T1, SEMA6A, SETD2, STIL, SYK, TAL1, TCF3, TFG, TLX1, TLX3, TP63, TSLP, TYK2, VAV1, ZCCHC7, ZNF384.\n\nDNA_genes: ABL1, ASXL1, BCOR, BCORL1, BRAF, CALR, CBL, CDKN2A, CEBPA, CSF3R, CUX1, DDX41, DNMT3A, EED, ETNK1, ETV6, EZH2, FBXW7, FLT3, GATA1, GATA2, GNAS, IDH1, IDH2, IKZF1, JAK2, JAK3, KDM6A, KIT, KMT2A, KRAS, LUC7L2, MPL, MYD88, NF1, NOTCH1, NPM1, NRAS, PAX5, PHF6, PIGA, PPM1D, PRPF8, PTEN, PTPN11, RAD21, RIT1, RUNX1, SETBP1, SF3B1, SH2B3, SMC1A, SMC3, SRSF2, STAG2, STAT3, STAT5B, SUZ12, TET2, TP53, U2AF1, WT1, ZRSR2. Aliquots are not accepted. ","ClinicalInfo":"DNA and RNA combination testing to evaluate for single nucleotide variants, small insertions and deletions, and common fusions in acute hematologic malignancies (acute myeloid and acute lymphoblastic leukemias); content includes all of the fusion targets of Hematologic Neoplasm Fusion NGS Panel as well as all of the DNA targets in the Chronic Myeloid NGS Panel.\n\n","ClinicalReference":null,"ClinicalLimitation":"Not to be ordered concurrently with the Hematologic Neoplasm Fusion NGS Panel or the Chronic Myeloid NGS Panel, since this panel includes all targeted regions from those panels.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13524,"ActiveDate":"2022-05-26T04:00:00","CreatedOn":"2022-02-04T16:47:48.9933333","CreatedById":14,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6662,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13524,"IsStat":false,"Comments":"The HDPNGS order requires both RNA and DNA extraction","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13144,"DictMethodologyId":461,"TdTestInfoSpecificId":13524,"DictMethodology":{"Id":461,"Name":"Next Gen Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13524,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":73,"DictDaysPerformed":"Mon - Fri","DictReported":"10 days"},"TdSpecimenRequirements":[{"Id":676655,"SpecialInstructions":"Refrigerate ASAP. 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Aids in the diagnosis, classification, prognosis and/or therapeutic options for these neoplasms; includes evaluation of FLT3 internal tandem duplication, which is resulted separately.","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":3,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":14013,"Aka":"CEBPA","TdTestInfoCommonId":6663},{"Id":14014,"Aka":"HDMNGS","TdTestInfoCommonId":6663},{"Id":14015,"Aka":"NPM1","TdTestInfoCommonId":6663},{"Id":14016,"Aka":"Hematologic Neoplasm Dual NGS, Bone Marrow","TdTestInfoCommonId":6663}],"TdBillingCommons":[{"Id":18122,"CptCode":"81455","Quantity":1,"Tmid":"31004425","CclTechComponentPrice":3000.00,"CclProfComponentPrice":null,"TestNameForCdm":"HDMNGS ACUTE LEUK NGS PNL BM","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6663,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6663,"SpecialInfo":"RNA_genes: ABL1, ABL2, AFDN (MLLT4), ALK, BCL11B, BCL2, BCL3, BCL6, BCR, BIRC3, BLNK, CBFB, CBL, CCND1, CCND2, CCND3, CD274, CD28, CDK6, CDKN2A, CEBPA, CEBPD, CEBPE, CEBPG, CHD1, CHIC2, CIITA, CREBBP, CRLF2, CSF1R, CTLA4, DEK, DGKH, DUSP22, EBF1, EIF4A1, EPOR, ERG, ETV6, FGFR1, FLT3, FOXP1, GLIS2, HLF, ID4, IKZF1, IKZF2, IKZF3, IL2RB, IRF4, IRF8, ITK, JAK2, KAT6A, KLF2, KMT2A, LMO1, LMO2, LYN, MALT1, MECOM, MEF2D, MLF1, MLLT10, MRTFA (MKL1), MUC1, MYC, MYH11, NF1, NFKB2, NOTCH1, NTRK3, NUP214, NUP98, NUTM1, P2RY8, PAG1, PAX5, PBX1, PDCD1, PDCD1LG2, PDGFRA,\nPDGFRB, PICALM, PML, PRDM16, PTK2B, RARA, RBM15, ROS1, RUNX1, RUNX1T1, SEMA6A, SETD2, STIL, SYK, TAL1, TCF3, TFG, TLX1, TLX3, TP63, TSLP, TYK2, VAV1, ZCCHC7, ZNF384.\n\nDNA_genes: ABL1, ASXL1, BCOR, BCORL1, BRAF, CALR, CBL, CDKN2A, CEBPA, CSF3R, CUX1, DDX41, DNMT3A, EED, ETNK1, ETV6, EZH2, FBXW7, FLT3, GATA1, GATA2, GNAS, IDH1, IDH2, IKZF1, JAK2, JAK3, KDM6A, KIT, KMT2A, KRAS, LUC7L2, MPL, MYD88, NF1, NOTCH1, NPM1, NRAS, PAX5, PHF6, PIGA, PPM1D, PRPF8, PTEN, PTPN11, RAD21, RIT1, RUNX1, SETBP1, SF3B1, SH2B3, SMC1A, SMC3, SRSF2, STAG2, STAT3, STAT5B, SUZ12, TET2, TP53, U2AF1, WT1, ZRSR2. Aliquots are not accepted. ","ClinicalInfo":"DNA and RNA combination testing to evaluate for single nucleotide variants, small insertions and deletions, and common fusions in acute hematologic malignancies (acute myeloid and acute lymphoblastic leukemias); content includes all of the fusion targets of Hematologic Neoplasm Fusion NGS Panel as well as all of the DNA targets in the Chronic Myeloid NGS Panel.","ClinicalReference":null,"ClinicalLimitation":"Not to be ordered concurrently with the Hematologic Neoplasm Fusion NGS Panel or the Chronic Myeloid NGS Panel, since this panel includes all targeted regions from those panels.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13525,"ActiveDate":"2022-05-26T04:00:00","CreatedOn":"2022-02-04T17:18:44.4833333","CreatedById":14,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6663,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13525,"IsStat":false,"Comments":"The HDMNGS order requires both RNA and DNA extraction","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13145,"DictMethodologyId":461,"TdTestInfoSpecificId":13525,"DictMethodology":{"Id":461,"Name":"Next Gen Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13525,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":73,"DictDaysPerformed":"Mon - Fri","DictReported":"10 days"},"TdSpecimenRequirements":[{"Id":676658,"SpecialInstructions":"Refrigerate ASAP. Aliquots are not accepted. ","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":141,"DictSpTypeName":"Aspirate, bone marrow","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":13525,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":29863,"Description":"Stored up to 3 days.\nIf testing is delayed, awaiting specimen triaging, store as NUCBUF","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13525,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29864,"Description":"If specimen is to be stored longer than 24 hours, it should be placed at 2-8 C for up to 3 days. \nIf testing is delayed, awaiting specimen triaging, store as NUCBUF","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13525,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":29865,"Description":"UNACCEPTABLE","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13525,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13525,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6664,"LISCode":"MYNGSO","PrimaryName":"Myeloid NGS Panel Other","LISName":"Myeloid NGS Panel Other","EMRName":"Myeloid NGS Panel Other","EMRCode":"SQMYNGSO","LOINC":null,"RecommendedUse":"Used in the evaluation of FFPE bone marrow clot sections or FFPE tissue sections for known or suspected chronic myeloid neoplasms, including but not limited to myeloproliferative neoplasms, myelodysplastic syndromes, and overlap myelodysplastic/myeloproliferative neoplasms. Aids in the diagnosis, classification, prognosis and/or therapeutic options for these neoplasms.","DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":3,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":13796,"Aka":"Chronic Myeloid Neoplasm NGS Panel Other","TdTestInfoCommonId":6664},{"Id":14011,"Aka":"CSF3R","TdTestInfoCommonId":6664},{"Id":14012,"Aka":"SF3B1","TdTestInfoCommonId":6664}],"TdBillingCommons":[{"Id":18123,"CptCode":"81455","Quantity":1,"Tmid":"31004465","CclTechComponentPrice":1512.00,"CclProfComponentPrice":null,"TestNameForCdm":"MYNGSO MYELOID PANEL NGS OTHER","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6664,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6664,"SpecialInfo":"the following genes are interrogated: ABL1, ASXL1, BCOR, BCORL1, BRAF, CALR, CBL, CDKN2A, CEBPA, CSF3R, CUX1, DDX41, DNMT3A, EED, ETNK1, ETV6, EZH2, FBXW7, FLT3, GATA1, GATA2,  GNAS, IDH1, IDH2, IKZF1, JAK2, JAK3, KDM6A, KIT, KMT2A, KRAS, LUC7L2, MPL, MYD88, NF1, NOTCH1, NPM1, NRAS, PAX5, PHF6, PIGA, PPMID, PRPF8, PTEN, PTPN11, RAD2, RIT1, RUNX1, SETBP1, SF3B1, SH2B3, SMC1A, SMC3, SRSF2, STAG2, STAT3, STAT5B, SUZ12, TET2, TP53, U2AF1, WT1, and ZRSR2.","ClinicalInfo":"Molecular evaluation of known or suspected chronic myeloid neoplasms, including but not limited to myeloproliferative neoplasms, myelodysplastic syndromes, and overlap myelodysplastic/myeloproliferative neoplasms.  Evaluates for single nucleotide variants, small insertions and deletions within the covered regions of the targeted genes.","ClinicalReference":null,"ClinicalLimitation":"This test does not evaluate for fusions. For a combined evaluation including fusions relevant to acute leukemias, the Acute Leukemia NGS panel is recommended.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13526,"ActiveDate":"2022-05-26T04:00:00","CreatedOn":"2022-02-14T15:47:34.2","CreatedById":16,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6664,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13526,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13146,"DictMethodologyId":449,"TdTestInfoSpecificId":13526,"DictMethodology":{"Id":449,"Name":"Next Generation DNA Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13526,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":73,"DictDaysPerformed":"Mon - Fri","DictReported":"10 days"},"TdSpecimenRequirements":[{"Id":676665,"SpecialInstructions":"Need 10 charged, unbaked, unstained slides plus 1 H&E slide. 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Informed consent forms are recommended and available through Client Services at 216.444.5755 or 800.628.6816.","ClinicalReference":null,"ClinicalLimitation":"Exons 26 and 34 are not covered by sequencing, and deletion/duplication analysis is not available for this gene.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13532,"ActiveDate":"2022-02-26T05:00:00","CreatedOn":"2022-01-26T12:10:17.57","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6670,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13532,"IsStat":false,"Comments":"Ordering restricted to hematology providers per Dr. Reyes Gil","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13153,"DictMethodologyId":500,"TdTestInfoSpecificId":13532,"DictMethodology":{"Id":500,"Name":"Massive Parallel Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13532,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":192,"DictDaysPerformed":"Varies","DictReported":"3 - 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If the lesion ruptures while swabbing, ensure to collect the lesion fluid.  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Additional specimens must be submitted when multiple tests are ordered.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":13594,"IsBeakerData":false},{"Id":677071,"SpecialInstructions":"Does not allow for repeat testing","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":13594,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":30067,"Description":"14 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13594,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30068,"Description":"60 days (1 freeze/thaw cycle)","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13594,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30069,"Description":"7 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13594,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13594,"TestCode":null,"IsReportable":false,"DictVendorId":71,"DictVendor":{"Id":71,"Name":"LabCorp","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6732,"LISCode":"THYRORF","PrimaryName":"Thyroglobulin, Serum with Reflex to IA or LC-MS/MS","LISName":"Thyroglobulin, Serum with Reflex to IA or LC-MS/MS","EMRName":"Thyroglobulin, Serum with Reflex to IA or LC-MS/MS","EMRCode":"SQTHYRORF","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":18322,"CptCode":"84432","Quantity":1,"Tmid":"30101745","CclTechComponentPrice":55.00,"CclProfComponentPrice":null,"TestNameForCdm":"Thyroglobulin","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6732,"IsBeakerData":false},{"Id":18323,"CptCode":"86800","Quantity":1,"Tmid":"30200755","CclTechComponentPrice":55.00,"CclProfComponentPrice":null,"TestNameForCdm":"Thyroglobulin Antibody","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6732,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6732,"SpecialInfo":"In this test, Thyroglobulin Antibody is analyzed by the Access Thyroglobulin Antibody assay (Beckman). If the result is negative (<4.0 IU/mL), the Thyroglobulin tests will be performed by immunoassay using the Access Thyroglobulin assay (Beckman). If the antibody result is positive (>=4.0 IU/mL), the Thyroglobulin tests will be performed by LC-MS/MS.  Results obtained from different assay method or kits cannot be used interchangeably.","ClinicalInfo":"Serum thyroglobulin levels correlate well with the volume of differentiated thyroid tissue, hence are increased in thyrotoxicosis, thyroiditis, iodine deficiency, benign thyroid adenomas, and thyroid cancer. Thus although it is unsuitable as a screening tool for differentiated thyroid cancer (DTC), it is a highly sensitive marker for the detection of residual or recurrent disease after a total thyroidectomy and successful radioiodine remnant ablation. Presence of thyroglobulin autoantibodies interfere in the assay and thyroglobulin levels are underestimated in the antibody positive patients. In the presence of anti-thyroglobulin antibodies, thyroglobulin measurement by LC-MS/MS provides accurate thyroglobulin results.\n\nThe thyroglobulin test is intended for surveillance of patients with differentiated thyroid cancer who have had a thyroidectomy with or without radioactive ablation. The presence of thyroglobulin antibodies may interfere with thyroglobulin measurement by immunoassay and cause falsely-low results. ","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":13595,"ActiveDate":"2022-11-29T05:00:00","CreatedOn":"2022-10-24T10:10:12.32","CreatedById":6,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6732,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13595,"IsStat":false,"Comments":null,"DictPerformingLabId":21,"DictPerformingLab":{"Id":21,"Name":"Immunopathology Lab (x49026)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13285,"DictMethodologyId":164,"TdTestInfoSpecificId":13595,"DictMethodology":{"Id":164,"Name":"Chemiluminescence Immunoassay (CLIA)","Description":null},"TdTestInfoSpecific":null},{"Id":13286,"DictMethodologyId":265,"TdTestInfoSpecificId":13595,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13595,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"Mon - 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External client shipping instructions: Ship “Priority Overnight;” do not ship on Fridays or the day preceding a holiday. Aliquots are not accepted. ","ClinicalInfo":"The t(9;22)(q32;q22) BCR-ABL  translocation is found by definition in cases of chronic myeloid leukemia (CML), and this abnormality is also found in approximately 25% of adult acute lymphoblastic leukemia (ALL).  The vast majority of transcripts in both cases are made up of three variants, e1a2, e13a2, and e14a2, resulting from translocations involving ABL intron 1 and BCR introns 1, 13, or 14.  In CML, 95% of the BCR-ABL transcripts are either e13a2 or e14a2 (p210 isoform).  In ALL, 70% of transcripts in BCR-ABL positive patients are e1a2 (p190 isoform), and 25% are either e13a2 or e14a2.  ","ClinicalReference":null,"ClinicalLimitation":"This assay does not detect minor or micro breakpoints, microdeletions, or mutations. This assay is designed to detect, but not distinguish between the BCR/ABL1 fusion transcripts e1a2, e13a2 (b2a2) and e14a2 (b3a2). Some specimens with very high levels of BCR/ABL1 major transcript (e13a2 and/or e14a2) may be displayed as a low p190 positive. \n","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13598,"ActiveDate":"2023-01-12T05:00:00","CreatedOn":"2022-10-13T13:52:24.9166667","CreatedById":20,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6735,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13598,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13290,"DictMethodologyId":482,"TdTestInfoSpecificId":13598,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13598,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":118,"DictDaysPerformed":"5 days per week","DictReported":"5 days"},"TdSpecimenRequirements":[{"Id":677094,"SpecialInstructions":"If patient has low white blood cell count, please collect up to an additional 10mL in EDTA (Lavender) and forward all tubes to performing lab. Aliquots are not accepted. ","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":97,"DictSpTypeName":"Blood, peripheral","DictSpVolumeId":24,"DictSpVolumeName":"10 mL","TdTestInfoSpecificId":13598,"IsBeakerData":false},{"Id":677095,"SpecialInstructions":"Aliquots are not accepted. 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","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13598,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30083,"Description":"Store at 2-8 C for up to 3 days.","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13598,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30084,"Description":"UNACCEPTABLE","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13598,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13598,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6739,"LISCode":"BCRBM1","PrimaryName":"BCR/ABL1 p210 and p190 Diagnostic PCR Bone Marrow","LISName":"BCR/ABL1 p210 and p190 Diagnostic PCR Bone Marrow","EMRName":"BCR/ABL1 p210 and p190 Diagnostic PCR Bone Marrow","EMRCode":"SQBCRBM1","LOINC":null,"RecommendedUse":null,"DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[{"Id":13939,"Aka":"SQBCRBM","TdTestInfoCommonId":6739},{"Id":14222,"Aka":"BCRQL","TdTestInfoCommonId":6739}],"TdBillingCommons":[{"Id":18340,"CptCode":"81206","Quantity":1,"Tmid":"31004635","CclTechComponentPrice":1020.00,"CclProfComponentPrice":null,"TestNameForCdm":"BCRBM BCR/ABL1 GENE MAJOR BP","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6739,"IsBeakerData":false},{"Id":18341,"CptCode":"81207","Quantity":1,"Tmid":"31004645","CclTechComponentPrice":570.00,"CclProfComponentPrice":null,"TestNameForCdm":"BCRBM BCR/ABL1 GENE MINOR BP","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6739,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":6739,"SpecialInfo":"Clearly indicate specimen type on label. External client shipping instructions: Ship “Priority Overnight;” do not ship on Fridays or the day preceding a holiday. Aliquots are not accepted. ","ClinicalInfo":"The t(9;22)(q32;q22) BCR-ABL  translocation is found by definition in cases of chronic myeloid leukemia (CML), and this abnormality is also found in approximately 25% of adult acute lymphoblastic leukemia (ALL).  The vast majority of transcripts in both cases are made up of three variants, e1a2, e13a2, and e14a2, resulting from translocations involving ABL intron 1 and BCR introns 1, 13, or 14.  In CML, 95% of the BCR-ABL transcripts are either e13a2 or e14a2 (p210 isoform).  In ALL, 70% of transcripts in BCR-ABL positive patients are e1a2 (p190 isoform), and 25% are either e13a2 or e14a2.  ","ClinicalReference":null,"ClinicalLimitation":"This assay does not detect minor or micro breakpoints, microdeletions, or mutations. This assay is designed to detect, but not distinguish between the BCR/ABL1 fusion transcripts e1a2, e13a2 (b2a2) and e14a2 (b3a2). Some specimens with very high levels of BCR/ABL1 major transcript (e13a2 and/or e14a2) may be displayed as a low p190 positive. \n","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13602,"ActiveDate":"2023-01-12T05:00:00","CreatedOn":"2022-10-13T14:42:44.4766667","CreatedById":20,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6739,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13602,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13294,"DictMethodologyId":482,"TdTestInfoSpecificId":13602,"DictMethodology":{"Id":482,"Name":"Polymerase Chain Reaction (PCR), Quant","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13602,"DictDaysPerformedId":16,"DictHoursPerformedId":null,"DictReportedId":118,"DictDaysPerformed":"5 days per week","DictReported":"5 days"},"TdSpecimenRequirements":[{"Id":677102,"SpecialInstructions":"If patient has low white blood cell count, please collect up to an additional 10mL in EDTA (Lavender) and forward all tubes to performing lab. Aliquots are not accepted. ","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":97,"DictSpTypeName":"Blood, peripheral","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":13602,"IsBeakerData":false},{"Id":677103,"SpecialInstructions":"Aliquots are not accepted. ","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":13602,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":30094,"Description":"If specimen is to be stored longer than 24 hours, it should be placed at 2-8 C for up to 3 days.","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13602,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30095,"Description":"Stored at 2-8 C for up to 3 days.","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13602,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":30096,"Description":"UNACCEPTABLE","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13602,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13602,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":6742,"LISCode":"CMVQL","PrimaryName":"Cytomegalovirus (CMV) DNA, Qualitative PCR, Non-Plasma","LISName":"Cytomegalovirus (CMV) DNA, Qualitative PCR, Non-Plasma","EMRName":"Cytomegalovirus (CMV) DNA, Qualitative PCR, Non-Plasma","EMRCode":"SQCMVQL","LOINC":"5000-5","RecommendedUse":null,"DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14557,"Aka":"cCMV","TdTestInfoCommonId":6742},{"Id":14558,"Aka":"CMVQL","TdTestInfoCommonId":6742},{"Id":14559,"Aka":"congenital CMV","TdTestInfoCommonId":6742},{"Id":14560,"Aka":"SQCMVQL","TdTestInfoCommonId":6742}],"TdBillingCommons":[{"Id":18383,"CptCode":"87496","Quantity":1,"Tmid":"30608135","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Amplified Probe, CMV","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":6742,"IsBeakerData":false}],"TdIncludes":[{"Id":26294,"TestName":"CMV DNA","Rank":1,"TdTestInfoCommonId":6742}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6742,"SpecialInfo":"CMVQL should only be used for saliva and urine. For EDTA plasma, utilize CMVQNT. For amniotic fluid, utilize CMVAMF. For all other specimen types (CSF, BAL, fluids, tissue, bone marrow), utilize CMVCSF.","ClinicalInfo":"Cytomegalovirus (CMV) is a common viral pathogen that can cause severe disease in immunocompromised patients, and lead to a range of presentations in congenitally-exposed infants. The cobas CMV assay is an FDA-approved test for human EDTA plasma, which has been modified and validated as a lab-develop test to accept alternative sample types of saliva swabs in viral transport media and urine for qualitative CMV detection. The assay is a real-time PCR assay that targets highly-conserved regions of the CMV DNA polymerase (UL54) gene. The results of this test should be interpreted within the context of all relevant clinical and laboratory findings.","ClinicalReference":"1. Leber AL. Maternal and congenital human cytomegalovirus infection: laboratory testing for detection and diagnosis. J Clin Microbiol. 2024 Apr 10;62(4):e0031323. doi: 10.1128/jcm.00313-23. Epub 2024 Feb 23. PMID: 38391188.\n2. U.S. Food and Drug Administration (FDA). Premarket Approval Summary of Safety and Effectiveness Data P160041. Accessed July 5, 2024. https://www.accessdata.fda.gov/cdrh_docs/pdf16/P160041B.pdf.","ClinicalLimitation":"For full limitations, refer to the assay instructions for use available on the manufacturer's website. The most important limitations are summarized as follows. Mutations within the highly-conserved regions of the CMV DNA polymerase (UL54) gene covered by cobas CMV may affect primers and/or probe binding resulting in the failure to detect the presence of virus. The cobas CMV mitigates this risk through the use of redundant amplification primers. Detection of CMV in patients >21 days of age is not specific for congenital CMV (cCMV), and could be the result of postnatal infection. Detection of CMV in saliva could be due to contamination from human milk feeding or other sources. Confirmation with a second specimen (ideally urine) is recommended. Samples containing mucin at concentrations >25 mg/mL may produce invalid results with the CMV assay. The results of this assay are not intended to be used as the sole basis for diagnosis, treatment, or other patient management decisions. 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Acceptable preservatives: Diazolidinyl Urea (Germall), 50% Acetic Acid, Boric Acid, 6M Hydrochloric Acid, or Thymol. Specimens with pH >8 may indicate bacterial contamination and testing will be cancelled. Do not attempt to adjust pH as it will adversely affect results. Record volume on sample and test request form. This test is New York DOH approved.","ClinicalInfo":"This test is useful for the diagnosis of the cause of acidosis and treatment of kidney stones. The kidney regulates acid excretion and systemic acid base balance. Changing the amount of ammonium in the urine is one important way the kidneys accomplish this task. Thus,  measuring the urine ammonium level can provide understanding of the cause of an acid base disturbance in individual patients. The urine ammonium level can also provide a lot of information about the daily acid production in a given patient. 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There are significant variations in measured plasma NfL levels among different methods and labs. Care must be taken when interpreting results obtained in different studies. Direct comparisons of absolute values can only be done on the same source fluid (plasma or serum). A rise in NfL is not specific for a specific disease factor and may be caused by both neurodegenerative diseases or a head impact during sports. Results should only be used in conjunction with other clinical information when evaluating patients with neurodegeneration. Due to a lack of specificity to a particular neurodegenerative disease, its role as a diagnostic marker is limited. There are numerous demographic, life style, and comorbidity factors that potentially influence NfL levels in plasma. Variables such as exercise,2 blood volume, body mass index may impact measured plasma NfL levels. NfL levels measured in the morning are more than 10% higher than those measured in the evening. Caution should be taken in interpreting NfL levels when disease treatment induced neurological complications that can potentially impact NfL levels. Plasma NfL levels can be decreased in patients with high immunoglobulin G (IgG) levels. Higher concentrations of NfL may be found in persons with history of stroke, atrial fibrillation, myocardial infarction, chronic kidney disease, pregnancy, and diabetes. Lower concentrations of NfL may be found in individuals who are obese (BMI > or =30).","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13738,"ActiveDate":"2024-02-01T05:00:00","CreatedOn":"2023-12-12T11:43:07.6933333","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6874,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13738,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13512,"DictMethodologyId":185,"TdTestInfoSpecificId":13738,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13738,"DictDaysPerformedId":1,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"Varies","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":678053,"SpecialInstructions":"Patient should avoid biotin consumption for at least 72 hours prior to collection. Separate plasma and transfer to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13738,"IsBeakerData":false},{"Id":678054,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":12,"DictSpVolumeName":"0.7 mL","TdTestInfoSpecificId":13738,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":30495,"Description":"14 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(AC)","Rank":7,"TdTestInfoCommonId":6877},{"Id":25820,"TestName":"AC/FC Ratio","Rank":8,"TdTestInfoCommonId":6877},{"Id":25821,"TestName":"Interpretation","Rank":9,"TdTestInfoCommonId":6877},{"Id":25822,"TestName":" Acetylcarnitine, C2","Rank":10,"TdTestInfoCommonId":6877},{"Id":25823,"TestName":"Acrylylcarnitine, C3:1","Rank":11,"TdTestInfoCommonId":6877},{"Id":25824,"TestName":"Propionylcarnitine, C3","Rank":12,"TdTestInfoCommonId":6877},{"Id":25825,"TestName":"Formiminoglutamate, FIGLU","Rank":13,"TdTestInfoCommonId":6877},{"Id":25826,"TestName":"Iso-/Butyrylcarnitine, C4","Rank":14,"TdTestInfoCommonId":6877},{"Id":25827,"TestName":"Tiglylcarnitine, C5:1","Rank":15,"TdTestInfoCommonId":6877},{"Id":25828,"TestName":"Isovaleryl-/2-Methylbutyrylcarn C5","Rank":16,"TdTestInfoCommonId":6877},{"Id":25829,"TestName":"3-OH-iso-/butyrylcarnitine, C4-OH","Rank":17,"TdTestInfoCommonId":6877},{"Id":25830,"TestName":"Hexenoylcarnitine, 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C16-OH","Rank":49,"TdTestInfoCommonId":6877},{"Id":25862,"TestName":"Octadecadienoylcarnitine, C18:2","Rank":50,"TdTestInfoCommonId":6877},{"Id":25863,"TestName":"Octadecenoylcarnitine, C18:1","Rank":51,"TdTestInfoCommonId":6877},{"Id":25864,"TestName":"Octadecanoylcarnitine, C18","Rank":52,"TdTestInfoCommonId":6877},{"Id":25865,"TestName":"Dodecanedioylcarnitine, C12-DC","Rank":53,"TdTestInfoCommonId":6877},{"Id":25866,"TestName":"3-OH-octadecadienoylcarn, C18:2-OH","Rank":54,"TdTestInfoCommonId":6877},{"Id":25867,"TestName":"3-OH-octadecenoylcarnitine C18:1-OH","Rank":55,"TdTestInfoCommonId":6877},{"Id":25868,"TestName":"3-OH-octadecanoylcarnitine, C18-OH","Rank":56,"TdTestInfoCommonId":6877},{"Id":25869,"TestName":"Comment (ACRN)","Rank":57,"TdTestInfoCommonId":6877},{"Id":26664,"TestName":"Free L-carnitine","Rank":1,"TdTestInfoCommonId":6877},{"Id":26665,"TestName":"Total L-carnitine","Rank":2,"TdTestInfoCommonId":6877},{"Id":26666,"TestName":"Esterified Carnitine","Rank":3,"TdTestInfoCommonId":6877},{"Id":26667,"TestName":"Esterified Carnitine / Free Carnitine Ratio","Rank":4,"TdTestInfoCommonId":6877}],"TdLaboratoryCommon":{"TdTestInfoCommonId":6877,"SpecialInfo":"Performing Labs: Special Chemistry, Client Services - Vendor Mayo. Indicate patient fasting hours when possible. Refer to individual tests Carnitine Free & Total, Plasma (CARNPL) and Acylcarnitines, Quantitative, Plasma (ACRNPL). Carnitine, fish oil, and omega-3 supplements affect test results; indicate supplement use on the requisition.","ClinicalInfo":"This test is useful in the evaluation of individuals at risk for a deficiency of free carnitine, which may occur during treatment with valproate, in persons receiving chronic renal dialysis, and in some forms of malnourishment. When combined with the profile of plasma acylcarnitine species, useful in the diagnostic evaluation of individuals suspected of having a disorder of mitochondrial fatty acid beta-oxidation and many genetic disorders of organic acid metabolism. It is also useful for diagnosis of fatty acid oxidation disorders and several organic acidurias, as well as evaluating treatment during follow-up of patients with fatty acid beta-oxidation disorders and several organic acidurias.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13741,"ActiveDate":"2024-03-26T04:00:00","CreatedOn":"2024-02-13T15:07:14.17","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":6877,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13741,"IsStat":false,"Comments":"Performing Labs: Special Chemistry (x42525), Client Services (x45755) - Vendor Mayo","DictPerformingLabId":50,"DictPerformingLab":{"Id":50,"Name":"Main Campus Performing Lab","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13521,"DictMethodologyId":484,"TdTestInfoSpecificId":13741,"DictMethodology":{"Id":484,"Name":"Flow Injection Analysis-Tandem Mass Spectrometry (FIA-MS/MS)","Description":null},"TdTestInfoSpecific":null},{"Id":13854,"DictMethodologyId":265,"TdTestInfoSpecificId":13741,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13741,"DictDaysPerformedId":25,"DictHoursPerformedId":null,"DictReportedId":21,"DictDaysPerformed":"Mon - Fri","DictReported":"Refer to individual components"},"TdSpecimenRequirements":[{"Id":678154,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Carnitine Free & Total, Plasma (CARNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. Centrifuge and transfer the plasma to a plastic CCL tube within 2 hours of collection and freeze.","LogicalOperation":"And","DictSpContainerId":221,"DictSpContainerName":"Green NaHep NOGEL","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":678155,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Acylcarnitines, Quantitative, Plasma (ACRNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. Centrifuge and aliquot plasma into standard aliquot tube.","LogicalOperation":"And","DictSpContainerId":28,"DictSpContainerName":"Sodium heparin (Green)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":5,"DictSpVolumeName":"0.1 mL","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":678156,"SpecialInstructions":"The aliquot for Carnitine Free & Total, Plasma (CARNPL) must have a minimum volume of 0.2 mL. The aliquot for Acylcarnitines, Quantitative, Plasma (ACRNPL) must have a minimum of 0.04 mL.","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":154,"DictSpVolumeName":"Variable","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":679502,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Carnitine Free & Total, Plasma (CARNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. Centrifuge and transfer the serum to a plastic CCL tube within 2 hours of collection and freeze.","LogicalOperation":"Or","DictSpContainerId":210,"DictSpContainerName":"Red Plain","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":679503,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Carnitine Free & Total, Plasma (CARNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. Centrifuge and transfer the plasma to a plastic CCL tube within 2 hours of collection and freeze.","LogicalOperation":"Or","DictSpContainerId":196,"DictSpContainerName":"Green LiHep Nogel","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":679504,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Carnitine Free & Total, Plasma (CARNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. Centrifuge and transfer the plasma to a plastic CCL tube within 2 hours of collection and freeze.","LogicalOperation":"Or","DictSpContainerId":209,"DictSpContainerName":"Mint PST LiHep","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":3,"DictSpTransportTemperatureName":"Frozen","DictSpTypeId":50,"DictSpTypeName":"Plasma","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13741,"IsBeakerData":false},{"Id":679505,"SpecialInstructions":"Multiple specimen tubes must be collected for this panel. This tube is for test: Carnitine Free & Total, Plasma (CARNPL). Collect specimen just prior to a scheduled meal or feeding. Patient age is required. 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Hydroxychloroquine is the mainstay of treatment for patients with lupus, with every patient requiring its use unless there are significant side effects. 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This test is New York state approved.","ClinicalInfo":"Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response or skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis. 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including Progressive Encephalomyelitis with Rigidity and Myoclonus, Serum","EMRCode":"SQSPSDEV","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":19085,"CptCode":"86341","Quantity":1,"Tmid":"30215045","CclTechComponentPrice":64.00,"CclProfComponentPrice":null,"TestNameForCdm":"SPSDEV GAD65 Ab","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7035,"IsBeakerData":false},{"Id":19086,"CptCode":"86255","Quantity":2,"Tmid":"30215055","CclTechComponentPrice":33.00,"CclProfComponentPrice":null,"TestNameForCdm":"SPSDEV Fluorescent Ab Screen","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7035,"IsBeakerData":false},{"Id":19087,"CptCode":"0431U","Quantity":1,"Tmid":"30215065","CclTechComponentPrice":630.00,"CclProfComponentPrice":null,"TestNameForCdm":"SPSDEV Glycine Receptor Alpha1 IgG","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7035,"IsBeakerData":false}],"TdIncludes":[{"Id":26440,"TestName":"Amphiphysin Ab","Rank":1,"TdTestInfoCommonId":7035},{"Id":26441,"TestName":"GAD65 Ab Assay","Rank":2,"TdTestInfoCommonId":7035},{"Id":26442,"TestName":"DPPX Ab CBA","Rank":3,"TdTestInfoCommonId":7035},{"Id":26443,"TestName":"Glycine Alpha1 LCBA","Rank":4,"TdTestInfoCommonId":7035},{"Id":26444,"TestName":"Stiff-Person/PERM Interp","Rank":5,"TdTestInfoCommonId":7035},{"Id":26445,"TestName":"IFA Notes","Rank":6,"TdTestInfoCommonId":7035}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7035,"SpecialInfo":"Reflex Algorithm: Each reflex test performed incurs additional charge. If client requests or if the indirect immunofluorescence assay (IFA) pattern suggests amphiphysin antibody, then amphiphysin immunoblot and amphiphysin IFA titer will be performed. If the dipeptidyl-peptidase-like protein-6 (DPPX) cell bound assay is positive, then DPPX antibody IFA titer will be performed. This test should not be requested for patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed or canceled if radioactivity remains. Grossly hemolyzed, lipemic or icteric specimens will be rejected. This test is New York state approved.","ClinicalInfo":"This test is useful for evaluating patients with suspected stiff-person syndrome (classical or focal forms, such as stiff-limb or stiff-trunk) and progressive encephalomyelitis with rigidity and myoclonus. Seropositivity supports the clinical diagnosis of stiff-person spectrum disorder (classical stiff-person, stiff-limb, stiff-trunk, or progressive encephalomyelitis with rigidity and myoclonus). A paraneoplastic basis should be considered. Negative results do not exclude the diagnosis of stiff-person spectrum disorder or progressive encephalomyelitis with rigidity and myoclonus (PERM). Glutamic acid decarboxylase 65 (GAD65) antibody positive values below 20 nmol/L should be interpreted with caution. Lower values are encountered in 8% of the general population. However, GAD65 autoimmunity (any antibody value) is associated with other autoimmune diseases that can cause neurological symptoms, including type 1 diabetes, pernicious anemia, hypothyroidism, and adrenal insufficiency.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13900,"ActiveDate":"2024-12-03T05:00:00","CreatedOn":"2024-09-24T12:35:09.4666667","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7035,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13900,"IsStat":false,"Comments":"Inpatient orders restricted to Neurology and outpatient orders restricted to the Mellen Center","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13785,"DictMethodologyId":487,"TdTestInfoSpecificId":13900,"DictMethodology":{"Id":487,"Name":"Cell Binding Assay (CBA)","Description":null},"TdTestInfoSpecific":null},{"Id":13786,"DictMethodologyId":77,"TdTestInfoSpecificId":13900,"DictMethodology":{"Id":77,"Name":"Indirect Immunofluorescence Assay (IFA) ","Description":null},"TdTestInfoSpecific":null},{"Id":13787,"DictMethodologyId":162,"TdTestInfoSpecificId":13900,"DictMethodology":{"Id":162,"Name":"Radioimmunoassay (RIA)","Description":null},"TdTestInfoSpecific":null},{"Id":13788,"DictMethodologyId":577,"TdTestInfoSpecificId":13900,"DictMethodology":{"Id":577,"Name":"Live Cell-Binding Assay (LCBA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13900,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":127,"DictDaysPerformed":"Sun - Sat","DictReported":"6 - 11 days"},"TdSpecimenRequirements":[{"Id":679232,"SpecialInstructions":"This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). Centrifuge and transfer serum to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":13900,"IsBeakerData":false},{"Id":679233,"SpecialInstructions":"This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). Centrifuge and transfer serum to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":30,"DictSpContainerName":"SST (Gold)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":13900,"IsBeakerData":false},{"Id":679234,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13900,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":30989,"Description":"28 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Pathology","Address1":null,"Address2":null,"City":null,"State":null,"Zip":null,"Phone":null,"Fax":null,"Clia":null,"TdVendors":[],"Vendors":[]},"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[{"TdTestInfoCommonId":6761,"PrimaryName":"Amphiphysin Antibody Titer Assay, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5867,"PrimaryName":"Amphiphysin Immunoblot, Serum (Reflex Only)","IsRequired":false},{"TdTestInfoCommonId":5811,"PrimaryName":"DPPX Ab IFA Titer, Serum (Reflex Only)","IsRequired":false}]},{"Id":7036,"LISCode":"MLPTHY","PrimaryName":"Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum","LISName":"Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum","EMRName":"Myelopathy, Autoimmune/Paraneoplastic Evaluation, Serum","EMRCode":"SQMLPTHY","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":19090,"CptCode":"86341","Quantity":1,"Tmid":"30215075","CclTechComponentPrice":106.00,"CclProfComponentPrice":null,"TestNameForCdm":"MLPTHY GAD65 Ab","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7036,"IsBeakerData":false},{"Id":19091,"CptCode":"84182","Quantity":1,"Tmid":"30123215","CclTechComponentPrice":131.00,"CclProfComponentPrice":null,"TestNameForCdm":"MLPTHY CRMP-5 WB","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7036,"IsBeakerData":false},{"Id":19092,"CptCode":"86255","Quantity":16,"Tmid":"30215085","CclTechComponentPrice":108.00,"CclProfComponentPrice":null,"TestNameForCdm":"MLPTHY Fluorescent Ab 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S","Rank":5,"TdTestInfoCommonId":7036},{"Id":26454,"TestName":"AP3B2 IFA, S","Rank":6,"TdTestInfoCommonId":7036},{"Id":26455,"TestName":"CRMP-5-IgG Western Blot, S","Rank":7,"TdTestInfoCommonId":7036},{"Id":26456,"TestName":"DPPX Ab CBA, S","Rank":8,"TdTestInfoCommonId":7036},{"Id":26457,"TestName":"GABA-B-R Ab CBA, S","Rank":9,"TdTestInfoCommonId":7036},{"Id":26458,"TestName":"GAD65 Ab Assay, S","Rank":10,"TdTestInfoCommonId":7036},{"Id":26459,"TestName":"GFAP IFA, S","Rank":11,"TdTestInfoCommonId":7036},{"Id":26460,"TestName":"mGluR1 Ab IFA, S","Rank":12,"TdTestInfoCommonId":7036},{"Id":26461,"TestName":"MOG FACS, S","Rank":13,"TdTestInfoCommonId":7036},{"Id":26462,"TestName":"Neurochondrin IFA, S","Rank":14,"TdTestInfoCommonId":7036},{"Id":26463,"TestName":"NIF IFA, S","Rank":15,"TdTestInfoCommonId":7036},{"Id":26464,"TestName":"NMO/AQP4 FACS, S","Rank":16,"TdTestInfoCommonId":7036},{"Id":26465,"TestName":"PCA-1, S","Rank":17,"TdTestInfoCommonId":7036},{"Id":26466,"TestName":"PCA-2, S","Rank":18,"TdTestInfoCommonId":7036},{"Id":26467,"TestName":"Septin-7 IFA, S","Rank":19,"TdTestInfoCommonId":7036},{"Id":26468,"TestName":"TRIM46 Ab IFA, S","Rank":20,"TdTestInfoCommonId":7036}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7036,"SpecialInfo":"Reflex Algorithm: Each reflex test performed incurs additional charge. If the indirect immunofluorescence assay (IFA) patterns suggest antiglial nuclear antibody (AGNA)-1, then the AGNA-1 immunoblot and AGNA-1 IFA titer will be performed. If the IFA patterns suggest amphiphysin antibody, then the amphiphysin immunoblot and amphiphysin IFA titer will be performed. If the IFA pattern suggests antineuronal nuclear antibody type 1 (ANNA-1), then the ANNA-1 IFA titer, ANNA-1 immunoblot, and ANNA-2 immunoblot will be performed. If the IFA pattern suggests ANNA-2 antibodies, then the ANNA-2 IFA titer, ANNA-2 immunoblot, and ANNA-1 immunoblot will be performed. If the client requests or the IFA pattern suggests ANNA-3 antibodies, then the ANNA-3 IFA titer will be performed. If the IFA pattern suggests adaptor protein 3 beta 2 (AP3B2) antibodies, then the AP3B2 cell-binding assay (CBA) and AP3B2 IFA titer will be performed. If the CRMP-5-IgG Western blot is positive, then the CRMP-5-IgG IFA titer will be performed. If the IFA pattern suggests Purkinje cytoplasmic antibody type 1 (PCA-1), then the PCA-1 immunoblot and PCA-1 IFA titer will be performed. If the IFA pattern suggests PCA-2 antibody, then the PCA-2 IFA titer will be performed. If gamma-aminobutyric acid B (GABA-B) receptor antibody CBA result is positive, then the GABA-B-receptor antibody IFA titer will be performed. If the dipeptidyl-peptidase-like protein-6 (DPPX) antibody CBA result is positive, then the DPPX antibody IFA titer will be performed. If the IFA pattern suggests metabotropic glutamate receptor 1 (mGluR1) antibody, then the mGluR1antibody CBA and mGluR1 antibody IFA titer will be performed. If the IFA pattern suggests glial fibrillary acidic protein (GFAP) antibody, then the GFAP antibody CBA and GFAP antibody IFA titer will be performed. If the neuromyelitis optica/aquaporin-4-IgG (NMO/AQP4-IgG) fluorescence-activated cell sorting (FACS) screen assay requires further investigation, then the NMO/AQP4-IgG FACS titration assay will be performed. If the myelin oligodendrocyte glycoprotein (MOG) FACS screen assay requires further investigation, then the MOG FACS titration assay will be performed. If the IFA pattern suggests neuronal intermediate filament (NIF) antibody, then the alpha internexin CBA, NIF heavy chain CBA, NIF light chain CBA, and NIF antibody IFA titer will be performed. If the IFA pattern suggests neurochondrin antibody, then the neurochondrin antibody CBA and neurochondrin IFA titer will be performed. If the IFA pattern suggests septin-7 antibody, then the septin-7 CBA and septin-7 IFA titer will be performed. If the IFA pattern suggests tripartite motif-containing protein 46 (TRIM46) antibody, then the TRIM46 antibody CBA and TRIM46 IFA titer will be performed. This test should not be requested for patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given, and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held 1 week and assayed if sufficiently decayed or canceled if radioactivity remains. Grossly hemolyzed, lipemic or icteric specimens will be rejected. This test is New York state approved.","ClinicalInfo":"This test is useful for evaluating patients with suspected autoimmune myelopathy, myelitis, and paraneoplastic myelopathy. Patients with autoimmune myelopathy present with subacute onset and rapid progression of spinal cord symptoms with one or more of the following: weakness, gait difficulties, loss of sensation, neuropathic pain, and bowel and bladder dysfunction. Clinical history and examination, spinal cord magnetic resonance imaging, and cerebrospinal fluid (CSF) testing may provide clues to an autoimmune diagnosis. Autoimmune myelopathy evaluation of both serum and CSF can assist in the diagnosis (paraneoplastic or idiopathic autoimmune) and aid distinction from other causes of myelopathy (multiple sclerosis, sarcoidosis, vascular disease). Early testing may assist in early diagnosis of occult cancer, prompt initiation of immune therapies, or both.","ClinicalReference":null,"ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13901,"ActiveDate":"2024-12-10T05:00:00","CreatedOn":"2024-09-24T14:33:47.44","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7036,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13901,"IsStat":false,"Comments":"Inpatient orders restricted to Neurology and outpatient orders restricted to the Mellen Center","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13790,"DictMethodologyId":487,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":487,"Name":"Cell Binding Assay (CBA)","Description":null},"TdTestInfoSpecific":null},{"Id":13791,"DictMethodologyId":401,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":401,"Name":"Flow Cytometry (FC)","Description":null},"TdTestInfoSpecific":null},{"Id":13792,"DictMethodologyId":195,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":195,"Name":"Immunoblot (IB)","Description":null},"TdTestInfoSpecific":null},{"Id":13793,"DictMethodologyId":77,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":77,"Name":"Indirect Immunofluorescence Assay (IFA) ","Description":null},"TdTestInfoSpecific":null},{"Id":13794,"DictMethodologyId":162,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":162,"Name":"Radioimmunoassay (RIA)","Description":null},"TdTestInfoSpecific":null},{"Id":13795,"DictMethodologyId":221,"TdTestInfoSpecificId":13901,"DictMethodology":{"Id":221,"Name":"Western Blot (WB)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13901,"DictDaysPerformedId":48,"DictHoursPerformedId":null,"DictReportedId":202,"DictDaysPerformed":"Sun - Sat","DictReported":"9 - 13 days"},"TdSpecimenRequirements":[{"Id":679242,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. Specimen collection is recommended before initiation of immunosuppressant medication. This test should not be requested in patients who have recently received radioisotopes (refer to Special Information). Centrifuge and transfer serum to standard aliquot tube.","LogicalOperation":null,"DictSpContainerId":25,"DictSpContainerName":"No additive (Red)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":51,"DictSpTypeName":"Serum","DictSpVolumeId":21,"DictSpVolumeName":"4 mL","TdTestInfoSpecificId":13901,"IsBeakerData":false},{"Id":679243,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":17,"DictSpVolumeName":"2 mL","TdTestInfoSpecificId":13901,"IsBeakerData":false},{"Id":679244,"SpecialInstructions":"Draw 2 tubes to ensure adequate serum volume. 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Adulterated: pH is less than 4 or greater than or equal to 11; Nitrite is greater than or equal to 500mg/L; Oxidant is greater than or equal to 200mg/L.","ClinicalReference":null,"ClinicalLimitation":"Assay does not differentiate between delta-8 or delta-9 carboxy-THC.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13906,"ActiveDate":"2025-01-07T05:00:00","CreatedOn":"2024-10-01T13:58:29.9033333","CreatedById":4,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7041,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13906,"IsStat":false,"Comments":null,"DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13812,"DictMethodologyId":265,"TdTestInfoSpecificId":13906,"DictMethodology":{"Id":265,"Name":"Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13906,"DictDaysPerformedId":17,"DictHoursPerformedId":null,"DictReportedId":24,"DictDaysPerformed":"6 days per week","DictReported":"2 - 4 days"},"TdSpecimenRequirements":[{"Id":679303,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":181,"DictSpContainerName":"Urine","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":13906,"IsBeakerData":false},{"Id":679304,"SpecialInstructions":"No preservatives","LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13906,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31005,"Description":"14 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13906,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31006,"Description":"14 days ","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13906,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31007,"Description":"7 days","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13906,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13906,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7042,"LISCode":"INSFT","PrimaryName":"Insulin, Free and Total, Serum","LISName":"Insulin, Free and Total, Serum","EMRName":"Insulin, Free and Total, Serum","EMRCode":"SQINSFT","LOINC":null,"RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":4,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":19391,"CptCode":"83527","Quantity":1,"Tmid":"30101315","CclTechComponentPrice":84.00,"CclProfComponentPrice":null,"TestNameForCdm":"INSULIN FREE","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7042,"IsBeakerData":false},{"Id":19392,"CptCode":"83525","Quantity":1,"Tmid":"30103635","CclTechComponentPrice":74.00,"CclProfComponentPrice":null,"TestNameForCdm":"INSULIN ASSAY","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7042,"IsBeakerData":false}],"TdIncludes":[{"Id":26581,"TestName":"Free Insulin","Rank":1,"TdTestInfoCommonId":7042},{"Id":26582,"TestName":"Total Insulin","Rank":2,"TdTestInfoCommonId":7042}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7042,"SpecialInfo":"Specimen collection should occur preferably from patients fasting for at least 8 hours and at minimum 8 hours after administration of multivitamins or dietary supplements, especially containing biotin (Vitamin B7).","ClinicalInfo":"Intended for the in vitro quantitative determination of human insulin in human serum and plasma. The determination of insulin is utilized in the diagnosis and therapy of various disorders of carbohydrate metabolism,\nincluding diabetes mellitus and hypoglycemia.","ClinicalReference":null,"ClinicalLimitation":"For diagnostic purposes, the results should always be assessed in conjunction with the patient’s medical history, clinical examination and other findings.","DictTestCategorizationId":null,"DictTestCategorization":{"Id":null,"Code":null,"Name":null}},"TdTestInfoSpecifics":[{"Id":13907,"ActiveDate":"2025-01-09T05:00:00","CreatedOn":"2024-10-31T01:17:43.3133333","CreatedById":4,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7042,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13907,"IsStat":false,"Comments":null,"DictPerformingLabId":4,"DictPerformingLab":{"Id":4,"Name":"Special Chemistry (x42525)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13814,"DictMethodologyId":185,"TdTestInfoSpecificId":13907,"DictMethodology":{"Id":185,"Name":"Electro Chemiluminescence Immunoassay (ECLIA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13907,"DictDaysPerformedId":13,"DictHoursPerformedId":null,"DictReportedId":15,"DictDaysPerformed":"2 days per week","DictReported":"1 - 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Other parasites such as Trypanosomes may be identified but molecular and serological testing is preferred for their higher sensitivity and accuracy in detection","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14795,"Aka":"Babesia smear","TdTestInfoCommonId":7045},{"Id":14796,"Aka":"Blood parasite smear","TdTestInfoCommonId":7045},{"Id":14797,"Aka":"Malaria smear","TdTestInfoCommonId":7045},{"Id":14798,"Aka":"Plasmodium species","TdTestInfoCommonId":7045}],"TdBillingCommons":[{"Id":19395,"CptCode":"87207","Quantity":1,"Tmid":"30602580","CclTechComponentPrice":39.00,"CclProfComponentPrice":null,"TestNameForCdm":"Smear, Blood Parasite","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7045,"IsBeakerData":false},{"Id":19471,"CptCode":"87015","Quantity":1,"Tmid":"30808765","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Processing, Thick smear preparation","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7045,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":7045,"SpecialInfo":"Malaria is a potentially life-threatening condition, and testing for this infection should be conducted as quickly as possible. Consequently, this test is not recommended as the primary screening method when specimens can be delivered within a few hours of collection. Laboratories that cannot ensure prompt specimen delivery should first conduct an initial screening for malaria and other blood parasites, such as a malaria antigen test, before sending the specimen for further analysis. This test is used to confirm a presumptive malaria diagnosis, identify the infecting Plasmodium and Babesia species, and determine the percent parasitemia. A percent parasitemia calculated more than 8 hours after blood collection may not accurately reflect the patient's current state of parasitemia. Additionally, if malaria parasites have degraded or their morphology has altered due to specimen age or suboptimal transportation conditions, the calculation of percent parasitemia may be either impossible or inaccurate.\n","ClinicalInfo":"Malaria is a mosquito-borne disease caused by Plasmodium parasites, which are a major cause of illness and death globally. Malaria can also affect travelers from non-endemic areas. The primary Plasmodium species responsible for malaria are P. falciparum, P. vivax, P. malariae, and P. ovale. P. knowlesi, a simian parasite, has also  been known to infect humans in parts of Southeast Asia and is significant due to its potential to cause severe illness. P. falciparum is particularly concerning due to its resistance to many antimalarial drugs.                                                                                                                                         In the U.S., Babesia microti is the main cause of human cases, with notable outbreaks in the Northeast and Midwest. Other species like Babesia duncani and Babesia divergens have also been reported in certain areas. Babesia microti is nationally notifiable.\n\nBabesia microti shares its tick vector with Borrelia burgdorferi (Lyme disease) and Anaplasma phagocytophilum (human granulocytic anaplasmosis), making concurrent testing for these diseases advisable in endemic regions. Additionally, babesiosis can be transmitted via blood transfusion, prompting the FDA to mandate donor screening for this parasite in 2018. While most cases of babesiosis are mild or asymptomatic, severe cases can occur, particularly in asplenic individuals. Thick film microscopy, is used for screening, while thin films help determine percent parasitemia, which indicates the severity and helps monitor treatment response. Percent parasitemia is calculated from microscopic fields on the thin blood film. Percent parasitemia exclude malarial gametocytes as they are not infectious and are not targeted by most antimalarial treatments and will be reported out within the comments. Microfilaria, Trypanosomes if seen will be reported but alternate molecular or serological testing is recommended.","ClinicalReference":"1. Centers for Disease Control (CDC). Evaluation and diagnosis of Malaria, June 24, 2024. https://www.cdc.gov/malaria/hcp/clinical-guidance/evaluation-diagnosis.html\n2. Bobbi S. Pritt, 2023. Plasmodium and Babesia, p.13-20. Manual of Clinical Microbiology, 13th Edition. ASM Press, Washington, DC.\n3. Mathison BA, Pritt BS. Update on malaria diagnostics and test utilization. J Clin Microbiol. 2017;55(7):2009-2017","ClinicalLimitation":"A single negative result does not exclude the possibility of parasitic infection. If there is strong suspicion testing should be conducted at least three times using samples collected at different times throughout the fever cycle. Delay in sample processing or transport can impact quality of smears thus the sensitivity and specificity of blood parasite detection. \nTesting can not be performed on grossly hemolysed, or clotted blood specimens.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":13910,"ActiveDate":"2025-01-16T05:00:00","CreatedOn":"2024-09-03T09:44:31.28","CreatedById":26,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7045,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13910,"IsStat":false,"Comments":null,"DictPerformingLabId":87,"DictPerformingLab":{"Id":87,"Name":"Clinical Microbiology (x45875)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13821,"DictMethodologyId":260,"TdTestInfoSpecificId":13910,"DictMethodology":{"Id":260,"Name":"Stain","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13910,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":8,"DictDaysPerformed":"7 days a week","DictReported":"1 - 2 days"},"TdSpecimenRequirements":[{"Id":679366,"SpecialInstructions":"Prompt delivery of specimens to the laboratory is crucial for accurate and reliable results. Laboratories that are unable to deliver specimens within a few hours of collection should conduct an initial screening for malaria, such as a Malaria Binax antigen test, before sending the specimen. This preliminary testing helps ensure timely diagnosis and effective patient management.","LogicalOperation":null,"DictSpContainerId":21,"DictSpContainerName":"EDTA (Lavender)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":114,"DictSpVolumeName":"2 - 3 mL","TdTestInfoSpecificId":13910,"IsBeakerData":false},{"Id":679367,"SpecialInstructions":"Minimum of 4 unstained slides - 2 thick and 2 thin slides should be prepared and submitted in addition to EDTA blood. Slides should be prepared per routine hematology processes and as described by the CDC protocol https://www.cdc.gov/dpdx/diagnosticProcedures/blood/specimenproc.html","LogicalOperation":null,"DictSpContainerId":5,"DictSpContainerName":"Slides, unstained","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":55,"DictSpTypeName":"Whole blood","DictSpVolumeId":158,"DictSpVolumeName":"4 slides","TdTestInfoSpecificId":13910,"IsBeakerData":false},{"Id":679368,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":10,"DictSpVolumeName":"0.5 mL","TdTestInfoSpecificId":13910,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31015,"Description":"24 hrs","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13910,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31016,"Description":"24 hrs","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13910,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31017,"Description":"Unacceptable","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13910,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13910,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7046,"LISCode":"MALAGS","PrimaryName":"Malaria Antigen, Screen and Microscopy Smear","LISName":"Malaria Binax Antigen, screen","EMRName":"Malaria Antigen, Screen and Microscopy Smear","EMRCode":"SQMALAGS","LOINC":"46094-9","RecommendedUse":"The BinaxNOW Malaria antigen test is recommended for rapid detection of malaria in patients with symptoms or travel history suggestive of the disease\n","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":14799,"Aka":"Binax Malaria","TdTestInfoCommonId":7046},{"Id":14800,"Aka":"Malaria antigen","TdTestInfoCommonId":7046},{"Id":14801,"Aka":"Malaria screen","TdTestInfoCommonId":7046},{"Id":14802,"Aka":"Plasmodium antigen","TdTestInfoCommonId":7046}],"TdBillingCommons":[{"Id":19397,"CptCode":"87899","Quantity":1,"Tmid":"30601545","CclTechComponentPrice":104.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, Malaria P. falciparum","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7046,"IsBeakerData":false},{"Id":19398,"CptCode":"87899","Quantity":1,"Tmid":"30601535","CclTechComponentPrice":104.00,"CclProfComponentPrice":null,"TestNameForCdm":"Immunoassay, Pan-malarial","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7046,"IsBeakerData":false}],"TdIncludes":[{"Id":26589,"TestName":"Blood Parasite Microscopy smear, including % parasitemia (BPMSM)","Rank":1,"TdTestInfoCommonId":7046}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7046,"SpecialInfo":"The malaria antigen test should be treated as a STAT test and processed immediately upon receipt in the lab. It is crucial to use this test for patients who have an appropriate travel history and a strong suspicion of malaria. Blood samples must also be delivered to the lab promptly after collection to ensure the accuracy, reliability and appropriate utilization of the test results. All malaria antigen screen tests will be reflexed to Blood parasite microscopy smear, regardless of a positive or negative result. \n","ClinicalInfo":"Malaria is a major parasitic disease, which is endemic in many countries in various areas of the world. Each year it causes up to 3 million deaths and close to 5 billion cases of clinical illness worldwide. The rapid malaria antigen screen has better sensitivity of detection for Plasmodium falciparum as compared to the other Plasmodium species. It provides rapid results and is designed to be used as a screening tests but all test results are paired with a blood parasite microscopy smear. The antigen test is not designed to be used for assessment of treatment efficacy or as a test-of-cure as residual plasmodium antigen may be detected several days following clearance as determined by microscopy.  \n","ClinicalReference":"1. Centers for Disease Control (CDC). Evaluation and diagnosis of Malaria, June 24, 2024. https://www.cdc.gov/malaria/hcp/clinical-guidance/evaluation-diagnosis.html\n2. Bobbi S. Pritt, 2023. Plasmodium and Babesia, p.13-20. Manual of Clinical Microbiology, 13th Edition. ASM Press, Washington, DC.\n3. Moody, Anthony. Rapid Diagnostic Tests for Malaria Parasites. Clinical Microbiology Reviews, Jan. 2002; 15: 66-78.  \n","ClinicalLimitation":"A negative test result does not exclude infection with malaria, particularly at low levels of parasitemia. Test performance depends on antigen load in the specimen and may not directly correlate with microscopy performed on the same specimen. Binax antigen test can cross react with rheumatoid factor, chronic viral infections such as hepatitis C and other parasitic infections. The Binax malaria test can be affected by the prozone effect, and both antigens may test positive due to dual infection or high levels of parasitemia. The antigen test may also remain positive for days after clearance of malarial parasitic infection. 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4 days"},"TdSpecimenRequirements":[{"Id":679725,"SpecialInstructions":"No additives or preservatives","LogicalOperation":null,"DictSpContainerId":269,"DictSpContainerName":"Urine (No Preservative)","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":54,"DictSpTypeName":"Urine, random","DictSpVolumeId":23,"DictSpVolumeName":"5 mL","TdTestInfoSpecificId":13959,"IsBeakerData":false},{"Id":679726,"SpecialInstructions":null,"LogicalOperation":null,"DictSpContainerId":null,"DictSpContainerName":null,"DictSpRequirementCategoryId":6,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":null,"DictSpTransportTemperatureName":null,"DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13959,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31153,"Description":"3 days","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13959,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31154,"Description":"7 days","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13959,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31155,"Description":"30 days","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13959,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13959,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7100,"LISCode":"EVPPCR","PrimaryName":"Enteric Viral Panel by PCR","LISName":"Enteric Viral Panel by PCR","EMRName":"Enteric Viral Panel by PCR","EMRCode":"SQEVPPCR","LOINC":"79390-1","RecommendedUse":null,"DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":15058,"Aka":"GIP","TdTestInfoCommonId":7100},{"Id":15059,"Aka":"adenovirus F40/41","TdTestInfoCommonId":7100},{"Id":15060,"Aka":"astrovirus","TdTestInfoCommonId":7100},{"Id":15061,"Aka":"gastrointestinal","TdTestInfoCommonId":7100},{"Id":15062,"Aka":"norovirus","TdTestInfoCommonId":7100},{"Id":15063,"Aka":"rotavirus","TdTestInfoCommonId":7100},{"Id":15064,"Aka":"sapovirus","TdTestInfoCommonId":7100},{"Id":15065,"Aka":"EVPPCR","TdTestInfoCommonId":7100},{"Id":15066,"Aka":"SQEVPPCR","TdTestInfoCommonId":7100},{"Id":15067,"Aka":"stool","TdTestInfoCommonId":7100}],"TdBillingCommons":[{"Id":19543,"CptCode":"87505","Quantity":1,"Tmid":"30608875","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Gastrointestinal Panel, 5 Viral Targets","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7100,"IsBeakerData":false}],"TdIncludes":[{"Id":26802,"TestName":"Adenovirus F 40/41 DNA","Rank":1,"TdTestInfoCommonId":7100},{"Id":26803,"TestName":"Astrovirus RNA","Rank":2,"TdTestInfoCommonId":7100},{"Id":26804,"TestName":"Norovirus GI/GII RNA","Rank":3,"TdTestInfoCommonId":7100},{"Id":26805,"TestName":"Rotavirus A RNA","Rank":4,"TdTestInfoCommonId":7100},{"Id":26806,"TestName":"Sapovirus (Genogroups I, II, IV, V) RNA","Rank":5,"TdTestInfoCommonId":7100}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7100,"SpecialInfo":null,"ClinicalInfo":"The BD Max Enteric Viral Panel is an FDA-cleared multiplex real-time PCR assay that qualitatively detects nucleic acids from the following targets in stool: Norovirus GI/GII, Rotavirus A, Adenovirus 40/41, Sapovirus (Genogroups I, II, IV, V), and Astrovirus.\n\nThe Infectious Diseases Society of America recommends stool viral pathogen testing in an outbreak setting and in immunocompromised hosts with diarrhea. Identification of the infectious etiology of diarrheal illness can help guide appropriate therapy, prevent unnecessary or harmful antibiotic exposure, and facilitate further workup. Repeat testing within 14 days of the same episode of diarrhea, or for test of cure, is not recommended.\n\nImmunocompromised individuals with persistent diarrhea may additionally benefit from additional testing (ie. SQSTLPCR: Enteric Bacterial by PCR or SQSTLPCR: Expanded Stool Gastrointestinal Panel by PCR, SQOVAP: Stool Ova/Parasite Exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora Exam, SQMICSPO: Microsporidia Exam, and gastrointestinal biopsy, among others). Individuals with travel history outside the United States with persistent diarrhea lasting >14 days may benefit from additional parasitic testing (ie. SQOVAP: Stool Ova/Parasite exam, SQCRYSPO: Cryptosporidium/Cyclospora/Cystoisospora exam). Individuals with onset of diarrhea after more than 3 days of hospital admission or with prior antibiotic exposure history may benefit from testing for C. difficile (SQCDPCR).","ClinicalReference":"1. Shane AL, Mody RK, Crump JA, Tarr PI, Steiner TS, Kotloff K, Langley JM, Wanke C, Warren CA, Cheng AC, Cantey J, Pickering LK. 2017 Infectious Diseases Society of America Clinical Practice Guidelines for the Diagnosis and Management of Infectious Diarrhea. Clin Infect Dis. 2017 Nov 29;65(12):e45-e80. doi: 10.1093/cid/cix669. PMID: 29053792.\n2. Stokes W, Simner PJ, Mortensen J, Oethinger M, Stellrecht K, Lockamy E, Lay T, Bouchy P, Pillai DR. Multicenter Clinical Validation of the Molecular BD Max Enteric Viral Panel for Detection of Enteric Pathogens. J Clin Microbiol. 2019 Aug 26;57(9):e00306-19. doi: 10.1128/JCM.00306-19. PMID: 31270179","ClinicalLimitation":"The BD Max Enteric Viral Panel results are meant to be used in conjunction with clinical presentation, laboratory findings, and epidemiological information. Results of this test should not be used as the sole basis for diagnosis, treatment, or other patient management decisions. Positive results do not rule out co-infection with other organisms that are not detected by this test, and may not be the sole or definitive cause of patient illness. Some targets on this panel have potential for false positives due to non-specific cross reactivity. Negative results in the setting of clinical illness compatible with gastroenteritis may be due to infection by pathogens that are not detected by this test or non-infectious causes such as ulcerative colitis, irritable bowel syndrome, or Crohn’s disease. Refer to the manufacturer package insert for full list of limitations.","DictTestCategorizationId":2,"DictTestCategorization":{"Id":2,"Code":"IVD","Name":"In Vitro Diagnostic"}},"TdTestInfoSpecifics":[{"Id":13966,"ActiveDate":"2025-09-23T04:00:00","CreatedOn":"2025-06-27T12:43:37.7333333","CreatedById":176,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7100,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13966,"IsStat":false,"Comments":null,"DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13915,"DictMethodologyId":422,"TdTestInfoSpecificId":13966,"DictMethodology":{"Id":422,"Name":"Qualitative Polymerase Chain Reaction","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13966,"DictDaysPerformedId":103,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"7 days a week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":679764,"SpecialInstructions":"The stool must be passed into a clean, dry, wide mouthed container and not contaminated by urine or water. A bed pan is an ideal initial collection container provided it has been thoroughly cleaned and the patient is cautioned against contaminating the specimen with urine. A plastic bag placed over the toilet seat is also acceptable. Select bloody, slimy, or watery portions of the stool using the collection spoon provided in the cap of the container. Place enough stool (~1g) in the Cary-Blair transport vial (Oracle #1124361, or #1570140 as part of STUL kit) to bring the liquid level up to the “fill to here” line. Mash and mix the stool with the spoon along the sides of the container. Tighten the cap and shake the vial until the mixture appears homogeneous.","LogicalOperation":null,"DictSpContainerId":97,"DictSpContainerName":"Cary-Blair kit","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":13966,"IsBeakerData":false},{"Id":679765,"SpecialInstructions":"The stool must be passed into a clean, dry, wide mouthed container and not contaminated by urine or water. A bed pan is an ideal initial collection container provided it has been thoroughly cleaned and the patient is cautioned against contaminating the specimen with urine. A plastic bag placed over the toilet seat is also acceptable. Select bloody, slimy, or watery portions of the stool using a clean transfer device. Place a minimum of 1g of stool into the sterile container (Oracle #1012787). ","LogicalOperation":null,"DictSpContainerId":68,"DictSpContainerName":"Sterile container","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":null,"DictSpTypeName":null,"DictSpVolumeId":100,"DictSpVolumeName":"One","TdTestInfoSpecificId":13966,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31173,"Description":"5 days  in Cary-Blair transport media or as unpreserved stool in a sterile container","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13966,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31174,"Description":"2 days in Cary-Blair transport media or as unpreserved stool in a sterile container","Rank":2,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13966,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13966,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7101,"LISCode":"POLEDD","PrimaryName":"POLE Mutation Detection by Droplet Digital PCR","LISName":"POLE Mutation Detection by Droplet Digital PCR","EMRName":"POLE Mutation Detection by Droplet Digital PCR","EMRCode":"SQPOLEDD","LOINC":null,"RecommendedUse":null,"DictDepartmentId":4,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":null,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":19544,"CptCode":"81479","Quantity":1,"Tmid":"31005105","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"POLE Droplet Digital PCR","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7101,"IsBeakerData":false}],"TdIncludes":[],"TdLaboratoryCommon":{"TdTestInfoCommonId":7101,"SpecialInfo":null,"ClinicalInfo":null,"ClinicalReference":"Ten unstained sections FFPE on charged, unbaked slides or scrolls plus one H&E stained section with best tumor area circled by a pathologist. Provide percentage of tumor cells present, minimum 10%.","ClinicalLimitation":null,"DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13967,"ActiveDate":"2025-09-30T04:00:00","CreatedOn":"2025-07-31T16:28:23.6633333","CreatedById":13,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7101,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13967,"IsStat":false,"Comments":"","DictPerformingLabId":5,"DictPerformingLab":{"Id":5,"Name":"Molecular PCR (x48283)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13916,"DictMethodologyId":547,"TdTestInfoSpecificId":13967,"DictMethodology":{"Id":547,"Name":"Droplet Digital Polymerase Chain Reaction (PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13967,"DictDaysPerformedId":13,"DictHoursPerformedId":null,"DictReportedId":118,"DictDaysPerformed":"2 days per week","DictReported":"5 days"},"TdSpecimenRequirements":[{"Id":679769,"SpecialInstructions":"Formalin-fixed paraffin embedded tissue slides. Transport and store slides at ambient temperature. Ten unstained sections FFPE on charged, unbaked slides or scrolls plus one H&E stained section with best tumor area circled by a pathologist. Provide percentage of tumor cells present, minimum 10%. Specimens that undergo heavy metal fixation or are decalcified with strong acids (i.e., formic acid) are not acceptable for molecular testing. Non-decalcified specimens or samples that undergo EDTA decalcification are acceptable.","LogicalOperation":null,"DictSpContainerId":118,"DictSpContainerName":"Formalin-fixed, paraffin-embedded block","DictSpRequirementCategoryId":4,"DictSpCollectionTemperatureId":18,"DictSpCollectionTemperatureName":"Ambient","DictSpTransportTemperatureId":18,"DictSpTransportTemperatureName":"Ambient","DictSpTypeId":121,"DictSpTypeName":"Block, Formalin fixed paraffin","DictSpVolumeId":89,"DictSpVolumeName":"10 mm square","TdTestInfoSpecificId":13967,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31176,"Description":"FFPE samples collected and stored at ambient temperature","Rank":1,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13967,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31177,"Description":"Refrigerated FFPE samples may be accepted","Rank":2,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13967,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31178,"Description":"Frozen FFPE samples will be rejected","Rank":3,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13967,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13967,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7104,"LISCode":"FLUSEQ","PrimaryName":"Influenza A Subtyping by Sequencing","LISName":"Influenza A Subtyping by Sequencing","EMRName":"Influenza A Subtyping by Sequencing","EMRCode":"SQFLUSEQ","LOINC":"22827-0","RecommendedUse":null,"DictDepartmentId":null,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[{"Id":15068,"Aka":"flu genotype","TdTestInfoCommonId":7104},{"Id":15069,"Aka":"flu subtype","TdTestInfoCommonId":7104},{"Id":15070,"Aka":"flu subtyping","TdTestInfoCommonId":7104},{"Id":15071,"Aka":"FLUSEQ","TdTestInfoCommonId":7104},{"Id":15072,"Aka":"influenza genotype","TdTestInfoCommonId":7104},{"Id":15073,"Aka":"influenza subtype","TdTestInfoCommonId":7104},{"Id":15074,"Aka":"influenza subtyping","TdTestInfoCommonId":7104},{"Id":15075,"Aka":"SQFLUSEQ","TdTestInfoCommonId":7104}],"TdBillingCommons":[{"Id":19547,"CptCode":"87502","Quantity":1,"Tmid":"30608775","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Sequencing, Influenza ","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7104,"IsBeakerData":false},{"Id":19548,"CptCode":"87503","Quantity":1,"Tmid":"30020615","CclTechComponentPrice":null,"CclProfComponentPrice":null,"TestNameForCdm":"Sequencing, Influenza Plus","SubComponent":null,"Rvu":null,"VariableCharges":true,"TdTestInfoCommonId":7104,"IsBeakerData":false}],"TdIncludes":[{"Id":26808,"TestName":"Influenza A Subtype","Rank":1,"TdTestInfoCommonId":7104}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7104,"SpecialInfo":null,"ClinicalInfo":"Influenza A viruses have segmented single-stranded RNA genomes and are divided into subtypes based on their hemagglutinin (H) and neuraminidase (N) subtypes. Current subtypes of influenza A viruses that routinely circulate in humans and cause seasonal influenza are A(H1N1)pdm09 and A(H3N2). Over 130 influenza A subtype combinations have been identified in other animals, predominantly in wild birds. Genetic reassortment or mutations in these novel influenza A viruses can lead to better adaptation for human infection, and are the basis of flu pandemics.\n\nIn 2020-2021, a new strain of highly pathogenic avian influenza A(H5N1) virus began affecting wild birds. In the United States, there have been outbreaks with these viruses among poultry and dairy cows, as well as sporadic human infections mostly tied to poultry and dairy cow exposure. In light of the ongoing avian influenza A(H5) virus animal outbreak in the United States, CDC now recommends that all influenza A positive respiratory specimens from hospitalized patients, especially from those in an ICU, be subtyped for seasonal influenza A viruses as soon as possible following admission, to support optimal patient care and proper infection prevention and control measures and to facilitate rapid public health investigation and action.\n\nThis Influenza A Subtyping by Sequencing assay is a lab-developed test that uses next-generation sequencing technology to sequence the entire influenza A genome, with subsequent analysis using a custom bioinformatic pipeline. This test reports influenza A(H1N1), influenza A(H3N2), or influenza A(H5N1) subtypes only if both hemagglutinin (H) and neuraminidase (N) gene segments are successfully sequenced. Infections with mixed subtypes or reassorted viruses with contributions of non-H/N segments from novel influenza A may not be reliably identified. This test should only be ordered on samples already-positive for influenza A by a nucleic acid amplification test. Sequencing may not be successful in specimens with low viral load.","ClinicalReference":"Centers for Disease Control Health Alert Network. CDCHAN-00520: Accelerated Subtyping of Influenza A in Hospitalized Patients. 2025 January 16. https://www.cdc.gov/han/2025/han00520.html.","ClinicalLimitation":"Infections with mixed subtypes or reassorted viruses with contributions of non-H/N segments from novel influenza A may not be reliably identified. \n\nThis test should only be ordered on samples already-positive for influenza A by a nucleic acid amplification test. Sequencing may not be successful in specimens with low viral load.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13970,"ActiveDate":"2025-10-28T04:00:00","CreatedOn":"2025-02-25T11:34:21.65","CreatedById":89,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7104,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13970,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13921,"DictMethodologyId":82,"TdTestInfoSpecificId":13970,"DictMethodology":{"Id":82,"Name":"Sequencing","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13970,"DictDaysPerformedId":65,"DictHoursPerformedId":null,"DictReportedId":158,"DictDaysPerformed":"Tue, Thu","DictReported":"7 days"},"TdSpecimenRequirements":[{"Id":679780,"SpecialInstructions":"Sterile saline may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":82,"DictSpContainerName":"Saline","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":13970,"IsBeakerData":false},{"Id":679781,"SpecialInstructions":"E-swabs in liquid amies may be used to collect swabs if UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":130,"DictSpContainerName":"E Swab","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":15,"DictSpVolumeName":"1 mL","TdTestInfoSpecificId":13970,"IsBeakerData":false},{"Id":679782,"SpecialInstructions":"Viral transport media (including VTM, M4RT, M5, or M6) may be used to collect swabs is UTM cannot be sourced.","LogicalOperation":null,"DictSpContainerId":113,"DictSpContainerName":"Viral Transport Media","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":119,"DictSpTypeName":"Swab(s)","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":13970,"IsBeakerData":false},{"Id":679783,"SpecialInstructions":"1. Insert the entire collection tip of the regular-tip flocked swab with a rigid shaft (i.e. Oracle 1063581) 1/2 - 3/4 of an inch or 1 - 1.5 cm inside the nostril. 2. Firmly sample the nasal wall by rotating the swab in a circular path against the nasal wall at least 4 times. 3. Take approximately 15 seconds to collect the specimen. Be sure to collect any nasal drainage that may be present on the swab. 4. Repeat in the other nostril using the same swab. 5. Place swab, tip first, into the transport tube provided. Break the swab shaft at the score line, discard the top portion of the stem, and close the cap.","LogicalOperation":null,"DictSpContainerId":165,"DictSpContainerName":"Universal Transport Media (UTM)","DictSpRequirementCategoryId":5,"DictSpCollectionTemperatureId":null,"DictSpCollectionTemperatureName":null,"DictSpTransportTemperatureId":4,"DictSpTransportTemperatureName":"Refrigerated","DictSpTypeId":69,"DictSpTypeName":"Nasal","DictSpVolumeId":19,"DictSpVolumeName":"3 mL","TdTestInfoSpecificId":13970,"IsBeakerData":false}],"TdSpecimenStabilities":[{"Id":31185,"Description":"7 days","Rank":1,"DictStabilityEnvironmentalConditionId":3,"TdTestInfoSpecificId":13970,"DictStabilityEnvironmentalCondition":{"Id":3,"Name":"Refrigerated"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31186,"Description":"30 days","Rank":2,"DictStabilityEnvironmentalConditionId":2,"TdTestInfoSpecificId":13970,"DictStabilityEnvironmentalCondition":{"Id":2,"Name":"Frozen"},"SpecimenStabilities":[],"TdTestInfoSpecific":null},{"Id":31187,"Description":"24 hours","Rank":3,"DictStabilityEnvironmentalConditionId":1,"TdTestInfoSpecificId":13970,"DictStabilityEnvironmentalCondition":{"Id":1,"Name":"Ambient"},"SpecimenStabilities":[],"TdTestInfoSpecific":null}],"TdTestInfoCommon":null,"User":null,"TdVendor":{"TdTestInfoSpecificId":13970,"TestCode":null,"IsReportable":false,"DictVendorId":null,"DictVendor":null,"TdTestInfoSpecific":null},"TestInfoSpecifics":[]}],"TdSupportDocuments":[],"TdReflexedTests":[]},{"Id":7110,"LISCode":"LYMCNS","PrimaryName":"Lyme Central Nervous System Infection IgG with Antibody Index Reflex, Serum and CSF","LISName":"Lyme Central Nervous System Infection IgG with Antibody Index Reflex, Serum and CSF","EMRName":"Lyme Central Nervous System Infection IgG with Antibody Index Reflex, Serum and CSF","EMRCode":"SQLYMCNS","LOINC":null,"RecommendedUse":"Per Gayle Wagner, a new TDMS was needed in order to add the reflex LYMRFX.","DictDepartmentId":2,"DictIntendedForId":3,"DictRestrictedOrderingFrequencyId":null,"DictTestClassificationId":1,"DictIntendedFor":null,"TdAlias":[],"TdBillingCommons":[{"Id":19558,"CptCode":"86618","Quantity":1,"Tmid":"30215115","CclTechComponentPrice":110.00,"CclProfComponentPrice":null,"TestNameForCdm":"Lyme IgG CSF","SubComponent":null,"Rvu":null,"VariableCharges":false,"TdTestInfoCommonId":7110,"IsBeakerData":false}],"TdIncludes":[{"Id":26826,"TestName":"Lyme CNS Infection IgG, CSF","Rank":1,"TdTestInfoCommonId":7110},{"Id":26827,"TestName":"Lyme CNS Infection IgG Interp","Rank":2,"TdTestInfoCommonId":7110},{"Id":26828,"TestName":"Lyme CNS Infection IgG, S","Rank":3,"TdTestInfoCommonId":7110}],"TdLaboratoryCommon":{"TdTestInfoCommonId":7110,"SpecialInfo":"Both CSF and serum are required for this test. CSF and serum must be collected within 24 hours (maximum) of each other and be rubber banded together prior to being sent to the performing laboratory. This test begins with IgG screening of the CSF specimen. If the screen is negative, no additional testing will be performed. If the screen is positive, the paired CSF and serum specimens will be used to establish the antibody index at additional cost. The additional quantitative assays determine levels for anti-Borrelia species IgG levels in CSF and serum, total IgG in CSF and serum, and albumin in CSF and serum. Grossly hemolyzed or lipemic specimens will be rejected. CSF contaminated with blood will be rejected. This test is New York state approved.","ClinicalInfo":"This test is useful for aiding in the diagnosis of neuroinvasive Lyme disease or neuroborreliosis due to Borrelia species associated with Lyme disease. It compares the level of IgG antibodies to Lyme disease-causing Borrelia species in spinal fluid (CSF) and serum. The level of anti-Borrelia species IgG is normalized to total IgG and albumin in CSF and serum. This test can help identify whether the presence of IgG to Borrelia species in the CSF is due to true intrathecal antibody synthesis, suggesting neuroinvasive Lyme disease, versus antibody presence due to passive diffusion through the blood-brain barrier or, possibly, due to blood contamination of the CSF as a result of a traumatic lumbar puncture.","ClinicalReference":null,"ClinicalLimitation":"A single negative result should not be used to exclude the diagnosis of neuroinvasive Lyme disease in a patient with appropriate exposure history and symptoms suggestive of infection.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13976,"ActiveDate":"2025-01-09T05:00:00","CreatedOn":"2024-11-13T09:39:33.0166667","CreatedById":185,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7110,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13976,"IsStat":false,"Comments":"","DictPerformingLabId":9,"DictPerformingLab":{"Id":9,"Name":"Client Services (x45755)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13933,"DictMethodologyId":170,"TdTestInfoSpecificId":13976,"DictMethodology":{"Id":170,"Name":"Enzyme-Linked Immunosorbent Assay (ELISA)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13976,"DictDaysPerformedId":37,"DictHoursPerformedId":null,"DictReportedId":14,"DictDaysPerformed":"Mon, Wed, Fri","DictReported":"1 - 5 days"},"TdSpecimenRequirements":[{"Id":679834,"SpecialInstructions":"Both CSF and serum are required for this test and must be collected within the same 24-hour period. 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HSV infections in humans can cause lesions at a variety of cutaneous and mucocutaneous sites. These lesions can be a result of the primary infection by the virus or they can result from a reactivation of the latent virus, causing recurrent episodes of the disease. While testing is typically performed on mucocutaneous swabs, more unusual presentations of disseminated disease, pneumonitis, central nervous system infection, or intraocular infection may require testing of alternative specimen types. Nucleic acid amplification tests are a sensitive method for detection of HSV in plasma, lower respiratory specimens, CSF, and ocular fluid.\n\nThis lab-developed multiplex real-time PCR assay simultaneously qualitatively detects and differentiates HSV-1 and HSV-2 DNA targets. Viral nucleic acid is extracted from clinical samples using the EZ2 Connect (Qiagen). HSV-1 and HSV-2 DNA are amplified and detected using the RealStar alpha Herpesvirus PCR kit 1.0 (Altona) using species-specific primers and fluorescently labeled hydrolysis probes on a RotorGene Q (Qiagen) thermocycler. \n\nThis specific procedure code (SQHSVPCR) can be used to order this test on plasma, bronchoalveolar lavage, bronchial wash, and ocular fluid specimens. Utilize alternative orders for the following specimen types: SQHSVVZV for mucocutaneous lesion swabs, SQHSPCRC for CSF, SQHSVNEO for neonatal surface swabs.","ClinicalReference":"1. Yip CCY, Sridhar S, Leung KH, Cheng AKW, Chan KH, Chan JFW, Cheng VCC, Yuen KY. Evaluation of RealStar® Alpha Herpesvirus PCR Kit for Detection of HSV-1, HSV-2, and VZV in Clinical Specimens. Biomed Res Int. 2019 Oct 9;2019:5715180. doi: 10.1155/2019/5715180. PMID: 31687393.\n2. Harper TW, Miller D, Schiffman JC, Davis JL. Polymerase chain reaction analysis of aqueous and vitreous specimens in the diagnosis of posterior segment infectious uveitis. Am J Ophthalmol. 2009 Jan;147(1):140-147.e2. doi: 10.1016/j.ajo.2008.07.043. Epub 2008 Oct 2. PMID: 18834576.","ClinicalLimitation":"As with any nucleic acid amplification test, positive results do not rule out coinfection with other organisms, detected organisms may not be the definite cause of disease, and negative results do not rule out infection. Dilution of ocular fluid at the point of collection may decrease assay sensitivity.","DictTestCategorizationId":3,"DictTestCategorization":{"Id":3,"Code":"LDT","Name":"Laboratory Developed Test"}},"TdTestInfoSpecifics":[{"Id":13986,"ActiveDate":"2026-01-20T05:00:00","CreatedOn":"2025-08-28T12:19:28.2933333","CreatedById":89,"DeletedOn":null,"DeletedById":null,"LocationId":1,"TdTestInfoCommonId":7120,"IsBeakerData":false,"Location":null,"TdBillingSpecifics":null,"TdCostCenters":null,"TdEventTrackings":null,"TdFinancialSpecific":null,"TdLaboratorySpecific":{"TdTestInfoSpecificId":13986,"IsStat":false,"Comments":"","DictPerformingLabId":38,"DictPerformingLab":{"Id":38,"Name":"Molecular Microbiology (x48033)","Functionality":"Service Area","LocationId":1,"Location":null,"LaboratorySpecifics":[],"TdLaboratorySpecifics":[],"Users":[]}},"TdMethodologies":[{"Id":13956,"DictMethodologyId":480,"TdTestInfoSpecificId":13986,"DictMethodology":{"Id":480,"Name":"Real-Time Polymerase Chain Reaction (RT-PCR)","Description":null},"TdTestInfoSpecific":null}],"TdReportingRequirements":null,"TdSchedule":{"TdTestInfoSpecificId":13986,"DictDaysPerformedId":14,"DictHoursPerformedId":null,"DictReportedId":5,"DictDaysPerformed":"3 days per week","DictReported":"1 - 3 days"},"TdSpecimenRequirements":[{"Id":680143,"SpecialInstructions":"Absolute minimum volume accepted is 0.25 mL (250 uL) for HSVPCR and VZVPCR combined. 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Primary VZV infection results in chickenpox (varicella), which may rarely result in complications including encephalitis or pneumonia. Even when clinical symptoms of chickenpox have resolved, VZV remains dormant in the nervous system of the infected person (virus latency). In approximately 10 to 20% of cases, VZV reactivates later in life producing shingles. While testing is typically performed on mucocutaneous swabs, more unusual presentations of disseminated disease, pneumonitis, central nervous system infection, or intraocular infection may require testing of alternative specimen types. Nucleic acid amplification tests are a sensitive method for detection of VZV in plasma, lower respiratory specimens, CSF, and ocular fluid.\n\nThis lab-developed real-time PCR assay qualitatively detects VZV DNA. Viral nucleic acid is extracted from clinical samples using the EZ2 Connect (Qiagen). VZV DNA  is amplified and detected using the RealStar alpha Herpesvirus PCR kit 1.0 (Altona) using species-specific primers and fluorescently labeled hydrolysis probes on a RotorGene Q (Qiagen) thermocycler.\n\nThis specific procedure code (SQVZVPCR) can be used to order this test on plasma, bronchoalveolar lavage, bronchial wash, CSF, and ocular fluid specimens. Utilize alternative orders for the following specimen types: SQHSVVZV for mucocutaneous lesion swabs.","ClinicalReference":"1. Yip CCY, Sridhar S, Leung KH, Cheng AKW, Chan KH, Chan JFW, Cheng VCC, Yuen KY. Evaluation of RealStar® Alpha Herpesvirus PCR Kit for Detection of HSV-1, HSV-2, and VZV in Clinical Specimens. Biomed Res Int. 2019 Oct 9;2019:5715180. doi: 10.1155/2019/5715180. PMID: 31687393.\n2. Harper TW, Miller D, Schiffman JC, Davis JL. Polymerase chain reaction analysis of aqueous and vitreous specimens in the diagnosis of posterior segment infectious uveitis. 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