Search our extensive Laboratory Test Directory to find test codes, ordering recommendations, specimen stability information, Test Fact Sheets, and more.
Recommendations when to order or not order the test. May include related or preferred tests.
Use to detect HLA antibodies for solid organ and stem cell transplantation.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
Testing is not New York state approved. Specimens from New York clients will be sent out to a New York state-approved laboratory.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Plain red.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Transfer 5 mL serum to ARUP Standard Transport Tubes. (Min. 2 mL) New York State Clients: Transfer 7 mL serum to ARUP Standard Transport Tubes. (Min. 3 mL)
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Refrigerated
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Ambient: 72 hours; Refrigerated: 1 month; Frozen: 2 years
Methodology
Process(es) used to perform the test.
Multiplex Bead Assay
Performed
Days of the week the test is performed.
Varies
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
3-7 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
By report
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Background Information for HLA Antibody Screen, Class I and Class II Purpose: To detect HLA Class I and Class II IgG antibodies. Analytical Sensitivity & Specificity: More sensitive than traditional lymphocyte cytotoxicity procedures. Limitations: Only detects IgG antibody isotype; IgM antibodies are not detected. This test does not provide information on the specificities of the HLA antibodies detected. Test Results: Results are reported as positive or negative for HLA Class I and Class II antibodies. This test was developed and its performance characteristics determined by the H&I laboratory at the University of Utah Health under the accreditation guidelines from the American Society for Histocompatibility and Immunogenetics (ASHI). Some tests or reagents have not been cleared or approved by the FDA.
Compliance Category
Performed by non-ARUP Laboratory
Note
Additional information related to the test.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
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