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Recommendations when to order or not order the test. May include related or preferred tests.
Use to identify unexpected red blood cell (RBC) antibodies in a patient's serum and, when applicable, in antibodies coating the patient's RBCs. For use in prenatal patients only to identify unexpected RBC antibodies and aid in determining the risk for hemolytic disease of the fetus and newborn (HDFN) and to evaluate the patient for Rh immunoglobulin administration. Do not use this test for nonprenatal patients. For nonprenatal patients, order Antibody Identification Package IRL (0013003).
New York DOH Approval Status
Indicates test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
3 (7mL) Lavender (K2EDTA) or Pink (K2EDTA) AND 1 (7mL) Plain Red.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Do not freeze. Transport 3 (7 mL) whole blood EDTA AND 1 (7 mL) whole blood plain red. (Min: 10 mL EDTA and 3 mL Plain Red)
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.
Separator tubes.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Expected turnaround time for a result, beginning when ARUP has received the specimen.
2-5 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Compliance Category
FDA
Note
Additional information related to the test.
This test is for prenatal patients only. Includes: ABO/Rh Type, Rh Phenotype, Direct Coombs, RBC Antibody Identification by various methods.
Titers will be performed, at an additional charge, on prenatal specimens for clinically significant antibodies.
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.
86900; 86901; 86906; 86880; 86870; additional CPT codes may apply
* 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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