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3021221
ABORH Discrepancy Investigation, IRL
ABORH DISC
Ordering Recommendation
Investigate a discrepancy in a patient's ABORh type. An ABO discrepancy occurs when the results of forward and reverse blood typing do not match.
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Lavender (K2EDTA), or pink (K2EDTA).
Specimen Preparation
Do not freeze red cells.
Transport 10 mL whole blood. (Min 5 mL)
Storage/Transport Temperature
Refrigerated.
Unacceptable Conditions
Separator tubes.
Remarks
Stability
Ambient: Unacceptable; Refrigerated: 1 week; Frozen: Unacceptable
Methodology
Qualitative Agglutination
Performed
Mon-Fri
Reported
3-5 days
Reference Interval
Refer to report
Interpretive Data
Compliance Category
FDA
Note
Depending on reactivity in the sample, additional testing will be required. Additional charges apply. Client must provide patient transfusion and transplant history along with issues noted in testing.
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
86900; 86901
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0010248 | ABORh | 882-1 |
* 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.
Aliases
- Blood Type Discrepancy
- Blood Typing Discrepancy
- ABO Investigation
ABORH Discrepancy Investigation, IRL
