Test Code ABONR ABO/Rh Newborn, Blood
Specimen Required
Container/Tube: Pink top (EDTA Micro tube)
Specimen Volume: 0.5 mL
Collection Instructions:
1. Invert several times to mix blood.
2. Send whole blood specimen in original tube. Do not aliquot.
Secondary ID
113498Useful For
Selecting compatible blood products for transfusion therapy
Determining the need for Rh immune globulin in mother of baby
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
ABIDR | Antibody Identification, RBC | Yes | No |
Testing Algorithm
Includes ABO and Rh blood group antigens.
Method Name
Hemagglutination
Reporting Name
Newborn ABORhSpecimen Type
Whole Blood EDTASpecimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole Blood EDTA | Refrigerated (preferred) | 10 days | |
Ambient | 4 days |
Reject Due To
Gross hemolysis | Reject |
Clinical Information
The ABO and Rh typing indicates the presence of 2 of the various blood group systems. The identification of antigens in the ABO and Rh system has its major application in the selection of blood and blood products of the appropriate ABO/Rh type for transfusion therapy and in the determination of the mother's candidacy for Rh immune globulin therapy.
Weak D testing will be performed on all Rh-negative babies.
Reference Values
ABO and Rh blood group antigens identified
Interpretation
Agglutination of red cells with an antiserum represents the presence of the corresponding antigen on the red cells.
Cautions
No significant cautionary statements
Clinical Reference
Cohn CS, Delaney DO, Johnson ST, Katz LM, Schwartz J, eds. Technical Manual. 21st ed. AABB; 2023
Method Description
Agglutination of red cells with an antiserum represents the presence of the corresponding antigen in the red cells.( Cohn CS, Delaney DO, Johnson ST, Katz LM, Schwartz J, eds. Technical Manual. 21st ed. AABB; 2023)
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysSpecimen Retention Time
14 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
ABONR | Newborn ABORh | 19057-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
ABONR | Newborn ABORh | 19057-9 |