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Test Code ABOMR ABO/Rh, Blood


Specimen Required


Container/Tube: Pink top (EDTA)

Specimen Volume: 6 mL

Collection Instructions:

1. Invert several times to mix blood.

2. Send whole blood specimen in original tube. Do not aliquot.


Secondary ID

113490

Useful For

Determining blood group ABO and Rh only

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
ABIDR Antibody Identification, RBC Yes No
ABOPR ABORh Problem RBC No No

Testing Algorithm

Includes identification of ABO and Rh blood group antigens. If indicated, antibody identification will be performed. If ABO/Rh discrepancy is detected, the ABO/Rh problem test may be ordered to result the final ABO/Rh interpretation.

Method Name

Hemagglutination

Reporting Name

ABORh, RBC

Specimen Type

Whole Blood EDTA

Specimen Minimum Volume

3 mL

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

This ABO and Rh blood typing test identifies the presence of specific red cell antigens and antibodies to determine the ABO/Rh type.

Reference Values

ABO and Rh blood group antigens identified

Interpretation

Standard ABO/Rh type will be reported. Routine types include: O pos, O neg, A pos, A neg, B pos, B neg, AB pos and AB neg. Any relevant discrepancies will be noted.

Cautions

Clinical evaluation of antibodies identified is necessary to determine their potential for harm to the patient at this time and to assess appropriate action to be taken in the future.

Clinical Reference

Cohn CS, Delaney DO, Johnson ST, Katz LM, Schwartz J, eds. Technical Manual. 21st ed. AABB; 2023

Method Description

Agglutination of patient red cells with an antiserum represents the presence of the corresponding antigen on the red cells. Agglutination of patient plasma with reagent red blood cells represents the presence of the corresponding antibodies.(Cohn CS, Delaney DO, Johnson ST, Katz LM, Schwartz J, eds. Technical Manual. 21st ed. AABB; 2023)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test 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.

CPT Code Information

86900-ABO

86901-Rh

LOINC Code Information

Test ID Test Order Name Order LOINC Value
ABOMR ABORh, RBC 882-1

 

Result ID Test Result Name Result LOINC Value
ABOMR ABORh, RBC 882-1

Day(s) Performed

Monday through Sunday

Report Available

Same day/1 to 2 days