Management of ABO Incompatibility in Transfusion and Transplantation
For ABO-incompatible transfusions: prevent them through rigorous verification protocols, and if they occur, immediately discontinue the transfusion as mortality correlates directly with volume transfused; for ABO-incompatible transplantation: utilize kidney paired donation programs when available, or proceed only with effective desensitization protocols including antibody removal strategies. 1, 2
Transfusion Medicine: Prevention is Paramount
Critical Prevention Strategies
- Perform ABO blood typing twice before any donation to eliminate unintended ABO-incompatible transfusions 1
- Verify two independent patient identifiers before phlebotomy and confirm identity at bedside immediately before transfusion 3
- Type and screen samples remain valid for only 72 hours (3 calendar days) in patients who received transfusion or were pregnant within the past 3 months, as new antibodies can develop rapidly 4
- For patients without recent transfusion/pregnancy, samples remain valid through day 3, but beyond this all patients require new samples regardless of history 4
When ABO-Incompatible Transfusion Occurs
The volume of incompatible blood directly determines outcomes: patients receiving >50 mL experienced symptoms in 64% of cases with 17% mortality, while those receiving ≤50 mL had only 25% symptom rate and zero deaths 2
Immediate management algorithm:
- Stop the transfusion immediately upon any suspicion 2
- Monitor for hypotension, hemoglobinuria, and hemoglobinemia—the most frequent findings in both survivors and fatalities 2
- Recognize that prompt discontinuation is the single most critical intervention to prevent death 2
Special Transfusion Considerations
- Provide ABO-compatible products whenever possible to optimize platelet increments and minimize hemolysis risk 5
- ABO incompatibility reduces post-transfusion platelet increments 3
- Exercise greater caution with ABO-incompatible platelets in pediatric patients due to higher hemolysis risk from incompatible plasma 5
- For sickle cell disease patients, extend matching beyond ABO/RhD to include Rh (C, E) and K antigens to reduce alloimmunization 1, 5
Transplantation Medicine: Algorithmic Approach
Kidney Transplantation Decision Tree
Step 1: Assess ABO Compatibility
- ABO compatibility is the primary consideration for donor suitability to prevent hyperacute rejection and graft failure 5
- Perform donor ABO blood typing twice before donation 1
- Conduct donor blood group A subtype testing when donation is planned to recipients with anti-A antibodies 1
Step 2: When ABO Incompatibility Exists
First-line approach: Kidney paired donation (KPD) programs 1
Second-line approach: ABO-incompatible transplantation with desensitization 1
Step 3: Mandatory Counseling
- Inform donor candidates who are ABO incompatible about all treatment options, including risks and benefits of both KPD and incompatibility management strategies 1
- Explain that incompatible transplantation is only available at select centers with appropriate expertise 1
Hematopoietic Stem Cell Transplantation
Nearly 50% of all HLA-matched stem cell transplants involve ABO incompatibility, classified as major, minor, or bidirectional 6, 7
Major ABO Incompatibility (recipient has antibodies against donor RBCs):
- Manage with combinations of plasma exchange, removal of donor-type RBCs from marrow before transplant 8
- Avoid transfusing incompatible donor-type RBCs before transplant—this caused delayed hemolysis in 78% (7/9) of patients in one series 8
- Risks include acute hemolysis, delayed RBC engraftment, and pure red cell aplasia 6, 7
Minor ABO Incompatibility (donor marrow contains antibodies against recipient RBCs):
- Centrifuge bone marrow to remove plasma and reduce antibody load, which retains 60-100% of stem cell activity 8
- Uncentrifuged marrow caused hemolysis in 29% (2/7) of patients 8
- Select blood components to avoid transfusing large amounts of incompatible plasma 8
Bidirectional Incompatibility:
Critical Pitfall to Avoid
The most common error location is at the patient's bedside (62% of ABO-incompatible transfusions), not in the laboratory 2. This underscores that even perfect laboratory processes fail without rigorous bedside verification protocols.