Objective:
To investigate the risk of allergic transfusion reactions (ATRs) in patients with blood type O receiving B or AB plasma or platelets compared to those receiving O products, particularly in regions with high alpha-gal syndrome (AGS) prevalence.
Approach:
- Study Design: International, multicenter, retrospective cohort study of platelet and plasma transfusions from 2020 to 2024 across 40 sites in the US, Australia, Japan, Germany, and France.
- Data Collection: Analysis of 558,823 transfusions with a focus on ATR rates among blood type O patients receiving different ABO products.
- Risk Assessment: Comparison of ATR rates in high vs low AGS prevalence clusters, examining reaction severity and ABO group of transfused products.
Key Findings:
- Patients with blood type O receiving B or AB products had 3.93 times the risk of ATRs compared to those receiving O products in high AGS prevalence areas.
- In low AGS prevalence areas, no excess ATRs were detected for B or AB products.
- B products were associated with 4.48 times the risk of ATRs and AB products with 2.53 times the risk in high AGS prevalence clusters.
- Moderate to severe ATRs were significantly higher in high AGS prevalence areas, with a risk of 9.14 times for B products.
Interpretation:
The study provides epidemiologic evidence suggesting that B antigen-containing products may pose a transfusion risk in regions with high AGS prevalence.
Limitations:
- Retrospective design limited the ability to confirm AGS as the cause of observed reactions.
- Potential underreporting of ATRs due to reliance on passive clinician reporting.
- Geographic misclassification and other unrelated factors could have influenced findings.
Conclusion:
The findings indicate a need for hospitals in high AGS prevalence regions to evaluate local reaction patterns regarding B antigen-containing products.
Sources:
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
