Associations between ABO non‐identical platelet transfusions and patient outcomes—A multicenter retrospective analysis

Author:

Bougie Daniel W.1ORCID,Reese Sarah E.2ORCID,Birch Rebecca J.2,Bookwalter Deborah B.2,Mitchell Patrick K.2,Roh David3ORCID,Kreuziger Lisa Baumann1,Cable Ritchard G.4,Goel Ruchika5ORCID,Gottschall Jerome6,Hauser Ronald George7,Hendrickson Jeanne E.78ORCID,Hod Eldad A.9ORCID,Josephson Cassandra D.10ORCID,Kahn Stacie11,Kleinman Steven H.12,Mast Alan E.1,Ness Paul M.4,Roubinian Nareg H.13ORCID,Sloan Steven14,

Affiliation:

1. Blood Research Institute Versiti Milwaukee WI Milwaukee Wisconsin USA

2. Public Health and Epidemiology Practice, Westat Rockville Maryland USA

3. Columbia University New York New York USA

4. American Red Cross Scientific Affairs Farmington Connecticut USA

5. Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland USA

6. Medical Sciences Institute, Versiti Milwaukee Wisconsin USA

7. Department of Laboratory Medicine Yale University School of Medicine New Haven Connecticut USA

8. Department of Pathology and Laboratory Medicine, Center for Transfusion and Cellular Therapies Emory University School of Medicine Atlanta Georgia USA

9. Columbia University Irving Medical Center New York New York USA

10. Cancer and Blood Disorders Institute, Johns Hopkins All Children's Hospital, St. Petersburg, FL., and Departments of Oncology and Pediatrics Johns Hopkins University School of Medicine Baltimore Maryland USA

11. New York‐Presbyterian New York New York USA

12. University of British Columbia Victoria British Columbia Canada

13. Vitalant Research Institute San Francisco California USA

14. Children's Hospital Boston Boston Massachusetts USA

Abstract

AbstractBackgroundDue to platelet availability limitations, platelet units ABO mismatched to recipients are often transfused. However, since platelets express ABO antigens and are collected in plasma which may contain ABO isohemagglutinins, it remains controversial as to whether ABO non‐identical platelet transfusions could potentially pose harm and/or have reduced efficacy.Study Design and MethodsThe large 4‐year publicly available Recipient Epidemiology and Donor Evaluation Study‐III (REDS‐III) database was used to investigate patient outcomes associated with ABO non‐identical platelet transfusions. Outcomes included mortality, sepsis, and subsequent platelet transfusion requirements.ResultsFollowing adjustment for possible confounding factors, no statistically significant association between ABO non‐identical platelet transfusion and increased risk of mortality was observed in the overall cohort of 21,176 recipients. However, when analyzed by diagnostic category and recipient ABO group, associations with increased mortality for major mismatched transfusions were noted in two of eight subpopulations. Hematology/Oncology blood group A and B recipients (but not group O) showed a Hazard Ratio (HR) of 1.29 (95%CI: 1.03–1.62) and intracerebral hemorrhage group O recipients (but not groups A and B) showed a HR of 1.75 (95%CI: 1.10–2.80). Major mismatched transfusions were associated with increased odds of receiving additional platelet transfusion each post‐transfusion day (through day 5) regardless of the recipient blood group.DiscussionWe suggest that prospective studies are needed to determine if specific patient populations would benefit from receiving ABO identical platelet units. Our findings indicate that ABO‐identical platelet products minimize patient exposure to additional platelet doses.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

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