Volume 59, Issue 6 pp. 1911-1915
BRIEF REPORT

Fatal acute hemolytic transfusion reaction due to anti-B from a platelet apheresis unit stored in platelet additive solution

Raisa Balbuena-Merle

Raisa Balbuena-Merle

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut

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F. Bernadette West

F. Bernadette West

American Red Cross, Farmington, Connecticut

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Christopher A. Tormey

Christopher A. Tormey

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut

Pathology & Laboratory Medicine Service, VA Connecticut Healthcare System, West Haven, Connecticut

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Jeanne E. Hendrickson

Corresponding Author

Jeanne E. Hendrickson

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut

Address reprint requests to: Jeanne E. Hendrickson, MD, Department of Laboratory Medicine, Yale University School of Medicine, 330 Cedar Street, CB 405, New Haven, CT 06520-8035; e-mail: [email protected]Search for more papers by this author
First published: 13 March 2019
Citations: 20

Abstract

BACKGROUND

Hemolytic transfusion reactions from out-of-group plasma in platelet (PLT) transfusions are uncommon, with most involving passive transfer of anti-A. Only rare reactions have ever been reported due to anti-B.

STUDY DESIGN AND METHODS

An apheresis PLT product was donated by a blood group O male, processed using PLT additive solution, and pathogen reduced. Postreaction recipient testing included an antibody screen using gel technology, a direct antiglobulin test (DAT) using immunoglobulin G and C3, and an eluate against group O and B cells. Postreaction donor testing included measuring anti-B titers in saline, with and without anti-human globulin.

RESULTS

A 60-year-old blood group B patient with relapsed acute myeloid leukemia developed confusion, fever, and hypotension within hours after a blood group O PLT transfusion. The posttransfusion reaction evaluation was remarkable for a positive DAT 3+ for C3; the eluate showed anti-B. Rapid extravascular hemolysis occurred, with a 50% decline in hemoglobin, a high lactate dehydrogenase, and a high bilirubin. She was resuscitated with fluids, blood products, pressors, and oxygen and died of asystole 60 hours later. The donor's anti-B titers were 128 by tube testing at immediate spin and 512 at the anti-human globulin phase. Notably, a group B patient at a different hospital received a split of the same apheresis unit, with no reaction.

CONCLUSION

To our knowledge, this is the first fatality reported from passively transfused anti-B. The fact that one transfusion recipient died whereas another did not have any reported reaction highlights the potential importance of recipient variables in isohemagglutinin-mediated hemolysis.

CONFLICT OF INTEREST

The authors have disclosed no conflicts of interest.

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