Acquired hemoglobin variants and exposure to glucose-6-phosphate dehydrogenase deficient red blood cell units during exchange transfusion for sickle cell disease in a patient requiring antigen-matched blood

Author:

Raciti Patricia M.1,Francis Richard O.1,Spitalnik Patrice F.1,Schwartz Joseph1,Jhang Jeffrey S.1

Affiliation:

1. Department of Pathology and Cell Biology; Columbia University Medical Center-NewYork-Presbyterian Hospital; New York; New York

Publisher

Wiley

Subject

Hematology,General Medicine

Reference31 articles.

1. Guidelines on the use of therapeutic apheresis in clinical practice-evidence-based approach from the Apheresis Applications Committee of the American Society for Apheresis;Szczepiorkowski;J Clin Apher,2010

2. Sickle cell disease: a review;Roseff;Immunohematology,2009

3. Phenotype matching of donor red blood cell units for nonalloimmunized sickle cell disease patients: a survey of 1182 North American laboratories;Osby;Arch Pathol Lab Med,2005

4. Antigen-matched donor blood in the transfusion management of patients with sickle cell disease;Tahhan;Transfusion,1994

5. Blood transfusions leading to apparent hemoglobin C, S, and O-Arab hemoglobinopathies;Kozarski;Arch Pathol Lab Med,2006

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