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- Title
Transfusing children with sickle cell disease using blood group genotyping when the pool of Black donors is limited.
- Authors
Leiva‐Torres, Gabriel André; Cigna, Maude; Constanzo‐Yanez, Jessica; St‐Louis, Maryse; Perreault, Josée; Lavoie, Josée; Laflamme, Geneviève; Lewin, Antoine; Pastore, Yves; Robitaille, Nancy
- Abstract
Background: Red blood cell transfusion is an effective treatment for patients with sickle cell disease (SCD). Alloimmunization can occur after a single transfusion, limiting further usage of blood transfusion. It is recommended to match for the ABO, D, C, E, and K antigens to reduce risks of alloimmunization. However, availability of compatible blood units can be challenging for blood providers with a limited number of Black donors. Study Design and Methods: A prospective cohort of 205 pediatric patients with SCD was genotyped for the RH and FY genes. Transfusion and alloimmunization history were collected. Our capacity to find RhCE‐matched donors was evaluated using a database of genotyped donors. Results: Nearly 9.8% of patients carried a partial D variant and 5.9% were D‐. Only 45.9% of RHCE alleles were normal, with the majority of variants affecting the RH5 (e) antigen. We found an alloimmunization prevalence of 20.7% and a Rh alloimmunization prevalence of 7.1%. Since Black donors represented only 1.40% of all blood donors in our province, D‐ Caucasian donors were mostly used to provide phenotype matched products. Compatible blood for patients with rare Rh variants was found only in Black donors. A donor with compatible RhCE could be identified for all patients. Conclusion: Although Rh‐compatible donors were identified, blood units might not be available when needed and/or the extended phenotype or ABO group might not match the patient. A greater effort has to be made for the recruitment of Black donors to accommodate patients with SCD.
- Subjects
SICKLE cell anemia; BLOOD groups; RED blood cell transfusion; BLOOD diseases; CHILD patients
- Publication
Transfusion, 2024, Vol 64, Issue 4, p716
- ISSN
0041-1132
- Publication type
Article
- DOI
10.1111/trf.17778