Adverse events of red blood cell transfusions in patients with sickle cell disease.

Transfus Apher Sci

The Children's Hospital of Philadelphia, Departments of Pediatrics and Pathology and Laboratory Medicine, The School of Medicine at the University of Pennsylvania, 3615 Civic Center Boulevard, Abramson Research Building Room 316D, Philadelphia, PA 19104, USA. Electronic address:

Published: October 2022

AI Article Synopsis

  • - Blood transfusions are frequently used to treat patients with sickle cell disease (SCD) and related complications, but these patients have specific risks during transfusions.
  • - The text reviews various adverse events related to blood transfusions, including alloimmunization, hemolytic reactions, hyperviscosity, and iron overload, which are especially relevant to SCD patients.
  • - It offers insights into risk factors, strategies to reduce these risks, and management tips for healthcare providers dealing with transfusions in patients with SCD.

Article Abstract

Blood transfusion is a common medical intervention for patients with sickle cell disease (SCD) and disease related complications. While patients with SCD are at risk for all transfusion related adverse events defined by the National Healthcare Safety Network (NHSN) Biovigilance Component Hemovigilance Module Surveillance Protocol, they are uniquely susceptible to certain adverse events. This review discusses risk factors, mitigation strategies, and management recommendations for alloimmunization, hemolytic transfusion reactions, hyperviscosity and transfusion-associated iron overload in the context of SCD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149091PMC
http://dx.doi.org/10.1016/j.transci.2022.103557DOI Listing

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