Management of Patients with Sickle Cell Disease Using Transfusion Therapy: Guidelines and Complications.

Hematol Oncol Clin North Am

Transfusion, Tissue, & Apheresis, Children's Healthcare of Atlanta and Grady Health System Transfusion Services, Departments of Clinical Pathology and Pediatric Hematology, Emory University School of Medicine, 7105B Woodruff Memorial Building, 101 Woodruff Circle, Atlanta, GA 30322, USA. Electronic address:

Published: June 2016

Red blood cell (RBC) transfusion therapy is a key component of comprehensive management of patients with sickle cell disease (SCD) and has increased over time as a means of primary and secondary stroke prevention. RBC transfusions also prove to be lifesaving for many acute sickle cell-related complications. Although episodic and chronic transfusion therapy has significantly improved the morbidity and mortality of patients with SCD, transfusions are not without adverse effects. This review addresses RBC transfusion methods, evidence-based and/or expert panel-based consensus on indications for chronic and episodic transfusion indications, and strategies to prevent and manage transfusion-related complications.

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Source
http://dx.doi.org/10.1016/j.hoc.2016.01.011DOI Listing

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