Navigating Transfusion Therapy in Sickle Cell Disease

This chapter explores the challenges of managing transfusion therapy for patients with sickle cell disease, detailing the risks of increased iron levels and alloimmunization. It underscores the importance of monitoring hemoglobin levels and the need for customized blood matching to prevent complications. Emerging treatments like stem cell transplants and gene therapy are also discussed, highlighting ongoing challenges in the field.