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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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A case of delayed hemolytic transfusion reaction in sickle cell disease patient

Ashu Dogra1, Meena Sidhu2

  • 1Department of Blood Bank, SBKSMIRC, Vadodara, Gujarat, India.

Asian Journal of Transfusion Science
|September 9, 2016
PubMed

Sickle cell disease (SCD) is autosomal recessive, genetically transmitted hemoglobinopathy responsible for considerable morbidity and mortality. It is prevalent in many parts of India including Central India, where the prevalence in different communities has ranged from 9.4% to 22%. Perioperative management may include transfusion of red blood cells. Hemolytic transfusion reactions can occur, and these can be either acute or delayed. We present a case of delayed hemolytic transfusion reaction in a patient with SCD.

Keywords:
Delayed hemolytic transfusion reactionhemolysissickle cell disease

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