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Post-transfusion hyperhemolysis syndrome in a patient with beta thalassemia major
Ganesh Kasinathan1, Jameela Sathar1
1Department of Haematology Ampang Hospital Ampang Malaysia.
Abstract:
Hyperhemolysis syndrome (HS) is characterized by the occurrence of severe anemia with post-transfusion hemoglobin and hematocrit levels being markedly lower than those present prior to transfusion. A high index of suspicion of HS in a multi-transfused thalassemia patient allows prompt institution of therapy resulting in improved survival outcome.
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