Abstract: Background: Thalassaemia is a autosomal recessive hereditary chronic blood disorder that does not allow the body to produce enough haemoglobin and red blood cells.The primary management is blood transfusions which leads to complications . Our study aims to to evaluate the clinical presentations and complications, observe the prescribing pattern , disease, to understand and improve the knowledge of study participants.
Materials and Methods: this is a prospective observational study, was conducted in the pediatrics department of tertiary care hospital(GGH-RIMS) in Kadapa, Andhra pradesh during the time period of 6 months, on 50 patients of both transfusion dependent and non-transfusion dependent thalassemia patients of all age groups involed in the study by taking informed consent form ..
Key words: Thalassemia major , deferasirox , deferiprone , blood transfusion..
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