Blood transfusion profile of Beta-Thalassemia Major patients attending a tertiary care hospital
Keywords:
β thalassemia, transfusion, chelation.Abstract
Background: Beta (β) thalassemia major is most common monogenic disorder in the world. Around 1,00,000 children are born each year with the severe homozygous state of the disease in India. The objectives of this study was to assess clinical data and the blood transfusion profile of Beta thalassemia major patients attending tertiary care hospital. This was undertaken as very few studies have been done in this region of the vast country.
Methods: The study was done at a tertiary care teaching hospital from January 2014 to December 2014. Universal sampling method was used and 35 β thalassemia major patients who received blood transfusions at 2 to 4 weeks interval in the hospital were included in this study. Clinical details and blood transfusion record was collected on proforma for all patients and data interpreted.
Result: Males (80%) outnumbered females (20%) with male to female ratio of 4:1. Nearly half of the study population was aged between 10 to 12 years (51.43). Majority of the patients had one blood transfusion per month (91.43%) and were on chelation therapy (71.43%). Majority of the patients received 100 to 125 blood transfusions during their lifetime        (28.57 %). Least number of blood transfusions of more than 250 transfusions was taken by one patient (2.86 %).
Conclusion: The present study describes the transfusion profile of β thalassemia major patients attending the tertiary care hospital and emphasizes on maintenance of transfusion record of b thalassemia major patients for better management of these patients.
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DOI:Â 10.21276/APALM.1269
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Copyright (c) 2017 Mallikarjun Adiveppa Pattanashetti, Ganga S Pilli, Laxmi Pattanashetti
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