Hydroxyurea in Sickle Cell Disease: Our Experience in Western India

被引:0
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作者
S. V. Deshpande
S. S. Bhatwadekar
Parth Desai
Tarang Bhavsar
Ankit Patel
Amey Koranne
Arpan Mehta
Shweta Khadse
机构
[1] GMERS Medical college Gotri,Department of Medicine
[2] Hemocare Centre,undefined
[3] Junior Resident GMERS Gotri,undefined
关键词
Sickle cell disesase; Hydroxyurea; Pain crisis;
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摘要
Sickle cell disease (SCD) is common in tribal belt of Gujarat, but not addressed effectively as it should be with effective use of Hydroxyurea, supportive care and counseling. In our single centre study of 70 patients of SCD who were only on Folic acid and Blood transfusion support, were analyzed and followed up for 1 year in terms of their clinical symptoms, Blood transfusion requirement, laboratory parameters before and after Hydroxyurea therapy. We found statistically significant improvement in clinical symptoms and positive changes in laboratory parameters studied. This validates the well established role of Hydroxyurea in SCD as seen in the various international trials. Hence it is imperative that the well documented benefits of Hydroxyurea in various International studies should be translated into clinical practice. SCD should be treated like a chronic disorder needing preventive therapy in form of Hydroxyurea and counseling with regular follow up.
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页码:215 / 220
页数:5
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