Literature DB >> 27065586

Hydroxyurea in Sickle Cell Disease: Our Experience in Western India.

S V Deshpande1, S S Bhatwadekar2, Parth Desai3, Tarang Bhavsar3, Ankit Patel3, Amey Koranne2, Arpan Mehta2, Shweta Khadse2.   

Abstract

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.

Entities:  

Keywords:  Hydroxyurea; Pain crisis; Sickle cell disesase

Year:  2015        PMID: 27065586      PMCID: PMC4788998          DOI: 10.1007/s12288-015-0542-1

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN: 0971-4502            Impact factor:   0.900


  22 in total

Review 1.  Hydroxyurea for the treatment of sickle cell anemia.

Authors:  Orah S Platt
Journal:  N Engl J Med       Date:  2008-03-27       Impact factor: 91.245

2.  Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease.

Authors:  Christopher D Reiter; Xunde Wang; Jose E Tanus-Santos; Neil Hogg; Richard O Cannon; Alan N Schechter; Mark T Gladwin
Journal:  Nat Med       Date:  2002-11-11       Impact factor: 53.440

3.  Treatment of sickle cell anemia with hydroxyurea and erythropoietin.

Authors:  M A Goldberg; C Brugnara; G J Dover; L Schapira; S Charache; H F Bunn
Journal:  N Engl J Med       Date:  1990-08-09       Impact factor: 91.245

4.  A multiparameter analysis of sickle erythrocytes in patients undergoing hydroxyurea therapy.

Authors:  K R Bridges; G D Barabino; C Brugnara; M R Cho; G W Christoph; G Dover; B M Ewenstein; D E Golan; C R Guttmann; J Hofrichter; R V Mulkern; B Zhang; W A Eaton
Journal:  Blood       Date:  1996-12-15       Impact factor: 22.113

5.  The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.

Authors:  Martin H Steinberg; William F McCarthy; Oswaldo Castro; Samir K Ballas; F Danny Armstrong; Wally Smith; Kenneth Ataga; Paul Swerdlow; Abdullah Kutlar; Laura DeCastro; Myron A Waclawiw
Journal:  Am J Hematol       Date:  2010-06       Impact factor: 10.047

6.  Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions.

Authors:  F D Armstrong; C H Pegelow; J C Gonzalez; A Martinez
Journal:  J Pediatr Psychol       Date:  1992-10

7.  Pain measurement in hospitalized adults with sickle cell painful episodes.

Authors:  S K Ballas; A Delengowski
Journal:  Ann Clin Lab Sci       Date:  1993 Sep-Oct       Impact factor: 1.256

8.  Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Authors:  S Charache; M L Terrin; R D Moore; G J Dover; F B Barton; S V Eckert; R P McMahon; D R Bonds
Journal:  N Engl J Med       Date:  1995-05-18       Impact factor: 91.245

Review 9.  Therapeutic approaches to hemoglobin switching in treatment of hemoglobinopathies.

Authors:  J A Stamatoyannopoulos; A W Nienhuis
Journal:  Annu Rev Med       Date:  1992       Impact factor: 13.739

Review 10.  The presentation, management and prophylaxis of sickle cell disease.

Authors:  S C Davies; M Brozović
Journal:  Blood Rev       Date:  1989-03       Impact factor: 8.250

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  4 in total

Review 1.  Fetal hemoglobin in sickle cell anemia.

Authors:  Martin H Steinberg
Journal:  Blood       Date:  2020-11-19       Impact factor: 22.113

2.  Paper-based microchip electrophoresis for point-of-care hemoglobin testing.

Authors:  Muhammad Noman Hasan; Arwa Fraiwan; Ran An; Yunus Alapan; Ryan Ung; Asya Akkus; Julia Z Xu; Amy J Rezac; Nicholas J Kocmich; Melissa S Creary; Tolulope Oginni; Grace Mfon Olanipekun; Fatimah Hassan-Hanga; Binta W Jibir; Safiya Gambo; Anil K Verma; Praveen K Bharti; Suchada Riolueang; Takdanai Ngimhung; Thidarat Suksangpleng; Priyaleela Thota; Greg Werner; Rajasubramaniam Shanmugam; Aparup Das; Vip Viprakasit; Connie M Piccone; Jane A Little; Stephen K Obaro; Umut A Gurkan
Journal:  Analyst       Date:  2020-03-03       Impact factor: 4.616

Review 3.  Sickle cell disease in India: a scoping review from a health systems perspective to identify an agenda for research and action.

Authors:  Vineet Raman; Prashanth N Srinivas; Tanya Seshadri; Sangeetha V Joice
Journal:  BMJ Glob Health       Date:  2021-02

Review 4.  Hydroxyurea and blood transfusion therapy for Sickle cell disease in South Asia: inconsistent treatment of a neglected disease.

Authors:  Thamal Darshana; David Rees; Anuja Premawardhena
Journal:  Orphanet J Rare Dis       Date:  2021-03-23       Impact factor: 4.123

  4 in total

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