Situational analysis of sickle cell disease in Gujarat, India

Background: Sickle cell disease (SCD) is a major public health concern in tribal community not only in Gujarat but also globally. Gujarat, a western state of India, has 89.12 lakh tribal populations and is expected to have at least 9,00,000 sickle cell trait and 70,000 SCD patients. The aim of the p...

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Main Authors: Deepak Saxena, Sandul Yasobant, Mahaveer Golechha
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Community Medicine
Subjects:
Online Access:http://www.ijcm.org.in/article.asp?issn=0970-0218;year=2017;volume=42;issue=4;spage=218;epage=221;aulast=Saxena
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spelling doaj-2e736687344c4c3788a11c9d3efeb6f92020-11-24T23:40:16ZengWolters Kluwer Medknow PublicationsIndian Journal of Community Medicine0970-02181998-35812017-01-0142421822110.4103/ijcm.IJCM_284_16Situational analysis of sickle cell disease in Gujarat, IndiaDeepak SaxenaSandul YasobantMahaveer GolechhaBackground: Sickle cell disease (SCD) is a major public health concern in tribal community not only in Gujarat but also globally. Gujarat, a western state of India, has 89.12 lakh tribal populations and is expected to have at least 9,00,000 sickle cell trait and 70,000 SCD patients. The aim of the present review is to document the prevalence of SCD in various communities and various screening methods adapted. Methodology: An in-depth literature review was carried out using available search engines such as Cochrane Library, PubMed, Scopus etc. and published articles, and government reports/policy documents with reference to SCD were gathered. Results: A total of 17 original research articles and 2 policy/program documents are included in this review. The review suggests a prevalence of 0.6%–35% studies conducted among medical students, tribal schoolchildren, and tribal adolescents, with diverse screening methodologies. Conclusion: A diverse prevalence is observed in this review. Various screening methods such as dithionite turbidity test/hemoglobin/high-performance liquid chromatography methods were used to estimate the prevalence, citing the need for standardization. It was also found that not only tribal population, but also nontribal population have the risk of getting SCD that needs to be further investigated properly. Qualitative studies with SCD patients are required to understand the quality of life and morbidity pattern.http://www.ijcm.org.in/article.asp?issn=0970-0218;year=2017;volume=42;issue=4;spage=218;epage=221;aulast=SaxenaGujaratsickle cellsickle cell diseases
collection DOAJ
language English
format Article
sources DOAJ
author Deepak Saxena
Sandul Yasobant
Mahaveer Golechha
spellingShingle Deepak Saxena
Sandul Yasobant
Mahaveer Golechha
Situational analysis of sickle cell disease in Gujarat, India
Indian Journal of Community Medicine
Gujarat
sickle cell
sickle cell diseases
author_facet Deepak Saxena
Sandul Yasobant
Mahaveer Golechha
author_sort Deepak Saxena
title Situational analysis of sickle cell disease in Gujarat, India
title_short Situational analysis of sickle cell disease in Gujarat, India
title_full Situational analysis of sickle cell disease in Gujarat, India
title_fullStr Situational analysis of sickle cell disease in Gujarat, India
title_full_unstemmed Situational analysis of sickle cell disease in Gujarat, India
title_sort situational analysis of sickle cell disease in gujarat, india
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Community Medicine
issn 0970-0218
1998-3581
publishDate 2017-01-01
description Background: Sickle cell disease (SCD) is a major public health concern in tribal community not only in Gujarat but also globally. Gujarat, a western state of India, has 89.12 lakh tribal populations and is expected to have at least 9,00,000 sickle cell trait and 70,000 SCD patients. The aim of the present review is to document the prevalence of SCD in various communities and various screening methods adapted. Methodology: An in-depth literature review was carried out using available search engines such as Cochrane Library, PubMed, Scopus etc. and published articles, and government reports/policy documents with reference to SCD were gathered. Results: A total of 17 original research articles and 2 policy/program documents are included in this review. The review suggests a prevalence of 0.6%–35% studies conducted among medical students, tribal schoolchildren, and tribal adolescents, with diverse screening methodologies. Conclusion: A diverse prevalence is observed in this review. Various screening methods such as dithionite turbidity test/hemoglobin/high-performance liquid chromatography methods were used to estimate the prevalence, citing the need for standardization. It was also found that not only tribal population, but also nontribal population have the risk of getting SCD that needs to be further investigated properly. Qualitative studies with SCD patients are required to understand the quality of life and morbidity pattern.
topic Gujarat
sickle cell
sickle cell diseases
url http://www.ijcm.org.in/article.asp?issn=0970-0218;year=2017;volume=42;issue=4;spage=218;epage=221;aulast=Saxena
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AT mahaveergolechha situationalanalysisofsicklecelldiseaseingujaratindia
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