Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional Study.

IF 1.2 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Hemoglobin Pub Date : 2023-11-01 Epub Date: 2024-01-22 DOI:10.1080/03630269.2023.2300675
Bontha V Babu, Yogita Sharma, Parikipandla Sridevi, Shaily B Surti, Deepa Bhat, Manoranjan Ranjit, Godi Sudhakar, Jatin Sarmah
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Abstract

Sickle cell disease (SCD) affects 5% of the global population, with over 300,000 infants born yearly. In India, 73% of those with the sickle hemoglobin gene belong to indigenous tribes in remote regions lacking proper healthcare. Despite the prevalence of SCD, India lacked state-led public health programs until recently, leaving a gap in screening and comprehensive care. Hence, the Indian Council of Medical Research conducted implementation research to address this gap. This paper discusses the development and impact of the program, including screening and treatment coverage for SCD in tribal areas. With a quasi-experimental design, this study was conducted in six tribal-dominated districts in three phases - formative, intervention, and evaluation. The intervention included advocacy, partnership building, building the health system's capacity and community mobilization, and enabling the health systems to screen and manage SCD patients. The capacity building included improving healthcare workers' skills through training and infrastructure development of primary healthcare (PHC) facilities. The impact of the intervention is visible in terms of people's participation (54%, 76% and 93% of the participants participated in some intervention activities, underwent symptomatic screening and demanded the continuity of the program, respectively), and improvement in SCD-related knowledge of the community and health workers (with more than 50% of net change in many of the knowledge-related outcomes). By developing screening and treatment models, this intervention model demonstrated the feasibility of SCD care at the PHC level in remote rural areas. This accessible approach allows the tribal population in India to routinely seek SCD care at their local PHCs, offering great convenience. Nevertheless, additional research employing rigorous methodology is required to fine-tune the model. National SCD program may adopt this model, specifically for community-level screening and management of SCD in remote and rural areas.

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加强印度部落人口镰状细胞病筛查和管理的卫生系统和社区动员:一项干预性研究。
镰状细胞病(SCD)影响着全球 5%的人口,每年有 30 多万婴儿出生。在印度,73% 的镰状血红蛋白基因携带者属于偏远地区的土著部落,他们缺乏适当的医疗保健。尽管 SCD 的发病率很高,但印度直到最近才开始实施由国家主导的公共卫生计划,因此在筛查和综合治疗方面存在空白。因此,印度医学研究理事会开展了实施研究,以弥补这一不足。本文讨论了该计划的发展和影响,包括 SCD 在部落地区的筛查和治疗覆盖率。这项研究采用准实验设计,在六个以部落为主的地区分三个阶段进行--形成、干预和评估。干预措施包括宣传、建立伙伴关系、建设卫生系统的能力和社区动员,以及使卫生系统能够筛查和管理 SCD 患者。能力建设包括通过培训和初级卫生保健(PHC)设施的基础设施建设来提高医护人员的技能。干预措施的影响体现在人们的参与度上(分别有 54%、76% 和 93% 的参与者参与了某些干预活动、接受了症状筛查并要求继续实施该计划),以及社区和医疗工作者对 SCD 相关知识的掌握程度上(许多知识相关结果的净变化超过了 50%)。通过开发筛查和治疗模式,该干预模式证明了在偏远农村地区的初级保健中心开展 SCD 护理的可行性。这种便捷的方法使印度的部落人口能够在当地的初级保健中心定期寻求 SCD 治疗,为他们提供了极大的便利。不过,还需要采用严格的方法进行更多的研究,以便对该模式进行微调。国家 SCD 计划可以采用这种模式,专门用于偏远和农村地区社区一级的 SCD 筛查和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hemoglobin
Hemoglobin 医学-生化与分子生物学
CiteScore
1.70
自引率
10.00%
发文量
59
审稿时长
3 months
期刊介绍: Hemoglobin is a journal in the English language for the communication of research and information concerning hemoglobin in humans and other species. Hemoglobin publishes articles, reviews, points of view The journal covers topics such as: structure, function, genetics and evolution of hemoglobins biochemical and biophysical properties of hemoglobin molecules characterization of hemoglobin disorders (variants and thalassemias), consequences and treatment of hemoglobin disorders epidemiology and prevention of hemoglobin disorders (neo-natal and adult screening) modulating factors methodology used for diagnosis of hemoglobin disorders
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