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印度镰状细胞病:从卫生系统视角出发的范围综述,旨在确定研究和行动议程。

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

机构信息

Health equity cluster, Institute of Public Health, Bangalore, India.

Tribal Health Resource Centre, Vivekananda Tribal Welfare Center, BR Hills, Karnataka, India.

出版信息

BMJ Glob Health. 2021 Feb;6(2). doi: 10.1136/bmjgh-2020-004322.

Abstract

INTRODUCTION

Sickle cell disease (SCD) disproportionately impacts Adivasi (tribal) communities in India. Current research has focused on epidemiological and biomedical aspects but there has been scarce research on social determinants and health systems aspects. Given its fragmented distribution, resources and programmes have emerged in west and central India. This scoping review seeks to identify geographical and evidence gaps for action on SCD from a health systems lens.

METHODS

We followed a scoping review protocol, using Google Scholar and PubMed for published literature. Keywords used included sickle cell anaemia/disease, health systems, tribal and India. We used Google search for grey literature. We compiled a list of 55 records (of which 35 were retained), with about half pertaining directly to India and others relevant to similar settings. Results were organised and analysed using the WHO health systems framework to identify geographical and evidence gaps.

RESULTS

We found substantial literature on biomedical and clinical aspects of SCD but little on the design and implementation of programmes in community and Adivasi-specific contexts as well as on social determinants of SCD. There were regional gaps in knowledge in southern and northeast India. Wherever community-based programmes exist, they have originated in civil society initiatives and relatively limited state-led primary healthcare-based efforts pointing to weak agenda setting.

CONCLUSION

Both research and action on SCD especially among tribal populations need immediate attention. While geospatial epidemiology has been well understood, gaps remain in context-specific knowledge for action in several parts, as well as evidence gaps across several health system building blocks, including governance and financing of care. Despite publication of a draft policy, delayed adoption and lapses in implementation have limited the response largely to local communities and non-governmental organisations.

摘要

简介

镰状细胞病(SCD)在印度的 Adivasi(部落)社区中不成比例地发生。目前的研究集中在流行病学和生物医学方面,但对社会决定因素和卫生系统方面的研究甚少。鉴于其分散的分布,资源和计划已经在印度西部和中部出现。本范围审查旨在从卫生系统角度确定 SCD 行动的地理和证据差距。

方法

我们遵循范围审查方案,使用 Google Scholar 和 PubMed 查找已发表的文献。使用的关键词包括镰状细胞贫血/疾病、卫生系统、部落和印度。我们使用 Google 搜索灰色文献。我们编制了一份 55 条记录的清单(其中 35 条被保留),其中约一半直接涉及印度,其他则与类似情况相关。使用世界卫生组织卫生系统框架对结果进行组织和分析,以确定地理和证据差距。

结果

我们发现了大量关于 SCD 的生物医学和临床方面的文献,但关于在社区和 Adivasi 特定背景下设计和实施计划以及 SCD 的社会决定因素的文献很少。在印度南部和东北部地区存在知识上的区域差距。只要存在基于社区的计划,它们就源于民间社会的倡议,而相对有限的国家主导的基层医疗保健为基础的努力表明议程设置薄弱。

结论

特别是在部落人口中,SCD 的研究和行动都需要立即关注。虽然地理空间流行病学已经得到很好的理解,但在几个地区的具体背景知识方面仍然存在差距,并且在几个卫生系统建设方面也存在证据差距,包括护理的治理和融资。尽管发布了政策草案,但延迟通过和执行中的失误在很大程度上限制了反应,主要是针对当地社区和非政府组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0027/7896595/f86f8618e4de/bmjgh-2020-004322f01.jpg

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