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肯尼亚严重儿童疾病遗传队列研究中的社区参与和知情同意经验。

Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya.

机构信息

Kenya Medical Research Institute (KEMRI) Wellcome Trust Research Programme, Kilifi, Kenya.

出版信息

BMC Med Ethics. 2010 Jul 15;11:13. doi: 10.1186/1472-6939-11-13.

Abstract

BACKGROUND

The potential contribution of community engagement to addressing ethical challenges for international biomedical research is well described, but there is relatively little documented experience of community engagement to inform its development in practice. This paper draws on experiences around community engagement and informed consent during a genetic cohort study in Kenya to contribute to understanding the strengths and challenges of community engagement in supporting ethical research practice, focusing on issues of communication, the role of field workers in 'doing ethics' on the ground and the challenges of community consultation.

METHODS

The findings are based on action research methods, including analysis of community engagement documentation and the observations of the authors closely involved in their development and implementation. Qualitative and quantitative content analysis has been used for documentation of staff meetings and trainings, a meeting with 24 community leaders, and 40 large public and 70 small community group meetings. Meeting minutes from a purposive sample of six community representative groups have been analysed using a thematic framework approach.

RESULTS

Field workers described challenges around misunderstandings about research, perceived pressure for recruitment and challenges in explaining the study. During consultation, leaders expressed support for the study and screening for sickle cell disease. In community meetings, there was a common interpretation of research as medical care. Concerns centred on unfamiliar procedures. After explanations of study procedures to leaders and community members, few questions were asked about export of samples or the archiving of samples for future research.

CONCLUSIONS

Community engagement enabled researchers to take account of staff and community opinions and issues during the study and adapt messages and methods to address emerging ethical challenges. Field workers conducting informed consent faced complex issues and their understanding, attitudes and communication skills were key influences on ethical practice. Community consultation was a challenging concept to put into practice, illustrating the complexity of assessing information needs and levels of deliberation that are appropriate to a given study.

摘要

背景

社区参与在解决国际生物医学研究中的伦理挑战方面具有潜在贡献,这一点已经得到了很好的描述,但在实践中为其发展提供信息的社区参与经验相对较少。本文借鉴了肯尼亚一项遗传队列研究中社区参与和知情同意方面的经验,旨在深入了解社区参与在支持伦理研究实践方面的优势和挑战,重点关注沟通、实地工作人员在“实践伦理”方面的作用以及社区咨询方面的挑战。

方法

研究结果基于行动研究方法,包括对社区参与文件的分析以及作者对其发展和实施的密切观察。工作人员会议和培训的文件、与 24 位社区领导的会议以及 40 次大型公众会议和 70 次小型社区会议都采用了定性和定量的内容分析方法。从六个社区代表小组中抽取了有针对性的样本,对会议记录进行了分析,采用了主题框架方法。

结果

实地工作人员描述了研究方面的误解、招募压力以及解释研究的困难等方面的挑战。在咨询过程中,领导们表示支持该研究和镰状细胞病筛查。在社区会议上,研究被普遍解释为医疗保健。关注的焦点是不熟悉的程序。在向领导和社区成员解释了研究程序之后,几乎没有人询问样本的出口或样本存档以备将来研究之用。

结论

社区参与使研究人员能够在研究过程中考虑到工作人员和社区的意见和问题,并调整信息和方法,以应对新出现的伦理挑战。进行知情同意的实地工作人员面临着复杂的问题,他们的理解、态度和沟通技巧是影响伦理实践的关键因素。社区咨询是一个具有挑战性的实践概念,说明了评估信息需求和适当的审议水平的复杂性,这对于给定的研究是很重要的。

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