为非洲病原体基因组研究和生物库制定一个与环境和文化相关的惠益分享框架:一种审慎的专家方法。

IF 3 1区 哲学 Q1 ETHICS
Pamela Emefa Selormey, Irene H Tsey, John Ganle, Patricia Akweongo, Paulina Tindana
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引用次数: 0

摘要

背景:在全球范围内,研究人员正在努力实施基因组学研究和生物银行的利益分享计划。在非洲的情况下,目前有有限的利益分享框架来指导研究人员,有些在做决定时往往依赖于个人关系和判断。因此,有人呼吁为非洲的病原研究和生物银行制定与环境和文化相关的惠益分享框架。本研究响应了这一呼吁,采用专家审议的方法,提出并制定了病原体基因组研究和生物银行的利益分享框架。方法:采用协商式专家关键举报人访谈法收集资料。共有25名与会者,包括基因组学研究人员、政策制定者、《名古屋议定书》联络人、机构审查委员会成员、赞助者以及基因组学和生物银行领域的专家,有意从12个国家取样。设计和使用了开放式主题指南,以促进访谈。访谈探讨了诸如利益分享框架的必要性、支持利益分享实践的原则以及可能的利益分享框架的主要特征等问题。采访以英语进行,录音和转录。将转录本导入Nvivo 14软件,使用框架方法进行编码和分析,以进行定性数据分析。结果:与会者报告了在制定利益分享框架时需要考虑的关键问题。其中包括分享惠益的动机、惠益分享框架的关键要素和监测框架执行情况的建议。基于这些专家的回应,我们提出并开发了一个三阶段框架。第一阶段提出了背景惠益分享过程,包括惠益分享过程、迭代惠益分享周期和惠益分享后的责任。第二阶段包括实施阶段,其中有关于逐步实现第一阶段三个领域的模板;第三阶段侧重于工作计划,以适应未来出现的问题,如制定战略,制定利益分享的最佳做法,努力公布选定的战略,并实施选定的利益分享。结论:本研究中使用的审议方法不仅允许识别上下文和文化相关因素,而且还允许反射性决策。制定的框架有可能为病原体基因组利益攸关方在其研究规划中确定和实施惠益分享机会提供实际指导。然而,需要更多的实证研究来测试和评估该框架。临床试验号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developing a contextually and culturally relevant benefit-sharing framework for pathogen genomic research and biobanking in africa: a deliberative expert approach.

Background: Globally, researchers are struggling to implement benefit-sharing plans in genomics research and biobanking. In the African context, there are currently limited benefit-sharing frameworks to guide researchers, and some often rely on personal relationships and judgments in making decisions. Consequently, there have been calls for the development of contextually and culturally relevant benefit-sharing frameworks for pathogenic research and biobanking in Africa. This study responds to that call by using a deliberative experts approach to propose and develop a benefit-sharing framework for pathogen genomic research and biobanking.

Methods: Data were collected through deliberative expert key informant interviews. A total of 25 participants, comprising genomics researchers, policymakers, Nagoya Protocol Focal persons, members of institutional review boards, Sponsors and Experts in the field of genomics and biobanking were purposively sampled from 12 countries. Open-ended topic guides were designed and used to facilitate the interviews. The interviews explored issues such as the need for a benefit-sharing framework, the principles underpinning the practice of benefit-sharing, and key features of a possible benefit-sharing framework. Interviews were conducted in English, audio-recorded, and transcribed. Transcripts were imported into Nvivo 14 software, coded and analysed using the framework approach for qualitative data analysis.

Results: The participants reported on the key issues to consider in the development of a benefit-sharing framework. These included motivations for sharing benefits, key elements of a benefit-sharing framework and suggestions for monitoring the implementation of the framework. Based on these expert responses, we proposed and developed a three-phase framework. The first phase presents the contextual benefit-sharing process, which includes the benefit-sharing process, iterative benefit-sharing cycles and post-benefit-sharing responsibilities. The second phase comprises the implementation phase with templates on a step-by-step approach to achieving the three areas in phase 1 and the third concentrates on workplans to accommodate future emerging issues such as designing strategies to map out best practices on benefit-sharing, making efforts to publish the selected strategy and implementing the selected benefit-sharing.

Conclusions: The deliberative approach used in this study allowed for not only contextually and culturally relevant factors to be identified but also enabled reflexive decision-making. The framework developed has the potential to provide practical guidance to pathogen genomic stakeholders in the identification and implementation of benefit-sharing opportunities in their research programmes. More empirical studies are however required to test and evaluate the framework.

Clinical trial number: Not applicable.

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来源期刊
BMC Medical Ethics
BMC Medical Ethics MEDICAL ETHICS-
CiteScore
5.20
自引率
7.40%
发文量
108
审稿时长
>12 weeks
期刊介绍: BMC Medical Ethics is an open access journal publishing original peer-reviewed research articles in relation to the ethical aspects of biomedical research and clinical practice, including professional choices and conduct, medical technologies, healthcare systems and health policies.
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