School of Medical and Health Sciences, Bangor University, Bangor, UK.
BMC Public Health. 2023 Jun 30;23(1):1271. doi: 10.1186/s12889-023-15937-9.
Patient and public involvement (PPI) is increasingly seen as something that is integral to research and of importance to research funders. There is general recognition that PPI is the right thing to do for both moral and practical reasons. The aim of this review of reviews is to examine how PPI can be done 'properly' by looking at the evidence that exists from published reviews and assessing it against the UK Standards for Public Involvement in Research, as well as examining the specific features of population health research that can make PPI more challenging.
A review of reviews and development of best practice guidance was carried out following the 5-stage Framework Synthesis method.
In total 31 reviews were included. There is a lack of current research or clarity around Governance and Impact when findings are mapped against UK Standards for Public Involvement in Research. It was also clear that there is little knowledge around PPI with under-represented groups. There are gaps in knowledge about how to ensure key specific attributes of population health research are addressed for PPI team members - particularly around how to deal with complexity and the data-driven nature of the research. Four tools were produced for researchers and PPI members to further improve their PPI activity within population health research and health research more generally, including a framework of recommended actions to address PPI in population health research, and guidance on integrating PPI based on the UK Standards for Public Involvement in Research.
Facilitating PPI in population health research is challenging due to the nature of this type of research and there is far less evidence on how to do PPI well in this context. The tools can help researchers identify key aspects of PPI that can be integrated when designing PPI within projects. Findings also highlight specific areas where more research or discussion is needed.
患者和公众参与(PPI)越来越被视为研究不可或缺的一部分,对研究资助者也很重要。人们普遍认识到,出于道德和实际原因,PPI 是正确的做法。本次综述的目的是通过查看已发表综述中的现有证据,并根据英国研究中公众参与的标准对其进行评估,以及研究人群健康研究的具体特征,这些特征可能使 PPI 更具挑战性,从而检查如何“正确”地进行 PPI。
采用 5 阶段框架综合方法进行综述和最佳实践指南的制定。
共纳入 31 项综述。当将研究结果与英国公众参与研究标准进行映射时,在治理和影响方面存在当前研究或缺乏明确性。此外,对于代表性不足的群体,PPI 知识也很少。关于如何确保 PPI 团队成员解决人群健康研究的特定属性的知识存在差距,特别是如何处理研究的复杂性和数据驱动性质。为研究人员和 PPI 成员制作了四个工具,以进一步提高他们在人群健康研究和更广泛的健康研究中的 PPI 活动,包括一个建议行动框架,以解决人群健康研究中的 PPI 问题,以及基于英国公众参与研究标准的 PPI 整合指南。
由于这种类型研究的性质,在人群健康研究中促进 PPI 具有挑战性,而且关于如何在这种情况下做好 PPI 的证据要少得多。这些工具可以帮助研究人员确定在项目中设计 PPI 时可以整合的 PPI 的关键方面。研究结果还突出了需要更多研究或讨论的特定领域。