1 Professor of Primary and Community Care, Centre for Health Services Studies, University of Kent, UK.
2 Research Fellow, Centre for Research in Primary and Community Care, University of Hertfordshire, UK.
J Health Serv Res Policy. 2018 Apr;23(2):98-106. doi: 10.1177/1355819617750688.
Objectives To explore how embedded patient and public involvement is within mainstream health research following two decades of policy-driven work to underpin health research with patient and public involvement in England. Methods Realist evaluation using Normalization Process Theory as a programme theory to understand what enabled patient and public involvement to be embedded as normal practice. Data were collected through a national scoping and survey, and qualitative methods to track patient and public involvement processes and impact over time within 22 nationally funded research projects. Results In research studies that were able to create reciprocal working relationships and to embed patient and public involvement this was contingent on: the purpose of patient and public involvement being clear; public contributors reflecting research end-beneficiaries; researchers understanding the value of patient and public involvement; patient and public involvement opportunities being provided throughout the research and ongoing evaluation of patient and public involvement. Key contested areas included: whether to measure patient and public involvement impact; seeking public contributors to maintain a balance between being research-aware and an outsider standpoint seen as 'authentically' lay; scaling-up patient and public involvement embedded within a research infrastructure rather than risk token presence and whether patient and public involvement can have a place within basic science. Conclusions While patient and public involvement can be well-integrated within all types of research, policy makers should take account of tensions that must be navigated in balancing moral and methodological imperatives.
目的 探索在英格兰通过政策驱动工作将患者和公众参与纳入主流健康研究二十年后,嵌入式患者和公众参与在主流健康研究中的实施情况。
方法 使用规范化进程理论作为方案理论进行真实评估,以了解使患者和公众参与能够嵌入正常实践的原因。通过全国范围的调查和定性方法收集数据,以跟踪 22 个国家资助的研究项目中患者和公众参与过程及其随时间推移的影响。
结果 在能够建立互惠工作关系并嵌入患者和公众参与的研究中,这取决于以下几个方面:患者和公众参与的目的明确;公众参与者反映研究的最终受益者;研究人员理解患者和公众参与的价值;在整个研究过程中提供患者和公众参与机会,并对患者和公众参与进行持续评估。关键的争议领域包括:是否衡量患者和公众参与的影响;寻求公众参与者在保持研究意识和作为“真正”外行的观点之间取得平衡,被视为“真实”的观点;在研究基础设施中扩大嵌入式患者和公众参与,而不是冒着象征性参与的风险,以及患者和公众参与是否可以在基础科学中占有一席之地。
结论 虽然患者和公众参与可以很好地融入各种类型的研究中,但政策制定者应该考虑在平衡道德和方法学要求时必须应对的紧张局势。