Nicholls Stuart G, Carroll Kelly, Weijer Charles, Goldstein Cory E, Brehaut Jamie, Sood Manish M, Al-Jaishi Ahmed, Basile Erika, Grimshaw Jeremy M, Garg Amit X, Taljaard Monica
Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Department of Philosophy, Western University, London, Canada.
Can J Kidney Health Dis. 2020 Oct 26;7:2054358120964119. doi: 10.1177/2054358120964119. eCollection 2020.
Pragmatic cluster randomized trials (CRTs) offer an opportunity to improve health care by answering important questions about the comparative effectiveness of treatments using a trial design that can be embedded in routine care. There is a lack of empirical research that addresses ethical issues generated by pragmatic CRTs in hemodialysis.
To identify stakeholder perceptions of ethical issues in pragmatic CRTs conducted in hemodialysis.
Qualitative study using semi-structured interviews.
In-person or telephone interviews with an international group of stakeholders.
Stakeholders (clinical investigators, methodologists, ethicists and research ethics committee members, and other knowledge users) who had been involved in the design or conduct of a pragmatic individual patient or cluster randomized trial in hemodialysis, or their role would require them to review and evaluate pragmatic CRTs in hemodialysis.
Interviews were conducted in-person or over the telephone and were audio-recorded with consent. Recorded interviews were transcribed verbatim prior to analysis. Transcripts and field notes were analyzed using a thematic analysis approach.
Sixteen interviews were conducted with 19 individuals. Interviewees were largely drawn from North America (84%) and were predominantly clinical investigators (42%). Six themes were identified in which pragmatic CRTs in hemodialysis raise ethical issues: (1) patients treated with hemodialysis as a vulnerable population, (2) appropriate approaches to informed consent, (3) research burdens, (4) roles and responsibilities of gatekeepers, (5) inequities in access to research, and (6) advocacy for patient-centered research and outcomes.
Participants were largely from North America and did not include research staff, who may have differing perspectives.
The six themes reflect concerns relating to individual rights, but also the need to consider population-level issues. To date, concerns regarding inequity of access to research and the need for patient-centered research have received less coverage than other, well-known, issues such as consent. Pragmatic CRTs offer a potential approach to address equity concerns and we suggest future ethical analyses and guidance for pragmatic CRTs in hemodialysis embed equity considerations within them. We further note the potential for the co-creation of health data infrastructure with patients which would aid care but also facilitate patient-centered research. These present results will inform planned future guidance in relation to the ethical design and conduct of pragmatic CRTs in hemodialysis.
Registration is not applicable as this is a qualitative study.
实用型整群随机试验(CRTs)提供了一个机会,通过采用一种可融入常规医疗的试验设计来回答有关治疗比较效果的重要问题,从而改善医疗保健。目前缺乏针对实用型CRTs在血液透析中产生的伦理问题的实证研究。
确定利益相关者对血液透析中实用型CRTs伦理问题的看法。
采用半结构化访谈的定性研究。
对一组国际利益相关者进行面对面或电话访谈。
参与过血液透析中实用型个体患者或整群随机试验设计或实施的利益相关者(临床研究人员、方法学家、伦理学家和研究伦理委员会成员以及其他知识使用者),或者其角色要求他们审查和评估血液透析中实用型CRTs的人员。
通过面对面或电话进行访谈,并在获得同意后进行录音。在分析之前,将录音访谈逐字转录。使用主题分析方法对转录本和现场笔记进行分析。
对19人进行了16次访谈。受访者主要来自北美(84%),主要是临床研究人员(42%)。确定了六个主题,其中血液透析中的实用型CRTs引发了伦理问题:(1)将接受血液透析治疗的患者视为弱势群体;(2)知情同意的适当方法;(3)研究负担;(4)把关人的角色和责任;(5)研究参与机会的不平等;(6)倡导以患者为中心的研究和结果。
参与者主要来自北美,未包括研究人员,他们可能有不同的观点。
这六个主题反映了对个人权利的关注,但也需要考虑人群层面的问题。迄今为止,与研究参与机会不平等以及以患者为中心的研究需求相关的问题,与其他诸如同意等知名问题相比,受到的关注较少。实用型CRTs提供了一种解决公平问题的潜在方法,我们建议未来对血液透析中实用型CRTs的伦理分析和指导将公平考虑纳入其中。我们还注意到与患者共同创建健康数据基础设施的潜力,这将有助于医疗护理,也便于开展以患者为中心的研究。这些研究结果将为未来关于血液透析中实用型CRTs伦理设计和实施的计划指导提供参考。
由于这是一项定性研究,因此不适用注册。