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《渥太华声明》在血液透析环境下进行整群随机试验的实施指南文件。

The Ottawa Statement implementation guidance document for cluster randomized trials in the hemodialysis setting.

机构信息

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Kidney Int. 2024 May;105(5):898-911. doi: 10.1016/j.kint.2024.03.001.

Abstract

Research teams are increasingly interested in using cluster randomized trial (CRT) designs to generate practice-guiding evidence for in-center maintenance hemodialysis. However, CRTs raise complex ethical issues. The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials, published in 2012, provides 15 recommendations to address ethical issues arising within 7 domains: justifying the CRT design, research ethics committee review, identifying research participants, obtaining informed consent, gatekeepers, assessing benefits and harms, and protecting vulnerable participants. But applying the Ottawa Statement recommendations to CRTs in the hemodialysis setting is complicated by the unique features of the setting and population. Here, with the help of content experts and patient partners, we co-developed this implementation guidance document to provide research teams, research ethics committees, and other stakeholders with detailed guidance on how to apply the Ottawa Statement recommendations to CRTs in the hemodialysis setting, the result of a 4-year research project. Thus, our work demonstrates how the voices of patients, caregivers, and all stakeholders may be included in the development of research ethics guidance.

摘要

研究团队越来越有兴趣使用整群随机试验 (cluster randomized trial, CRT) 设计来为中心维持性血液透析产生实践指导证据。然而,CRT 引发了复杂的伦理问题。2012 年发表的《关于整群随机试验的伦理设计和实施的渥太华声明》提出了 15 项建议,以解决在 7 个领域中出现的伦理问题:证明 CRT 设计的合理性、研究伦理委员会审查、确定研究参与者、获得知情同意、把关者、评估获益和危害,以及保护弱势群体参与者。但是,由于该环境和人群的独特性,将渥太华声明建议应用于血液透析环境中的 CRT 是复杂的。在这里,在内容专家和患者伙伴的帮助下,我们共同制定了这份实施指南文件,为研究团队、研究伦理委员会和其他利益攸关方提供了详细的指导,说明如何将渥太华声明建议应用于血液透析环境中的 CRT,这是一个为期 4 年的研究项目的成果。因此,我们的工作表明,患者、护理人员和所有利益攸关方的声音可以如何被纳入研究伦理指导的制定。

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