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对适应性平台试验和公共卫生紧急情况替代设计试验的社区参与及知情同意过程的快速回顾。

A rapid review of community engagement and informed consent processes for adaptive platform trials and alternative design trials for public health emergencies.

作者信息

Davies Alun, Ormel Ilja, Bernier Alexe, Harriss Eli, Mumba Noni, Gobat Nina, Schwartz Lisa, Cheah Phaik Yeong

机构信息

Health Systems Collaborative, Nuffield Department of Medicine, University of Oxford, Oxford, England, UK.

Faculty of Health Sciences, Department of Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.

出版信息

Wellcome Open Res. 2023 May 2;8:194. doi: 10.12688/wellcomeopenres.19318.1. eCollection 2023.

Abstract

Public Health Emergencies (PHE) demand expeditious research responses to evaluate new or repurposed therapies and prevention strategies. Alternative Design Trials (ADTs) and Adaptive Platform Trials (APTs) have enabled efficient large-scale testing of biomedical interventions during recent PHEs. Design features of these trials may have implications for engagement and/or informed consent processes. We aimed to rapidly review evidence on engagement and informed consent for ADTs and APTs during PHE to consider what (if any) recommendations can inform practice. In 2022, we searched 8 prominent databases for relevant peer reviewed publications and guidelines for ADTs/APTs in PHE contexts. Articles were selected based on pre-identified inclusion and exclusion criteria. We reviewed protocols and informed consent documents for a sample of large platform trials and consulted with key informants from ADTs/APT trial teams. Data were extracted and summarised using narrative synthesis. Of the 49 articles included, 10 were guidance documents, 14 discussed engagement, 10 discussed informed consent, and 15 discussed both. Included articles addressed ADTs delivered during the West African Ebola epidemic and APTs delivered during COVID-19. PHE clinical research guidance documents highlight the value of ADTs/APTs and the importance of community engagement, but do not provide practice-specific guidance for engagement or informed consent. Engagement and consent practice for ADTs conducted during the West African Ebola epidemic have been well-documented. For COVID-19, engagement and consent practice was described for APTs primarily delivered in high income countries with well-developed health service structures. A key consideration is strong communication of the complexity of trial design in clear, accessible ways. : We highlight key considerations for best practice in community engagement and informed consent relevant to ADTs and APTs for PHEs which may helpfully be included in future guidance. : The review protocol is published online at Prospero on 15/06/2022: registration number CRD42022334170.

摘要

突发公共卫生事件(PHE)需要迅速开展研究应对措施,以评估新的或重新利用的治疗方法及预防策略。替代设计试验(ADT)和适应性平台试验(APT)在近期突发公共卫生事件期间实现了对生物医学干预措施的高效大规模测试。这些试验的设计特点可能会对参与和/或知情同意程序产生影响。我们旨在快速回顾关于突发公共卫生事件期间替代设计试验和适应性平台试验的参与和知情同意的证据,以考虑哪些(如果有的话)建议可为实践提供指导。2022年,我们在8个著名数据库中搜索了关于突发公共卫生事件背景下替代设计试验/适应性平台试验的相关同行评审出版物和指南。根据预先确定的纳入和排除标准选择文章。我们审查了大型平台试验样本的方案和知情同意文件,并咨询了替代设计试验/适应性平台试验团队的关键信息提供者。使用叙述性综合方法提取和总结数据。在纳入的49篇文章中,10篇是指导文件,14篇讨论了参与,10篇讨论了知情同意,15篇同时讨论了两者。纳入的文章涉及西非埃博拉疫情期间开展的替代设计试验以及新冠疫情期间开展的适应性平台试验。突发公共卫生事件临床研究指导文件强调了替代设计试验/适应性平台试验的价值以及社区参与的重要性,但没有提供针对参与或知情同意的具体实践指导。西非埃博拉疫情期间开展的替代设计试验的参与和同意实践已有充分记录。对于新冠疫情,主要在卫生服务结构完善的高收入国家开展的适应性平台试验的参与和同意实践已有描述。一个关键考虑因素是以清晰、易懂的方式大力传达试验设计的复杂性。我们强调了与突发公共卫生事件的替代设计试验和适应性平台试验相关的社区参与和知情同意最佳实践的关键考虑因素,这些因素可能有助于纳入未来的指导意见。审查方案于2022年6月15日在国际前瞻性系统评价注册库(Prospero)在线发表:注册号CRD42022334170。

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