快速审查方法系列:关于快速审查报告的临时指南
Adrienne Stevens1, Mona Hersi2, Chantelle Garritty3,4
1Centre for Immunization Programs, Infectious Diseases & Vaccination Programs Branch, Public Health Agency of Canada, Ottawa, Ontario, Canada adrienne.stevens@gmail.com.
BMJ evidence-based medicine
|July 22, 2024
概括
本指南有助于快速审查 (RR) 制造商完全报告他们的调查结果. 它建议使用现有的指导方针,如PRISMA 2020,并详细介绍了RRs的六个基本报告项目.
科学领域:
- 健康科学 卫生科学 卫生科学
- 证据综合 证据综合
- 研究方法研究方法研究方法学
背景情况:
- 快速审查 (RRs) 为决策提供了加速的证据综合.
- 标准系统性审查 (SRs) 是耗时的,需要适应RRs的方法.
- 关于RR的不完整报告可能会阻碍其有效使用.
研究的目的:
- 为快速审查 (RRs) 的完整报告提供临时指导.
- 为RRs建立最低一组报告项目.
- 为未来对RRs的合并报告准则的制定提供信息.
主要方法:
- 根据对RR生产商的调查和经验研究得出的建议.
- 利用现有的报告准则,如PRISMA 2020和PRIOR.
- 确定RRs的至少六个基本报告项目.
主要成果:
- 资源资源应该建立在像PRISMA 2020这样的既定指导方针上.
- 推六个关键项目:三个是方法 (代方法,RR与SR区分,知识用户参与) 和三个是出版伦理 (作者,贡献者,同行评审).
- 完整的报告可能涵盖多个链接的,开放访问的文档.
结论:
- 遵守这些报告建议将提高RRs的透明度和实用性.
- 对方法和对SRs的偏差进行明确报告至关重要.
- 进一步鼓励社区反,以完善RR报告标准.
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