Yang Donghua, Zhou Yongjia, Tang Xiao, Zhang Tianyi, Li Yiyi, Zhang Jun, Tian Jinhui, Yang Limei
Evidence-Based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou, 730000, Germany.
Qinghai University Affiliated Hospital, Xi Ning, 810000, China.
Syst Rev. 2025 Jun 10;14(1):127. doi: 10.1186/s13643-025-02870-8.
The aim of this study was to assess the reporting quality of rapid reviews (RRs) against the Cochrane Rapid Reviews Methodological Guidance to identify areas for improvement.
A literature quality assessment was conducted through systematic searches in PubMed, the Cochrane Library, and Web of Science until February 28, 2023. An expert guided the search strategy, and the reporting quality of RRs was evaluated. Descriptive statistics were used to summarize reporting quality, and subgroup analyses were performed to examine differences between groups. Categorical variables were compared using the chi-square (χ) test to identify statistically significant differences in reporting adherence across different subgroups.
Among the 112 rapid reviews analyzed, fewer than 50% fully reported four key methodological components: topic refinement with stakeholders, eligibility criteria co-definition, risk of bias assessment tools, and protocol/software reporting. Reports published after 2021 demonstrated slightly higher overall quality compared to those published before 2020, with significant improvements in protocol development (Item 2: χ = 10.434, P < 0.0001), PICOS specification (Item 3: χ = 5.378, P = 0.02), and protocol registration (Item 23: χ = 6.638, P = 0.01). Cochrane Rapid Reviews (CRRs) achieved 100% compliance in several key areas, including setting restrictions with justification (Item 4: χ = 52.923, P < 0.001) and study selection (Item 14: χ = 14.897, P < 0.001). The impact of journal prestige was also evident: publications in high-impact factor (IF > 5) journals showed significantly better compliance in stakeholder involvement (Item 1: χ = 8.856, P = 0.003) but comparable adherence to protocol registration (Item 23: ≤ 20.3%).
While RR quality is improving post-2021, critical gaps persist in stakeholder engagement and protocol transparency. Mandatory adoption of Cochrane guidelines-particularly protocol registration (Item23) and dual data extraction (Item17)-should be prioritized in journal submission policies.
本研究旨在根据Cochrane快速综述方法学指南评估快速综述(RRs)的报告质量,以确定需要改进的领域。
通过在PubMed、Cochrane图书馆和科学网进行系统检索,直至2023年2月28日,开展文献质量评估。由一位专家指导检索策略,并对RRs的报告质量进行评估。使用描述性统计来总结报告质量,并进行亚组分析以检验组间差异。使用卡方(χ)检验比较分类变量,以确定不同亚组在报告依从性方面的统计学显著差异。
在分析的112篇快速综述中,不到50%的综述完整报告了四个关键方法学组成部分:与利益相关者进行主题细化、共同定义纳入标准、偏倚风险评估工具以及方案/软件报告。与2020年之前发表的报告相比,2021年之后发表的报告总体质量略有提高,在方案制定(第2项:χ = 10.434,P < 0.0001)、PICOS规范(第3项:χ = 5.378,P = 0.02)和方案注册(第23项:χ = 6.638,P = 0.01)方面有显著改善。Cochrane快速综述(CRRs)在几个关键领域实现了100%的合规,包括合理设置限制(第4项:χ = 52.923,P < 0.001)和研究选择(第14项:χ = 14.897,P < 0.001)。期刊影响力的影响也很明显:在高影响因子(IF > 5)期刊上发表的文章在利益相关者参与方面的合规性显著更好(第1项:χ = 8.856,P = 0.003),但在方案注册方面的依从性相当(第23项:≤ 20.3%)。
虽然2021年之后RR质量有所提高,但在利益相关者参与和方案透明度方面仍存在关键差距。在期刊投稿政策中,应优先强制采用Cochrane指南,特别是方案注册(第23项)和双重数据提取(第17项)。