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Improving the quality of reporting of systematic reviews of dose-response meta-analyses: a cross-sectional survey

机译:提高剂量反应荟萃分析系统评价报告的质量:横断面调查

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摘要

Dose-response meta-analysis (DRMA) is a useful tool to investigate potential dose-response relationship between certain exposure or intervention and the outcome of interest. A large number of DRMAs have been published in the past several years. However, the standard of reporting for such studies is not known. Medline, Embase, and Wiley Library were searched for systematic reviews with DRMAs (SR-DRMAs) published from January 2011 to July 2017. We used the combination of PRISMA and MOOSE statements, containing 33 items, to assess the reporting of included SR-DRMAs. The adherence of reporting was defined as the proportion of SR-DRMAs meeting the reporting requirement of an item. We explored the association between five pre-specified variables with the total score of reporting on both fully as well as each domain of the checklist. In total, 529 SR-DRMAs were eligible. Ten out of 33 items were under reported, and this mainly refers to the methods domain: only a small proportion of SR-DRMAs stated whether a review protocol existed (45, 8.5%); clarified the qualifications of searchers (1.7%); presented full electronic search strategy (25.9%); described any effort to include all available studies (22.9%), described methods for languages other than English (27.4%), and stated the process for selecting studies (20.2%). Multiple regression analysis suggested that studies with more authors (regression coefficient?=?0.78; 95% CI: 0.35, 1.20; P? 0.001), published more recently (regression coefficient?=?0.38; 95% CI: 0.28 to 0.47; trend P? 0.001), used reporting guideline (regression coefficient?=?0.98; 95% CI: 0.68 to 1.32; P? 0.001), and involvement of methodologist (regression coefficient?=?0.86; 95% CI: 0.42 to 1.32; P? 0.001) were associated with higher score of reporting. Further regression suggested that the improvement on the quality mainly concentrated on the methods and results domains. The reporting of SR-DRMAs needs to be further improved, particularly in the issues refer to the methods. The quality of reporting may improve when involving more authors and methodologists and employing any reporting guidelines.
机译:剂量反应荟萃分析(DRMA)是一种有用的工具,可用于研究某些暴露或干预与目标结果之间潜在的剂量反应关系。在过去的几年中已经发布了许多DRMA。但是,此类研究的报告标准尚不清楚。搜索了Medline,Embase和Wiley库,以查找2011年1月至2017年7月发布的DRMA(SR-DRMA)的系统评价。我们使用PRISMA和MOOSE语句的组合(包含33个项目)来评估包括的SR-DRMA的报告。遵守报告的定义是满足项目报告要求的SR-DRMA的比例。我们探索了五个预先指定的变量与完整清单以及清单中每个域的报告总得分之间的关​​联。总共有529个SR-DRMA有资格。在33个项目中,有10个报告不足,主要涉及方法领域:只有一小部分SR-DRMA声明是否存在审查协议(45,8.5%);阐明搜索者的资格(1.7%);提出了完整的电子搜索策略(25.9%);描述了包括所有可用研究的任何努力(22.9%),描述了除英语以外的其他语言的方法(27.4%),并指出了选择研究的过程(20.2%)。多元回归分析表明,作者较多的研究(回归系数?=?0.78; 95%CI:0.35,1.20; P?<0.001)最近发表(回归系数?=?0.38; 95%CI:0.28至0.47;回归系数?=?0.38; 95%CI:?0.28至0.47)。趋势P?<0.001),使用的报告准则(回归系数?=?0.98; 95%CI:0.68至1.32; P?<0.001)和方法学家的参与度(回归系数?=?0.86; 95%CI:0.42至1.32; P <0.001)与较高的报告分数相关。进一步的回归表明,质量的提高主要集中在方法和结果领域。 SR-DRMA的报告需要进一步改进,特别是在涉及方法的问题中。当更多的作者和方法学家参与进来并采用任何报告准则时,报告的质量可能会提高。

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