School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Research Institute of Rehabilitation Information, China Rehabilitation Science Institute, Beijing, China; China Rehabilitation Research Center, Beijing, China.
J Clin Epidemiol. 2019 Nov;115:133-140. doi: 10.1016/j.jclinepi.2019.07.008. Epub 2019 Jul 18.
The objective of this study was to investigate the characteristics, methodological quality, and reporting of statistical analyses of published dose-response meta-analyses (DRMAs).
We searched PubMed to identify DRMAs published in 2017. The reporting characteristics and methodological qualities were assessed by the PRISMA (27 items) and AMSTAR (11 items), respectively. We also summarized the reporting of statistical analyses of included DRMAs.
We identified 93 DRMAs, most of which (59/93) were conducted by Chinese researchers and the main outcome was the incidence of cancers. Of the PRISMA and AMSTAR items, twenty and five were well complied (80% or more), respectively. The compliance rates of several PRISMA checklist items, such as structured summary, objectives, protocol and registration, and funding, were less than 50%. There were no criteria to estimate the doses for the open-ended intervals of exposure or intervention doses. When the restricted cubic splines were used to fit nonlinear dose-response relationships, there were also no criteria to determine the fixed knots.
The adherence to the methodological items of reporting guidelines and statistical analysis of published DRMAs were suboptimal. Development of reporting guidelines to assist authors in writing and readers in critically appraising the reports of DRMAs is timely.
本研究旨在调查已发表的剂量-反应荟萃分析(DRMAs)中统计分析的特点、方法学质量和报告情况。
我们在 PubMed 中搜索了 2017 年发表的 DRMAs。分别采用 PRISMA(27 项)和 AMSTAR(11 项)评估报告特征和方法学质量。我们还总结了纳入 DRMAs 中统计分析的报告情况。
我们确定了 93 项 DRMAs,其中大多数(59/93)是由中国研究人员进行的,主要结局是癌症的发病率。在 PRISMA 和 AMSTAR 项目中,分别有二十项和五项得到了很好的遵守(80%或以上)。一些 PRISMA 清单项目的遵守率,如结构化摘要、目标、方案和注册以及资金,低于 50%。对于暴露或干预剂量的开放式间隔,没有标准来估计剂量。当使用限制立方样条拟合非线性剂量-反应关系时,也没有标准来确定固定结。
发表的 DRMAs 中报告指南的方法学项目和统计分析的遵循情况并不理想。及时制定报告指南,以帮助作者撰写和读者批判性评估 DRMAs 的报告是适时的。