背景:对研究(IfR)部分的影响是系统评价(SRs)的重要组成部分,以告知医疗保健研究人员和政策制定者。PRISMA2020建议报告IfR,而Cochrane评论需要关于IfR的单独一章。然而,目前尚不清楚SRs在多大程度上讨论IfR。我们的目标是i)评估SR是否包括IfR声明,以及ii)评估哪些要素为IfR声明提供了信息。
方法:我们根据先前项目(CRD42019134904)对晚期癌症患者的干预措施进行了一项荟萃研究。正如Cochrane手册所建议的,我们评估了IfR语句中是否引用了以下预定义变量:患者,干预,control,结果(PICO)和研究设计;建议分级的基本概念,评估,开发和评估(等级)领域:偏差风险,不一致,间接性,不精确,出版偏见。在试用数据提取表后,由三名审阅者独立提取数据。在每周的深入讨论中解决了差异。
结果:我们包括261个SR。大多数人评估了药物干预(n=244,93.5%);29个是Cochrane评论(11.1%)。五个SR中有四个包含IfR语句(n=210,80.5%)。IfR语句通常涉及“干预”(n=121,57.6%),\'病人\'(n=113,53.8%),和“研究设计”(n=107,51.0%)。最常见的PICO和研究设计组合是“患者和干预”(n=71,33.8%)和“患者,干预和研究设计(n=34,16.2%)。等级域的基本概念很少用于通知IfR建议:“偏见风险”(n=2,1.0%),和“不精确”(n=1,0.5%),“不一致”(n=1,0.5%)。通知IfR的其他要素是对成本效益的考虑(n=9,4.3%),报告标准(n=4,1.9%),和个体患者数据荟萃分析(n=4,1.9%)。
结论:尽管大约80%的SR包含IfR声明,PICO元素的报告因SRs而异。GRADE域的基础概念很少用于推导IfR。需要进一步的工作来评估在晚期癌症患者中超越SR的普遍性。我们建议需要制定更具体的指导意见,说明在干预措施的SR中报告哪些IfR要素以及如何报告。根据Cochrane手册,利用PICO元素和GRADE基础概念来陈述IfR似乎是过渡期间的合理方法。
背景:CRD42011134904.
Implications for research (IfR) sections are an important part of systematic reviews (SRs) to inform health care researchers and policy makers. PRISMA 2020 recommends reporting IfR, while Cochrane Reviews require a separate chapter on IfR. However, it is unclear to what extent SRs discuss IfR. We aimed i) to assess whether SRs include an IfR statement and ii) to evaluate which elements informed IfR statements.
We conducted a meta-research study based on SRs of interventions in advanced cancer patients from a previous project (CRD42019134904). As suggested in the Cochrane Handbook, we assessed if the following predefined variables were referred to in IfR statements: patient, intervention, control, outcome (PICO) and study design; concepts underlying Grading of Recommendations, Assessment, Development and Evaluation (
GRADE) domains: risk of bias, inconsistency, indirectness, imprecision, publication bias. Data were independently extracted by three reviewers after piloting the data extraction form. Discrepancies were resolved in weekly in-depth discussions.
We included 261 SRs. The majority evaluated a pharmacological intervention (n = 244, 93.5%); twenty-nine were Cochrane Reviews (11.1%). Four out of five SRs included an IfR statement (n = 210, 80.5%). IfR statements commonly addressed \'intervention\' (n = 121, 57.6%), \'patient \' (n = 113, 53.8%), and \'study design\' (n = 107, 51.0%). The most frequent PICO and study design combinations were \'patient and intervention \' (n = 71, 33.8%) and \'patient, intervention and
study design \' (n = 34, 16.2%). Concepts underlying
GRADE domains were rarely used for informing IfR recommendations: \'risk of bias \' (n = 2, 1.0%), and \'imprecision \' (n = 1, 0.5%), \'inconsistency \' (n = 1, 0.5%). Additional elements informing IfR were considerations on cost effectiveness (n = 9, 4.3%), reporting standards (n = 4, 1.9%), and individual patient data meta-analysis (n = 4, 1.9%).
Although about 80% of SRs included an IfR statement, the reporting of PICO elements varied across SRs. Concepts underlying
GRADE domains were rarely used to derive IfR. Further work needs to assess the generalizability beyond SRs in advanced cancer patients. We suggest that more specific guidance on which and how IfR elements to report in SRs of interventions needs to be developed. Utilizing PICO elements and concepts underlying
GRADE according to the Cochrane Handbook to state IfR seems to be a reasonable approach in the interim.
CRD42019134904.