Department of Biostatistics, University of Liverpool, Shelley's Cottage, Brownlow Street, Liverpool L69 3GS, UK.
Trials. 2013 Jan 22;14:21. doi: 10.1186/1745-6215-14-21.
Missing outcome data or the inconsistent reporting of outcome data in clinical research can affect the quality of evidence within a systematic review. A potential solution is an agreed standardized set of outcomes known as a core outcome set (COS) to be measured in all studies for a specific condition. We investigated the amount of missing patient data for primary outcomes in Cochrane systematic reviews, and surveyed the Co-ordinating Editors of Cochrane Review Groups (CRGs) on issues related to the standardization of outcomes in their CRG's reviews. These groups are responsible for the more than 7,000 protocols and full versions of Cochrane Reviews that are currently available, and the several hundred new reviews published each year, presenting the world's largest collection of standardized systematic reviews in health care.
Using an unselected cohort of Cochrane Reviews, we calculated and presented the percentage of missing patient data for the primary outcome measure chosen for each review published by each CRG. We also surveyed the CRG Co-ordinating Editors to see what their policies are with regards to outcome selection and outcomes to include in the Summary of Finding (SoF) tables in their Cochrane Reviews. They were also asked to list the main advantages and challenges of standardizing outcomes across all reviews within their CRG.
In one fifth of the 283 reviews in the sample, more than 50% of the patient data for the primary outcome was missing. Responses to the survey were received from 90% of Co-ordinating Editors. Thirty-six percent of CRGs have a centralized policy regarding which outcomes to include in the SoF table and 73% of Co-ordinating Editors thought that a COS for effectiveness trials should be used routinely for a SoF table.
The reliability of systematic reviews, in particular meta-analyses they contain, can be improved if more attention is paid to missing outcome data. The availability of COSs for specific health conditions might help with this and the concept has support from the majority of Co-ordinating Editors in CRGs.
临床研究中缺失的结局数据或结局数据报告不一致会影响系统评价中证据的质量。一种潜在的解决方案是制定一套经过共识的标准化结局,称为核心结局集(COS),以便在特定疾病的所有研究中进行测量。我们调查了 Cochrane 系统评价中主要结局的缺失患者数据量,并对 Cochrane 评价组(CRG)的协调编辑进行了调查,内容涉及他们评价中结局标准化的相关问题。这些小组负责目前可获得的 7000 多个方案和完整的 Cochrane 评价版本,以及每年发表的数百个新评价,展示了全球最大的医疗保健标准化系统评价集合。
使用未经选择的 Cochrane 评价队列,我们计算并呈现了每个 CRG 发表的每个评价中选择的主要结局测量的缺失患者数据的百分比。我们还调查了 CRG 协调编辑,了解他们在评价中的结局选择和纳入总结结局表格(SoF)的政策。他们还被要求列出在他们的 CRG 内的所有评价中标准化结局的主要优势和挑战。
在样本中的 283 项评价中,有五分之一以上的评价中超过 50%的主要结局患者数据缺失。对调查的回应来自 90%的协调编辑。36%的 CRG 有一个关于纳入 SoF 表格的结局的集中政策,73%的协调编辑认为应该常规使用 COS 用于 SoF 表格。
如果更多地关注缺失的结局数据,系统评价,特别是其中包含的荟萃分析,的可靠性可以得到提高。针对特定健康状况的 COS 的可用性可能有助于解决这个问题,而且这个概念得到了大多数 CRG 协调编辑的支持。