Research Information Specialist, Canadian Agency for Drugs and Technologies in Health (CADTH), Ottawa, ON, Canada,
Manager, Research Information Services, Canadian Agency for Drugs and Technologies in Health (CADTH), Ottawa, ON, Canada,
J Med Libr Assoc. 2019 Apr;107(2):187-193. doi: 10.5195/jmla.2019.629. Epub 2019 Apr 1.
The research sought to determine the prevalence of errata for drug trial publications that are included in systematic reviews, their potential value to reviews, and their accessibility via standard information retrieval methods.
The authors conducted a retrospective review of included studies from forty systematic reviews of drugs evaluated by the Canadian Agency for Drugs and Technologies in Health (CADTH) Common Drug Review (CDR) in 2015. For each article that was included in the systematic reviews, we conducted searches for associated errata using the CDR review report, PubMed, and the journal publishers' websites. The severity of errors described in errata was evaluated using a three-category scale: trivial, minor, or major. The accessibility of errata was determined by examining inclusion in bibliographic databases, costs of obtaining errata, time lag between article and erratum publication, and correction of online articles.
The 40 systematic reviews included 127 articles in total, for which 26 errata were identified. These errata described 38 errors. When classified by severity, 6 errors were major; 20 errors were minor; and 12 errors were trivial. No one database contained all the errata. On average, errata were published 211 days after the original article (range: 15-1,036 days). All were freely available. Over one-third (9/24) of online articles were uncorrected after errata publication.
Errata frequently described non-trivial errors that would either impact the interpretation of data in the article or, in fewer cases, impact the conclusions of the study. As such, it seems useful for reviewers to identify errata associated with included studies. However, publication time lag and inconsistent database indexing impair errata accessibility.
本研究旨在确定纳入系统评价的药物试验出版物中错误的发生率、这些错误对评价的潜在价值,以及通过标准信息检索方法获取这些错误的难易程度。
作者对加拿大药品和技术评估机构(CADTH)通用药物评价(CDR)2015 年进行的 40 项药物系统评价中纳入的研究进行了回顾性审查。对于每项纳入系统评价的文章,我们使用 CDR 评价报告、PubMed 和期刊出版商的网站,对相关错误进行了检索。使用三分类量表评估错误的严重程度:微不足道、轻微或严重。通过检查错误是否包含在书目数据库中、获取错误的成本、文章与错误发布之间的时间滞后以及在线文章的更正,确定错误的可获取性。
这 40 项系统评价共纳入 127 篇文章,其中发现 26 篇错误。这些错误描述了 38 个错误。按严重程度分类,6 个错误为严重;20 个错误为轻微;12 个错误为微不足道。没有一个数据库包含所有的错误。平均而言,错误在原始文章发表后 211 天(范围:15-1036 天)发布。所有错误均免费提供。错误发布后,24 篇在线文章中有超过三分之一(9/24)未更正。
错误经常描述非微不足道的错误,这些错误要么会影响文章中数据的解释,要么在少数情况下会影响研究的结论。因此,评价者识别与纳入研究相关的错误似乎是有用的。然而,发表时间滞后和数据库索引不一致会影响错误的可获取性。