The use of clinical study reports to enhance the quality of systematic reviews: a survey of systematic review authors

被引:22
|
作者
Hodkinson, Alex [1 ]
Dietz, Kristina Charlotte [2 ]
Lefebvre, Carol [3 ]
Golder, Su [4 ]
Jones, Mark [5 ]
Doshi, Peter [6 ]
Heneghan, Carl [7 ]
Jefferson, Tom [7 ]
Boutron, Isabelle [8 ]
Stewart, Lesley [2 ]
机构
[1] LCtr Primary Care, Div Populat Hlth Hlth Serv Res & Primary Care, Williamson Bldg,Oxford Rd, Manchester M13 9PL, Lancs, England
[2] Univ York, Alcuin Coll, Ctr Reviews & Disseminat, A-B Block, York YO10 5DD, N Yorkshire, England
[3] Lefebvre Associates Ltd, Oxford, England
[4] Univ York, Dept Hlth Sci, York, N Yorkshire, Australia
[5] Univ Queensland, Sch Publ Hlth, Brisbane, Qld, Australia
[6] Univ Maryland, Sch Pharm, Dept Pharmaceut Hlth Serv Res, Baltimore, MD 21201 USA
[7] Univ Oxford, Primary Sci Div, Nuffield Dept Primary Care Hlth Sci, Ctr Evidence Based Med, Oxford, England
[8] Univ Paris 05, Ctr Res Epidemiol & Stat, METHODs Team, Sorbonne Paris Cite,INSERM UMR, Paris, France
关键词
Clinical Study Reports (CSRs); Future Systematic Reviews; Regulatory Documents; Cochrane Review Authors; Marketing Authorization Application;
D O I
10.1186/s13643-018-0766-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Clinical study reports (CSRs) are produced for marketing authorisation applications. They often contain considerably more information about, and data from, clinical trials than corresponding journal publications. Use of data from CSRs might help circumvent reporting bias, but many researchers appear to be unaware of their existence or potential value. Our survey aimed to gain insight into the level of familiarity, understanding and use of CSRs, and to raise awareness of their potential within the systematic review community. We also aimed to explore the potential barriers faced when obtaining and using CSRs in systematic reviews. Methods: Online survey of systematic reviewers who (i) had requested or used CSRs, (ii) had considered but not used CSRs and (iii) had not considered using CSRs was conducted. Cochrane reviewers were contacted twice via the Cochrane monthly digest. Non-Cochrane reviewers were reached via journal and other website postings. Results: One hundred sixty respondents answered an open invitation and completed the questionnaire; 20/160 (13%) had previously requested or used CSRs and other regulatory documents, 7/160 (4%) had considered but not used CSRs and 133/160 (83%) had never considered this data source. Survey respondents mainly sought data from the European Medicines Agency (EMA) and/or the Food and Drug Administration (FDA). Motivation for using CSRs stemmed mainly from concerns about reporting bias 11/20 (55%), specifically outcome reporting bias 11/20 (55%) and publication bias 5/20 (25%). The barriers to using CSRs noted by all types of respondents included current limited access to these documents (43 respondents), the time and resources needed to obtain and include these data in evidence syntheses (n = 25) and lack of guidance about how to use these sources in systematic reviews (n = 26). Conclusions: Most respondents (irrespective of whether they had previously used them) agreed that access to CSRs is important, and suggest that further guidance on how to use and include these data would help to promote their use in future systematic reviews. Most respondents who received CSRs considered them to be valuable in their systematic review and/or meta-analysis.
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页数:12
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