A systematic review of core outcome set development studies demonstrates difficulties in defining unique outcomes

被引:51
|
作者
Young, Amber E. [1 ]
Brookes, Sara T. [2 ]
Avery, Kerry N. L. [3 ]
Davies, Anna [4 ]
Metcalfe, Chris [5 ]
Blazeby, Jane M. [3 ]
机构
[1] Univ Bristol, Bristol Med Sch, Populat Hlth Sci, Bristol Ctr Surg Res, Canynge Hall,39 Whatley Rd, Bristol BS8 2PS, Avon, England
[2] Univ Birmingham, Inst Canc & Gen Sci, Canc Res UK Clin Trials Unit CRCTU, Birmingham B15 2TT, W Midlands, England
[3] Univ Bristol, Med Res Council ConDuCT II Hub Trials Methodol Re, Bristol Biomed Res Ctr,Bristol Ctr Surg Res, Bristol Med Sch Populat Hlth Sci,Natl Inst Hlth R, 39 Whatley Rd, Bristol BS8 1NU, Avon, England
[4] Univ Bristol, Ctr Acad Child Hlth, 1-5 Whiteladies Rd, Bristol BS8 1NU, Avon, England
[5] Univ Bristol, Bristol Med Sch, Populat Hlth Sci, Canynge Hall,39 Whatley Rd, Bristol BS8 2PS, Avon, England
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Outcomes; Research methodology; Core outcome set; Clinical trials; Systematic review; COMET; RANDOMIZED-TRIALS; DATABASE; THERAPY; UPDATE; TIME; PAIN;
D O I
10.1016/j.jclinepi.2019.06.016
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objectives: Core outcome set (COS) development often begins with a systematic review to identify outcomes. Reviews frequently show heterogeneity in numbers of outcomes reported across trials. Contributing to this is a lack of a uniform definition for an outcome. This study proposes a first working definition for a unique trial outcome to support reporting a quantitative assessment of outcome reporting heterogeneity (ORH). Study Design and Setting: Eligible COS literature (development papers, protocols, and reviews) were identified using the COMET database, Ovid MEDLINE, and PubMed. Outcome numbers, definitions, timing, and grouping methodology were examined. Results: One hundred and thirty two studies were included. 82 (88.1%) studies (excluding protocols) reported a total number of unique outcomes (median, 82; range, 12-5776; IQR, 261). Timing of assessment was reported in 32 (31.4%) studies. Methods to group similar outcomes were reported in 8 (7.8%) articles. No study defined how outcomes were agreed as different and how final numbers of unique outcomes were determined. It is proposed that a unique outcome requires original meaning and context. Thus ORH is suggested to be the reporting of multiple unique outcomes across trials related to one health care condition. Conclusion: This review identified inconsistencies in how authors define, extract, group, and count trial outcomes. Further work is needed to refine our proposed definitions to optimize COS development and allow a quantifiable measure of ORH. Crown Copyright (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:14 / 24
页数:11
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