Justification and reporting of subgroup analyses were lacking or inadequate in randomized controlled trials

被引:18
|
作者
Fan, Jingchun [1 ,2 ]
Song, Fujian [2 ]
Bachmann, Max O. [2 ]
机构
[1] Gansu Univ Chinese Med, Epidemiol & Evidence Based Med, Sch Publ Hlth, Lanzhou, Gansu, Peoples R China
[2] Univ East Anglia, Publ Hlth & Hlth Serv Res, Norwich Med Sch, Norwich, Norfolk, England
关键词
Subgroup analysis; Subgroup effect; Prespecification; Clinical trial; Study protocol; Study reporting; CLINICAL-TRIALS; PROTOCOL; HETEROGENEITY; MEDICINE; IMPACT;
D O I
10.1016/j.jclinepi.2018.12.009
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: The aim of the article was to assess the appropriateness and rationales of subgroup analyses planned in protocols of randomized controlled trials and reported in subsequent corresponding trial publications. Study Design and Setting: We searched PubMed to identify trial protocols published in journals during 2006-2017. From a total of 3,774 initially identified records, we included a random sample of 479 protocols and identified 280 trial publications corresponding to the included protocols. Results: Subgroup analyses were specified in 19% of the protocols and reported in 21% of the trial publications. Of the 94 protocols with planned subgroup analyses, 32% mentioned testing for interaction, and only three considered statistical power. Subgroup analyses were not prespecified in 56% of the 59 trial publications with subgroup analyses. Subgroup analyses were stated as prespecified in nine trial publications, without support evidence from the corresponding protocols. Subgroup analyses were often reported insufficiently for assessing the consistency of subgroup effects across studies. Justifications for subgroup analyses were provided in only four trial protocols and seven trial publications. Conclusion: Inappropriate specification and reporting of subgroup analyses remain problematic in protocols and reports of randomized controlled trials. Justifications or rationales for subgroup analyses were only rarely provided in trial protocols and reports. (C) 2018 The Authors. Published by Elsevier Inc.
引用
收藏
页码:17 / 25
页数:9
相关论文
共 50 条
  • [21] The quality of reporting of randomized controlled trials
    McGowan, David R.
    Norris, Joseph M.
    Bennett, Grace L.
    [J]. CURRENT MEDICAL RESEARCH AND OPINION, 2015, 31 (08) : 1609 - 1610
  • [22] The reporting of randomized controlled trials in prosthodontics
    Jokstad, A
    Esposito, M
    Coulthard, P
    Worthington, HV
    [J]. INTERNATIONAL JOURNAL OF PROSTHODONTICS, 2002, 15 (03) : 230 - 242
  • [23] The reporting quality of randomized controlled trials
    Cobourne, Martyn T.
    [J]. JOURNAL OF ORTHODONTICS, 2015, 42 (03) : 181 - 182
  • [24] SAFETY REPORTING IN RANDOMIZED CONTROLLED TRIALS
    Yeahia, Rubaya
    Gennarelli, Renee
    Morgan, Daniel J.
    Korenstein, Deborah R.
    [J]. JOURNAL OF GENERAL INTERNAL MEDICINE, 2020, 35 (SUPPL 1) : S264 - S264
  • [25] Adherence reporting in randomized controlled trials
    Zhang, Ze
    Peluso, Michael J.
    Gross, Cary P.
    Viscoli, Catherine M.
    Kernan, Walter N.
    [J]. CLINICAL TRIALS, 2014, 11 (02) : 195 - 204
  • [26] REPORTING RANDOMIZED CONTROLLED TRIALS - REPLY
    MOHER, D
    RENNIE, D
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (17): : 1342 - 1343
  • [27] Reporting process of randomized controlled trials
    Maksymowych, WP
    [J]. CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 170 (09) : 1375 - 1375
  • [28] STANDARDIZATION FOR SUBGROUP ANALYSIS IN RANDOMIZED CONTROLLED TRIALS
    Varadhan, Ravi
    Wang, Sue-Jane
    [J]. JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2014, 24 (01) : 154 - 167
  • [29] Subgroup analyses in randomized trials—more rigour needed
    Douglas G. Altman
    [J]. Nature Reviews Clinical Oncology, 2015, 12 : 506 - 507
  • [30] Trials within trials:: Confirmatory subgroup analyses in controlled clinical experiments
    Moyé, LA
    Deswal, A
    [J]. CONTROLLED CLINICAL TRIALS, 2001, 22 (06): : 605 - 619