Evidence of selective reporting bias in hematology journals: A systematic review

被引:36
作者
Wayant, Cole [1 ]
Scheckel, Caleb [2 ]
Hicks, Chandler [1 ]
Nissen, Timothy [1 ]
Leduc, Linda [3 ]
Som, Mousumi [3 ]
Vassar, Matt [1 ]
机构
[1] Oklahoma State Univ, Ctr Hlth Sci, Dept Inst Res, Tulsa, OK 74106 USA
[2] Mayo Clin, Internal Med, Scottsdale, AZ USA
[3] Oklahoma State Univ, Med Ctr, Internal Med, Tulsa, OK USA
来源
PLOS ONE | 2017年 / 12卷 / 06期
基金
美国国家卫生研究院;
关键词
RANDOMIZED CONTROLLED-TRIALS; PUBLISHED PRIMARY OUTCOMES; CLINICAL-TRIALS; SUBGROUP ANALYSES; REGISTRATION; PUBLICATIONS; PROTOCOLS; STATEMENT; PRIMER; COHORT;
D O I
10.1371/journal.pone.0178379
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction Selective reporting bias occurs when chance or selective outcome reporting rather than the intervention contributes to group differences. The prevailing concern about selective reporting bias is the possibility of results being modified towards specific conclusions. In this study, we evaluate randomized controlled trials (RCTs) published in hematology journals, a group in which selective outcome reporting has not yet been explored. Methods Our primary goal was to examine discrepancies between the reported primary and secondary outcomes in registered and published RCTs concerning hematological malignancies reported in hematology journals with a high impact factor. The secondary goals were to address whether outcome reporting discrepancies favored statistically significant outcomes, whether a pattern existed between the funding source and likelihood of outcome reporting bias, and whether temporal trends were present in outcome reporting bias. For trials with major outcome discrepancies, we contacted trialists to determine reasons for these discrepancies. Trials published between January 1, 2010 and December 31, 2015 in Blood; British Journal of Haematology; American Journal of Hematology; Leukemia; and Haematologica were included. Results Of 499 RCTs screened, 109 RCTs were included. Our analysis revealed 118 major discrepancies and 629 total discrepancies. Among the 118 discrepancies, 30 (25.4%) primary outcomes were demoted, 47 (39.8%) primary outcomes were omitted, and 30 (25.4%) primary outcomes were added. Three (2.5%) secondary outcomes were upgraded to a primary outcome. The timing of assessment for a primary outcome changed eight (6.8%) times. Thirty-one major discrepancies were published with a P-value and twenty-five (80.6%) favored statistical significance. A majority of authors whom we contacted cited a pre-planned subgroup analysis as a reason for outcome changes. Conclusion Our results suggest that outcome changes occur frequently in hematology trials. Because RCTs ultimately underpin clinical judgment and guide policy implementation, selective reporting could pose a threat to medical decision making.
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页数:13
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共 52 条
  • [1] [Anonymous], 2016, STANDARDS SYSTEMATIC
  • [2] [Anonymous], 2016, SAMPL GUIDELINES
  • [3] [Anonymous], 2016, PRISMA STATEMENT CHE
  • [4] [Anonymous], 2016, WHO INT CLIN TRIALS
  • [5] [Anonymous], 2016, NIH OUTREACH TOOLKIT
  • [6] [Anonymous], 2014, Cochrane handbook for systematic reviews of interventions
  • [7] Value of infliximab (Remicade®) in patients with low-risk myelodysplastic syndrome: final results of a randomized phase II trial (EORTC trial 06023) of the EORTC Leukemia Group
    Baron, Frederic
    Suciu, Stefan
    Amadori, Sergio
    Muus, Petra
    Zwierzina, Heinz
    Denzlinger, Claudio
    Delforge, Michel
    Thyss, Antoine
    Selleslag, Dominik
    Indrak, Karel
    Ossenkoppele, Gert
    de Witte, Theo
    [J]. HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2012, 97 (04): : 529 - 533
  • [8] Biostatistics Primer What a Clinician Ought to Know: Subgroup Analyses
    Barraclough, Helen
    Govindan, Ramaswamy
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (05) : 741 - 746
  • [9] Legitimate division of large datasets, salami slicing and dual publication. Where does a fraud begin?
    Beaufils, P.
    Karlsson, J.
    [J]. ORTHOPAEDICS & TRAUMATOLOGY-SURGERY & RESEARCH, 2013, 99 (02) : 121 - 122
  • [10] Besselink MGH, 2005, JAMA-J AM MED ASSOC, V293, P157, DOI 10.1001/jama.293.2.157-c