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Evidence of unexplained discrepancies between planned and conducted statistical analyses: a review of randomised trials.
Cro, Suzie; Forbes, Gordon; Johnson, Nicholas A; Kahan, Brennan C.
Afiliação
  • Cro S; Imperial Clinical Trials Unit, School of Public Health, Imperial College London, 1st Floor, Stadium House, London, W12 7RH, UK. s.cro@imperial.ac.uk.
  • Forbes G; Department of Biostatistics and Health Informatics, Kings College London, London, UK.
  • Johnson NA; Imperial Clinical Trials Unit, School of Public Health, Imperial College London, 1st Floor, Stadium House, London, W12 7RH, UK.
  • Kahan BC; MRC Clinical Trials Unit at UCL, London, UK.
BMC Med ; 18(1): 137, 2020 05 29.
Article em En | MEDLINE | ID: mdl-32466758
BACKGROUND: Choosing or altering the planned statistical analysis approach after examination of trial data (often referred to as 'p-hacking') can bias the results of randomised trials. However, the extent of this issue in practice is currently unclear. We conducted a review of published randomised trials to evaluate how often a pre-specified analysis approach is publicly available, and how often the planned analysis is changed. METHODS: A review of randomised trials published between January and April 2018 in six leading general medical journals. For each trial, we established whether a pre-specified analysis approach was publicly available in a protocol or statistical analysis plan and compared this to the trial publication. RESULTS: Overall, 89 of 101 eligible trials (88%) had a publicly available pre-specified analysis approach. Only 22/89 trials (25%) had no unexplained discrepancies between the pre-specified and conducted analysis. Fifty-four trials (61%) had one or more unexplained discrepancies, and in 13 trials (15%), it was impossible to ascertain whether any unexplained discrepancies occurred due to incomplete reporting of the statistical methods. Unexplained discrepancies were most common for the analysis model (n = 31, 35%) and analysis population (n = 28, 31%), followed by the use of covariates (n = 23, 26%) and the approach for handling missing data (n = 16, 18%). Many protocols or statistical analysis plans were dated after the trial had begun, so earlier discrepancies may have been missed. CONCLUSIONS: Unexplained discrepancies in the statistical methods of randomised trials are common. Increased transparency is required for proper evaluation of results.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação Estatística de Dados Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Revista: BMC Med Assunto da revista: MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação Estatística de Dados Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Revista: BMC Med Assunto da revista: MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de publicação: Reino Unido