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Trends in study design and the statistical methods employed in a leading general medicine journal.
Gosho, M; Sato, Y; Nagashima, K; Takahashi, S.
Afiliação
  • Gosho M; Department of Clinical Trial and Clinical Epidemiology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Sato Y; Department of Global Clinical Research, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Nagashima K; Department of Global Clinical Research, Graduate School of Medicine, Chiba University, Chiba, Japan.
  • Takahashi S; Clinical Research Centre, Chiba University Hospital, Chiba, Japan.
J Clin Pharm Ther ; 43(1): 36-44, 2018 Feb.
Article em En | MEDLINE | ID: mdl-28749016
ABSTRACT
WHAT IS KNOWN AND

OBJECTIVE:

Study design and statistical methods have become core components of medical research, and the methodology has become more multifaceted and complicated over time. The study of the comprehensive details and current trends of study design and statistical methods is required to support the future implementation of well-planned clinical studies providing information about evidence-based medicine. Our purpose was to illustrate study design and statistical methods employed in recent medical literature.

METHODS:

This was an extension study of Sato et al. (N Engl J Med 2017; 376 1086-1087), which reviewed 238 articles published in 2015 in the New England Journal of Medicine (NEJM) and briefly summarized the statistical methods employed in NEJM. Using the same database, we performed a new investigation of the detailed trends in study design and individual statistical methods that were not reported in the Sato study. RESULTS AND

DISCUSSION:

Due to the CONSORT statement, prespecification and justification of sample size are obligatory in planning intervention studies. Although standard survival methods (eg Kaplan-Meier estimator and Cox regression model) were most frequently applied, the Gray test and Fine-Gray proportional hazard model for considering competing risks were sometimes used for a more valid statistical inference. With respect to handling missing data, model-based methods, which are valid for missing-at-random data, were more frequently used than single imputation methods. These methods are not recommended as a primary analysis, but they have been applied in many clinical trials. Group sequential design with interim analyses was one of the standard designs, and novel design, such as adaptive dose selection and sample size re-estimation, was sometimes employed in NEJM. WHAT IS NEW AND

CONCLUSION:

Model-based approaches for handling missing data should replace single imputation methods for primary analysis in the light of the information found in some publications. Use of adaptive design with interim analyses is increasing after the presentation of the FDA guidance for adaptive design.
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Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Pesquisa Biomédica Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Pesquisa Biomédica Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article