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Data-Driven Simulations to Assess the Impact of Study Imperfections in Time-to-Event Analyses.
Abrahamowicz, Michal; Beauchamp, Marie-Eve; Boulesteix, Anne-Laure; Morris, Tim P; Sauerbrei, Willi; Kaufman, Jay S; Stratos Simulation Panel, On Behalf Of The.
Afiliación
  • Abrahamowicz M; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.
  • Beauchamp ME; Centre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
  • Boulesteix AL; Centre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
  • Morris TP; Institute for Medical Information Processing, Biometry, and Epidemiology, Ludwig-Maximilians-Universität München, München, Germany.
  • Sauerbrei W; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, University College London, London, UK.
  • Kaufman JS; Institute of Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Stefan-Meier-Str.26, 79104, Freiburg, Germany.
  • Stratos Simulation Panel OBOT; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.
Am J Epidemiol ; 2024 May 06.
Article en En | MEDLINE | ID: mdl-38717330
ABSTRACT
Quantitative bias analysis (QBA) permits assessment of the expected impact of various imperfections of the available data on the results and conclusions of a particular real-world study. This article extends QBA methodology to multivariable time-to-event analyses with right-censored endpoints, possibly including time-varying exposures or covariates. The proposed approach employs data-driven simulations, which preserve important features of the data at hand while offering flexibility in controlling the parameters and assumptions that may affect the results. First, the steps required to perform data-driven simulations are described, and then two examples of real-world time-to-event analyses illustrate their implementation and the insights they may offer. The first example focuses on the omission of an important time-invariant predictor of the outcome in a prognostic study of cancer mortality, and permits separating the expected impact of confounding bias from non-collapsibility. The second example assesses how imprecise timing of an interval-censored event - ascertained only at sparse times of clinic visits - affects its estimated association with a time-varying drug exposure. The simulation results also provide a basis for comparing the performance of two alternative strategies for imputing the unknown event times in this setting. The R scripts that permit the reproduction of our examples are provided.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Am J Epidemiol / Am. j. epidemiol / American journal of epidemiology Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Am J Epidemiol / Am. j. epidemiol / American journal of epidemiology Año: 2024 Tipo del documento: Article