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Bias due to coarsening of time intervals in the inference for the effectiveness of colorectal cancer screening.
Karmakar, Bikram; Zauber, Ann G; Hahn, Anne I; Lau, Yan Kwan; Doubeni, Chyke A; Joffe, Marshall M.
Afiliação
  • Karmakar B; Department of Statistics, College of Liberal Arts and Sciences, University of Florida, Gainesville, FL, USA.
  • Zauber AG; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Hahn AI; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Lau YK; Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
  • Doubeni CA; Family and Community Medicine, Arthur G. James Cancer Hospital and Solove Research Institute, Columbus, OH, USA.
  • Joffe MM; Department of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics, The University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Int J Epidemiol ; 53(4)2024 Jun 12.
Article em En | MEDLINE | ID: mdl-39002174
ABSTRACT

BACKGROUND:

Observational studies are frequently used to estimate the comparative effectiveness of different colorectal cancer (CRC) screening methods due to the practical limitations and time needed to conduct large clinical trials. However, time-varying confounders, e.g. polyp detection in the last screening, can bias statistical results. Recently, generalized methods, or G-methods, have been used for the analysis of observational studies of CRC screening, given their ability to account for such time-varying confounders. Discretization, or the process of converting continuous functions into discrete counterparts, is required for G-methods when the treatment and outcomes are assessed at a continuous scale. DEVELOPMENT This paper evaluates the interplay between time-varying confounding and discretization, which can induce bias in assessing screening effectiveness. We investigate this bias in evaluating the effect of different CRC screening methods that differ from each other in typical screening frequency. APPLICATION First, using theory, we establish the direction of the bias. Then, we use simulations of hypothetical settings to study the bias magnitude for varying levels of discretization, frequency of screening and length of the study period. We develop a method to assess possible bias due to coarsening in simulated situations.

CONCLUSIONS:

The proposed method can inform future studies of screening effectiveness, especially for CRC, by determining the choice of interval lengths where data are discretized to minimize bias due to coarsening while balancing computational costs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Viés / Detecção Precoce de Câncer Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Viés / Detecção Precoce de Câncer Idioma: En Ano de publicação: 2024 Tipo de documento: Article