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Propensity score analysis for time-dependent exposure
Propensity score analysis (PSA) is widely used in medical literature to account for confounders. Conventionally, the propensity score (PS) is calculated by a binary logistic regression model using time-fixed covariates. In the presence of time-varying treatment or exposure, the conventional method m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154493/ https://www.ncbi.nlm.nih.gov/pubmed/32309393 http://dx.doi.org/10.21037/atm.2020.01.33 |
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author | Zhang, Zhongheng Li, Xiuyang Wu, Xiao Qiu, Huixian Shi, Hongying |
author_facet | Zhang, Zhongheng Li, Xiuyang Wu, Xiao Qiu, Huixian Shi, Hongying |
author_sort | Zhang, Zhongheng |
collection | PubMed |
description | Propensity score analysis (PSA) is widely used in medical literature to account for confounders. Conventionally, the propensity score (PS) is calculated by a binary logistic regression model using time-fixed covariates. In the presence of time-varying treatment or exposure, the conventional method may cause bias because subjects with early and late exposure are treated as the same. In effect, subjects who are treated latter can be different from those who are treated early. Thus, the conventional PSA must be modified to address this bias. In this paper, we illustrate how to perform analysis in the presence of time-dependent exposure. We conduct a simulation study with a known treatment effect. In the simulation study, we find the PSA method that directly adjust PS estimated by either a binary logistic regression model or a Cox regression model using time-fixed covariates still introduce significant bias. On the other hand, the time-dependent PS matching can help to achieve a result approaching the true effect. After time-dependent PS matching, the matched cohort can be analyzed with conventional Cox regression model or conditional logistic regression (CLR) model with time strata. The performance is comparable to the correctly specified Cox regression model with time-varying covariates (i.e., adjusting the exposure in a multivariable model as a time-varying covariate). We further develop a function called TDPSM() for time-dependent PS matching and it is applied to a real world dataset. |
format | Online Article Text |
id | pubmed-7154493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-71544932020-04-17 Propensity score analysis for time-dependent exposure Zhang, Zhongheng Li, Xiuyang Wu, Xiao Qiu, Huixian Shi, Hongying Ann Transl Med Big-data Clinical Trial Column Propensity score analysis (PSA) is widely used in medical literature to account for confounders. Conventionally, the propensity score (PS) is calculated by a binary logistic regression model using time-fixed covariates. In the presence of time-varying treatment or exposure, the conventional method may cause bias because subjects with early and late exposure are treated as the same. In effect, subjects who are treated latter can be different from those who are treated early. Thus, the conventional PSA must be modified to address this bias. In this paper, we illustrate how to perform analysis in the presence of time-dependent exposure. We conduct a simulation study with a known treatment effect. In the simulation study, we find the PSA method that directly adjust PS estimated by either a binary logistic regression model or a Cox regression model using time-fixed covariates still introduce significant bias. On the other hand, the time-dependent PS matching can help to achieve a result approaching the true effect. After time-dependent PS matching, the matched cohort can be analyzed with conventional Cox regression model or conditional logistic regression (CLR) model with time strata. The performance is comparable to the correctly specified Cox regression model with time-varying covariates (i.e., adjusting the exposure in a multivariable model as a time-varying covariate). We further develop a function called TDPSM() for time-dependent PS matching and it is applied to a real world dataset. AME Publishing Company 2020-03 /pmc/articles/PMC7154493/ /pubmed/32309393 http://dx.doi.org/10.21037/atm.2020.01.33 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Big-data Clinical Trial Column Zhang, Zhongheng Li, Xiuyang Wu, Xiao Qiu, Huixian Shi, Hongying Propensity score analysis for time-dependent exposure |
title | Propensity score analysis for time-dependent exposure |
title_full | Propensity score analysis for time-dependent exposure |
title_fullStr | Propensity score analysis for time-dependent exposure |
title_full_unstemmed | Propensity score analysis for time-dependent exposure |
title_short | Propensity score analysis for time-dependent exposure |
title_sort | propensity score analysis for time-dependent exposure |
topic | Big-data Clinical Trial Column |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154493/ https://www.ncbi.nlm.nih.gov/pubmed/32309393 http://dx.doi.org/10.21037/atm.2020.01.33 |
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