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Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models

Clinical prediction models (CPMs) can inform decision making about treatment initiation, which requires predicted risks assuming no treatment is given. However, this is challenging since CPMs are usually derived using data sets where patients received treatment, often initiated postbaseline as “trea...

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Autores principales: Sperrin, Matthew, Martin, Glen P., Pate, Alexander, Van Staa, Tjeerd, Peek, Niels, Buchan, Iain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282523/
https://www.ncbi.nlm.nih.gov/pubmed/30073700
http://dx.doi.org/10.1002/sim.7913
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author Sperrin, Matthew
Martin, Glen P.
Pate, Alexander
Van Staa, Tjeerd
Peek, Niels
Buchan, Iain
author_facet Sperrin, Matthew
Martin, Glen P.
Pate, Alexander
Van Staa, Tjeerd
Peek, Niels
Buchan, Iain
author_sort Sperrin, Matthew
collection PubMed
description Clinical prediction models (CPMs) can inform decision making about treatment initiation, which requires predicted risks assuming no treatment is given. However, this is challenging since CPMs are usually derived using data sets where patients received treatment, often initiated postbaseline as “treatment drop‐ins.” This study proposes the use of marginal structural models (MSMs) to adjust for treatment drop‐in. We illustrate the use of MSMs in the CPM framework through simulation studies that represent randomized controlled trials and real‐world observational data and the example of statin initiation for cardiovascular disease prevention. The simulations include a binary treatment and a covariate, each recorded at two timepoints and having a prognostic effect on a binary outcome. The bias in predicted risk was examined in a model ignoring treatment, a model fitted on treatment‐naïve patients (at baseline), a model including baseline treatment, and the MSM. In all simulation scenarios, all models except the MSM underestimated the risk of outcome given absence of treatment. These results were supported in the statin initiation example, which showed that ignoring statin initiation postbaseline resulted in models that significantly underestimated the risk of a cardiovascular disease event occurring within 10 years. Consequently, CPMs that do not acknowledge treatment drop‐in can lead to underallocation of treatment. In conclusion, when developing CPMs to predict treatment‐naïve risk, researchers should consider using MSMs to adjust for treatment drop‐in, and also seek to exploit the ability of MSMs to allow estimation of individual treatment effects.
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spelling pubmed-62825232018-12-11 Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models Sperrin, Matthew Martin, Glen P. Pate, Alexander Van Staa, Tjeerd Peek, Niels Buchan, Iain Stat Med Research Articles Clinical prediction models (CPMs) can inform decision making about treatment initiation, which requires predicted risks assuming no treatment is given. However, this is challenging since CPMs are usually derived using data sets where patients received treatment, often initiated postbaseline as “treatment drop‐ins.” This study proposes the use of marginal structural models (MSMs) to adjust for treatment drop‐in. We illustrate the use of MSMs in the CPM framework through simulation studies that represent randomized controlled trials and real‐world observational data and the example of statin initiation for cardiovascular disease prevention. The simulations include a binary treatment and a covariate, each recorded at two timepoints and having a prognostic effect on a binary outcome. The bias in predicted risk was examined in a model ignoring treatment, a model fitted on treatment‐naïve patients (at baseline), a model including baseline treatment, and the MSM. In all simulation scenarios, all models except the MSM underestimated the risk of outcome given absence of treatment. These results were supported in the statin initiation example, which showed that ignoring statin initiation postbaseline resulted in models that significantly underestimated the risk of a cardiovascular disease event occurring within 10 years. Consequently, CPMs that do not acknowledge treatment drop‐in can lead to underallocation of treatment. In conclusion, when developing CPMs to predict treatment‐naïve risk, researchers should consider using MSMs to adjust for treatment drop‐in, and also seek to exploit the ability of MSMs to allow estimation of individual treatment effects. John Wiley and Sons Inc. 2018-08-02 2018-12-10 /pmc/articles/PMC6282523/ /pubmed/30073700 http://dx.doi.org/10.1002/sim.7913 Text en © 2018 The Authors. Statistics in Medicine Published by John Wiley & Sons, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sperrin, Matthew
Martin, Glen P.
Pate, Alexander
Van Staa, Tjeerd
Peek, Niels
Buchan, Iain
Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title_full Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title_fullStr Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title_full_unstemmed Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title_short Using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
title_sort using marginal structural models to adjust for treatment drop‐in when developing clinical prediction models
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282523/
https://www.ncbi.nlm.nih.gov/pubmed/30073700
http://dx.doi.org/10.1002/sim.7913
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