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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6282523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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