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Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation
In trials comparing the rate of chronic obstructive pulmonary disease exacerbation between treatment arms, the rate is typically calculated on the basis of the whole of each patient's follow‐up period. However, the true time a patient is at risk should exclude periods in which an exacerbation e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434805/ https://www.ncbi.nlm.nih.gov/pubmed/27966248 http://dx.doi.org/10.1002/pst.1798 |
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author | Law, M. Sweeting, M.J. Donaldson, G.C. Wedzicha, J.A. |
author_facet | Law, M. Sweeting, M.J. Donaldson, G.C. Wedzicha, J.A. |
author_sort | Law, M. |
collection | PubMed |
description | In trials comparing the rate of chronic obstructive pulmonary disease exacerbation between treatment arms, the rate is typically calculated on the basis of the whole of each patient's follow‐up period. However, the true time a patient is at risk should exclude periods in which an exacerbation episode is occurring, because a patient cannot be at risk of another exacerbation episode until recovered. We used data from two chronic obstructive pulmonary disease randomized controlled trials and compared treatment effect estimates and confidence intervals when using two different definitions of the at‐risk period. Using a simulation study we examined the bias in the estimated treatment effect and the coverage of the confidence interval, using these two definitions of the at‐risk period. We investigated how the sample size required for a given power changes on the basis of the definition of at‐risk period used. Our results showed that treatment efficacy is underestimated when the at‐risk period does not take account of exacerbation duration, and the power to detect a statistically significant result is slightly diminished. Correspondingly, using the correct at‐risk period, some modest savings in required sample size can be achieved. Using the proposed at‐risk period that excludes recovery times requires formal definitions of the beginning and end of an exacerbation episode, and we recommend these be always predefined in a trial protocol. |
format | Online Article Text |
id | pubmed-5434805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54348052017-06-01 Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation Law, M. Sweeting, M.J. Donaldson, G.C. Wedzicha, J.A. Pharm Stat Main Papers In trials comparing the rate of chronic obstructive pulmonary disease exacerbation between treatment arms, the rate is typically calculated on the basis of the whole of each patient's follow‐up period. However, the true time a patient is at risk should exclude periods in which an exacerbation episode is occurring, because a patient cannot be at risk of another exacerbation episode until recovered. We used data from two chronic obstructive pulmonary disease randomized controlled trials and compared treatment effect estimates and confidence intervals when using two different definitions of the at‐risk period. Using a simulation study we examined the bias in the estimated treatment effect and the coverage of the confidence interval, using these two definitions of the at‐risk period. We investigated how the sample size required for a given power changes on the basis of the definition of at‐risk period used. Our results showed that treatment efficacy is underestimated when the at‐risk period does not take account of exacerbation duration, and the power to detect a statistically significant result is slightly diminished. Correspondingly, using the correct at‐risk period, some modest savings in required sample size can be achieved. Using the proposed at‐risk period that excludes recovery times requires formal definitions of the beginning and end of an exacerbation episode, and we recommend these be always predefined in a trial protocol. John Wiley and Sons Inc. 2016-12-14 2017 /pmc/articles/PMC5434805/ /pubmed/27966248 http://dx.doi.org/10.1002/pst.1798 Text en Copyright © 2016 The Authors. Pharmaceutical Statistics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (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 | Main Papers Law, M. Sweeting, M.J. Donaldson, G.C. Wedzicha, J.A. Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title | Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title_full | Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title_fullStr | Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title_full_unstemmed | Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title_short | Misspecification of at‐risk periods and distributional assumptions in estimating COPD exacerbation rates: The resultant bias in treatment effect estimation |
title_sort | misspecification of at‐risk periods and distributional assumptions in estimating copd exacerbation rates: the resultant bias in treatment effect estimation |
topic | Main Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434805/ https://www.ncbi.nlm.nih.gov/pubmed/27966248 http://dx.doi.org/10.1002/pst.1798 |
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