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Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials
BACKGROUND: Vascular prevention trials typically use dichotomous event outcomes although this may be inefficient statistically and gives no indication of event severity. We assessed whether ordinal outcomes would be more efficient and how to best analyse them. METHODS: Chief investigators of vascula...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520648/ https://www.ncbi.nlm.nih.gov/pubmed/34657596 http://dx.doi.org/10.1186/s12874-021-01388-6 |
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author | Woodhouse, Lisa J. Montgomery, Alan A. Mant, Jonathan Davis, Barry R. Algra, Ale Mas, Jean-Louis Staessen, Jan A. Thijs, Lutgarde Tonkin, Andrew Kirby, Adrienne Pocock, Stuart J. Chalmers, John Hankey, Graeme J. Spence, J. David Sandercock, Peter Diener, Hans-Christoph Uchiyama, Shinichiro Sprigg, Nikola Bath, Philip M. |
author_facet | Woodhouse, Lisa J. Montgomery, Alan A. Mant, Jonathan Davis, Barry R. Algra, Ale Mas, Jean-Louis Staessen, Jan A. Thijs, Lutgarde Tonkin, Andrew Kirby, Adrienne Pocock, Stuart J. Chalmers, John Hankey, Graeme J. Spence, J. David Sandercock, Peter Diener, Hans-Christoph Uchiyama, Shinichiro Sprigg, Nikola Bath, Philip M. |
author_sort | Woodhouse, Lisa J. |
collection | PubMed |
description | BACKGROUND: Vascular prevention trials typically use dichotomous event outcomes although this may be inefficient statistically and gives no indication of event severity. We assessed whether ordinal outcomes would be more efficient and how to best analyse them. METHODS: Chief investigators of vascular prevention randomised controlled trials that showed evidence of either benefit or harm, or were included in a systematic review that overall showed benefit or harm, shared individual participant data from their trials. Ordered categorical versions of vascular event outcomes (such as stroke and myocardial infarction) were analysed using 15 statistical techniques and their results then ranked, with the result with the smallest p-value given the smallest rank. Friedman and Duncan’s multiple range tests were performed to assess differences between tests by comparing the average ranks for each statistical test. RESULTS: Data from 35 trials (254,223 participants) were shared with the collaboration. 13 trials had more than two treatment arms, resulting in 59 comparisons. Analysis approaches (Mann Whitney U, ordinal logistic regression, multiple regression, bootstrapping) that used ordinal outcome data had a smaller average rank and therefore appeared to be more efficient statistically than those that analysed the original binary outcomes. CONCLUSIONS: Ordinal vascular outcome measures appear to be more efficient statistically than binary outcomes and provide information on the severity of event. We suggest a potential role for using ordinal outcomes in vascular prevention trials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01388-6. |
format | Online Article Text |
id | pubmed-8520648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85206482021-10-20 Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials Woodhouse, Lisa J. Montgomery, Alan A. Mant, Jonathan Davis, Barry R. Algra, Ale Mas, Jean-Louis Staessen, Jan A. Thijs, Lutgarde Tonkin, Andrew Kirby, Adrienne Pocock, Stuart J. Chalmers, John Hankey, Graeme J. Spence, J. David Sandercock, Peter Diener, Hans-Christoph Uchiyama, Shinichiro Sprigg, Nikola Bath, Philip M. BMC Med Res Methodol Research BACKGROUND: Vascular prevention trials typically use dichotomous event outcomes although this may be inefficient statistically and gives no indication of event severity. We assessed whether ordinal outcomes would be more efficient and how to best analyse them. METHODS: Chief investigators of vascular prevention randomised controlled trials that showed evidence of either benefit or harm, or were included in a systematic review that overall showed benefit or harm, shared individual participant data from their trials. Ordered categorical versions of vascular event outcomes (such as stroke and myocardial infarction) were analysed using 15 statistical techniques and their results then ranked, with the result with the smallest p-value given the smallest rank. Friedman and Duncan’s multiple range tests were performed to assess differences between tests by comparing the average ranks for each statistical test. RESULTS: Data from 35 trials (254,223 participants) were shared with the collaboration. 13 trials had more than two treatment arms, resulting in 59 comparisons. Analysis approaches (Mann Whitney U, ordinal logistic regression, multiple regression, bootstrapping) that used ordinal outcome data had a smaller average rank and therefore appeared to be more efficient statistically than those that analysed the original binary outcomes. CONCLUSIONS: Ordinal vascular outcome measures appear to be more efficient statistically than binary outcomes and provide information on the severity of event. We suggest a potential role for using ordinal outcomes in vascular prevention trials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-021-01388-6. BioMed Central 2021-10-17 /pmc/articles/PMC8520648/ /pubmed/34657596 http://dx.doi.org/10.1186/s12874-021-01388-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Woodhouse, Lisa J. Montgomery, Alan A. Mant, Jonathan Davis, Barry R. Algra, Ale Mas, Jean-Louis Staessen, Jan A. Thijs, Lutgarde Tonkin, Andrew Kirby, Adrienne Pocock, Stuart J. Chalmers, John Hankey, Graeme J. Spence, J. David Sandercock, Peter Diener, Hans-Christoph Uchiyama, Shinichiro Sprigg, Nikola Bath, Philip M. Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title | Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title_full | Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title_fullStr | Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title_full_unstemmed | Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title_short | Statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
title_sort | statistical reanalysis of vascular event outcomes in primary and secondary vascular prevention trials |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520648/ https://www.ncbi.nlm.nih.gov/pubmed/34657596 http://dx.doi.org/10.1186/s12874-021-01388-6 |
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