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Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol

INTRODUCTION: Recent publications have called for substantial improvements in the design, conduct, analysis and reporting of prediction models. Publication of study protocols, with prespecification of key aspects of the analysis plan, can help to improve transparency, increase quality and protect ag...

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Autores principales: Taljaard, Monica, Tuna, Meltem, Bennett, Carol, Perez, Richard, Rosella, Laura, Tu, Jack V, Sanmartin, Claudia, Hennessy, Deirdre, Tanuseputro, Peter, Lebenbaum, Michael, Manuel, Douglas G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208046/
https://www.ncbi.nlm.nih.gov/pubmed/25341454
http://dx.doi.org/10.1136/bmjopen-2014-006701
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author Taljaard, Monica
Tuna, Meltem
Bennett, Carol
Perez, Richard
Rosella, Laura
Tu, Jack V
Sanmartin, Claudia
Hennessy, Deirdre
Tanuseputro, Peter
Lebenbaum, Michael
Manuel, Douglas G
author_facet Taljaard, Monica
Tuna, Meltem
Bennett, Carol
Perez, Richard
Rosella, Laura
Tu, Jack V
Sanmartin, Claudia
Hennessy, Deirdre
Tanuseputro, Peter
Lebenbaum, Michael
Manuel, Douglas G
author_sort Taljaard, Monica
collection PubMed
description INTRODUCTION: Recent publications have called for substantial improvements in the design, conduct, analysis and reporting of prediction models. Publication of study protocols, with prespecification of key aspects of the analysis plan, can help to improve transparency, increase quality and protect against increased type I error. Valid population-based risk algorithms are essential for population health planning and policy decision-making. The purpose of this study is to develop, evaluate and apply cardiovascular disease (CVD) risk algorithms for the population setting. METHODS AND ANALYSIS: The Ontario sample of the Canadian Community Health Survey (2001, 2003, 2005; 77 251 respondents) will be used to assess risk factors focusing on health behaviours (physical activity, diet, smoking and alcohol use). Incident CVD outcomes will be assessed through linkage to administrative healthcare databases (619 886 person-years of follow-up until 31 December 2011). Sociodemographic factors (age, sex, immigrant status, education) and mediating factors such as presence of diabetes and hypertension will be included as predictors. Algorithms will be developed using competing risks survival analysis. The analysis plan adheres to published recommendations for the development of valid prediction models to limit the risk of overfitting and improve the quality of predictions. Key considerations are fully prespecifying the predictor variables; appropriate handling of missing data; use of flexible functions for continuous predictors; and avoiding data-driven variable selection procedures. The 2007 and 2009 surveys (approximately 50 000 respondents) will be used for validation. Calibration will be assessed overall and in predefined subgroups of importance to clinicians and policymakers. ETHICS AND DISSEMINATION: This study has been approved by the Ottawa Health Science Network Research Ethics Board. The findings will be disseminated through professional and scientific conferences, and in peer-reviewed journals. The algorithm will be accessible electronically for population and individual uses. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov NCT02267447.
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spelling pubmed-42080462014-10-27 Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol Taljaard, Monica Tuna, Meltem Bennett, Carol Perez, Richard Rosella, Laura Tu, Jack V Sanmartin, Claudia Hennessy, Deirdre Tanuseputro, Peter Lebenbaum, Michael Manuel, Douglas G BMJ Open Cardiovascular Medicine INTRODUCTION: Recent publications have called for substantial improvements in the design, conduct, analysis and reporting of prediction models. Publication of study protocols, with prespecification of key aspects of the analysis plan, can help to improve transparency, increase quality and protect against increased type I error. Valid population-based risk algorithms are essential for population health planning and policy decision-making. The purpose of this study is to develop, evaluate and apply cardiovascular disease (CVD) risk algorithms for the population setting. METHODS AND ANALYSIS: The Ontario sample of the Canadian Community Health Survey (2001, 2003, 2005; 77 251 respondents) will be used to assess risk factors focusing on health behaviours (physical activity, diet, smoking and alcohol use). Incident CVD outcomes will be assessed through linkage to administrative healthcare databases (619 886 person-years of follow-up until 31 December 2011). Sociodemographic factors (age, sex, immigrant status, education) and mediating factors such as presence of diabetes and hypertension will be included as predictors. Algorithms will be developed using competing risks survival analysis. The analysis plan adheres to published recommendations for the development of valid prediction models to limit the risk of overfitting and improve the quality of predictions. Key considerations are fully prespecifying the predictor variables; appropriate handling of missing data; use of flexible functions for continuous predictors; and avoiding data-driven variable selection procedures. The 2007 and 2009 surveys (approximately 50 000 respondents) will be used for validation. Calibration will be assessed overall and in predefined subgroups of importance to clinicians and policymakers. ETHICS AND DISSEMINATION: This study has been approved by the Ottawa Health Science Network Research Ethics Board. The findings will be disseminated through professional and scientific conferences, and in peer-reviewed journals. The algorithm will be accessible electronically for population and individual uses. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov NCT02267447. BMJ Publishing Group 2014-10-23 /pmc/articles/PMC4208046/ /pubmed/25341454 http://dx.doi.org/10.1136/bmjopen-2014-006701 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Cardiovascular Medicine
Taljaard, Monica
Tuna, Meltem
Bennett, Carol
Perez, Richard
Rosella, Laura
Tu, Jack V
Sanmartin, Claudia
Hennessy, Deirdre
Tanuseputro, Peter
Lebenbaum, Michael
Manuel, Douglas G
Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title_full Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title_fullStr Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title_full_unstemmed Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title_short Cardiovascular Disease Population Risk Tool (CVDPoRT): predictive algorithm for assessing CVD risk in the community setting. A study protocol
title_sort cardiovascular disease population risk tool (cvdport): predictive algorithm for assessing cvd risk in the community setting. a study protocol
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208046/
https://www.ncbi.nlm.nih.gov/pubmed/25341454
http://dx.doi.org/10.1136/bmjopen-2014-006701
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