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Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study

Most cardiovascular disease (CVD) events can be prevented with appropriate risk management. Existing evidence suggests women are less likely than men to receive guideline-recommended medications, however data on sex-differences in preventive medication use following a CVD event are lacking. Relative...

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Autores principales: Barrett, Eden, Paige, Ellie, Welsh, Jennifer, Korda, Rosemary J., Joshy, Grace, Martin, Melonie, Banks, Emily
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985714/
https://www.ncbi.nlm.nih.gov/pubmed/33777665
http://dx.doi.org/10.1016/j.pmedr.2021.101342
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author Barrett, Eden
Paige, Ellie
Welsh, Jennifer
Korda, Rosemary J.
Joshy, Grace
Martin, Melonie
Banks, Emily
author_facet Barrett, Eden
Paige, Ellie
Welsh, Jennifer
Korda, Rosemary J.
Joshy, Grace
Martin, Melonie
Banks, Emily
author_sort Barrett, Eden
collection PubMed
description Most cardiovascular disease (CVD) events can be prevented with appropriate risk management. Existing evidence suggests women are less likely than men to receive guideline-recommended medications, however data on sex-differences in preventive medication use following a CVD event are lacking. Relative risks (RRs) comparing use of blood pressure- and lipid-lowering medications in men and women at 3-, 6-, 9- and 12-months following hospitalisation for myocardial infarction (MI) or stroke from 2012 to 2017 were quantified using linked data from 8,278 participants enrolled in the Australian 45 and Up Study. Overall, 51% of women and 58% of men were using both blood-pressure- and lipid-lowering medications three months after a MI or stroke event, decreasing to 48% and 53%, respectively, at 12 months after an event. Adjusting for potential confounders, women were 9% less likely than men (RR = 0.91 [95% CI: 0.87, 0.95]) to be using both medications and 19% more likely (RR = 1.19 [95% CI: 1.07, 1.32]) to use neither medication three months after a MI or stroke event. At the 12-month mark, women were 8% less likely (RR = 0.92 [95% CI: 0.88, 0.97]) to be using both medications and 14% more likely (RR = 1.14 [95% CI: 1.03, 1.26]) to use neither medication. Women were consistently less likely to use both preventive medications and more likely to use neither medication at each follow-up time point. Overall, there were major shortfalls in basic preventive medication use post-CVD event and sex disparities are likely to further jeopardise efforts to reduce CVD events in the community.
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spelling pubmed-79857142021-03-25 Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study Barrett, Eden Paige, Ellie Welsh, Jennifer Korda, Rosemary J. Joshy, Grace Martin, Melonie Banks, Emily Prev Med Rep Regular Article Most cardiovascular disease (CVD) events can be prevented with appropriate risk management. Existing evidence suggests women are less likely than men to receive guideline-recommended medications, however data on sex-differences in preventive medication use following a CVD event are lacking. Relative risks (RRs) comparing use of blood pressure- and lipid-lowering medications in men and women at 3-, 6-, 9- and 12-months following hospitalisation for myocardial infarction (MI) or stroke from 2012 to 2017 were quantified using linked data from 8,278 participants enrolled in the Australian 45 and Up Study. Overall, 51% of women and 58% of men were using both blood-pressure- and lipid-lowering medications three months after a MI or stroke event, decreasing to 48% and 53%, respectively, at 12 months after an event. Adjusting for potential confounders, women were 9% less likely than men (RR = 0.91 [95% CI: 0.87, 0.95]) to be using both medications and 19% more likely (RR = 1.19 [95% CI: 1.07, 1.32]) to use neither medication three months after a MI or stroke event. At the 12-month mark, women were 8% less likely (RR = 0.92 [95% CI: 0.88, 0.97]) to be using both medications and 14% more likely (RR = 1.14 [95% CI: 1.03, 1.26]) to use neither medication. Women were consistently less likely to use both preventive medications and more likely to use neither medication at each follow-up time point. Overall, there were major shortfalls in basic preventive medication use post-CVD event and sex disparities are likely to further jeopardise efforts to reduce CVD events in the community. 2021-03-07 /pmc/articles/PMC7985714/ /pubmed/33777665 http://dx.doi.org/10.1016/j.pmedr.2021.101342 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Barrett, Eden
Paige, Ellie
Welsh, Jennifer
Korda, Rosemary J.
Joshy, Grace
Martin, Melonie
Banks, Emily
Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title_full Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title_fullStr Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title_full_unstemmed Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title_short Differences between men and women in the use of preventive medications following a major cardiovascular event: Australian prospective cohort study
title_sort differences between men and women in the use of preventive medications following a major cardiovascular event: australian prospective cohort study
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985714/
https://www.ncbi.nlm.nih.gov/pubmed/33777665
http://dx.doi.org/10.1016/j.pmedr.2021.101342
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