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The Association of Cardioprotective Medications with Pneumonia-Related Outcomes

INTRODUCTION: Little research has examined whether cardiovascular medications, other than statins, are associated with improved outcomes after pneumonia. Our aim was to examine the association between the use of beta-blockers, statins, angiotensin converting enzyme (ACE) inhibitors, and angiotensin...

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Autores principales: Wu, Albert, Good, Chester, Downs, John R., Fine, Michael J., Pugh, Mary Jo V., Anzueto, Antonio, Mortensen, Eric M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904855/
https://www.ncbi.nlm.nih.gov/pubmed/24489672
http://dx.doi.org/10.1371/journal.pone.0085797
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author Wu, Albert
Good, Chester
Downs, John R.
Fine, Michael J.
Pugh, Mary Jo V.
Anzueto, Antonio
Mortensen, Eric M.
author_facet Wu, Albert
Good, Chester
Downs, John R.
Fine, Michael J.
Pugh, Mary Jo V.
Anzueto, Antonio
Mortensen, Eric M.
author_sort Wu, Albert
collection PubMed
description INTRODUCTION: Little research has examined whether cardiovascular medications, other than statins, are associated with improved outcomes after pneumonia. Our aim was to examine the association between the use of beta-blockers, statins, angiotensin converting enzyme (ACE) inhibitors, and angiotensin II receptor blockers (ARBs) with pneumonia-related outcomes. MATERIALS AND METHODS: We conducted a retrospective population-based study on male patients ≥65 years of age hospitalized with pneumonia and who did not have pre-existing cardiac disease. Our primary analyses were multilevel regression models that examined the association between cardiovascular medication classes and either mortality or cardiovascular events. RESULTS: Our cohort included 21,985 patients: 22% died within 90 days of admission, and 22% had a cardiac event within 90 days. The cardiovascular medications studied that were associated with decreased 90-day mortality included: statins (OR 0.70, 95% CI 0.63–0.77), ACE inhibitors (OR 0.82, 95% CI 0.74–0.91), and ARBs (OR 0.58, 95% CI 0.44–0.77). However, none of the medications were significantly associated with decreased cardiovascular events. DISCUSSION: While statins, ACE inhibitors, and ARBs, were associated with decreased mortality, there was no significant association with decreased CV events. These results indicate that this decreased mortality is unlikely due to their potential cardioprotective effects.
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spelling pubmed-39048552014-01-31 The Association of Cardioprotective Medications with Pneumonia-Related Outcomes Wu, Albert Good, Chester Downs, John R. Fine, Michael J. Pugh, Mary Jo V. Anzueto, Antonio Mortensen, Eric M. PLoS One Research Article INTRODUCTION: Little research has examined whether cardiovascular medications, other than statins, are associated with improved outcomes after pneumonia. Our aim was to examine the association between the use of beta-blockers, statins, angiotensin converting enzyme (ACE) inhibitors, and angiotensin II receptor blockers (ARBs) with pneumonia-related outcomes. MATERIALS AND METHODS: We conducted a retrospective population-based study on male patients ≥65 years of age hospitalized with pneumonia and who did not have pre-existing cardiac disease. Our primary analyses were multilevel regression models that examined the association between cardiovascular medication classes and either mortality or cardiovascular events. RESULTS: Our cohort included 21,985 patients: 22% died within 90 days of admission, and 22% had a cardiac event within 90 days. The cardiovascular medications studied that were associated with decreased 90-day mortality included: statins (OR 0.70, 95% CI 0.63–0.77), ACE inhibitors (OR 0.82, 95% CI 0.74–0.91), and ARBs (OR 0.58, 95% CI 0.44–0.77). However, none of the medications were significantly associated with decreased cardiovascular events. DISCUSSION: While statins, ACE inhibitors, and ARBs, were associated with decreased mortality, there was no significant association with decreased CV events. These results indicate that this decreased mortality is unlikely due to their potential cardioprotective effects. Public Library of Science 2014-01-28 /pmc/articles/PMC3904855/ /pubmed/24489672 http://dx.doi.org/10.1371/journal.pone.0085797 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Wu, Albert
Good, Chester
Downs, John R.
Fine, Michael J.
Pugh, Mary Jo V.
Anzueto, Antonio
Mortensen, Eric M.
The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title_full The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title_fullStr The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title_full_unstemmed The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title_short The Association of Cardioprotective Medications with Pneumonia-Related Outcomes
title_sort association of cardioprotective medications with pneumonia-related outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904855/
https://www.ncbi.nlm.nih.gov/pubmed/24489672
http://dx.doi.org/10.1371/journal.pone.0085797
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