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RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19

The COVID-19 pandemic led to an enormous burden on healthcare systems worldwide. Causal therapy is still in its infancy. Contrary to initial views that the use of angiotensin-converting enzyme inhibitors (ACEi)/angiotensin II receptor blockers (ARBs) may increase the risk for a deleterious disease c...

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Autores principales: Dutsch, Alexander, Schunkert, Heribert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127983/
https://www.ncbi.nlm.nih.gov/pubmed/37097476
http://dx.doi.org/10.1007/s00059-023-05168-4
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author Dutsch, Alexander
Schunkert, Heribert
author_facet Dutsch, Alexander
Schunkert, Heribert
author_sort Dutsch, Alexander
collection PubMed
description The COVID-19 pandemic led to an enormous burden on healthcare systems worldwide. Causal therapy is still in its infancy. Contrary to initial views that the use of angiotensin-converting enzyme inhibitors (ACEi)/angiotensin II receptor blockers (ARBs) may increase the risk for a deleterious disease course, it has been shown that these agents may actually be beneficial for patients affected by COVID-19. In this article, we provide an overview of the three most commonly used classes of drugs in cardiovascular disease (ACEi/ARB, statins, beta-blockers) and their potential role in COVID-19 therapy. More results from randomized clinical trials are necessary to identify patients that can benefit most from the use of the respective drugs.
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spelling pubmed-101279832023-04-27 RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19 Dutsch, Alexander Schunkert, Heribert Herz Main Topic The COVID-19 pandemic led to an enormous burden on healthcare systems worldwide. Causal therapy is still in its infancy. Contrary to initial views that the use of angiotensin-converting enzyme inhibitors (ACEi)/angiotensin II receptor blockers (ARBs) may increase the risk for a deleterious disease course, it has been shown that these agents may actually be beneficial for patients affected by COVID-19. In this article, we provide an overview of the three most commonly used classes of drugs in cardiovascular disease (ACEi/ARB, statins, beta-blockers) and their potential role in COVID-19 therapy. More results from randomized clinical trials are necessary to identify patients that can benefit most from the use of the respective drugs. Springer Medizin 2023-04-25 2023 /pmc/articles/PMC10127983/ /pubmed/37097476 http://dx.doi.org/10.1007/s00059-023-05168-4 Text en © The Author(s), under exclusive licence to Springer Medizin Verlag GmbH, ein Teil von Springer Nature 2023 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Main Topic
Dutsch, Alexander
Schunkert, Heribert
RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title_full RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title_fullStr RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title_full_unstemmed RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title_short RAAS inhibition and beyond—cardiovascular medications in patients at risk of or affected by COVID-19
title_sort raas inhibition and beyond—cardiovascular medications in patients at risk of or affected by covid-19
topic Main Topic
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127983/
https://www.ncbi.nlm.nih.gov/pubmed/37097476
http://dx.doi.org/10.1007/s00059-023-05168-4
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