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Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19

Continued receipt of Renin–Angiotensin–Aldosterone inhibitors in patients with COVID-19 has shown potential in producing better clinical outcomes. However, superiority between ACEi (angiotensin-converting enzyme inhibitors) and ARB (angiotensin II receptor blockers) regarding clinical outcomes in th...

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Autores principales: Hamada, Seiji, Suzuki, Tomoharu, Tokuda, Yasuharu, Taniguchi, Kiyosu, Shibuya, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361955/
https://www.ncbi.nlm.nih.gov/pubmed/37479767
http://dx.doi.org/10.1038/s41598-023-38838-8
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author Hamada, Seiji
Suzuki, Tomoharu
Tokuda, Yasuharu
Taniguchi, Kiyosu
Shibuya, Kenji
author_facet Hamada, Seiji
Suzuki, Tomoharu
Tokuda, Yasuharu
Taniguchi, Kiyosu
Shibuya, Kenji
author_sort Hamada, Seiji
collection PubMed
description Continued receipt of Renin–Angiotensin–Aldosterone inhibitors in patients with COVID-19 has shown potential in producing better clinical outcomes. However, superiority between ACEi (angiotensin-converting enzyme inhibitors) and ARB (angiotensin II receptor blockers) regarding clinical outcomes in this setting remains unknown. We retrospectively collected data on patients hospitalized for acute COVID-19 using the nationwide administrative database (Diagnosis and Procedure Combinations, DPC). The DPC data covered around 25% of all acute care hospitals in Japan. Patient outcomes, with focus on inpatient mortality, were compared between patients previously prescribed ACEi and those prescribed ARB. Comparisons based on crude, multivariate and propensity-score adjusted analysis were conducted. We examined a total of 7613 patients (ARB group, 6903; ACEi group 710). The ARB group showed lower crude in-hospital mortality, compared to the ACEi group (5% vs 8%; odds ratio, 0.65; 95% CI 0.48–0.87), however not in the multivariate-adjusted model (odds ratio, 0.95; 95% CI 0.69–1.3) or propensity-score adjusted models (odds ratio, 0.86; 95% CI 0.63–1.2). ARB shows potential in reducing hospital stay duration over ACEi in patients admitted for COVID-19, but does not significantly reduce in-hospital mortality. Further prospective studies are needed to draw a definitive conclusion, but continuation of either of these medications is warranted to improve clinical outcomes.
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spelling pubmed-103619552023-07-23 Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19 Hamada, Seiji Suzuki, Tomoharu Tokuda, Yasuharu Taniguchi, Kiyosu Shibuya, Kenji Sci Rep Article Continued receipt of Renin–Angiotensin–Aldosterone inhibitors in patients with COVID-19 has shown potential in producing better clinical outcomes. However, superiority between ACEi (angiotensin-converting enzyme inhibitors) and ARB (angiotensin II receptor blockers) regarding clinical outcomes in this setting remains unknown. We retrospectively collected data on patients hospitalized for acute COVID-19 using the nationwide administrative database (Diagnosis and Procedure Combinations, DPC). The DPC data covered around 25% of all acute care hospitals in Japan. Patient outcomes, with focus on inpatient mortality, were compared between patients previously prescribed ACEi and those prescribed ARB. Comparisons based on crude, multivariate and propensity-score adjusted analysis were conducted. We examined a total of 7613 patients (ARB group, 6903; ACEi group 710). The ARB group showed lower crude in-hospital mortality, compared to the ACEi group (5% vs 8%; odds ratio, 0.65; 95% CI 0.48–0.87), however not in the multivariate-adjusted model (odds ratio, 0.95; 95% CI 0.69–1.3) or propensity-score adjusted models (odds ratio, 0.86; 95% CI 0.63–1.2). ARB shows potential in reducing hospital stay duration over ACEi in patients admitted for COVID-19, but does not significantly reduce in-hospital mortality. Further prospective studies are needed to draw a definitive conclusion, but continuation of either of these medications is warranted to improve clinical outcomes. Nature Publishing Group UK 2023-07-21 /pmc/articles/PMC10361955/ /pubmed/37479767 http://dx.doi.org/10.1038/s41598-023-38838-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Hamada, Seiji
Suzuki, Tomoharu
Tokuda, Yasuharu
Taniguchi, Kiyosu
Shibuya, Kenji
Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title_full Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title_fullStr Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title_full_unstemmed Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title_short Comparing clinical outcomes of ARB and ACEi in patients hospitalized for acute COVID-19
title_sort comparing clinical outcomes of arb and acei in patients hospitalized for acute covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361955/
https://www.ncbi.nlm.nih.gov/pubmed/37479767
http://dx.doi.org/10.1038/s41598-023-38838-8
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