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Administration of macrolide antibiotics increases cardiovascular risk
BACKGROUND: The increased risk of cardiovascular events in patients prescribed macrolides has been subject to debate for decades. METHODS: Medline, EMBASE databases and ClinicalTrials.gov were searched from inception until August 31, 2022 for studies investigating the link between macrolides and car...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996752/ https://www.ncbi.nlm.nih.gov/pubmed/36910529 http://dx.doi.org/10.3389/fcvm.2023.1117254 |
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author | Wu, Yang Bi, Wen-Tao Qu, Li-Ping Fan, Jun Kong, Xiang-Jun Ji, Cheng-Cheng Chen, Xu-Miao Yao, Feng-Juan Liu, Li-Juan Cheng, Yun-Jiu Wu, Su-Hua |
author_facet | Wu, Yang Bi, Wen-Tao Qu, Li-Ping Fan, Jun Kong, Xiang-Jun Ji, Cheng-Cheng Chen, Xu-Miao Yao, Feng-Juan Liu, Li-Juan Cheng, Yun-Jiu Wu, Su-Hua |
author_sort | Wu, Yang |
collection | PubMed |
description | BACKGROUND: The increased risk of cardiovascular events in patients prescribed macrolides has been subject to debate for decades. METHODS: Medline, EMBASE databases and ClinicalTrials.gov were searched from inception until August 31, 2022 for studies investigating the link between macrolides and cardiovascular risk. A meta-analysis was performed using a random-effects model. RESULTS: A total of 80 studies involving 39,374,874 patients were included. No association was found between macrolides and all-cause death. However, compared with the non-macrolide group, macrolides were associated with a significantly increased risk of ventricular arrhythmia or sudden cardiac death (VA or SCD) (azithromycin, relative ratio [RR]: 1.53; 95% confidence interval [CI]: 1.19 to 1.97; clarithromycin, RR: 1.52; 95% CI: 1.07 to 2.16). Besides, administration of macrolides was associated with a higher risk of cardiovascular disease (CVD) death (azithromycin, RR: 1.63; 95% CI: 1.17 to 2.27) and a slightly increased risk of myocardial infarction (MI) (azithromycin, RR: 1.08; 95% CI: 1.02 to 1.15). Interestingly, no association was observed between roxithromycin and adverse cardiac outcomes. Increased risk of VA or SCD was observed for recent or current use of macrolides, MI for former use, and CVD death for current use. CONCLUSION: Administration of macrolide antibiotics and timing of macrolide use are associated with increased risk for SCD or VTA and cardiovascular death, but not all-cause death. |
format | Online Article Text |
id | pubmed-9996752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99967522023-03-10 Administration of macrolide antibiotics increases cardiovascular risk Wu, Yang Bi, Wen-Tao Qu, Li-Ping Fan, Jun Kong, Xiang-Jun Ji, Cheng-Cheng Chen, Xu-Miao Yao, Feng-Juan Liu, Li-Juan Cheng, Yun-Jiu Wu, Su-Hua Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: The increased risk of cardiovascular events in patients prescribed macrolides has been subject to debate for decades. METHODS: Medline, EMBASE databases and ClinicalTrials.gov were searched from inception until August 31, 2022 for studies investigating the link between macrolides and cardiovascular risk. A meta-analysis was performed using a random-effects model. RESULTS: A total of 80 studies involving 39,374,874 patients were included. No association was found between macrolides and all-cause death. However, compared with the non-macrolide group, macrolides were associated with a significantly increased risk of ventricular arrhythmia or sudden cardiac death (VA or SCD) (azithromycin, relative ratio [RR]: 1.53; 95% confidence interval [CI]: 1.19 to 1.97; clarithromycin, RR: 1.52; 95% CI: 1.07 to 2.16). Besides, administration of macrolides was associated with a higher risk of cardiovascular disease (CVD) death (azithromycin, RR: 1.63; 95% CI: 1.17 to 2.27) and a slightly increased risk of myocardial infarction (MI) (azithromycin, RR: 1.08; 95% CI: 1.02 to 1.15). Interestingly, no association was observed between roxithromycin and adverse cardiac outcomes. Increased risk of VA or SCD was observed for recent or current use of macrolides, MI for former use, and CVD death for current use. CONCLUSION: Administration of macrolide antibiotics and timing of macrolide use are associated with increased risk for SCD or VTA and cardiovascular death, but not all-cause death. Frontiers Media S.A. 2023-02-23 /pmc/articles/PMC9996752/ /pubmed/36910529 http://dx.doi.org/10.3389/fcvm.2023.1117254 Text en Copyright © 2023 Wu, Bi, Qu, Fan, Kong, Ji, Chen, Yao, Liu, Cheng and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Wu, Yang Bi, Wen-Tao Qu, Li-Ping Fan, Jun Kong, Xiang-Jun Ji, Cheng-Cheng Chen, Xu-Miao Yao, Feng-Juan Liu, Li-Juan Cheng, Yun-Jiu Wu, Su-Hua Administration of macrolide antibiotics increases cardiovascular risk |
title | Administration of macrolide antibiotics increases cardiovascular risk |
title_full | Administration of macrolide antibiotics increases cardiovascular risk |
title_fullStr | Administration of macrolide antibiotics increases cardiovascular risk |
title_full_unstemmed | Administration of macrolide antibiotics increases cardiovascular risk |
title_short | Administration of macrolide antibiotics increases cardiovascular risk |
title_sort | administration of macrolide antibiotics increases cardiovascular risk |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996752/ https://www.ncbi.nlm.nih.gov/pubmed/36910529 http://dx.doi.org/10.3389/fcvm.2023.1117254 |
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