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Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction

AIMS: Little is known regarding factors that predict the occurrence of lethal ventricular arrhythmias (VAs) occurring after acute myocardial infarction (AMI). This observational cohort study aimed to identify factors that predicted lethal VAs during the late phase after AMI in patients with reduced...

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Autores principales: Saito, Kan, Kondo, Yusuke, Takahashi, Masashi, Kitahara, Hideki, Nakayama, Takashi, Fujimoto, Yoshihide, Kobayashi, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497219/
https://www.ncbi.nlm.nih.gov/pubmed/34173350
http://dx.doi.org/10.1002/ehf2.13499
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author Saito, Kan
Kondo, Yusuke
Takahashi, Masashi
Kitahara, Hideki
Nakayama, Takashi
Fujimoto, Yoshihide
Kobayashi, Yoshio
author_facet Saito, Kan
Kondo, Yusuke
Takahashi, Masashi
Kitahara, Hideki
Nakayama, Takashi
Fujimoto, Yoshihide
Kobayashi, Yoshio
author_sort Saito, Kan
collection PubMed
description AIMS: Little is known regarding factors that predict the occurrence of lethal ventricular arrhythmias (VAs) occurring after acute myocardial infarction (AMI). This observational cohort study aimed to identify factors that predicted lethal VAs during the late phase after AMI in patients with reduced left ventricular ejection fraction (LVEF). METHODS AND RESULTS: Data were collected from our AMI database regarding consecutive patients with an LVEF of ≤40% after AMI (January 2012 to July 2018). The ‘late phase’ was defined as ≥7 days after AMI onset, and the primary endpoint was defined as lethal VAs in the late phase. The study included 136 patients (82% men; mean age: 66 ± 13 years). The average LVEF at admission was 32.7 ± 8.2%. During a mean follow‐up period of 20.7 months, 14 patients (10%) experienced lethal VAs, including ventricular fibrillation (n = 8) and sustained ventricular tachycardia (n = 10). Univariate analyses revealed that lethal VAs were predicted by age and LVEF at admission. Receiver operating characteristic curve analysis indicated that the optimal cut‐off value was 23% for using the LVEF at admission to predict the primary endpoint (area under the curve: 0.77, P < 0.0001). Multivariable analysis also demonstrated that LVEF at admission was an independent predictor of the primary endpoint (risk ratio = 7.12, P = 0.001). CONCLUSIONS: Lethal VAs in the late phase are common in patients with AMI, and reduced LVEF and cardiac function at admission play a significant role in the risk stratification for future lethal VAs in this population.
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spelling pubmed-84972192021-10-12 Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction Saito, Kan Kondo, Yusuke Takahashi, Masashi Kitahara, Hideki Nakayama, Takashi Fujimoto, Yoshihide Kobayashi, Yoshio ESC Heart Fail Original Research Articles AIMS: Little is known regarding factors that predict the occurrence of lethal ventricular arrhythmias (VAs) occurring after acute myocardial infarction (AMI). This observational cohort study aimed to identify factors that predicted lethal VAs during the late phase after AMI in patients with reduced left ventricular ejection fraction (LVEF). METHODS AND RESULTS: Data were collected from our AMI database regarding consecutive patients with an LVEF of ≤40% after AMI (January 2012 to July 2018). The ‘late phase’ was defined as ≥7 days after AMI onset, and the primary endpoint was defined as lethal VAs in the late phase. The study included 136 patients (82% men; mean age: 66 ± 13 years). The average LVEF at admission was 32.7 ± 8.2%. During a mean follow‐up period of 20.7 months, 14 patients (10%) experienced lethal VAs, including ventricular fibrillation (n = 8) and sustained ventricular tachycardia (n = 10). Univariate analyses revealed that lethal VAs were predicted by age and LVEF at admission. Receiver operating characteristic curve analysis indicated that the optimal cut‐off value was 23% for using the LVEF at admission to predict the primary endpoint (area under the curve: 0.77, P < 0.0001). Multivariable analysis also demonstrated that LVEF at admission was an independent predictor of the primary endpoint (risk ratio = 7.12, P = 0.001). CONCLUSIONS: Lethal VAs in the late phase are common in patients with AMI, and reduced LVEF and cardiac function at admission play a significant role in the risk stratification for future lethal VAs in this population. John Wiley and Sons Inc. 2021-06-25 /pmc/articles/PMC8497219/ /pubmed/34173350 http://dx.doi.org/10.1002/ehf2.13499 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Saito, Kan
Kondo, Yusuke
Takahashi, Masashi
Kitahara, Hideki
Nakayama, Takashi
Fujimoto, Yoshihide
Kobayashi, Yoshio
Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title_full Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title_fullStr Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title_full_unstemmed Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title_short Factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
title_sort factors that predict ventricular arrhythmias in the late phase after acute myocardial infarction
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497219/
https://www.ncbi.nlm.nih.gov/pubmed/34173350
http://dx.doi.org/10.1002/ehf2.13499
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