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Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome

Premature atrial complexes (PACs) have been suggested to increase the risk of adverse events. The distribution of PAC burden and its dose–response effects on all-cause mortality and cardiovascular death had not been elucidated clearly. We analyzed 15,893 patients in a medical referral center from Ju...

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Autores principales: Huang, Ting-Chun, Lee, Po-Tseng, Huang, Mu-Shiang, Su, Pei-Fang, Liu, Ping-Yen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190115/
https://www.ncbi.nlm.nih.gov/pubmed/34108588
http://dx.doi.org/10.1038/s41598-021-91800-4
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author Huang, Ting-Chun
Lee, Po-Tseng
Huang, Mu-Shiang
Su, Pei-Fang
Liu, Ping-Yen
author_facet Huang, Ting-Chun
Lee, Po-Tseng
Huang, Mu-Shiang
Su, Pei-Fang
Liu, Ping-Yen
author_sort Huang, Ting-Chun
collection PubMed
description Premature atrial complexes (PACs) have been suggested to increase the risk of adverse events. The distribution of PAC burden and its dose–response effects on all-cause mortality and cardiovascular death had not been elucidated clearly. We analyzed 15,893 patients in a medical referral center from July 1st, 2011, to December 31st, 2018. Multivariate regression driven by ln PAC (beats per 24 h plus 1) or quartiles of PAC burden were examined. Older group had higher PAC burden than younger group (p for trend < 0.001), and both genders shared similar PACs distribution. In Cox model, ln PAC remained an independent risk factor for all-cause mortality (hazard ratio (HR) = 1.09 per ln PAC increase, 95% CI = 1.06‒1.12, p < 0.001). PACs were a significant risk factor in cause-specific model (HR = 1.13, 95% CI = 1.05‒1.22, p = 0.001) or sub-distribution model (HR = 1.12, 95% CI = 1.04‒1.21, p = 0.004). In ordinal PAC model, 4th quartile group had significantly higher risk of all-cause mortality than those in 1st quartile group (HR = 1.47, 95% CI = 1.13‒1.94, p = 0.005), but no difference in cardiovascular death were found in competing risk analysis. In subgroup analysis, the risk of high PAC burden was consistently higher than in low-burden group across pre-specified subgroups. In conclusion, PAC burden has a dose response effect on all-cause mortality and cardiovascular death.
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spelling pubmed-81901152021-06-10 Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome Huang, Ting-Chun Lee, Po-Tseng Huang, Mu-Shiang Su, Pei-Fang Liu, Ping-Yen Sci Rep Article Premature atrial complexes (PACs) have been suggested to increase the risk of adverse events. The distribution of PAC burden and its dose–response effects on all-cause mortality and cardiovascular death had not been elucidated clearly. We analyzed 15,893 patients in a medical referral center from July 1st, 2011, to December 31st, 2018. Multivariate regression driven by ln PAC (beats per 24 h plus 1) or quartiles of PAC burden were examined. Older group had higher PAC burden than younger group (p for trend < 0.001), and both genders shared similar PACs distribution. In Cox model, ln PAC remained an independent risk factor for all-cause mortality (hazard ratio (HR) = 1.09 per ln PAC increase, 95% CI = 1.06‒1.12, p < 0.001). PACs were a significant risk factor in cause-specific model (HR = 1.13, 95% CI = 1.05‒1.22, p = 0.001) or sub-distribution model (HR = 1.12, 95% CI = 1.04‒1.21, p = 0.004). In ordinal PAC model, 4th quartile group had significantly higher risk of all-cause mortality than those in 1st quartile group (HR = 1.47, 95% CI = 1.13‒1.94, p = 0.005), but no difference in cardiovascular death were found in competing risk analysis. In subgroup analysis, the risk of high PAC burden was consistently higher than in low-burden group across pre-specified subgroups. In conclusion, PAC burden has a dose response effect on all-cause mortality and cardiovascular death. Nature Publishing Group UK 2021-06-09 /pmc/articles/PMC8190115/ /pubmed/34108588 http://dx.doi.org/10.1038/s41598-021-91800-4 Text en © The Author(s) 2021 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
Huang, Ting-Chun
Lee, Po-Tseng
Huang, Mu-Shiang
Su, Pei-Fang
Liu, Ping-Yen
Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title_full Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title_fullStr Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title_full_unstemmed Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title_short Higher premature atrial complex burden from the Holter examination predicts poor cardiovascular outcome
title_sort higher premature atrial complex burden from the holter examination predicts poor cardiovascular outcome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190115/
https://www.ncbi.nlm.nih.gov/pubmed/34108588
http://dx.doi.org/10.1038/s41598-021-91800-4
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