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Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry

AIMS: Persistent and permanent atrial fibrillation (AF) often occurs in the presence of multiple comorbidities and is linked to adverse outcomes. It is unclear whether the sustained pattern of AF itself is prognostic or if it is confounded by underlying comorbidities. Here, we tested the association...

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Autores principales: Apiyasawat, Sirin, Kornbongkotmas, Sakaorat, Chichareon, Ply, Krittayaphong, Rungroj
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/PMC8637082/
https://www.ncbi.nlm.nih.gov/pubmed/34887947
http://dx.doi.org/10.1002/joa3.12643
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author Apiyasawat, Sirin
Kornbongkotmas, Sakaorat
Chichareon, Ply
Krittayaphong, Rungroj
author_facet Apiyasawat, Sirin
Kornbongkotmas, Sakaorat
Chichareon, Ply
Krittayaphong, Rungroj
author_sort Apiyasawat, Sirin
collection PubMed
description AIMS: Persistent and permanent atrial fibrillation (AF) often occurs in the presence of multiple comorbidities and is linked to adverse outcomes. It is unclear whether the sustained pattern of AF itself is prognostic or if it is confounded by underlying comorbidities. Here, we tested the association between the temporal patterns of AF and the risks of ischemic stroke and all‐cause mortality. METHODS AND RESULTS: In a prospective multicenter cohort, 3046 non‐valvular AF patients were consecutively enrolled and followed for adverse outcomes of all‐cause mortality and ischemic stroke. The risks of both outcomes were adjusted for underlying comorbidities, and compared between the patterns of AF. At baseline, the patients were classified as paroxysmal (N = 963, 31.6%), persistent (N = 604, 19.8%), and permanent AF (N = 1479, 45.6%) according to the standard definition. Anticoagulants were administered in 75% of all patients and 83% of those with CHA(2)DS(2)‐VAS(c) score ≥2 in males or ≥3 in females. During a mean follow up of 26 (SD 10.5) months, all‐cause mortality occurred less in paroxysmal AF (2.5 per 100 patient‐years) than in persistent AF (4.4 per 100 patient‐years; adjusted hazard ratio [HR] 0.66, 95% CI, 0.46‐0.96; P = .029) and permanent AF (4.1 per 100 patient‐years; adjusted HR 0.71, 95% CI, 0.52‐0.98; P = .036). The risk of ischemic stroke was similar across all patterns of AF. CONCLUSIONS: In this multicenter cohort of AF patients, persistent and permanent AF was associated with higher all‐cause mortality than paroxysmal AF, independent of baseline comorbidities. CLINICAL TRIAL REGISTRATION: Thai Clinical Trial Registration; Study ID: TCTR20160113002 (http://www.thaiclinicaltrials.org/show/TCTR20160113002).
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spelling pubmed-86370822021-12-08 Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry Apiyasawat, Sirin Kornbongkotmas, Sakaorat Chichareon, Ply Krittayaphong, Rungroj J Arrhythm Original Article AIMS: Persistent and permanent atrial fibrillation (AF) often occurs in the presence of multiple comorbidities and is linked to adverse outcomes. It is unclear whether the sustained pattern of AF itself is prognostic or if it is confounded by underlying comorbidities. Here, we tested the association between the temporal patterns of AF and the risks of ischemic stroke and all‐cause mortality. METHODS AND RESULTS: In a prospective multicenter cohort, 3046 non‐valvular AF patients were consecutively enrolled and followed for adverse outcomes of all‐cause mortality and ischemic stroke. The risks of both outcomes were adjusted for underlying comorbidities, and compared between the patterns of AF. At baseline, the patients were classified as paroxysmal (N = 963, 31.6%), persistent (N = 604, 19.8%), and permanent AF (N = 1479, 45.6%) according to the standard definition. Anticoagulants were administered in 75% of all patients and 83% of those with CHA(2)DS(2)‐VAS(c) score ≥2 in males or ≥3 in females. During a mean follow up of 26 (SD 10.5) months, all‐cause mortality occurred less in paroxysmal AF (2.5 per 100 patient‐years) than in persistent AF (4.4 per 100 patient‐years; adjusted hazard ratio [HR] 0.66, 95% CI, 0.46‐0.96; P = .029) and permanent AF (4.1 per 100 patient‐years; adjusted HR 0.71, 95% CI, 0.52‐0.98; P = .036). The risk of ischemic stroke was similar across all patterns of AF. CONCLUSIONS: In this multicenter cohort of AF patients, persistent and permanent AF was associated with higher all‐cause mortality than paroxysmal AF, independent of baseline comorbidities. CLINICAL TRIAL REGISTRATION: Thai Clinical Trial Registration; Study ID: TCTR20160113002 (http://www.thaiclinicaltrials.org/show/TCTR20160113002). John Wiley and Sons Inc. 2021-10-06 /pmc/articles/PMC8637082/ /pubmed/34887947 http://dx.doi.org/10.1002/joa3.12643 Text en © 2021 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of Japanese Heart Rhythm Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Apiyasawat, Sirin
Kornbongkotmas, Sakaorat
Chichareon, Ply
Krittayaphong, Rungroj
Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title_full Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title_fullStr Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title_full_unstemmed Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title_short Mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
title_sort mortality risk and temporal patterns of atrial fibrillation in the nationwide registry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637082/
https://www.ncbi.nlm.nih.gov/pubmed/34887947
http://dx.doi.org/10.1002/joa3.12643
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