Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events. / Rasmussen, Peter Vibe; Blanche, Paul; Dalgaard, Frederik; Gislason, Gunnar Hilmar; Torp-Pedersen, Christian; Tønnesen, Jacob; Ruwald, Martin H.; Pallisgaard, Jannik Langtved; Hansen, Morten Lock.

In: American Heart Journal, Vol. 244, 2022, p. 42-49.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rasmussen, PV, Blanche, P, Dalgaard, F, Gislason, GH, Torp-Pedersen, C, Tønnesen, J, Ruwald, MH, Pallisgaard, JL & Hansen, ML 2022, 'Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events', American Heart Journal, vol. 244, pp. 42-49. https://doi.org/10.1016/j.ahj.2021.10.182

APA

Rasmussen, P. V., Blanche, P., Dalgaard, F., Gislason, G. H., Torp-Pedersen, C., Tønnesen, J., Ruwald, M. H., Pallisgaard, J. L., & Hansen, M. L. (2022). Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events. American Heart Journal, 244, 42-49. https://doi.org/10.1016/j.ahj.2021.10.182

Vancouver

Rasmussen PV, Blanche P, Dalgaard F, Gislason GH, Torp-Pedersen C, Tønnesen J et al. Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events. American Heart Journal. 2022;244:42-49. https://doi.org/10.1016/j.ahj.2021.10.182

Author

Rasmussen, Peter Vibe ; Blanche, Paul ; Dalgaard, Frederik ; Gislason, Gunnar Hilmar ; Torp-Pedersen, Christian ; Tønnesen, Jacob ; Ruwald, Martin H. ; Pallisgaard, Jannik Langtved ; Hansen, Morten Lock. / Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events. In: American Heart Journal. 2022 ; Vol. 244. pp. 42-49.

Bibtex

@article{8f1fef42028a4d67a451ddebf3c3d4fd,
title = "Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events",
abstract = "Background: Electrical cardioversion (ECV) is a common procedure for terminating atrial fibrillation (AF). ECV is associated with brady-arrhythmic events, however, the age-specific risks of clinically significant brady-arrhythmic events are unknown. Methods: Using Danish nationwide registers, we identified patients with AF at their first non-emergent ECV between 2005 and 2018 and estimated their 30-day risk of brady-arrhythmic events. Moreover, factors associated with increased risks of brady-arrhythmias were identified. Absolute risks were estimated using logistic regression models fitted with natural splines as well as standardization (G-formula). Results: We identified 20,725 eligible patients with a median age of 66 years (IQR 60-72) and most males (73%). The 30-day risks of brady-arrhythmic events after ECV were highly dependent on age with estimated risks ranging from 0.5% (95% CI 0.2-1.7) and 1.2% (95% CI 0.99-1.5) to 2.7% (95% CI 2.1-3.3) and 5.1% (95% CI 2.6-9.7) in patients aged 40, 65, 80, and 90 years, respectively. Factors associated with brady-arrhythmias were generally related to cardiovascular disease (eg, ischemic heart disease, heart failure, valvular AF) or a history of syncope. We found no indications that pre-treatment with anti-arrhythmic drugs conferred increased risks of brady-arrhythmic events (standardized absolute risk difference -0.25% [95% CI -0.67 to 0.17]). Conclusions: ECV conferred clinically relevant 30-day risks of brady-arrhythmic events, especially in older patients. Anti-arrhythmic drug treatment was not found to increase the risk of brady-arrhythmias. Given the widespread use of ECV, these data should provide insights regarding the potential risks of brady-arrhythmic events.",
author = "Rasmussen, {Peter Vibe} and Paul Blanche and Frederik Dalgaard and Gislason, {Gunnar Hilmar} and Christian Torp-Pedersen and Jacob T{\o}nnesen and Ruwald, {Martin H.} and Pallisgaard, {Jannik Langtved} and Hansen, {Morten Lock}",
note = "Publisher Copyright: {\textcopyright} 2021",
year = "2022",
doi = "10.1016/j.ahj.2021.10.182",
language = "English",
volume = "244",
pages = "42--49",
journal = "American Heart Journal",
issn = "0002-8703",
publisher = "Mosby Inc.",

}

RIS

TY - JOUR

T1 - Electrical cardioversion of atrial fibrillation and the risk of brady-arrhythmic events

AU - Rasmussen, Peter Vibe

AU - Blanche, Paul

AU - Dalgaard, Frederik

AU - Gislason, Gunnar Hilmar

AU - Torp-Pedersen, Christian

AU - Tønnesen, Jacob

AU - Ruwald, Martin H.

AU - Pallisgaard, Jannik Langtved

AU - Hansen, Morten Lock

N1 - Publisher Copyright: © 2021

PY - 2022

Y1 - 2022

N2 - Background: Electrical cardioversion (ECV) is a common procedure for terminating atrial fibrillation (AF). ECV is associated with brady-arrhythmic events, however, the age-specific risks of clinically significant brady-arrhythmic events are unknown. Methods: Using Danish nationwide registers, we identified patients with AF at their first non-emergent ECV between 2005 and 2018 and estimated their 30-day risk of brady-arrhythmic events. Moreover, factors associated with increased risks of brady-arrhythmias were identified. Absolute risks were estimated using logistic regression models fitted with natural splines as well as standardization (G-formula). Results: We identified 20,725 eligible patients with a median age of 66 years (IQR 60-72) and most males (73%). The 30-day risks of brady-arrhythmic events after ECV were highly dependent on age with estimated risks ranging from 0.5% (95% CI 0.2-1.7) and 1.2% (95% CI 0.99-1.5) to 2.7% (95% CI 2.1-3.3) and 5.1% (95% CI 2.6-9.7) in patients aged 40, 65, 80, and 90 years, respectively. Factors associated with brady-arrhythmias were generally related to cardiovascular disease (eg, ischemic heart disease, heart failure, valvular AF) or a history of syncope. We found no indications that pre-treatment with anti-arrhythmic drugs conferred increased risks of brady-arrhythmic events (standardized absolute risk difference -0.25% [95% CI -0.67 to 0.17]). Conclusions: ECV conferred clinically relevant 30-day risks of brady-arrhythmic events, especially in older patients. Anti-arrhythmic drug treatment was not found to increase the risk of brady-arrhythmias. Given the widespread use of ECV, these data should provide insights regarding the potential risks of brady-arrhythmic events.

AB - Background: Electrical cardioversion (ECV) is a common procedure for terminating atrial fibrillation (AF). ECV is associated with brady-arrhythmic events, however, the age-specific risks of clinically significant brady-arrhythmic events are unknown. Methods: Using Danish nationwide registers, we identified patients with AF at their first non-emergent ECV between 2005 and 2018 and estimated their 30-day risk of brady-arrhythmic events. Moreover, factors associated with increased risks of brady-arrhythmias were identified. Absolute risks were estimated using logistic regression models fitted with natural splines as well as standardization (G-formula). Results: We identified 20,725 eligible patients with a median age of 66 years (IQR 60-72) and most males (73%). The 30-day risks of brady-arrhythmic events after ECV were highly dependent on age with estimated risks ranging from 0.5% (95% CI 0.2-1.7) and 1.2% (95% CI 0.99-1.5) to 2.7% (95% CI 2.1-3.3) and 5.1% (95% CI 2.6-9.7) in patients aged 40, 65, 80, and 90 years, respectively. Factors associated with brady-arrhythmias were generally related to cardiovascular disease (eg, ischemic heart disease, heart failure, valvular AF) or a history of syncope. We found no indications that pre-treatment with anti-arrhythmic drugs conferred increased risks of brady-arrhythmic events (standardized absolute risk difference -0.25% [95% CI -0.67 to 0.17]). Conclusions: ECV conferred clinically relevant 30-day risks of brady-arrhythmic events, especially in older patients. Anti-arrhythmic drug treatment was not found to increase the risk of brady-arrhythmias. Given the widespread use of ECV, these data should provide insights regarding the potential risks of brady-arrhythmic events.

U2 - 10.1016/j.ahj.2021.10.182

DO - 10.1016/j.ahj.2021.10.182

M3 - Journal article

C2 - 34666012

AN - SCOPUS:85119382404

VL - 244

SP - 42

EP - 49

JO - American Heart Journal

JF - American Heart Journal

SN - 0002-8703

ER -

ID: 286504829