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Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation

BACKGROUND: The low voltage zone (LVZ) detected with three‐dimensional electroanatomical mapping is a surrogate marker of atrial scar in patients with persistent atrial fibrillation (PeAF) and is associated with poor clinical outcomes after catheter ablation. However, fewer studies have reported the...

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Autores principales: Yakabe, Daisuke, Fukuyama, Yusuke, Araki, Masahiro, Nakamura, Toshihiro
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/PMC7896463/
https://www.ncbi.nlm.nih.gov/pubmed/33664889
http://dx.doi.org/10.1002/joa3.12492
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author Yakabe, Daisuke
Fukuyama, Yusuke
Araki, Masahiro
Nakamura, Toshihiro
author_facet Yakabe, Daisuke
Fukuyama, Yusuke
Araki, Masahiro
Nakamura, Toshihiro
author_sort Yakabe, Daisuke
collection PubMed
description BACKGROUND: The low voltage zone (LVZ) detected with three‐dimensional electroanatomical mapping is a surrogate marker of atrial scar in patients with persistent atrial fibrillation (PeAF) and is associated with poor clinical outcomes after catheter ablation. However, fewer studies have reported the relationship between responsiveness to antiarrhythmic drugs and the LVZ. METHODS: We retrospectively analyzed 76 patients who underwent catheter ablation for PeAF at our center. Rhythm control with bepridil was initiated before ablation in all patients, and electrical cardioversion was performed in cases of failure to restore sinus rhythm with bepridil alone. Patients with successful sinus restoration with bepridil alone (≤200 mg/d) were defined as “responders”, while those who required electrical cardioversion as well were defined as “non‐responders”. We compared the LVZ ratio (ratio of the LVZ surface area to the left atrium surface area on three‐dimensional electroanatomical mapping) and the recurrence‐free rate after ablation between the two groups. RESULTS: Of the 76 patients, 48 (63.2%) were responders to bepridil. The median LVZ ratio was significantly lower in the responder group than in the nonresponder group (7.5% vs 14.0%, P = .009). Multivariate analysis revealed that response to bepridil was an independent predictor of normal voltage (P = .02, odds ratio = 0.20, 95% confidence interval = 0.04‐0.76). The recurrence‐free rate at 1 year after catheter ablation was significantly higher in the responder group than in the nonresponder group (87.1% vs 62.3%, P = .03). CONCLUSIONS: Response to bepridil is a marker of normal voltage in electroanatomical mapping and is significantly associated with better clinical outcomes after catheter ablation.
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spelling pubmed-78964632021-03-03 Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation Yakabe, Daisuke Fukuyama, Yusuke Araki, Masahiro Nakamura, Toshihiro J Arrhythm Original Articles BACKGROUND: The low voltage zone (LVZ) detected with three‐dimensional electroanatomical mapping is a surrogate marker of atrial scar in patients with persistent atrial fibrillation (PeAF) and is associated with poor clinical outcomes after catheter ablation. However, fewer studies have reported the relationship between responsiveness to antiarrhythmic drugs and the LVZ. METHODS: We retrospectively analyzed 76 patients who underwent catheter ablation for PeAF at our center. Rhythm control with bepridil was initiated before ablation in all patients, and electrical cardioversion was performed in cases of failure to restore sinus rhythm with bepridil alone. Patients with successful sinus restoration with bepridil alone (≤200 mg/d) were defined as “responders”, while those who required electrical cardioversion as well were defined as “non‐responders”. We compared the LVZ ratio (ratio of the LVZ surface area to the left atrium surface area on three‐dimensional electroanatomical mapping) and the recurrence‐free rate after ablation between the two groups. RESULTS: Of the 76 patients, 48 (63.2%) were responders to bepridil. The median LVZ ratio was significantly lower in the responder group than in the nonresponder group (7.5% vs 14.0%, P = .009). Multivariate analysis revealed that response to bepridil was an independent predictor of normal voltage (P = .02, odds ratio = 0.20, 95% confidence interval = 0.04‐0.76). The recurrence‐free rate at 1 year after catheter ablation was significantly higher in the responder group than in the nonresponder group (87.1% vs 62.3%, P = .03). CONCLUSIONS: Response to bepridil is a marker of normal voltage in electroanatomical mapping and is significantly associated with better clinical outcomes after catheter ablation. John Wiley and Sons Inc. 2021-01-04 /pmc/articles/PMC7896463/ /pubmed/33664889 http://dx.doi.org/10.1002/joa3.12492 Text en © 2021 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Heart Rhythm Society. This is an open access article under the terms of the http://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 Articles
Yakabe, Daisuke
Fukuyama, Yusuke
Araki, Masahiro
Nakamura, Toshihiro
Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title_full Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title_fullStr Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title_full_unstemmed Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title_short Responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
title_sort responsiveness to bepridil predicts atrial substrate in patients with persistent atrial fibrillation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896463/
https://www.ncbi.nlm.nih.gov/pubmed/33664889
http://dx.doi.org/10.1002/joa3.12492
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