Pulmonary vein isolation alone vs. more extensive ablation with defragmentation and linear ablation of persistent atrial fibrillation: the EARNEST-PVI trial.


Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
06 04 2021
Historique:
received: 10 07 2020
accepted: 12 09 2020
pubmed: 18 11 2020
medline: 10 8 2021
entrez: 17 11 2020
Statut: ppublish

Résumé

Previous studies could not demonstrate any benefit of more intensive ablation in addition to pulmonary vein isolation (PVI) including complex fractionated atrial electrogram (CFAE) and linear ablation for recurrence in the initial catheter ablation of persistent atrial fibrillation (AF). This study aimed to establish the non-inferiority of PVI alone to PVI plus these additional ablation strategies. Patients with persistent AF who underwent an initial catheter ablation (n = 512, long-standing persistent AF; 128 cases) were randomly assigned in a 1:1 ratio to either PVI alone (PVI-alone group) or PVI plus CFAE and/or linear ablation (PVI-plus group). After excluding 15 cases who did not receive procedures, we analysed 249 and 248 patients, respectively. The primary endpoint was recurrence of AF, atrial flutter, and/or atrial tachycardia, and the non-inferior margin was set at a hazard ratio of 1.43. In the PVI-plus group, 85.1% of patients had linear ablation and 15.3% CFAE ablation. After 12 months, freedom from the primary endpoint occurred in 71.3% of patients in the PVI-alone group and in 78.3% in the PVI-plus group [hazard ratio = 1.56 (95% confidence interval: 1.10-2.24), non-inferior P = 0.3062]. The procedure-related complication rates were 2.0% in the PVI-alone group and 3.6% in the PVI-plus group (P = 0.199). This randomized trial did not establish the non-inferiority of PVI alone to PVI plus linear ablation or CFAE ablation in patients with persistent AF, but implied that the PVI plus strategy was promising to improve the clinical efficacy (NCT03514693).

Identifiants

pubmed: 33200213
pii: 5983833
doi: 10.1093/europace/euaa293
doi:

Banques de données

ClinicalTrials.gov
['NCT03514693']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

565-574

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com.

Auteurs

Koichi Inoue (K)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Shungo Hikoso (S)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Masaharu Masuda (M)

Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.

Yoshio Furukawa (Y)

Cardiovascular Center, Kansai Rosai Hospital, Amagasaki, Japan.

Akio Hirata (A)

Division of Cardiology, Osaka General Medical Center, Osaka, Japan.

Yasuyuki Egami (Y)

Cardiovascular Division, Osaka Police Hospital, Osaka, Japan.

Tetsuya Watanabe (T)

Division of Cardiology, Osaka Rosai Hospital, Sakai, Japan.

Hitoshi Minamiguchi (H)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Miwa Miyoshi (M)

Department of Cardiovascular Medicine, Yao Municipal Hospital, Yao, Japan.

Nobuaki Tanaka (N)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Takafumi Oka (T)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Masato Okada (M)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Takashi Kanda (T)

Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.

Yasuhiro Matsuda (Y)

Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.

Masato Kawasaki (M)

Cardiovascular Center, Kansai Rosai Hospital, Amagasaki, Japan.

Kenichi Hayashi (K)

Department of Cardiology, Osaka Hospital, Japan Community Healthcare Organization, Osaka, Japan.

Tetsuhisa Kitamura (T)

Division of Environmental Medicine and Population Sciences, Department of Social and Environmental Medicine, Osaka University Graduate School of Medicine, Suita, Japan.

Tomoharu Dohi (T)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Akihiro Sunaga (A)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Hiroya Mizuno (H)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Daisaku Nakatani (D)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

Yasushi Sakata (Y)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, 2-4-32 Umeda, Kita-ku, Osaka 530-0001, Japan.

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