Impact of early vs. delayed atrial fibrillation catheter ablation on atrial arrhythmia recurrences.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
14 Jul 2023
Historique:
received: 22 03 2023
revised: 10 04 2023
accepted: 13 04 2023
medline: 17 7 2023
pubmed: 17 4 2023
entrez: 16 4 2023
Statut: ppublish

Résumé

Catheter ablation is an effective strategy in atrial fibrillation (AF). However, its timing in the course of management remains unclear. The aim of this study was to determine if an early vs. delayed AF ablation strategy is associated with differences in arrhythmia outcomes during 12-month follow-up. One hundred patients with symptomatic AF referred to a tertiary centre for management were randomized in a 1:1 ratio to either an early ablation strategy (within 1 month of recruitment) or a delayed ablation strategy (optimized medical therapy followed by catheter ablation at 12 months post recruitment). The primary endpoint was atrial arrhythmia free survival at 12 months post-ablation. Secondary outcomes included: (i) AF burden, (ii) AF burden by AF phenotype, and (iii) antiarrhythmic drug (AAD) use at 12 months. Overall, 89 patients completed the study protocol (Early vs. Delayed: 48 vs. 41). Mean age was 59 ± 12.9 years (29% women). Pulmonary vein isolation was achieved in 100% of patients. At 12 months, 56.3% of patients in the early ablation group were free from recurrent arrhythmia, compared with 58.6% in the delayed ablation group (HR 1.12, 95% CI 0.59-2.13, P = 0.7). All secondary outcomes showed no significant difference including median AF burden (Early vs. Delayed: 0% [IQR 3.2] vs. 0% [5], P = 0.66), median AF burden amongst paroxysmal AF patients (0% [IQR 1.1] vs. 0% [4.5], P = 0.78), or persistent AF patients (0% [IQR 22.8] vs. 0% [5.6], P = 0.45) or AAD use (33% vs. 37%, P = 0.8). Compared with an early ablation strategy, delaying AF ablation by 12 months for AAD management did not result in reduced ablation efficacy.

Sections du résumé

BACKGROUND BACKGROUND
Catheter ablation is an effective strategy in atrial fibrillation (AF). However, its timing in the course of management remains unclear. The aim of this study was to determine if an early vs. delayed AF ablation strategy is associated with differences in arrhythmia outcomes during 12-month follow-up.
METHODS AND RESULTS RESULTS
One hundred patients with symptomatic AF referred to a tertiary centre for management were randomized in a 1:1 ratio to either an early ablation strategy (within 1 month of recruitment) or a delayed ablation strategy (optimized medical therapy followed by catheter ablation at 12 months post recruitment). The primary endpoint was atrial arrhythmia free survival at 12 months post-ablation. Secondary outcomes included: (i) AF burden, (ii) AF burden by AF phenotype, and (iii) antiarrhythmic drug (AAD) use at 12 months. Overall, 89 patients completed the study protocol (Early vs. Delayed: 48 vs. 41). Mean age was 59 ± 12.9 years (29% women). Pulmonary vein isolation was achieved in 100% of patients. At 12 months, 56.3% of patients in the early ablation group were free from recurrent arrhythmia, compared with 58.6% in the delayed ablation group (HR 1.12, 95% CI 0.59-2.13, P = 0.7). All secondary outcomes showed no significant difference including median AF burden (Early vs. Delayed: 0% [IQR 3.2] vs. 0% [5], P = 0.66), median AF burden amongst paroxysmal AF patients (0% [IQR 1.1] vs. 0% [4.5], P = 0.78), or persistent AF patients (0% [IQR 22.8] vs. 0% [5.6], P = 0.45) or AAD use (33% vs. 37%, P = 0.8).
CONCLUSION CONCLUSIONS
Compared with an early ablation strategy, delaying AF ablation by 12 months for AAD management did not result in reduced ablation efficacy.

Identifiants

pubmed: 37062010
pii: 7123666
doi: 10.1093/eurheartj/ehad247
doi:

Substances chimiques

Anti-Arrhythmia Agents 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2447-2454

Subventions

Organisme : National Health and Medical Research Council
Organisme : advisory board of Medtronic
Organisme : Abbott Medical
Organisme : Boston Scientific
Organisme : CathRx
Organisme : PaceMate
Organisme : University of Adelaide
Organisme : Becton Dickenson
Organisme : Biosense Webster
Organisme : Medtronic

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Conflict of interest All authors declare no conflict of interest for this contribution.

Auteurs

Jonathan M Kalman (JM)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.

Ahmed M Al-Kaisey (AM)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.
Heart Centre, Alfred Hospital, 55 Commercial Rd, Melbourne, VIC 3004, Australia.

Ramanathan Parameswaran (R)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.
Heart Centre, Alfred Hospital, 55 Commercial Rd, Melbourne, VIC 3004, Australia.

Joshua Hawson (J)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.

Robert D Anderson (RD)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.

Michael Lim (M)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.

David Chieng (D)

Heart Centre, Alfred Hospital, 55 Commercial Rd, Melbourne, VIC 3004, Australia.
Baker IDI, Heart & Diabetes Institute, 75 Commercial Rd, Melbourne, VIC 3004, Australia.

Stephen A Joseph (SA)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.

Alex McLellan (A)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.

Joseph B Morton (JB)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.

Paul B Sparks (PB)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.

Geoffrey Lee (G)

Department of Cardiology, Royal Melbourne Hospital, Level 2, 300 Grattan Street, Melbourne, VIC 3050, Australia.
Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.

Prashanthan Sanders (P)

Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, Port Rd, Adelaide, SA 5000, Australia.

Peter M Kistler (PM)

Department of Medicine, University of Melbourne, Grattan Street, Parkville, VIC 3010, Australia.
Heart Centre, Alfred Hospital, 55 Commercial Rd, Melbourne, VIC 3004, Australia.
Baker IDI, Heart & Diabetes Institute, 75 Commercial Rd, Melbourne, VIC 3004, Australia.

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