Diagnosis to Ablation in Persistent AF: Any Time Can Be a Good Time to Ablate.


Journal

JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 29 04 2024
revised: 24 05 2024
accepted: 25 05 2024
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 31 7 2024
Statut: ppublish

Résumé

Nonrandomized data suggest that longer diagnosis-to-ablation time (DAT) is associated with poorer outcomes; however, a recent randomized trial found no difference in recurrences when ablation was delayed by 12 months. This study sought to assess the impact of DAT on atrial fibrillation (AF) recurrence in patients undergoing catheter ablation for persistent AF. CAPLA (Effect of Catheter Ablation Using Pulmonary Vein Isolation With vs Without Posterior Left Atrial Wall Isolation on Atrial Arrhythmia Recurrence in Patients With Persistent Atrial Fibrillation: The CAPLA randomized clinical trial) was a multicenter trial that randomized patients with persistent AF to pulmonary vein isolation + posterior wall isolation or pulmonary vein isolation alone. Follow-up was 12 months. Outcomes were assessed after a 3-month blanking period. Median DAT in the 334 patients was 28 months (Q1-Q3: 12-66 months). Patients were divided into quartile groups: Q1 was DAT 0 to 12 months (n = 84, median DAT 7 months), Q2 was DAT 13 to 28 months (n = 85, median DAT 20 months), Q3 was DAT 29 to 66 months (n = 84, median DAT 41 months), and Q4 was DAT ≥67 months (n = 81, median DAT 119 months). AF recurrence rate was 36.9% for Q1, 44.7% for Q2, 47.6% for Q3, and 56.8% for Q4 (P = 0.082). On multivariable analysis, DAT Q4 was the only factor significantly associated with risk of recurrence (HR: 1.607; 95% CI: 1.005-2.570; P = 0.048). Median AF burden was 0% (Q1-Q3: 0%-0.47%) in Q1 and 0.33% (Q1-Q3: 0%-4.6%) in Q4 (P = 0.002). Quality of life (assessed by the Atrial Fibrillation Effect on Quality-of-Life questionnaire) improved markedly in all quartiles (Q1: Δ28.8 ± 24, Q2: Δ24.4 ± 23.4, Q3: Δ21.7 ± 26.6, Q4: Δ24.6 ± 21.4; P = 0.331). In a cohort of patients with persistent AF undergoing ablation in a prospective trial with standardized entry criteria and intensive electrocardiogram monitoring, those with shorter DAT had lower rates of AF recurrence. However, differences were modest, and all quartiles demonstrated very low AF burden and improvements in quality of life.

Sections du résumé

BACKGROUND BACKGROUND
Nonrandomized data suggest that longer diagnosis-to-ablation time (DAT) is associated with poorer outcomes; however, a recent randomized trial found no difference in recurrences when ablation was delayed by 12 months.
OBJECTIVES OBJECTIVE
This study sought to assess the impact of DAT on atrial fibrillation (AF) recurrence in patients undergoing catheter ablation for persistent AF.
METHODS METHODS
CAPLA (Effect of Catheter Ablation Using Pulmonary Vein Isolation With vs Without Posterior Left Atrial Wall Isolation on Atrial Arrhythmia Recurrence in Patients With Persistent Atrial Fibrillation: The CAPLA randomized clinical trial) was a multicenter trial that randomized patients with persistent AF to pulmonary vein isolation + posterior wall isolation or pulmonary vein isolation alone. Follow-up was 12 months. Outcomes were assessed after a 3-month blanking period.
RESULTS RESULTS
Median DAT in the 334 patients was 28 months (Q1-Q3: 12-66 months). Patients were divided into quartile groups: Q1 was DAT 0 to 12 months (n = 84, median DAT 7 months), Q2 was DAT 13 to 28 months (n = 85, median DAT 20 months), Q3 was DAT 29 to 66 months (n = 84, median DAT 41 months), and Q4 was DAT ≥67 months (n = 81, median DAT 119 months). AF recurrence rate was 36.9% for Q1, 44.7% for Q2, 47.6% for Q3, and 56.8% for Q4 (P = 0.082). On multivariable analysis, DAT Q4 was the only factor significantly associated with risk of recurrence (HR: 1.607; 95% CI: 1.005-2.570; P = 0.048). Median AF burden was 0% (Q1-Q3: 0%-0.47%) in Q1 and 0.33% (Q1-Q3: 0%-4.6%) in Q4 (P = 0.002). Quality of life (assessed by the Atrial Fibrillation Effect on Quality-of-Life questionnaire) improved markedly in all quartiles (Q1: Δ28.8 ± 24, Q2: Δ24.4 ± 23.4, Q3: Δ21.7 ± 26.6, Q4: Δ24.6 ± 21.4; P = 0.331).
CONCLUSIONS CONCLUSIONS
In a cohort of patients with persistent AF undergoing ablation in a prospective trial with standardized entry criteria and intensive electrocardiogram monitoring, those with shorter DAT had lower rates of AF recurrence. However, differences were modest, and all quartiles demonstrated very low AF burden and improvements in quality of life.

Identifiants

pubmed: 39084743
pii: S2405-500X(24)00456-0
doi: 10.1016/j.jacep.2024.05.031
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1689-1699

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Chieng was supported by a National heart foundation (NHF) Post-Doctoral Fellowship. Dr William was supported by a NHF postgraduate PhD scholarship. Dr Crowley was supported by a Baker Institute PhD scholarship. Dr Segan was supported by a cofunded National Health and Medical Research Council (NHMRC)/NHF postgraduate PhD scholarship. Dr Kalman has received research and fellowship support from Medtronic, Abbott, Zoll, and Biosense Webster. Dr Kistler has received an Investigator grant from the NHMRC; received funding for consultancy and speaking engagements from Abbott Medical; and served on the advisory board with fellowship support from Biosense Webster. Dr Sanders has served on the advisory board for Medtronic, Abbott Medical, CathRx, Pacemate, and Boston Scientific; and received a practitioner fellowship from the NHMRC and NHF. Dr Lee has received consulting fees from Biosense Webster. Dr Prabhu has received a NHMRC Post-Doctoral Research Fellowship; and received consulting fees, fellowship support, and educational grants from Biosense Webster, Abbott Medical, and Boston Scientific. Dr Ling has received grants from Abbott Australia. Dr Sterns has received personal fees from Biosense Webster. Dr Ginks has served on the Speakers Bureau for Biosense Webster; and as a speaker for Abbott. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Rose Crowley (R)

University of Melbourne, Melbourne, Victoria, Australia; Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia.

Michael W Lim (MW)

University of Melbourne, Melbourne, Victoria, Australia; Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Royal Melbourne Hospital, Melbourne, Victoria, Australia.

David Chieng (D)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Louise Segan (L)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Jeremy William (J)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Joseph B Morton (JB)

Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Geoffrey Lee (G)

University of Melbourne, Melbourne, Victoria, Australia; Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Paul Sparks (P)

Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Alex J McLellan (AJ)

University of Melbourne, Melbourne, Victoria, Australia; Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Hariharan Sugumar (H)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Sandeep Prabhu (S)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Liang-Han Ling (LH)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Aleksandr Voskoboinik (A)

Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Rajeev K Pathak (RK)

Canberra Hospital, Australian Capital Territory, Australia.

Laurence Sterns (L)

Royal Jubilee Hospital, Victoria, British Columbia, Canada.

Matthew Ginks (M)

John Radcliffe Hospital, Oxford, United Kingdom.

Prashanthan Sanders (P)

Royal Adelaide Hospital, Adelaide, South Australia, Australia.

Peter M Kistler (PM)

University of Melbourne, Melbourne, Victoria, Australia; Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Alfred Hospital, Melbourne, Victoria, Australia; Monash University, Melbourne, Victoria, Australia.

Jonathan M Kalman (JM)

University of Melbourne, Melbourne, Victoria, Australia; Baker Heart and Diabetes Research Institute, Melbourne, Victoria, Australia; Royal Melbourne Hospital, Melbourne, Victoria, Australia. Electronic address: jon.kalman@mh.org.au.

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Classifications MeSH