Hybrid epicardial-endocardial ablation for long-standing persistent atrial fibrillation: A subanalysis of the CONVERGE Trial.

Antiarrhythmic drug Endocardial ablation Epicardial Hybrid ablation Long-standing persistent atrial fibrillation

Journal

Heart rhythm O2
ISSN: 2666-5018
Titre abrégé: Heart Rhythm O2
Pays: United States
ID NLM: 101768511

Informations de publication

Date de publication:
Feb 2023
Historique:
entrez: 6 3 2023
pubmed: 7 3 2023
medline: 7 3 2023
Statut: epublish

Résumé

Favorable clinical outcomes are difficult to achieve in long-standing persistent atrial fibrillation (LSPAF) with catheter ablation (CA). The CONVERGE (Convergence of Epicardial and Endocardial Ablation for the Treatment of Symptomatic Persistent Atrial FIbrillation) trial evaluated the effectiveness of hybrid convergent (HC) ablation vs endocardial CA. The study sought to evaluate the safety and effectiveness of HC vs CA in the LSPAF subgroup from the CONVERGE trial. The CONVERGE trial was a prospective, multicenter, randomized trial that enrolled 153 patients at 27 sites. A post hoc analysis was performed on LSPAF patients. The primary effectiveness was freedom from atrial arrhythmias off new or increased dose of previously failed or intolerant antiarrhythmic drugs (AADs) through 12 months. The primary safety endpoint was major adverse event incidence through 30 days with HC. Key secondary effectiveness measures included (1) percent of patients achieving ≥90% AF burden reduction vs baseline and (2) AF freedom. Sixty-five patients (42.5% of total enrollment) had LSPAF; 38 in HC and 27 in CA. Primary effectiveness was 65.8% (95% confidence interval [CI] 50.7%-80.9%) with HC vs 37.0% (95% CI 5.1%-52.4%) with CA ( Post hoc analysis demonstrated effectiveness and acceptable safety of HC compared with CA in LSPAF.

Sections du résumé

Background UNASSIGNED
Favorable clinical outcomes are difficult to achieve in long-standing persistent atrial fibrillation (LSPAF) with catheter ablation (CA). The CONVERGE (Convergence of Epicardial and Endocardial Ablation for the Treatment of Symptomatic Persistent Atrial FIbrillation) trial evaluated the effectiveness of hybrid convergent (HC) ablation vs endocardial CA.
Objective UNASSIGNED
The study sought to evaluate the safety and effectiveness of HC vs CA in the LSPAF subgroup from the CONVERGE trial.
Methods UNASSIGNED
The CONVERGE trial was a prospective, multicenter, randomized trial that enrolled 153 patients at 27 sites. A post hoc analysis was performed on LSPAF patients. The primary effectiveness was freedom from atrial arrhythmias off new or increased dose of previously failed or intolerant antiarrhythmic drugs (AADs) through 12 months. The primary safety endpoint was major adverse event incidence through 30 days with HC. Key secondary effectiveness measures included (1) percent of patients achieving ≥90% AF burden reduction vs baseline and (2) AF freedom.
Results UNASSIGNED
Sixty-five patients (42.5% of total enrollment) had LSPAF; 38 in HC and 27 in CA. Primary effectiveness was 65.8% (95% confidence interval [CI] 50.7%-80.9%) with HC vs 37.0% (95% CI 5.1%-52.4%) with CA (
Conclusion UNASSIGNED
Post hoc analysis demonstrated effectiveness and acceptable safety of HC compared with CA in LSPAF.

Identifiants

pubmed: 36873309
doi: 10.1016/j.hroo.2022.11.007
pii: S2666-5018(22)00343-9
pmc: PMC9975017
doi:

Types de publication

Journal Article

Langues

eng

Pagination

111-118

Informations de copyright

© 2022 Heart Rhythm Society. Published by Elsevier Inc.

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Auteurs

David B DeLurgio (DB)

St. Joseph's Hospital, Emory University, Atlanta, Georgia.

Christopher Blauth (C)

Guy's and St. Thomas' Foundation Trust, London, United Kingdom.

Michael E Halkos (ME)

St. Joseph's Hospital, Emory University, Atlanta, Georgia.

Karl J Crossen (KJ)

Cardiology Associates Research, LLC, Tupelo, Mississippi.

David Talton (D)

Cardiology Associates Research, LLC, Tupelo, Mississippi.

Saumil R Oza (SR)

St. Vincent's Healthcare, Jacksonville, Florida.

Anthony R Magnano (AR)

St. Vincent's Healthcare, Jacksonville, Florida.

Mark A Mostovych (MA)

St. Vincent's Healthcare, Jacksonville, Florida.

Sreedhar Billakanty (S)

Riverside Methodist Hospital, OhioHealth, Columbus, Ohio.

Steven Duff (S)

Riverside Methodist Hospital, OhioHealth, Columbus, Ohio.

Christopher Stees (C)

HealthOne Cardiothoracic Surgery Associates, Aurora, Colorado.

Jason Sperling (J)

HealthOne Cardiothoracic Surgery Associates, Aurora, Colorado.

Syed Ahsan (S)

Barts Heart Centre, St. Bartholomew's Hospital, London, United Kingdom.

John Yap (J)

Barts Heart Centre, St. Bartholomew's Hospital, London, United Kingdom.

Christian Shults (C)

MedStar Washington Hospital Center, Washington, DC.

David Pederson (D)

STAR Clinical Trials/Methodist Cardiology Clinic San Antonio, San Antonio, Texas.

James Garrison (J)

STAR Clinical Trials/Methodist Cardiology Clinic San Antonio, San Antonio, Texas.

Paul Tabereaux (P)

Heart Center Research, LLC, Huntsville, Alabama.

David M Gilligan (DM)

Virginia Cardiovascular Specialists, Richmond, Virginia.

Graham Bundy (G)

Virginia Cardiovascular Specialists, Richmond, Virginia.

Otto Costantini (O)

Summa Health Medical Group, Akron, Ohio.

Eric Espinal (E)

Summa Health Medical Group, Akron, Ohio.

Angelo La Pietra (A)

Mount Sinai Medical Center, Miami Beach, Florida.

Felix Yang (F)

Maimonides Medical Center, Brooklyn, New York.

Yisachar Greenberg (Y)

Maimonides Medical Center, Brooklyn, New York.

Israel Jacobowitz (I)

Maimonides Medical Center, Brooklyn, New York.

Jaswinder Gill (J)

Guy's and St. Thomas' Foundation Trust, London, United Kingdom.

Classifications MeSH