Your browser doesn't support javascript.
loading
Hybrid epicardial-endocardial ablation for long-standing persistent atrial fibrillation: A subanalysis of the CONVERGE Trial.
DeLurgio, David B; Blauth, Christopher; Halkos, Michael E; Crossen, Karl J; Talton, David; Oza, Saumil R; Magnano, Anthony R; Mostovych, Mark A; Billakanty, Sreedhar; Duff, Steven; Stees, Christopher; Sperling, Jason; Ahsan, Syed; Yap, John; Shults, Christian; Pederson, David; Garrison, James; Tabereaux, Paul; Gilligan, David M; Bundy, Graham; Costantini, Otto; Espinal, Eric; La Pietra, Angelo; Yang, Felix; Greenberg, Yisachar; Jacobowitz, Israel; Gill, Jaswinder.
Afiliação
  • DeLurgio DB; St. Joseph's Hospital, Emory University, Atlanta, Georgia.
  • Blauth C; Guy's and St. Thomas' Foundation Trust, London, United Kingdom.
  • Halkos ME; St. Joseph's Hospital, Emory University, Atlanta, Georgia.
  • Crossen KJ; Cardiology Associates Research, LLC, Tupelo, Mississippi.
  • Talton D; Cardiology Associates Research, LLC, Tupelo, Mississippi.
  • Oza SR; St. Vincent's Healthcare, Jacksonville, Florida.
  • Magnano AR; St. Vincent's Healthcare, Jacksonville, Florida.
  • Mostovych MA; St. Vincent's Healthcare, Jacksonville, Florida.
  • Billakanty S; Riverside Methodist Hospital, OhioHealth, Columbus, Ohio.
  • Duff S; Riverside Methodist Hospital, OhioHealth, Columbus, Ohio.
  • Stees C; HealthOne Cardiothoracic Surgery Associates, Aurora, Colorado.
  • Sperling J; HealthOne Cardiothoracic Surgery Associates, Aurora, Colorado.
  • Ahsan S; Barts Heart Centre, St. Bartholomew's Hospital, London, United Kingdom.
  • Yap J; Barts Heart Centre, St. Bartholomew's Hospital, London, United Kingdom.
  • Shults C; MedStar Washington Hospital Center, Washington, DC.
  • Pederson D; STAR Clinical Trials/Methodist Cardiology Clinic San Antonio, San Antonio, Texas.
  • Garrison J; STAR Clinical Trials/Methodist Cardiology Clinic San Antonio, San Antonio, Texas.
  • Tabereaux P; Heart Center Research, LLC, Huntsville, Alabama.
  • Gilligan DM; Virginia Cardiovascular Specialists, Richmond, Virginia.
  • Bundy G; Virginia Cardiovascular Specialists, Richmond, Virginia.
  • Costantini O; Summa Health Medical Group, Akron, Ohio.
  • Espinal E; Summa Health Medical Group, Akron, Ohio.
  • La Pietra A; Mount Sinai Medical Center, Miami Beach, Florida.
  • Yang F; Maimonides Medical Center, Brooklyn, New York.
  • Greenberg Y; Maimonides Medical Center, Brooklyn, New York.
  • Jacobowitz I; Maimonides Medical Center, Brooklyn, New York.
  • Gill J; Guy's and St. Thomas' Foundation Trust, London, United Kingdom.
Heart Rhythm O2 ; 4(2): 111-118, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36873309
ABSTRACT

Background:

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:

The study sought to evaluate the safety and effectiveness of HC vs CA in the LSPAF subgroup from the CONVERGE trial.

Methods:

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:

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 (P = .022). Through 18 months, these rates were 60.5% (95% CI 50.0%-76.1%) with HC vs 25.9% (95% CI 9.4%-42.5%) with CA (P = .006). Secondary effectiveness rates were higher than CA with HC at 12 and 18 months. Freedom from atrial arrhythmias off AADs was 52.6% (95% CI 36.8%-68.5%) and 47.4% (95% CI 31.5%-63.2%) with HC at 12 and 18 months vs 25.9% (95% CI 9.4%-42.5%) and 22.2% (95% CI 6.5%-37.9%) with CA, respectively (12 months P = .031; 18 months P = .038). Three (7.9%) major adverse events occurred within 30 days of HC.

Conclusion:

Post hoc analysis demonstrated effectiveness and acceptable safety of HC compared with CA in LSPAF.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Heart Rhythm O2 Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Geórgia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Heart Rhythm O2 Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Geórgia