Intramural Venous Ethanol Infusion for Refractory Ventricular Arrhythmias: Outcomes of a Multicenter Experience.


Journal

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

Informations de publication

Date de publication:
26 10 2020
Historique:
received: 22 06 2020
revised: 22 07 2020
accepted: 27 07 2020
entrez: 30 10 2020
pubmed: 31 10 2020
medline: 19 8 2021
Statut: ppublish

Résumé

The aim of this study was to assess the long-term efficacy and outcomes of retrograde venous ethanol ablation in treating ventricular arrhythmias (VAs). Retrograde coronary venous ethanol ablation (RCVEA) can be effective for radiofrequency ablation (RFA)-refractory VAs, particularly those arising in the LV summit (LVS). Patients with drug and RFA-refractory VAs were considered for RCVEA after RF failure attempts. Intramural coronary veins (tributaries of the great cardiac, anterior interventricular, lateral cardiac, posterolateral, and middle cardiac) were mapped using an angioplasty wire. Ethanol infusion was delivered in veins with appropriate signals. Of 63 patients (age 63 ± 14 years; 60% men) with VAs (71% extrasystole, 29% ventricular tachycardia, 76% LVS origin), RCVEA was performed in 56 patients who had suitable vein branches. These were defined as those amenable to cannulation and with intramural signals that preceded those mapped in the epicardium or endocardium and had better matching pace maps or entrainment responses. Seven patients had no suitable veins and underwent RFA. In 38 of 56 (68%) patients, the VAs were successfully terminated exclusively with ethanol infusion. In 17 of 56 (30%) patients, successful ablation was achieved using ethanol with adjunctive RFA in the vicinity of the infused vein due to acute recurrence or ethanol-induced change in VA morphology. Overall, isolated or adjuvant RCVEA was successful in 55 of 56 (98%) patients. At 1-year follow-up, 77% of patients were free of recurrent arrhythmias. Procedural complications included 2 venous dissections that led to pericardial effusions. RCVEA offers a significant long-term effective treatment for patients with drug and RF-refractory VAs.

Sections du résumé

OBJECTIVES
The aim of this study was to assess the long-term efficacy and outcomes of retrograde venous ethanol ablation in treating ventricular arrhythmias (VAs).
BACKGROUND
Retrograde coronary venous ethanol ablation (RCVEA) can be effective for radiofrequency ablation (RFA)-refractory VAs, particularly those arising in the LV summit (LVS).
METHODS
Patients with drug and RFA-refractory VAs were considered for RCVEA after RF failure attempts. Intramural coronary veins (tributaries of the great cardiac, anterior interventricular, lateral cardiac, posterolateral, and middle cardiac) were mapped using an angioplasty wire. Ethanol infusion was delivered in veins with appropriate signals.
RESULTS
Of 63 patients (age 63 ± 14 years; 60% men) with VAs (71% extrasystole, 29% ventricular tachycardia, 76% LVS origin), RCVEA was performed in 56 patients who had suitable vein branches. These were defined as those amenable to cannulation and with intramural signals that preceded those mapped in the epicardium or endocardium and had better matching pace maps or entrainment responses. Seven patients had no suitable veins and underwent RFA. In 38 of 56 (68%) patients, the VAs were successfully terminated exclusively with ethanol infusion. In 17 of 56 (30%) patients, successful ablation was achieved using ethanol with adjunctive RFA in the vicinity of the infused vein due to acute recurrence or ethanol-induced change in VA morphology. Overall, isolated or adjuvant RCVEA was successful in 55 of 56 (98%) patients. At 1-year follow-up, 77% of patients were free of recurrent arrhythmias. Procedural complications included 2 venous dissections that led to pericardial effusions.
CONCLUSIONS
RCVEA offers a significant long-term effective treatment for patients with drug and RF-refractory VAs.

Identifiants

pubmed: 33121671
pii: S2405-500X(20)30705-2
doi: 10.1016/j.jacep.2020.07.023
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1420-1431

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL115003
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Liliana Tavares (L)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Adi Lador (A)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Stephanie Fuentes (S)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Akanibo Da-Wariboko (A)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Krzysztof Blaszyk (K)

Poznan University of Medical Sciences, Poznan, Poland.

Katarzyna Malaczynska-Rajpold (K)

Poznan University of Medical Sciences, Poznan, Poland.

Giorgi Papiashvili (G)

Arrhythmia Unit, Jo Ann Medical Center, Tbilisi, Georgia, USA.

Sergey Korolev (S)

Federal Research and Clinical Center of the FMBA of Russia, Moscow, Russia.

Petr Peichl (P)

Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech Republic.

Josef Kautzner (J)

Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech Republic.

Matthew Webber (M)

Wellington Hospital, Wellington, New Zealand.

Darren Hooks (D)

Wellington Hospital, Wellington, New Zealand.

Moisés Rodríguez-Mañero (M)

Arrhythmia Unit, Complexo Hospitalario de Santiago de Compostela, A Coruña, Spain.

Darío Di Toro (D)

Hospital CEMIC, Buenos Aires, Argentina.

Carlos Labadet (C)

Hospital CEMIC, Buenos Aires, Argentina.

Takeshi Sasaki (T)

Heart Rhythm Center, National Hospital Organization Disaster Medical Center, Tokyo, Japan.

Kaoru Okishige (K)

Heart Center, Japan Red Cross Yokohama City Bay Hospital, Yokohama, Japan.

Apoor Patel (A)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Paul A Schurmann (PA)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Amish S Dave (AS)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Tapan G Rami (TG)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.

Miguel Valderrábano (M)

Division of Cardiac Electrophysiology, Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA. Electronic address: mvalderrabano@houstonmethodist.org.

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