Cryocure-VT: the safety and effectiveness of ultra-low-temperature cryoablation of monomorphic ventricular tachycardia in patients with ischaemic and non-ischaemic cardiomyopathies.

Ablation Clinical trial Cryoablation Outcomes Ultra-low Ventricular tachycardia

Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
30 Mar 2024
Historique:
received: 29 02 2024
accepted: 18 03 2024
medline: 7 4 2024
pubmed: 7 4 2024
entrez: 7 4 2024
Statut: ppublish

Résumé

The ultra-low-temperature cryoablation (ULTC) ablation system using -196°C N2 cryogen has been reported to create lesions with freeze duration-dependent depth titratable to over 10 mm with minimum attenuation by scar. Cryocure-VT (NCT04893317) was a first-in-human clinical trial evaluating the safety and efficacy of a novel, purpose-built ULTC catheter in endocardial ablation of scar-dependent ventricular tachycardias (VTs). This prospective, multi-centre study enrolled patients referred for de novo or second ablations of recurrent monomorphic VT of both ischaemic and non-ischaemic aetiologies. Primary safety and efficacy endpoints of the study were freedom from device- or procedure-related major adverse events (MAEs) up to 30 days post-ablation, acute non-inducibility of clinical VTs at the end of the procedure, and freedom from sustained VT or implantable defibrillator intervention at 6 months. Ultra-low-temperature cryoablation was performed in 64 patients (age 67 ± 11 years, 78% ischaemic, ejection fraction = 35 ± 10%) at 9 centres. The primary acute effectiveness endpoint was achieved in 94% (51/54) of patients in whom post-ablation induction was attempted. There were no protocol-defined MAEs; four procedure-related serious adverse events resolved without clinical sequelae. At 6-month follow-up, 38 patients (60.3%) remained VT-free, and freedom from defibrillator shock was 81.0%, with no significant difference between ischaemic and non-ischaemic cohorts. In 47 patients with defibrillator for at least 6 months prior to the ablation, the VT burden was reduced from median of 4, inter-quartile range (IQR, 1-9) to 0, IQR (0-2). In this first-in-human multi-centre experience, endocardial ULTC ablation of monomorphic VT appears safe and effective in patients with both ischaemic-cardiomyopathy and non-ischaemic-cardiomyopathy. NCT04893317.

Identifiants

pubmed: 38582974
pii: 7641150
doi: 10.1093/europace/euae076
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04893317']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Adagio Medical Inc

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Déclaration de conflit d'intérêts

Conflict of interest: A.V. reports being a consultant for Biosense Webster, Medtronic, Adagio Medical, Medlumics, and Abbott. L.B. reports being a consultant for Medtronic, Boston Scientific, and Adagio Medical. All fees go to the cardiology department. V.E. is supported by a Clinical Research Scholar Award from the Fonds de Recherche du Quebec Santé (FRQS) and reports honoraria from Abbott, Biosense Webster, Boston Scientific, and Medtronic. V.Y.R. reports serving as a consultant to Adagio Medical, unrelated to this manuscript. V.Y.R. has served as a consultant for and has equity in Ablacon, Acutus Medical, Affera-Medtronic, Anumana, Apama Medical-Boston Scientific, APN Health, Aquaheart, Atacor, Autonomix, Axon Therapies, Backbeat, BioSig, CardiaCare, CardioNXT/AFTx, Circa Scientific, CoRISMA, Corvia Medical, Dinova-Hangzhou DiNovA EP Technology, East End Medical, EPD-Philips, EP Frontiers, Epix Therapeutics-Medtronic, EpiEP, Eximo, Farapulse-Boston Scientific, Field Medical, Focused Therapeutics, HRT, Intershunt, Javelin, Kardium, Keystone Heart, LuxMed, Medlumics, Middlepeak, Neutrace, Nuvera-Biosense Webster, Oracle Health, Restore Medical, Sirona Medical, SoundCath, and Valcare, unrelated to this work. V.R. has served as a consultant for Abbott, AtriAN, Biosense-Webster, BioTel Heart, Biotronik, Boston Scientific, Cairdac, Cardiofocus, Cardionomic, CoreMap, Fire1, Gore & Associates, Impulse Dynamics, Medtronic, Novartis, Philips, and Pulse Biosciences, unrelated to this work, V.R. has equity in Atraverse, Manual Surgical Sciences, Newpace, Nyra Medical, Surecor, and Vizaramed. I.G. is an employee of Adagio Medical. T.D.P. reports receiving institutional payments related to study activities from Adagio Medical, unrelated to this manuscript and reports receiving institutional payments for consultancy from Abbott, Boston Scientific, GE, J&J, and Medlumics. All remaining authors have declared no conflicts of interest.

Auteurs

Atul Verma (A)

Division of Cardiology, McGill University Health Centre, D13.173, 1650 Cedar Avenue, Montreal, QC H3G 1A4, Canada.

Vidal Essebag (V)

Division of Cardiology, McGill University Health Centre, D13.173, 1650 Cedar Avenue, Montreal, QC H3G 1A4, Canada.

Petr Neuzil (P)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.

Katia Dyrda (K)

Department of Medicine, Montreal Heart Institute, Montreal, QC, Canada.

Jippe Balt (J)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, The Netherlands.

Borislav Dinov (B)

Department of Electrophysiology, Leipzig Heart Center, Leipzig, Germany.

Angeliki Darma (A)

Department of Electrophysiology, Leipzig Heart Center, Leipzig, Germany.

Arash Arya (A)

Department for Internal Medicine, University Hospital Halle, Halle, Germany.

Frederic Sacher (F)

Bordeaux University Hospital, IHU LIRYC, University of Bordeaux, Bordeaux, France.

Vivek Y Reddy (VY)

Department of Cardiology, Na Homolce Hospital, Prague, Czech Republic.
Helmsley Electrophysiology Center, Mount Sinai Fuster Heart Hospital, New York, NY, USA.

Lucas Boersma (L)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Department of Heart Failure and Arrhythmias,Amsterdam University Medical Center, Amsterdam, The Netherlands.

Ilya Grigorov (I)

Adagio Medical, Inc., Laguna Hills, CA, USA.

Tom De Potter (T)

Cardiovascular Center, OLV Hospital, Moorselbaan 164, 9300 Aalst, Belgium.

Classifications MeSH