Efficacy and safety of novel temperature-controlled radiofrequency ablation system during pulmonary vein isolation in patients with paroxysmal atrial fibrillation: TRAC-AF study.

Atrial fibrillation Catheter radiofrequency ablation Diamond tip irrigated catheter High-resolution electrograms Safety and efficacy Temperature contol ablation

Journal

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
ISSN: 1572-8595
Titre abrégé: J Interv Card Electrophysiol
Pays: Netherlands
ID NLM: 9708966

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 25 09 2020
accepted: 22 03 2021
pubmed: 6 6 2021
medline: 26 8 2022
entrez: 5 6 2021
Statut: ppublish

Résumé

Saline-irrigated radiofrequency ablation (RFA) for atrial fibrillation (AF) is limited by the absence of reliable thermal feedback limiting the utility of temperature monitoring for power titration. The DiamondTemp (DT) ablation catheter was designed to allow efficient temperature-controlled irrigated ablation. We sought to assess the 1-year clinical safety and efficacy of the DT catheter in treating drug-refractory paroxysmal AF. The TRAC-AF trial (NCT02821351) is a prospective, multi-center (n = 4), single-arm study which enrolled patients with symptomatic, drug-refractory, paroxysmal AF. Using the DT catheter, point-by-point ablation was performed around all pulmonary veins (PVs) to achieve PV isolation (PVI). Ablation was performed in a temperature-controlled mode (60 °C, max 50 W). Acute and chronic efficacy and safety was evaluated. Seventy-one patients (age 69.9 ± 11.0 years; 60.6% male) were ablated using the DT catheter. The mean fluoroscopy and RF ablation times were 9.3 ± 6.1 min and 20.6 ± 8.9 min, respectively. Acute isolation of all PVs was achieved in 100% of patients, and freedom from AF after 1 year was 70.6%. There were no steam pops, char, or coagulum on the catheter tip after ablation. There were few serious procedure/device-related adverse events including a single case of cardiac tamponade (1.4%) and transient ischemic attack (1.4). This first in man series demonstrates that temperature-controlled irrigated RFA with the DT catheter is efficient, safe, and effective in the treatment of paroxysmal AF. Randomized controlled trials are ongoing and will evaluate better the role of this catheter in relation to standard RFA. Registered on the site ClinicalTrials.gov January 2016 with identifier: NCT02821351.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Saline-irrigated radiofrequency ablation (RFA) for atrial fibrillation (AF) is limited by the absence of reliable thermal feedback limiting the utility of temperature monitoring for power titration. The DiamondTemp (DT) ablation catheter was designed to allow efficient temperature-controlled irrigated ablation. We sought to assess the 1-year clinical safety and efficacy of the DT catheter in treating drug-refractory paroxysmal AF.
METHODS METHODS
The TRAC-AF trial (NCT02821351) is a prospective, multi-center (n = 4), single-arm study which enrolled patients with symptomatic, drug-refractory, paroxysmal AF. Using the DT catheter, point-by-point ablation was performed around all pulmonary veins (PVs) to achieve PV isolation (PVI). Ablation was performed in a temperature-controlled mode (60 °C, max 50 W). Acute and chronic efficacy and safety was evaluated.
RESULTS RESULTS
Seventy-one patients (age 69.9 ± 11.0 years; 60.6% male) were ablated using the DT catheter. The mean fluoroscopy and RF ablation times were 9.3 ± 6.1 min and 20.6 ± 8.9 min, respectively. Acute isolation of all PVs was achieved in 100% of patients, and freedom from AF after 1 year was 70.6%. There were no steam pops, char, or coagulum on the catheter tip after ablation. There were few serious procedure/device-related adverse events including a single case of cardiac tamponade (1.4%) and transient ischemic attack (1.4).
CONCLUSION CONCLUSIONS
This first in man series demonstrates that temperature-controlled irrigated RFA with the DT catheter is efficient, safe, and effective in the treatment of paroxysmal AF. Randomized controlled trials are ongoing and will evaluate better the role of this catheter in relation to standard RFA.
TRIAL REGISTRATION BACKGROUND
Registered on the site ClinicalTrials.gov January 2016 with identifier: NCT02821351.

Identifiants

pubmed: 34089431
doi: 10.1007/s10840-021-00986-0
pii: 10.1007/s10840-021-00986-0
doi:

Banques de données

ClinicalTrials.gov
['NCT02821351']

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-381

Informations de copyright

© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Références

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Auteurs

Zdenek Starek (Z)

International Clinical Research Center, Interventional cardiac electrophysiology group, St. Anne's University Hospital Brno, Pekařská 53, 656 91, Brno, Czech Republic. zdenek.starek@fnusa.cz.
First Department of Internal Medicine/Cardioangiology, St. Anne's Hospital, Masaryk University, Pekařská 53, 656 91, Brno, Czech Republic. zdenek.starek@fnusa.cz.

Frantisek Lehar (F)

International Clinical Research Center, Interventional cardiac electrophysiology group, St. Anne's University Hospital Brno, Pekařská 53, 656 91, Brno, Czech Republic.
First Department of Internal Medicine/Cardioangiology, St. Anne's Hospital, Masaryk University, Pekařská 53, 656 91, Brno, Czech Republic.

Jiri Jez (J)

International Clinical Research Center, Interventional cardiac electrophysiology group, St. Anne's University Hospital Brno, Pekařská 53, 656 91, Brno, Czech Republic.
First Department of Internal Medicine/Cardioangiology, St. Anne's Hospital, Masaryk University, Pekařská 53, 656 91, Brno, Czech Republic.

Martin Pesl (M)

International Clinical Research Center, Interventional cardiac electrophysiology group, St. Anne's University Hospital Brno, Pekařská 53, 656 91, Brno, Czech Republic.
First Department of Internal Medicine/Cardioangiology, St. Anne's Hospital, Masaryk University, Pekařská 53, 656 91, Brno, Czech Republic.
Department of Biology, Faculty of Medicine, Masaryk University, Kamenice 753/5, 625 00, Brno, Czech Republic.

Petr Neuzil (P)

Department of Cardiology, Na Homolce Hospital, Roentgenova 2, 15030, Prague, Czech Republic.

Lucie Sediva (L)

Department of Cardiology, Na Homolce Hospital, Roentgenova 2, 15030, Prague, Czech Republic.

Jan Petru (J)

Department of Cardiology, Na Homolce Hospital, Roentgenova 2, 15030, Prague, Czech Republic.

Libor Dujka (L)

Department of Cardiology, Na Homolce Hospital, Roentgenova 2, 15030, Prague, Czech Republic.

Moritoshi Funasako (M)

Department of Cardiology, Na Homolce Hospital, Roentgenova 2, 15030, Prague, Czech Republic.

Josef Kautzner (J)

Department of Cardiology, Institute for Clinical and Experimental Medicine, Vídeňská 1958/9, 140 21, Prague 4, Czech Republic.
Department of Medicine I, Palacky University Hospital, Olomouc, Czech Republic.

Petr Peichl (P)

Department of Cardiology, Institute for Clinical and Experimental Medicine, Vídeňská 1958/9, 140 21, Prague 4, Czech Republic.

Bashar Aldhoon (B)

Department of Cardiology, Institute for Clinical and Experimental Medicine, Vídeňská 1958/9, 140 21, Prague 4, Czech Republic.

Jean-Paul Albenque (JP)

Cardiology - Heart Rhythm Management Department, Clinique Pasteur, 45 Avenue de Lombez, 31076, Toulouse, France.

Stephane Combes (S)

Cardiology - Heart Rhythm Management Department, Clinique Pasteur, 45 Avenue de Lombez, 31076, Toulouse, France.

Serge Boveda (S)

Cardiology - Heart Rhythm Management Department, Clinique Pasteur, 45 Avenue de Lombez, 31076, Toulouse, France.
Universiteit Ziekenhuis, Vrije Universiteit Brussel (VUB), Laarbeeklaan 101, 1090, Jette, Brussels, Belgium.

Srinivas R Dukkipati (SR)

Helmsley Electrophysiology Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1030, New York, NY, 10029, USA.

Vivek Y Reddy (VY)

Helmsley Electrophysiology Center, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1030, New York, NY, 10029, USA.

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