Efficacy and safety of the GOLD FORCE multicentre randomized clinical trial: multielectrode phased radiofrequency vs. irrigated radiofrequency single-tip catheter with contact force ablation for treatment of symptomatic paroxysmal atrial fibrillation

Author:

Wintgens Lisette I S1ORCID,Klaver Martijn N1,Maarse Moniek1,Spitzer Stefan G23,Langbein Anke2,Swaans Martin J1,Van Dijk Vincent F1,Balt Jippe C1,Wijffels Maurits C E F1,Tijssen Jan G P4,Elvan Arif5ORCID,Boersma Lucas V A14ORCID

Affiliation:

1. St. Antonius Hospital, Department of Cardiology, Koekoekslaan 1, 3435 Nieuwegein, The Netherlands

2. Praxisklinik Herz und Gefäße Dresden, Akademische Lehrpraxisklinik der TU Dresden, Department of Cardiology, Dresden, Germany

3. Brandenburg University of Technology Cottbus-Senftenberg, Institute of Medical Technology, Department of Cardiology, Cottbus, Germany

4. Amsterdam UMC, Department of Cardiology, Amsterdam, The Netherlands

5. Isala Clinics, Department of Cardiology, Zwolle, the Netherlands

Abstract

Abstract Aims Pulmonary vein isolation (PVI) for atrial fibrillation (AF) has become increasingly safe and effective with the evolution of single-tip ablation catheters aided by contact force sensing (ST-CF) and single-shot devices such as the second-generation pulmonary vein ablation catheter (PVAC) Gold multi-electrode array. The multicentre randomized GOLD FORCE trial was conducted to evaluate non-inferiority of safety and efficacy of PVAC Gold PVI compared to ST-CF ablation for paroxysmal AF. Methods and results The primary efficacy endpoint documented AF recurrence ≥30 s was assessed by time-to-first-event analysis after a 90-day blanking period using repeated 7-day Holters. Secondary endpoints include acute success and procedural characteristics. Safety endpoints included procedural complications, stroke/transient ischaemic attack (TIA), tamponade, bleeding, and access site complications. Two hundred and eight patients underwent randomization and PVI (103 assigned to PVAC Gold, 105 to ST-CF). Acute success rates were 95% and 97% for PVAC Gold and ST-CF, respectively. At 12 months, AF recurrence was observed in 46.6% of the PVAC Gold group and in 26.2% of the ST-CF group [absolute efficacy difference 20.4% (95% confidence interval, CI 7.5–33.2%), hazard ratio 2.05 (95% CI 1.28–3.29), P = 0.003]. PVAC Gold had significantly shorter procedure and ablation times. Complication rates were 5.7% and 4.9% for PVAC Gold and ST-CF, respectively (P = 0.782). Conclusion In this multicentre randomized clinical trial, ablation with ST-CF and PVAC Gold ablation catheters non-inferiority for efficacy was not met. AF recurrence was significantly more frequent in the PVAC Gold group compared to single-tip contact force group. Both groups had similarly low rates of adverse events. PVAC Gold ablation had significantly shorter procedure and ablation times.

Funder

ZonMw Topzorg

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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