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.
J Interv Card Electrophysiol. 2022 Aug;64(2):375-381. doi: 10.1007/s10840-021-00986-0. Epub 2021 Jun 5.
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.
盐水灌洗射频消融(RFA)治疗心房颤动(AF)的应用受到限制,因为缺乏可靠的热反馈,使得温度监测在功率滴定中的作用受限。DiamondTemp(DT)消融导管的设计目的是实现高效的温度控制灌洗消融。我们旨在评估 DT 导管在治疗药物难治性阵发性 AF 中的 1 年临床安全性和有效性。
TRAC-AF 试验(NCT02821351)是一项前瞻性、多中心(n=4)、单臂研究,纳入了有症状、药物难治性、阵发性 AF 的患者。使用 DT 导管,在所有肺静脉(PVs)周围进行点式消融,以实现 PV 隔离(PVI)。消融采用温度控制模式(60°C,最大 50 W)。评估急性和慢性疗效及安全性。
71 例患者(年龄 69.9±11.0 岁;60.6%为男性)使用 DT 导管进行了消融。平均透视和 RF 消融时间分别为 9.3±6.1 min 和 20.6±8.9 min。所有患者均实现了 100%的 PV 急性隔离,1 年后 AF 无复发率为 70.6%。消融后导管尖端无蒸汽爆破、炭化或凝血块。只有 1 例(1.4%)心脏压塞和 1 例(1.4%)短暂性脑缺血发作为严重的手术/器械相关不良事件。
这项首次人体研究表明,使用 DT 导管的温度控制灌洗 RFA 治疗阵发性 AF 既高效又安全且有效。正在进行随机对照试验,将更好地评估该导管在标准 RFA 中的作用。
2016 年 1 月在 ClinicalTrials.gov 网站注册,标识符为:NCT02821351。