Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Clinique Pasteur, Toulouse, France.
JACC Clin Electrophysiol. 2021 Mar;7(3):352-363. doi: 10.1016/j.jacep.2020.11.009. Epub 2021 Jan 27.
DIAMOND-AF (DiamondTemp™ Ablation System for the Treatment of Paroxysmal Atrial Fibrillation) was a prospective, multicenter, noninferiority, randomized trial that compared the safety and effectiveness of the DTA system versus those of a force-sensing RF ablation system (control) for the treatment of patients with drug-refractory, recurrent, symptomatic paroxysmal atrial fibrillation (AF).
Irrigated radiofrequency (RF) ablation catheters lose tissue temperature acuity, which is vital in assessing lesion formation. DiamondTemp Ablation (DTA) was designed to re-establish accurate tissue temperature measurements during ablation.
A total of 482 patients with paroxysmal AF were randomized (239 DTA, 243 control) to undergo pulmonary vein isolation and were followed up at 23 sites. Patients were screened for disease progression, cardiac characteristics, and prior interventions. Primary endpoints were effectiveness (freedom from atrial arrhythmia recurrence) and safety (composite of procedure- and device-related serious adverse events).
The primary safety event rate was 3.3% in the DTA group versus 6.6% in the control group (p < 0.001 vs. 6.5% noninferiority margin). Primary effectiveness was met in 79.1% of DTA subjects and 75.7% of control subjects (p < 0.001 vs. -12.5% noninferiority margin). Secondary endpoint analysis found that off-drug effectiveness favored DTA compared with the control (142 [59.4%] vs. 120 [49.4%], respectively; p = 0.03). Total RF time and individual RF ablation duration were significantly shorter with less saline infused through the DTA catheter (p < 0.001). Both arms saw clinically meaningful improvements in quality of life at 12 months.
Safety and efficacy of the DTA system proved noninferior to force-sensing RF ablation in a paroxysmal AF population. Efficiencies were observed using DTA with shorter total RF times, individual RF ablation durations, and less saline infusion. (DiamondTemp™ Ablation System for the Treatment of Paroxysmal Atrial Fibrillation; NCT03334630).
DIAMOND-AF(DiamondTemp™ 消融系统治疗阵发性心房颤动)是一项前瞻性、多中心、非劣效性、随机试验,比较了 DTA 系统与力感应射频消融系统(对照)治疗药物难治性、复发性、有症状阵发性心房颤动(房颤)患者的安全性和有效性。
灌流射频(RF)消融导管失去组织温度感知能力,这对于评估病变形成至关重要。DiamondTemp Ablation(DTA)旨在重新建立消融过程中的准确组织温度测量。
共有 482 名阵发性房颤患者被随机分为(DTA 组 239 例,对照组 243 例)进行肺静脉隔离,并在 23 个部位进行随访。患者接受疾病进展、心脏特征和既往干预措施的筛查。主要终点是有效性(无房性心律失常复发)和安全性(包括程序和器械相关严重不良事件的复合事件)。
DTA 组主要安全性事件发生率为 3.3%,对照组为 6.6%(p<0.001,优于 6.5%的非劣效性边界)。DTA 组 79.1%的患者和对照组 75.7%的患者达到主要有效性终点(p<0.001,优于-12.5%的非劣效性边界)。次要终点分析发现,停药后有效性方面,DTA 优于对照组(分别为 142[59.4%]和 120[49.4%];p=0.03)。DTA 导管的总 RF 时间和单个 RF 消融时间显著缩短,通过导管输注的盐水也更少(p<0.001)。两组患者在 12 个月时的生活质量均有显著改善。
在阵发性房颤人群中,DTA 系统的安全性和有效性被证明不劣于力感应射频消融。使用 DTA 时,总 RF 时间、单个 RF 消融时间和盐水输注量均减少,观察到效率提高。(DiamondTemp™ 消融系统治疗阵发性心房颤动;NCT03334630)。