Barts Heart Centre, Barts Health National Health Service Trust, London, United Kingdom.
Barts Heart Centre, Barts Health National Health Service Trust, London, United Kingdom.
JACC Clin Electrophysiol. 2019 Jul;5(7):817-829. doi: 10.1016/j.jacep.2019.04.007. Epub 2019 May 8.
The aim of this study was to demonstrate that a stochastic vector-based mapping approach could guide ablation of atrial fibrillation (AF) drivers as evidenced by ablation response and long-term follow-up outcomes.
The optimal method for mapping and ablation of AF drivers is yet to be defined.
Patients undergoing persistent AF ablation were recruited. Patients underwent pulmonary vein isolation (PVI) with further ablation guided by the stochastic trajectory analysis of ranked signals (STAR) mapping method. The proportion of the time an electrode's activation was seen to precede its neighboring electrodes activation was used to determine early sites of activation (ESA). A positive ablation response at ESA was defined as AF termination or cycle length slowing of ≥30 ms. Clinical outcome was defined as recurrence of AF/atrial tachycardia (AT) during a follow-up of 12 months.
Thirty-five patients were included (AF duration of 14.4 ± 5.3 months). After PVI, an average of 2.6 ± 0.8 ESA were ablated per patient with study-defined ablation response achieved in all patients. Of the 86 STAR maps created post-PVI, the same ESA was identified on 73.8 ± 26.1% of maps. ESA that resulted in AF termination were more likely to be identified on both pre- and post-PVI maps than those associated with cycle length slowing (23 of 24 vs. 16 of 49; p < 0.001). During a follow-up of 18.5 ± 3.7 months, 28 (80%) patients were free from AF/AT.
The ablation response at ESA suggests they may be drivers of AF. Ablation guided by STAR mapping produced a favorable clinical outcome and warrants testing through a randomized controlled trial. (Identification, Electro-mechanical Characterisation and Ablation of Driver Regions in Persistent Atrial Fibrillation [STAR MAPPING]; NCT02950844).
本研究旨在证明基于随机向量的映射方法可以指导房颤(AF)驱动灶的消融,其依据是消融反应和长期随访结果。
目前仍未确定用于 AF 驱动灶标测和消融的最佳方法。
招募接受持续性 AF 消融的患者。患者接受肺静脉隔离(PVI),进一步的消融由排序信号随机轨迹分析(STAR)标测方法指导。电极激活早于相邻电极激活的时间比例用于确定早期激活部位(ESA)。ESA 处的阳性消融反应定义为 AF 终止或周长缩短≥30ms。临床结果定义为 12 个月随访期间 AF/房性心动过速(AT)的复发。
共纳入 35 例患者(AF 病程 14.4±5.3 个月)。PVI 后,平均每位患者消融 2.6±0.8 个 ESA,所有患者均达到研究定义的消融反应。在 86 份 PVI 后的 STAR 图中,有 73.8±26.1%的图上出现相同的 ESA。与周长缩短相关的 ESA (23 个中的 16 个)比导致 AF 终止的 ESA (24 个中的 23 个)更有可能在 PVI 前后的图上识别出来(p<0.001)。在 18.5±3.7 个月的随访期间,28(80%)例患者无 AF/AT。
ESA 处的消融反应提示其可能为 AF 的驱动灶。基于 STAR 标测的消融产生了良好的临床结果,值得通过随机对照试验进行检验。(Identification,Electro-mechanical Characterisation and Ablation of Driver Regions in Persistent Atrial Fibrillation [STAR MAPPING];NCT02950844)。