Division of Cardiology, Section of Electrophysiology, Emory University, Atlanta, Georgia, USA.
Michigan Heart, Ypsilanti, Michigan, USA.
J Cardiovasc Electrophysiol. 2021 Mar;32(3):832-841. doi: 10.1111/jce.14881. Epub 2021 Jan 23.
The feasibility and outcomes of concomitant atrioventricular node ablation (AVNA) and leadless pacemaker implant are not well studied. We report outcomes in patients undergoing Micra implant with concomitant AVNA.
Patients undergoing AVNA at the time of Micra implant from the Micra Transcatheter Pacing (IDE) Study, Continued Access (CA) study, and Post-Approval Registry (PAR) were included in the analysis and compared to Micra patients without AVNA. Baseline characteristics, acute and follow-up outcomes, and electrical performance were compared between patients with and without AVNA during the follow-up period.
A total of 192 patients (mean age 77.4 ± 8.9 years, 72% female) underwent AVNA at the time of Micra implant and were followed for 20.4 ± 15.6 months. AVNA patients were older, more frequently female, and tended to have more co-morbid conditions compared with non-AVNA patients (N = 2616). Implant was successful in 191 of 192 patients (99.5%). The mean pacing threshold at implant was 0.58 ± 0.35 V and remained stable during follow-up. Major complications within 30 days occurred more frequently in AVNA patients than non-AVNA patients (7.3% vs. 2.0%, p < .001). The risk of major complications through 36-months was higher in AVNA patients (hazard ratio: 3.81, 95% confidence interval: 2.33-6.23, p < .001). Intermittent loss of capture occurred in three AVNA patients (1.6%), all were within 30 days of implant and required system revision. There were no device macrodislodgements or unexpected device malfunctions.
Concomitant AVN ablation and leadless pacemaker implant is feasible. Pacing thresholds are stable over time. However, patient comorbidities and the risk of major complications are higher in patients undergoing AVNA.
同期房室结消融(AVNA)和无导线起搏器植入的可行性和结果尚未得到充分研究。我们报告了在接受 Micra 植入的同时进行 AVNA 的患者的结果。
从 Micra 经导管起搏(IDE)研究、持续接入(CA)研究和上市后注册(PAR)中纳入同时接受 AVNA 和 Micra 植入的患者进行分析,并与未行 AVNA 的 Micra 患者进行比较。比较了 AVNA 患者和非 AVNA 患者在随访期间的基线特征、急性和随访结果以及电性能。
共 192 例(平均年龄 77.4±8.9 岁,72%为女性)患者在接受 Micra 植入时同期行 AVNA,随访时间为 20.4±15.6 个月。AVNA 患者年龄较大,女性比例较高,合并症较多,与非 AVNA 患者(N=2616 例)相比差异有统计学意义。192 例患者中有 191 例(99.5%)植入成功。植入时的平均起搏阈值为 0.58±0.35V,随访期间保持稳定。AVNA 患者 30 天内主要并发症发生率高于非 AVNA 患者(7.3%比 2.0%,p<.001)。AVNA 患者 36 个月时主要并发症风险较高(风险比:3.81,95%置信区间:2.33-6.23,p<.001)。3 例 AVNA 患者(1.6%)出现间歇性捕获丢失,均发生在植入后 30 天内,需要系统修订。无设备宏观移位或意外设备故障。
同期房室结消融和无导线起搏器植入是可行的。起搏阈值随时间稳定。然而,行 AVNA 的患者合并症和发生重大并发症的风险较高。