Doshi Rahul N, Ip James E, Defaye Pascal, Exner Derek V, Reddy Vivek Y, Hindricks Gerhard, Canby Robert, Shoda Morio, Bongiorni Maria G, Neužil Petr, Callahan Thomas, Badie Nima, Ligon David, Knops Reinoud E
HonorHealth Cardiac Arrhythmia Group, Scottsdale, Arizona.
Weill Cornell Medicine/New York Presbyterian Hospital, New York, New York.
Heart Rhythm. 2025 Apr;22(4):1010-1020. doi: 10.1016/j.hrthm.2024.10.020. Epub 2024 Oct 19.
Aveir DR (Abbott, Abbott Park, IL) is a dual-chamber leadless pacemaker (LP) system with distinct atrial and ventricular LPs (ALP, VLP) that communicate wirelessly to deliver atrioventricular synchronous pacing. Success rates of these implant-to-implant (i2i) transmissions have not been systematically evaluated.
This study aims to evaluate chronic i2i success rates in a clinical setting.
Patients meeting standard dual-chamber pacing indications were enrolled and implanted with dual-chamber LP systems as part of a prospective international clinical trial (Aveir DR i2i Study). The percent of successful i2i transmissions from ALP-to-VLP (A-to-V) and VLP-to-ALP (V-to-A) were interrogated from LPs in de novo patients using the device programmer at implant, discharge, and at 1, 3, and 6 months postimplant (1M, 3M, 6M).
A total of 399 patients completed device implant and i2i diagnostic interrogation (62% male; age 69 years; 65% sinus node dysfunction, 32% atrioventricular [AV] block). Median A-to-V and V-to-A i2i success rates exceeded 90% of beats at all time-points from implant to 6M. The minority of patients with A-to-V or V-to-A i2i success in <70% of beats at implant (A-to-V: 19% of patients, V-to-A: 31% of patients) showed roughly 40% improvement by 1M, with this minority dropping to roughly 5% of patients by 6M. Improvement in i2i communication success may be attributed to reprogramming of i2i setting levels, natural changes in dominant posture, and device stabilization.
Wireless implant-to-implant communication in the new dual-chamber leadless pacemaker system demonstrated successful transmissions in >90% of beats throughout the 6-month evaluation period. Communication success improved significantly over time postimplant for specific subgroups.
Aveir DR i2i Study, ClinicalTrials.gov ID NCT05252702.
Aveir DR(雅培公司,伊利诺伊州雅培公园)是一种双腔无导线起搏器(LP)系统,具有独特的心房和心室无导线起搏器(ALP、VLP),它们通过无线通信来实现房室同步起搏。这些植入物到植入物(i2i)传输的成功率尚未得到系统评估。
本研究旨在评估临床环境中慢性i2i成功率。
符合标准双腔起搏指征的患者入组,并植入双腔LP系统,作为一项前瞻性国际临床试验(Aveir DR i2i研究)的一部分。在植入时、出院时以及植入后1个月、3个月和6个月(1M、3M、6M),使用设备编程器从初治患者的无导线起搏器中查询从ALP到VLP(A到V)和VLP到ALP(V到A)的i2i传输成功率。
共有399例患者完成了设备植入和i2i诊断查询(男性占62%;年龄69岁;65%为窦房结功能障碍,32%为房室[AV]阻滞)。从植入到6个月的所有时间点,A到V和V到A的i2i成功率中位数均超过90%。在植入时A到V或V到A的i2i成功率低于70%的少数患者(A到V:19%的患者,V到A:31%的患者)在1个月时显示出约40%的改善,到6个月时这一少数患者降至约5%。i2i通信成功率的提高可能归因于i2i设置水平的重新编程、主导姿势的自然变化以及设备的稳定。
新型双腔无导线起搏器系统中的无线植入物到植入物通信在整个6个月的评估期内,超过90%的搏动实现了成功传输。对于特定亚组,植入后随着时间推移,通信成功率显著提高。
Aveir DR i2i研究,ClinicalTrials.gov标识符NCT05252702。