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采用浮动心房环(偶极)的单通道(VDD)起搏导线进行双腔(DDD)起搏的可行性:病例系列、未来考量及改进

Feasibility of dual-chamber (DDD) pacing via a single-pass (VDD) pacing lead employing a floating atrial ring (dipole): case series, future considerations, and refinements.

作者信息

Kassotis John, Voigt Louis, Mongwa Mbu, Reddy C V R

机构信息

Clinical Electrophysiologic Services, New York Methodist Hospital, Clinical Affiliate of New York Presbyterian Hospital System, Brooklyn, 11215, USA.

出版信息

Angiology. 2005 May-Jun;56(3):323-9. doi: 10.1177/000331970505600313.

Abstract

The objective of this study was to assess the feasibility of DDD pacing from a standard single-pass VDD pacemaker system. Over the past 2 decades significant advances have been made in the development of single-pass VDD pacing systems. These have been shown in long-term prospective studies to effectively preserve atrioventricular (AV)synchrony in patients with AV block and normal sinus node function. What remains problematic is the development of a single-pass pacing system capable of DDD pacing. Such a lead configuration would be useful in those patients with peripheral venous anomalies and in younger patients with congenital anomalies, which may require lead revisions in the future. In addition, with the increased use of resynchronization (biventricular pacing) therapy, the availability of a reliable single-pass lead will minimize operative time, enhance patient safety, and minimize the amount of hardware within the heart. The feasibility of DDD pacing via a Medtronic Capsure VDD-2 (Model #5038) pacing lead was evaluated. Twenty patients who presented with AV block and normal sinus node function were recruited for this study. Atrial pacing thresholds and sensitivities were assessed intraoperatively in the supine position with various respiratory maneuvers. Five patients who agreed to participate in long-term follow-up received a dual-chamber generator and were evaluated periodically over a 12-month period. Mean atrial sensitivity was 2.35 +/- 0.83 mV at the time of implantation. Effective atrial stimulation was possible in all patients at the time of implantation (mean stimulation threshold 3.08 +/- 1.04 V at 0.5 ms [bipolar], 3.34 +/- 0.95 V at 0.5 ms [unipolar]). Five of the 20 patients received a Kappa KDR701 generator, and atrial electrical properties were followed up over a 1-year period. There was no significant change in atrial pacing threshold or incidence of phrenic nerve stimulation over the 1-year follow-up. A standard single-pass VDD pacing lead system was capable of DDD pacing intraoperatively and during long-term follow-up. Despite higher than usual thresholds via the atrial dipole, pacemaker telemetry revealed < 10% use of atrial pacing dipole over a 12-month period, which would minimally deplete the pacemaker's battery. In addition, the telemetry confirmed appropriate sensing and pacing of the atrial dipole throughout the study period. At this time such systems can serve as back-up DDD pacing systems with further refinements required to optimize atrial thresholds in all patients.

摘要

本研究的目的是评估采用标准单极VDD起搏器系统进行DDD起搏的可行性。在过去20年里,单极VDD起搏系统的研发取得了重大进展。长期前瞻性研究表明,这些系统能有效维持房室传导阻滞且窦房结功能正常患者的房室(AV)同步性。目前仍存在问题的是开发一种能够进行DDD起搏的单极起搏系统。这种导线配置对那些存在外周静脉异常的患者以及可能在未来需要更换导线的年轻先天性异常患者有用。此外,随着再同步化(双心室起搏)治疗的使用增加,可靠的单极导线将减少手术时间,提高患者安全性,并减少心脏内的硬件数量。评估了通过美敦力Capsure VDD - 2(型号#5038)起搏导线进行DDD起搏的可行性。招募了20名患有房室传导阻滞且窦房结功能正常的患者参与本研究。术中在仰卧位通过各种呼吸动作评估心房起搏阈值和感知灵敏度。5名同意参加长期随访的患者接受了双腔起搏器,并在12个月内定期进行评估。植入时平均心房感知灵敏度为2.35±0.83 mV。所有患者在植入时均能实现有效的心房刺激(平均刺激阈值在0.5 ms时为3.08±1.04 V[双极],在0.5 ms时为3.34±0.95 V[单极])。20名患者中有5名接受了Kappa KDR701起搏器,并对心房电学特性进行了为期1年的随访。在1年随访期间心房起搏阈值或膈神经刺激发生率无显著变化。标准单极VDD起搏导线系统在术中及长期随访期间均能进行DDD起搏。尽管通过心房偶极的阈值高于平常,但起搏器遥测显示在12个月期间心房起搏偶极的使用率<10%,这只会使起搏器电池电量轻微消耗。此外,遥测证实了在整个研究期间心房偶极的感知和起搏适当。目前此类系统可作为备用DDD起搏系统,不过还需要进一步改进以优化所有患者的心房阈值。

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