Ritter Philippe, Duray Gabor Z, Zhang Shu, Narasimhan Calambur, Soejima Kyoko, Omar Razali, Laager Verla, Stromberg Kurt, Williams Eric, Reynolds Dwight
Department of Cardiac Pacing and Electrophysiology, CHU/Université de Bordeaux, Avenue Magellan, 33604 Pessac, France L'Institut de Rythmologie et de Modélisation Cardiaque LIRYC, CHU/Université de Bordeaux/INSERM U1045, Pessac, France
Clinical Electrophysiology Department of Cardiology, Medical Centre, Hungarian Defence Forces, Budapest, Hungary.
Europace. 2015 May;17(5):807-13. doi: 10.1093/europace/euv026. Epub 2015 Apr 7.
Recent advances in miniaturization technologies and battery chemistries have made it possible to develop a pacemaker small enough to implant within the heart while still aiming to provide similar battery longevity to conventional pacemakers. The Micra Transcatheter Pacing System is a miniaturized single-chamber pacemaker system that is delivered via catheter through the femoral vein. The pacemaker is implanted directly inside the right ventricle of the heart, eliminating the need for a device pocket and insertion of a pacing lead, thereby potentially avoiding some of the complications associated with traditional pacing systems.
The Micra Transcatheter Pacing Study is currently undergoing evaluation in a prospective, multi-site, single-arm study. Approximately 720 patients will be implanted at up to 70 centres around the world. The study is designed to have a continuously growing body of evidence and data analyses are planned at various time points. The primary safety and efficacy objectives at 6-month post-implant are to demonstrate that (i) the percentage of Micra patients free from major complications related to the Micra system or implant procedure is significantly higher than 83% and (ii) the percentage of Micra patients with both low and stable thresholds is significantly higher than 80%. The safety performance benchmark is based on a reference dataset of 977 subjects from 6 recent pacemaker studies.
The Micra Transcatheter Pacing Study will assess the safety and efficacy of a miniaturized, totally endocardial pacemaker in patients with an indication for implantation of a single-chamber ventricular pacemaker.
NCT02004873.
小型化技术和电池化学领域的最新进展使得开发一种足够小的起搏器成为可能,这种起搏器小到可以植入心脏内部,同时仍旨在提供与传统起搏器相似的电池使用寿命。Micra经导管起搏系统是一种小型化的单腔起搏器系统,通过导管经股静脉输送。该起搏器直接植入心脏右心室内,无需设备囊袋和插入起搏导线,从而有可能避免一些与传统起搏系统相关的并发症。
Micra经导管起搏研究目前正在一项前瞻性、多中心、单臂研究中进行评估。全球约70个中心将为约720名患者植入该起搏器。该研究旨在不断积累证据,并计划在不同时间点进行数据分析。植入后6个月的主要安全性和有效性目标是证明:(i)Micra患者中与Micra系统或植入手术无关的主要并发症发生率显著高于83%;(ii)Micra患者中阈值低且稳定的比例显著高于80%。安全性性能基准基于最近6项起搏器研究中977名受试者的参考数据集。
Micra经导管起搏研究将评估一种小型化、完全心内膜起搏器在有单腔心室起搏器植入指征患者中的安全性和有效性。
NCT02004873。