医学
并发症
危险系数
置信区间
外科
心内注射
指南
人工心脏起搏器
铅(地质)
植入
心脏病学
内科学
地貌学
地质学
病理
作者
Gábor Zoltán Duray,Philippe Ritter,Mikhael F. El‐Chami,Calambur Narasimhan,Razali Omar,José Marı́a Tolosana,Shu Zhang,Kyoko Soejima,Clemens Steinwender,Leonardo Rapallini,Aida Cicic,Dedra H. Fagan,Shufeng Liu,DWIGHT W. REYNOLDS
出处
期刊:Heart Rhythm
[Elsevier BV]
日期:2017-02-10
卷期号:14 (5): 702-709
被引量:306
标识
DOI:10.1016/j.hrthm.2017.01.035
摘要
BACKGROUND: Early performance of the Micra transcatheter pacemaker from the global clinical trial reported a 99.2% implant success rate, low and stable pacing capture thresholds, and a low (4.0%) rate of major complications up to 6 months. OBJECTIVE: The purpose of this report was to describe the prespecified long-term safety objective of Micra at 12 months and electrical performance through 24 months. METHODS: The Micra Transcatheter Pacing Study was a prospective single-arm study designed to assess the safety and efficacy of the Micra VVIR leadless/intracardiac pacemaker. Enrolled patients met class I or II guideline recommendations for de novo ventricular pacing. The long-term safety objective was freedom from a system- or procedure-related major complication at 12 months. A predefined historical control group of 2667 patients with transvenous pacemakers was used to compare major complication rates. RESULTS: The long-term safety objective was achieved with a freedom from major complication rate of 96.0% at 12 months (95% confidence interval 94.2%-97.2%; P < .0001 vs performance goal). The risk of major complications for patients with Micra (N = 726) was 48% lower than that for patients with transvenous systems through 12 months postimplant (hazard ratio 0.52; 95% confidence interval 0.35-0.77; P = .001). Across subgroups of age, sex, and comorbidities, Micra reduced the risk of major complications compared to transvenous systems. Electrical performance was excellent through 24 months, with a projected battery longevity of 12.1 years. CONCLUSION: Long-term performance of the Micra transcatheter pacemaker remains consistent with previously reported data. Few patients experienced major complications through 12 months of follow-up, and all patient subgroups benefited as compared to transvenous pacemaker historical control group.
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