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完全皮下植入式心脏除颤器的安全性和有效性。

Safety and efficacy of a totally subcutaneous implantable-cardioverter defibrillator.

机构信息

Ohio State University, Columbus, OH, USA.

出版信息

Circulation. 2013 Aug 27;128(9):944-53. doi: 10.1161/CIRCULATIONAHA.113.003042.

Abstract

BACKGROUND

The most frequent complications associated with implantable cardioverter-defibrillators (ICDs) involve the transvenous leads. A subcutaneous implantable cardioverter-defibrillator (S-ICD) has been developed as an alternative system. This study evaluated the safety and effectiveness of the S-ICD System (Cameron Health/Boston Scientific) for the treatment of life-threatening ventricular arrhythmias (ventricular tachycardia/ventricular fibrillation).

METHODS AND RESULTS

This prospective, nonrandomized, multicenter trial included adult patients with a standard indication for an ICD, who neither required pacing nor had documented pace-terminable ventricular tachycardia. The primary safety end point was the 180-day S-ICD System complication-free rate compared with a prespecified performance goal of 79%. The primary effectiveness end point was the induced ventricular fibrillation conversion rate compared with a prespecified performance goal of 88%, with success defined as 2 consecutive ventricular fibrillation conversions of 4 attempts. Detection and conversion of spontaneous episodes were also evaluated. Device implantation was attempted in 321 of 330 enrolled patients, and 314 patients underwent successful implantation. The cohort was followed for a mean duration of 11 months. The study population was 74% male with a mean age of 52±16 years and mean left ventricular ejection fraction of 36±16%. A previous transvenous ICD had been implanted in 13%. Both primary end points were met: The 180-day system complication-free rate was 99%, and sensitivity analysis of the acute ventricular fibrillation conversion rate was >90% in the entire cohort. There were 38 discrete spontaneous episodes of ventricular tachycardia/ventricular fibrillation recorded in 21 patients (6.7%), all of which successfully converted. Forty-one patients (13.1%) received an inappropriate shock.

CONCLUSIONS

The findings support the efficacy and safety of the S-ICD System for the treatment of life-threatening ventricular arrhythmias.

摘要

背景

与植入式心脏复律除颤器(ICD)相关的最常见并发症涉及经静脉导线。已开发出一种皮下植入式心脏复律除颤器(S-ICD)作为替代系统。这项研究评估了 S-ICD 系统(Cameron Health/Boston Scientific)治疗危及生命的室性心律失常(室性心动过速/心室颤动)的安全性和有效性。

方法和结果

这项前瞻性、非随机、多中心试验纳入了具有 ICD 标准适应证的成年患者,这些患者既不需要起搏,也没有记录到可由起搏终止的室性心动过速。主要安全性终点是与预先指定的 79%性能目标相比,180 天 S-ICD 系统无并发症发生率。主要有效性终点是诱发性心室颤动转复率与预先指定的 88%性能目标相比,成功定义为 4 次尝试中连续 2 次心室颤动转复。还评估了自发发作的检测和转复。在 330 名入组患者中尝试了 321 名患者的设备植入,314 名患者成功植入。该队列的平均随访时间为 11 个月。研究人群中 74%为男性,平均年龄为 52±16 岁,平均左心室射血分数为 36±16%。13%的患者之前植入过经静脉 ICD。两个主要终点都达到了:180 天系统无并发症发生率为 99%,整个队列的急性心室颤动转复率的敏感性分析>90%。在 21 名患者(6.7%)中记录到 38 次离散的室性心动过速/心室颤动自发发作,均成功转复。41 名患者(13.1%)接受了不适当的电击。

结论

研究结果支持 S-ICD 系统治疗危及生命的室性心律失常的疗效和安全性。

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