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植入式心房除颤器和房室联合除颤器的临床经验。

Clinical experience with implantable atrial and combined atrioventricular defibrillators.

作者信息

Jung W, Wolpert C, Esmailzadeh B, Spehl S, Herwig S, Schumacher B, Lewalter T, Omran H, Schimpf R, Vahlhaus C, Welz A, Lüderitz B

机构信息

Departments of Medicine-Cardiology, University of Bonn, Germany.

出版信息

J Interv Card Electrophysiol. 2000 Jan;4 Suppl 1:185-95. doi: 10.1023/a:1009819707643.

Abstract

UNLABELLED

The high prevalence of atrial fibrillation (AF) and its clinical complications, the poor efficacy of medical therapy for preventing recurrences, and dissatisfaction with alternative modes of therapy stimulated interest in implantable atrial and combined atrioventricular defibrillators. In a multicenter study, the safety and efficacy of a stand alone implantable atrial defibrillator, the Metrix system, were evaluated. The device was implanted in 51 patients with highly symptomatic episodes of AF refractory to pharmacological treatment. During a follow-up of 9 months, 96% of 227 spontaneous AF episodes were successfully converted to sinus rhythm in 41 patients. In 62 episodes (27%), several shocks and/or additional drug treatment were required to maintain stable sinus rhythm because of early recurrences of AF. A total of 3719 shocks were delivered and no induction of ventricular proarrhythmia or inaccurately synchronized shocks occurred. The AF detection algorithm exhibited a 100% specificity for the recognition of sinus rhythm and a 92.3% sensitivity for the detection of AF. The combined atrioventricular defibrillator, Jewel AF 7250, was evaluated in a multicenter, randomized, cross-over trial. The primary study objectives included: overall safety as determined by complications-free survival at 6 months, efficacy of tiered atrial pacing and defibrillation therapies for termination of spontaneous atrial tachycardias (AT) and AF, and relative sensitivity of a new dual-chamber detection algorithm. The device was implanted in 211 patients with either a history of ventricular tachyarrhythmias (VT/VF) alone or with a history of both AT/AF and VT/VF. During a mean follow-up of 4.5 months, it has been shown that the Jewel AF is safe and effective in treating atrial and ventricular tachyarrhythmias. Pace termination of 85% of AT episodes were achieved with painless delivery of antitachycardia pacing; additional 35% of AT episodes were terminated by high frequency burst pacing.

CONCLUSIONS

The stand alone implantable atrial defibrillator may be safe and clinically useful in selected patients for the treatment of highly symptomatic, drug resistant recurrences of AF. The combined atrioventricular defibrillator may be particularly indicated in patients presenting with both a history of atrial and ventricular tachyarrhythmias.

摘要

未标记

心房颤动(AF)的高患病率及其临床并发症、药物治疗预防复发的疗效不佳以及对替代治疗方式的不满激发了人们对植入式心房除颤器和房室联合除颤器的兴趣。在一项多中心研究中,对一种独立的植入式心房除颤器Metrix系统的安全性和有效性进行了评估。该装置被植入51例对药物治疗难治的高度症状性房颤发作患者体内。在9个月的随访期间,41例患者中227次自发性房颤发作的96%成功转为窦性心律。在62次发作(27%)中,由于房颤早期复发,需要多次电击和/或额外的药物治疗来维持稳定的窦性心律。共发放了3719次电击,未诱发室性心律失常或出现同步不准确的电击。房颤检测算法对窦性心律识别的特异性为100%,对房颤检测的敏感性为92.3%。房室联合除颤器Jewel AF 7250在一项多中心、随机、交叉试验中进行了评估。主要研究目标包括:通过6个月无并发症生存率确定的总体安全性、分级心房起搏和除颤治疗终止自发性房性心动过速(AT)和房颤的有效性以及一种新的双腔检测算法的相对敏感性。该装置被植入211例仅有心室快速心律失常(VT/VF)病史或同时有AT/AF和VT/VF病史的患者体内。在平均4.5个月的随访期间,已证明Jewel AF在治疗房性和室性快速心律失常方面是安全有效的。85%的AT发作通过无痛发放抗心动过速起搏实现起搏终止;另外35%的AT发作通过高频猝发起搏终止。

结论

独立的植入式心房除颤器在选定患者中治疗高度症状性、耐药性房颤复发可能是安全且具有临床实用性的。房室联合除颤器可能特别适用于既有房性又有心室快速心律失常病史的患者。

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