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使用新一代单导联VDD起搏器在房室传导阻滞中维持生理性起搏。

Maintaining physiological pacing in AV block using a new generation single lead VDD pacemaker.

作者信息

Lau C, Nishimura S C, Harrison A W, Goldman B S

机构信息

Division of Cardiology, Sunnybrook Health Science Centre, University of Toronto, Ontario.

出版信息

Can J Cardiol. 1996 Jun;12(6):579-83.

PMID:8665420
Abstract

OBJECTIVE

A prospective evaluation of patients with AV block using a single pass lead, VDD pacing system.

DESIGN

Fifteen patients with AV block, eight males, seven females, average age 68.1 years (range 22.3 to 86.5) were implanted with the THERA VDD 8948 pacemaker and 5032 single pass steroid eluting lead (Medtronic, Inc). P wave sensing and ventricular thresholds were done predischarge and at one, three, and six months and subsequent six-month periods postimplant. P wave sensing was evaluated with exercise testing and other provocative tests. Twenty-four hour Holter monitoring was done before discharge. Patients were given a quality of life questionnaire pre- and postimplant.

SETTING

Tertiary care hospital.

RESULTS

Average follow-up was 6.4 months (1.5 to 18). Ventricular thresholds remained stable. P wave amplitude at implant (average 2.2 mV; 1.6 to 3.6) showed a significant decrease at the initial visit (average 1.1 mV, 0.5 to 2.4), however, it remained stable at subsequent visits. This initial decrease had no clinical significance as the maximum atrial sensitivity of the device is 0.18 mV. The 24 hr Holter monitoring confirmed reliable AV synchronous pacing in 14 of 15 patient pacemakers programmed in the VDD mode. The sleep function maintained AV synchrony during nocturnal bradycardia; atrial rate histograms available at follow-up imply appropriate intrinsic rate variation and provocative sensing tests and exercise protocol demonstrated reliable atrial sensing. There was a significant improvement in overall patient well-being score using a quality of life questionnaire.

CONCLUSIONS

During the follow-up period, this new generation VDD pacemaker, using a single pass lead, provided reliable AV synchronous pacing for patients diagnosed with AV block and normal sinus node function, as well as improved patient well-being.

摘要

目的

使用单极导线VDD起搏系统对房室传导阻滞患者进行前瞻性评估。

设计

15例房室传导阻滞患者,8例男性,7例女性,平均年龄68.1岁(范围22.3至86.5岁),植入了THERA VDD 8948起搏器和5032单极类固醇洗脱导线(美敦力公司)。在出院前、植入后1个月、3个月、6个月以及随后的6个月期间测定P波感知和心室阈值。通过运动试验和其他激发试验评估P波感知。出院前进行24小时动态心电图监测。在植入前后给患者发放生活质量问卷。

地点

三级护理医院。

结果

平均随访6.4个月(1.5至18个月)。心室阈值保持稳定。植入时P波振幅(平均2.2mV;1.6至3.6)在初次随访时显著降低(平均1.1mV,0.5至2.4),但在随后的随访中保持稳定。由于该装置的最大心房感知灵敏度为0.18mV,所以这种最初的降低无临床意义。24小时动态心电图监测证实,15例采用VDD模式程控的患者起搏器中有14例实现了可靠的房室同步起搏。睡眠功能在夜间心动过缓期间维持房室同步;随访时可获得的心房率直方图显示固有心率变化适当,激发感知试验和运动方案证明心房感知可靠。使用生活质量问卷评估,患者总体幸福感得分有显著改善。

结论

在随访期间,这种新一代的使用单极导线的VDD起搏器为诊断为房室传导阻滞且窦房结功能正常的患者提供了可靠的房室同步起搏,并改善了患者的幸福感。

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