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首次植入时评估的心动过缓起搏器受者的预后:一项全国性队列研究。

Prognosis of the bradycardia pacemaker recipient assessed at first implantation: a nationwide cohort study.

机构信息

Department of Cardiology, UMC Utrecht, , Utrecht, The Netherlands.

出版信息

Heart. 2013 Nov;99(21):1573-8. doi: 10.1136/heartjnl-2013-304445. Epub 2013 Aug 22.

Abstract

OBJECTIVE

Pacing technology and care have improved notably over the past decade, justifying an update on the long-term prognosis and pre-implantation determinants of prognosis of bradycardia pacemaker (PM) recipients.

DESIGN

Prospective cohort study.

SETTING

23 Dutch pacemaker centres

PATIENTS

Pre-implantation characteristics of 1517 patients receiving a first bradycardia PM between 2003-2007 were studied in relation to survival.

INTERVENTIONS

None; patients were followed up during routine clinical practice.

MAIN OUTCOME MEASURES

Cause and time to death.

RESULTS

At the end of a mean follow-up of 5.8 (SD 1.1) years, 512 patients (33%) died, mostly of non-cardiac cause (67%). There were two PM related deaths. Survival rates were 93%, 81%, 69%, and 61% after 1, 3, 5 and 7 years, respectively. PM recipients without concomitant cardiovascular disease at implantation showed survival rates comparable to age and sex matched controls. Predictors at time of implantation associated with cardiac mortality were: age, coronary artery disease (CAD), diabetes, heart failure, valve disease, and the indication for PM implantation. Predictors for all cause mortality were: male gender, age, body mass index, CAD, cardiac surgery, diabetes, heart failure, and maintained atrioventricular synchrony.

CONCLUSIONS

A pre-implantation history of heart failure, CAD, and diabetes are the most important predictors for worse prognosis in PM recipients. Without baseline heart disease, survival rates equal that of the general population, suggesting that the prognosis of contemporary PM recipients is mainly determined by comorbid diseases and a bradycardia pacing indication as such does not influence survival.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT00135174.

摘要

目的

在过去的十年中,起搏技术和护理得到了显著改善,这使得有必要更新关于缓慢性心律失常起搏器(PM)受者的长期预后和植入前预后决定因素的信息。

设计

前瞻性队列研究。

地点

23 家荷兰起搏器中心。

患者

研究了 2003-2007 年间植入第一枚缓慢性 PM 的 1517 例患者的植入前特征与生存的关系。

干预措施

无;患者在常规临床实践中接受随访。

主要观察指标

死因和死亡时间。

结果

平均随访 5.8(SD 1.1)年后,512 例(33%)患者死亡,主要死于非心脏原因(67%)。有 2 例与 PM 相关的死亡。分别在 1、3、5 和 7 年后,生存率为 93%、81%、69%和 61%。植入时无合并心血管疾病的 PM 受者的生存率与年龄和性别匹配的对照组相当。植入时与心脏死亡率相关的预测因素包括:年龄、冠状动脉疾病(CAD)、糖尿病、心力衰竭、瓣膜疾病和 PM 植入的适应证。全因死亡率的预测因素包括:性别、年龄、体重指数、CAD、心脏手术、糖尿病、心力衰竭和保持房室同步。

结论

植入前心力衰竭、CAD 和糖尿病病史是 PM 受者预后不良的最重要预测因素。在没有基线心脏病的情况下,生存率与普通人群相当,这表明当代 PM 受者的预后主要由合并症和缓慢性起搏适应证决定,而适应证本身并不影响生存率。

临床试验注册

ClinicalTrials.gov 标识符:NCT00135174。

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