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

医学 内科学 心脏病学 冠状动脉疾病 心力衰竭 体质指数 队列 心动过缓 队列研究 糖尿病 人口 心率 血压 环境卫生 内分泌学
作者
Erik O. Udo,Norbert M. van Hemel,Nicolaas P. A. Zuithoff,Pieter A. Doevendans,Karel G.M. Moons
出处
期刊:Heart [BMJ]
卷期号:99 (21): 1573-1578 被引量:33
标识
DOI:10.1136/heartjnl-2013-304445
摘要

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.

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