Suppr超能文献

先天性完全性房室传导阻滞患儿的心室功能与长期起搏

Ventricular function and long-term pacing in children with congenital complete atrioventricular block.

作者信息

Kim Jeffrey J, Friedman Richard A, Eidem Benjamin W, Cannon Bryan C, Arora Gaurav, Smith E O'Brian, Fenrich Arnold L, Kertesz Naomi J

机构信息

Section of Pediatric Cardiology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas 77030, USA.

出版信息

J Cardiovasc Electrophysiol. 2007 Apr;18(4):373-7. doi: 10.1111/j.1540-8167.2006.00741.x.

Abstract

OBJECTIVE

To determine the sequela of right ventricular pacing in children with congenital complete atrioventricular block.

BACKGROUND

Pacing is a well-accepted therapy for patients with congenital complete atrioventricular block. The long-term sequela of right ventricular pacing in this population has not been well described.

METHODS

We performed a cohort study on all patients with congenital complete atrioventricular block who underwent pacemaker implantation at our institution from 1972 to 2004. Patients with associated congenital heart disease or ventricular dysfunction prior to pacemaker implantation were excluded.

RESULTS

A total of 63 patients were included in the study. The median age at pacemaker implantation was 6.5 years, with an average follow-up of 9.9 years. The cumulative dysfunction free survival at 20 years was 92%. In total, four patients (6%) were noted to develop LV dysfunction an average of 15.1 years after pacemaker implantation. Of 30 patients who were paced for >10 years, only three (10%) developed echocardiographic evidence of LV dysfunction. Right ventricular apex pacing and prolonged QRS duration were found to be predictive of decreased long-term LV systolic function (P < 0.05).

CONCLUSIONS

Left ventricular dysfunction in patients with congenital complete atrioventricular block is a rare finding, even in those who have been paced for more than 10 years. Right ventricular apex pacing and prolonged QRS duration may be associated with decreased ventricular function over time. At this time, with such a low incidence of cardiac dysfunction, right ventricular pacing should be considered an acceptable first-line therapy in this population.

摘要

目的

确定先天性完全性房室传导阻滞患儿右心室起搏的后遗症。

背景

起搏是先天性完全性房室传导阻滞患者广泛接受的治疗方法。该人群右心室起搏的长期后遗症尚未得到充分描述。

方法

我们对1972年至2004年在我院接受起搏器植入的所有先天性完全性房室传导阻滞患者进行了队列研究。排除起搏器植入前伴有先天性心脏病或心室功能障碍的患者。

结果

共63例患者纳入研究。起搏器植入时的中位年龄为6.5岁,平均随访9.9年。20年时累积无功能障碍生存率为92%。共有4例患者(6%)在起搏器植入后平均15.1年出现左心室功能障碍。在30例起搏时间超过10年的患者中,只有3例(10%)出现超声心动图证实的左心室功能障碍。右心室心尖起搏和QRS时限延长被发现可预测长期左心室收缩功能下降(P<0.05)。

结论

先天性完全性房室传导阻滞患者的左心室功能障碍是一种罕见的发现,即使是那些起搏超过10年的患者。随着时间的推移,右心室心尖起搏和QRS时限延长可能与心室功能下降有关。目前,由于心脏功能障碍的发生率如此之低,右心室起搏应被视为该人群可接受的一线治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验