Permanent Cardiac Pacing in Children: A 30-Year Follow-Up Retrospective Study in a Single Pediatric Asian Center

IF 1.9 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Jiahui Charmaine Chan, Dyan Zhewei Zhang, Koh Zhi Xuan, Sreekanthan Sundararaghavan, Jonathan Tze Liang Choo, Kah Leng Ho, Eric Tien Siang Lim, Ju Le Tan, Nurhafizah Binte Abdul Aziz, Wan Ting Chan, Monika Kotecha, Jan Hau Lee, Teng Hong Tan
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Abstract

Background

Permanent cardiac pacing in children is commonly indicated in high-grade atrioventricular block. These patients require long-term ventricular pacing (Vp), multiple device changes, and lead revisions.

Objectives

To describe a single pediatric center's 30-year experience with permanent pacemaker implantation, focusing on long-term device-associated complications (DACs) and pacing-induced cardiomyopathy (PIC).

Methods

We conducted a retrospective observational study at KK Women's and Children's Hospital, Singapore. Patients with permanent pacemakers followed between January 1, 1994 and December 31, 2024 were included. Primary outcomes were DAC and PIC.

Results

Fifty-three patients underwent 113 pacemaker lead implantations; 51 (96.2%) had epicardial systems. Median follow-up was 12 years (interquartile range [IQR] 9–19 years). Median age at first pacemaker implantation was 16 months (IQR 2 months to 7.7 years). Congenital complete heart block was the most common indication (26 [49%]), followed by postoperative complete heart block (17 [32%]). Freedom from lead-associated complications was 85% and 83% at 5 and 10 years, respectively. Eight (15%) patients developed PIC. All patients with PIC had concomitant congenital heart disease (CHD) (8/8). CHD was present in 28.9% (13/45) of patients without PIC. Recovery of ventricular function occurred in two patients following pacing modification, but not in those managed with medical therapy alone.

Conclusion

In this pediatric cohort with predominantly epicardial pacing systems, long-term DAC rates were acceptable. PIC occurred primarily in patients with CHD. These findings support careful pacing strategy selection and long-term surveillance in children requiring permanent pacing.

儿童永久性心脏起搏:一个亚洲儿科中心的30年随访回顾性研究
背景:儿童永久性心脏起搏通常指的是高级别房室传导阻滞。这些患者需要长期心室起搏(Vp)、多次更换装置和导联修复。目的介绍某儿科中心30年来在永久性起搏器植入方面的经验,重点介绍长期装置相关并发症(DACs)和起搏器诱发心肌病(PIC)。方法我们在新加坡KK妇女儿童医院进行回顾性观察研究。1994年1月1日至2024年12月31日期间使用永久性起搏器的患者纳入研究。主要结局为DAC和PIC。结果53例患者接受了113次起搏器导联植入;51例(96.2%)有心外膜系统。中位随访时间为12年(四分位数间距[IQR] 9-19年)。首次植入起搏器的中位年龄为16个月(IQR为2个月至7.7岁)。先天性完全性心脏传导阻滞是最常见的适应症(26例[49%]),其次是术后完全性心脏传导阻滞(17例[32%])。5年和10年的铅相关并发症发生率分别为85%和83%。8例(15%)患者发生PIC。所有PIC患者均伴有先天性心脏病(CHD)(8/8)。没有PIC的患者中有28.9%(13/45)存在冠心病。2例患者在调整起搏后出现心室功能恢复,但在单独药物治疗的患者中没有。结论:在这个主要采用心外膜起搏系统的儿科队列中,长期DAC率是可以接受的。PIC主要发生在冠心病患者中。这些发现支持对需要永久起搏的儿童进行谨慎的起搏策略选择和长期监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Arrhythmia
Journal of Arrhythmia CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.90
自引率
10.00%
发文量
127
审稿时长
45 weeks
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