Atrioventricular node ablation and the pathological findings of a refractory ectopic atrial tachycardia in a small infant with hypoplastic left heart syndrome: a case report.

Pub Date : 2024-09-10 eCollection Date: 2024-09-01 DOI:10.1093/ehjcr/ytae493
Masayoshi Mori, Chihiro Ichikawa, Taka-Aki Matsuyama, Risa Nawa-Hasegawa, Hisaaki Aoki
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Abstract

Background: An atrioventricular node (AVN) ablation and permanent pacing have been previously reported as effective treatments for patients with atrial tachyarrhythmias. However single-ventricle patients requiring chronic ventricular pacing are at a higher risk of developing ventricular dysfunction and atrioventricular valve regurgitation. We report a case of successful AVN ablation in a 3-month-old infant with hypoplastic left heart syndrome and ectopic atrial tachycardia (EAT).

Case summary: A boy with hypoplastic left heart syndrome who had a refractory EAT resistant to various medications. At 2 months old, we performed an urgent radiofrequency (RF) catheter ablation of the EAT and the applications delivered at the cavo-atrial junction. Although it disappeared after the first catheter ablation for 2 weeks, it recurred on the next day after the diaphragm plication. At 3 months old and weighed 3.1 kg, we decided to perform an urgent AVN ablation of the EAT. The application was performed on the mid-septum of the tricuspid septum. A permanent pacemaker was implanted after the ablation. After the AVN ablation, the haemodynamics stabilized during the EAT. However, he died from a bacteraemia infection at 4 months.

Discussion: This patient received an AVN ablation due to failure to previous RF catheter ablation and was haemodynamically stable with the dual-chamber pacemaker. The AV block was successfully created by RF energy on the mid-septum of the tricuspid annulus in this hypoplastic left heart syndrome patient. Pathological findings exhibited that the compact AVN was totally ablated without damage to the tricuspid leaflets or coronary artery.

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左心发育不全综合征小婴儿难治性异位房性心动过速的房室结消融和病理发现:病例报告。
背景:据报道,房室结(AVN)消融和永久起搏是治疗房性快速性心律失常患者的有效方法。然而,需要长期心室起搏的单心室患者发生心室功能障碍和房室瓣反流的风险较高。我们报告了一例在 3 个月大的患有左心发育不全综合征和异位房性心动过速(EAT)的婴儿中成功进行房室瓣消融的病例。病例摘要:一名患有左心发育不全综合征的男孩,其异位房性心动过速对各种药物均有耐药性。2 个月大时,我们对 EAT 进行了紧急射频导管消融术,并在腔房交界处进行了应用。虽然第一次导管消融术后症状消失了两周,但在膈肌成形术后的第二天又复发了。孩子出生 3 个月、体重 3.1 千克时,我们决定对 EAT 进行紧急 AVN 消融。手术在三尖瓣中隔进行。消融术后植入了永久起搏器。房室结消融术后,EAT 期间的血流动力学趋于稳定。然而,他在 4 个月后死于菌血症感染:讨论:该患者因之前的射频导管消融术失败而接受了房室结消融术,使用双腔起搏器后血流动力学稳定。射频能量成功地在这位左心发育不全综合征患者的三尖瓣环中隔形成了房室传导阻滞。病理结果显示,紧凑型房室结被完全消融,三尖瓣叶或冠状动脉未受损伤。
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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