Liu Fuqiang, Li Yifei, Yan Song, Liu Lijun, Zhou Kaiyu, Hua Yimin
Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE, Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Department of Nursing, West China Second University Hospital, Sichuan University, Chengdu, China.
Front Cardiovasc Med. 2025 Jan 8;11:1424187. doi: 10.3389/fcvm.2024.1424187. eCollection 2024.
Focal atrial tachycardia (FAT) is predominant in the pediatric population. Recent research has identified cases of sustained FAT originating from the interatrial septum (IAS); a subset of cases presents a unique challenge, with foci originating from the peri-patent foramen ovale (peri-PFO), requiring specialized management during catheter ablation. Here, we present a rare case of peri-PFO-associated FAT that resulted in tachycardia-related cardiomyopathy and propose a comprehensive multipath joint strategy for the successful treatment of PFO-associated FAT.
A 10-year-old boy presented with refractory cardiomyopathy associated with incessant atrial tachycardia, unresponsive to metoprolol. A 12-lead electrocardiogram revealed a narrow QRS complex tachycardia with a rate of 157 beats per minute and a prolonged RP relationship. Echocardiography indicated a severely reduced ejection fraction of 22%. Subsequent electrophysiological study findings identified the tachycardia as originating from the anterior limbus of the PFO. Radiofrequency ablation was performed at the earliest activation site and surrounding structures, encompassing the right atrial septum, non-coronary sinus of Valsalva, and the left atrium peri-PFO. Post-procedure, the patient remained free from arrhythmia and showed restored normal cardiac function and was prescribed a low-dose β-blocker for 1 month. Remarkably, the patient continued to be well without the need for any medications for the subsequent 3 months.
The structure of the PFO brought significant challenges in performing successful ablation. The multipath strategy was beneficial in managing peri-PFO-associated FAT based on its anatomical vicinity of the target.
局灶性房性心动过速(FAT)在儿科人群中占主导地位。最近的研究发现了起源于房间隔(IAS)的持续性FAT病例;其中一部分病例带来了独特的挑战,即病灶起源于卵圆孔未闭(PFO)周围,在导管消融过程中需要特殊处理。在此,我们报告一例罕见的与PFO相关的FAT病例,该病例导致了心动过速相关性心肌病,并提出了一种全面的多路径联合策略以成功治疗与PFO相关的FAT。
一名10岁男孩因持续性房性心动过速伴难治性心肌病就诊,对美托洛尔无反应。12导联心电图显示窄QRS波群心动过速,心率为每分钟157次,RP间期延长。超声心动图显示射血分数严重降低至22%。随后的电生理研究结果确定心动过速起源于PFO的前边缘。在最早激活部位及周围结构进行了射频消融,包括右心房隔、无冠窦和左心房PFO周围。术后,患者未再发生心律失常,心脏功能恢复正常,并给予低剂量β受体阻滞剂治疗1个月。值得注意的是,在随后的3个月里,患者持续状况良好,无需任何药物治疗。
PFO的结构给成功消融带来了重大挑战。基于其与靶点的解剖位置关系,多路径策略在处理与PFO相关的FAT方面是有益的。