Department of Paediatric Cardiology, Hacettepe Universty Ihsan Dogramacı Children's Hospital, Ankara, Turkey.
Department of Paediatric Cardiology, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Centre and Research Hospital, Istanbul Saglik Bilimleri University, Istanbul, Turkey.
Cardiol Young. 2022 Mar;32(3):437-443. doi: 10.1017/S1047951121002353. Epub 2021 Jun 21.
Accessory pathways are commonly seen due to delamination of tricuspid valve leaflets. In addition to accessory pathways, an enlarged right atrium due to tricuspid regurgitation and incisional scars creates substrates for atrial re-entries and ectopic tachycardia. We sought to describe our experience with catheter ablation in children with Ebstein's anomaly.
During the study period, of 89 patients diagnosed with Ebstein's anomaly, 26 (30.9%) of them who underwent 33 ablation procedures were included in the study. Accessory pathways were observed in the majority of procedures (n = 27), whereas atrial flutter was observed in five, atrioventricular nodal reentrant tachycardia in five, and atrial tachycardia in two procedures. Accessory pathways were commonly localised in the right posteroseptal (n = 10 patients), right posterolateral (n = 14 patients), septal (n = two patients), and left posteroseptal (n = one patient) areas. Multiple accessory pathways and coexistent arrhythmia were observed in six procedures. All ablation attempts related to the accessory pathways were successful, but recurrence was observed in five (19%) of the ablations. Ablation for atrial flutter was performed in five patients; two of them were ablated successfully. One of the atrial tachycardia cases was ablated successfully.
Ablation in patients with Ebstein's anomaly is challenging, and due to nature of the disease, it is not a rare occasion in this group of patients. Ablation of accessory pathways has high success, but also relatively high recurrence rates, whereas ablation of atrial arrhythmias has lower success rates, especially in operated patients.
由于三尖瓣瓣叶分层,常可见到附加旁路。除了附加旁路之外,由于三尖瓣反流和切口疤痕导致的右心房增大为心房折返和异位性心动过速创造了基质。我们旨在描述我们在患有Ebstein 畸形的儿童中进行导管消融的经验。
在研究期间,在 89 例被诊断为 Ebstein 畸形的患者中,有 26 例(30.9%)接受了 33 次消融手术,这些患者被纳入了研究。在大多数手术中都观察到了附加旁路(n=27),而在 5 次手术中观察到了心房扑动,5 次手术中观察到房室结折返性心动过速,2 次手术中观察到了房性心动过速。附加旁路通常位于右后间隔(n=10 例)、右后外侧(n=14 例)、间隔(n=2 例)和左后间隔(n=1 例)区域。在 6 次手术中观察到了多个附加旁路和共存的心律失常。所有与附加旁路相关的消融尝试均成功,但在 5 次消融中(19%)观察到了复发。在 5 例患者中进行了心房扑动的消融;其中 2 例成功消融。1 例房性心动过速病例成功消融。
Ebstein 畸形患者的消融具有挑战性,而且由于疾病的性质,在这群患者中并不罕见。旁路消融的成功率很高,但复发率也相对较高,而心房性心律失常的消融成功率较低,尤其是在已接受手术的患者中。