Brem Ofir, Buturlin Kirill, Kolker Shimon, Schamroth Pravda Nili
Faculty of Medicine, Tel Aviv University, PO Box 39040, Klatzkin 35, Tel Aviv 6997801, Israel.
Department of Cardiology, Rabin Medical Center, Zeev Jabotinsky 39, Petah Tikva 4941492, Israel.
Eur Heart J Case Rep. 2024 Sep 23;8(10):ytae520. doi: 10.1093/ehjcr/ytae520. eCollection 2024 Oct.
This case report details the application of left bundle branch pacing in a patient with congenitally corrected transposition of the great arteries (cc-TGA), a rare congenital heart defect characterized by anatomical complexities that pose unique challenges in the management of device-related complications and heart failure. The patient's history is notable for complex anatomical considerations, cardiovascular implantable electronic device (CIED) infection, and heart failure.
The patient underwent a series of interventions, including treatment for pocket-site infections, abandonment of epicardial leads, and an unsuccessful attempt at trans-catheter leadless pacemaker implantation. Given the patient's complex anatomy and prior CIED infection, traditional pacing methods were deemed unsuitable, leading to the selection of left bundle branch pacing. The lead implantation was guided using 3D electro-anatomical mapping to ensure synchronous physiologic pacing in a patient with heart failure.
The case underscores the heightened risks faced by cc-TGA patients, with a focus on systemic right ventricular dysfunction and pacing-induced ventricular dysfunction. In these patients, ventricular synchrony is critical and can be achieved with biventricular pacing. Physiologic pacing emerges as a promising alternative to cardiac resynchronization therapy (CRT), especially in cases where endovascular CRT is unfeasible. This case demonstrates the utilization of 3D electro-anatomical mapping for achieving successful physiologic pacing in complex congenital heart lesions. At the 12-month follow-up, the patient presented with stable clinical status and a narrow QRS complex. Echocardiography indicated improvement in the right systemic ventricular function.
本病例报告详细介绍了左束支起搏在一名先天性矫正型大动脉转位(cc-TGA)患者中的应用,cc-TGA是一种罕见的先天性心脏缺陷,其解剖结构复杂,在处理与器械相关的并发症和心力衰竭方面带来了独特的挑战。该患者的病史因复杂的解剖学因素、心血管植入式电子设备(CIED)感染和心力衰竭而值得关注。
患者接受了一系列干预措施,包括治疗囊袋部位感染、放弃心外膜导线,以及经导管无导线起搏器植入尝试失败。鉴于患者复杂的解剖结构和既往CIED感染,传统起搏方法被认为不合适,因此选择了左束支起搏。使用三维电解剖标测引导导线植入,以确保在心力衰竭患者中实现同步生理性起搏。
该病例强调了cc-TGA患者面临的更高风险,重点是系统性右心室功能障碍和起搏诱导的心室功能障碍。在这些患者中,心室同步性至关重要,可通过双心室起搏实现。生理性起搏成为心脏再同步治疗(CRT)的一种有前景的替代方法,特别是在血管内CRT不可行的情况下。本病例展示了利用三维电解剖标测在复杂先天性心脏病变中实现成功的生理性起搏。在12个月的随访中,患者临床状态稳定,QRS波群变窄。超声心动图显示右系统性心室功能有所改善。