Ngan Ho Ting Abe, Fabbricatore Davide, Regan William, Rosenthal Eric, Wong Tom
Department of Cardiac Electrophyioslogy, Royal Brompton and Harefield Hospitals, Guys and St Thomas' NHS Foundation Trust, Sydney Street, London SW3 6NP, UK.
Department of Cardiac Electrophysiology, Evelina London Children's Hospital, Guys and St Thomas' NHS Foundation Trust, Westminster Bridge Rd, London SE1 7EH, UK.
Eur Heart J Case Rep. 2024 Sep 17;8(10):ytae506. doi: 10.1093/ehjcr/ytae506. eCollection 2024 Oct.
Atrioventricular block is common with adult congenital heart disease and pacemaker implantation is challenging. Atrioventricular synchronous pacing is important for better haemodynamics. This case reports the implantation of a dual-chamber leadless pacemaker in a patient with univentricular heart physiology and contributes to the literature regarding the management option in complex adult congenital heart disease patients with conduction abnormalities.
A 25-year-old male with double inlet left ventricular, transposition of great arteries, hypoplastic aortic arch receive multiple surgeries including the Glenn shunt at the age of 1. He presented with 2:1 and 3:1 heart block at the age of 13 with a transvenous dual-chamber pacemaker implanted by pacing the superior vena cava stump and puncturing the Glenn shunt for the ventricular lead. A decade later, lead malfunctioned and the patient progressed to complete heart block. A subcutaneous implantable cardioverter defibrillator was implanted when he was 23 for monomorphic ventricular tachycardia. Given the anticipated challenges with transvenous lead extraction and epicardial pacemaker implantation, we implanted the novel dual-chamber leadless pacemakers which resulted in satisfactory atrioventricular synchronous pacing performance immediately post-op and 2 weeks after the procedure.
We present a case of a novel dual-chamber leadless pacemaker implantation to maintain atrioventricular synchrony in the patient with complete heart block and univentricular physiology. This case illustrates an additional pacing option in complex adult congenital heart to maintain atrioventricular synchrony.
房室传导阻滞在成人先天性心脏病中很常见,起搏器植入具有挑战性。房室同步起搏对于改善血流动力学很重要。本病例报告了在一名单心室心脏生理患者中植入双腔无导线起搏器的情况,并为有关复杂成人先天性心脏病合并传导异常患者管理选择的文献做出了贡献。
一名25岁男性,患有左心室双入口、大动脉转位、主动脉弓发育不全,1岁时接受了包括格林分流术在内的多次手术。他13岁时出现2:1和3:1房室传导阻滞,通过对上腔静脉残端进行起搏并穿刺格林分流术以植入心室导线,植入了经静脉双腔起搏器。十年后,导线出现故障,患者进展为完全性房室传导阻滞。23岁时因单形性室性心动过速植入了皮下植入式心律转复除颤器。鉴于经静脉导线拔除和心外膜起搏器植入预期的挑战,我们植入了新型双腔无导线起搏器,术后即刻及术后2周均获得了令人满意的房室同步起搏性能。
我们报告了一例在完全性房室传导阻滞和单心室生理患者中植入新型双腔无导线起搏器以维持房室同步的病例。该病例说明了在复杂成人先天性心脏病中维持房室同步的另一种起搏选择。