Rogers Dominic P S, Walker Fiona, Chow Anthony W C, Lambiase Pier D
The Heart Hospital, University College London, London, UK.
Pacing Clin Electrophysiol. 2008 Apr;31(4):499-502. doi: 10.1111/j.1540-8159.2008.01021.x.
An increasing number of patients with congenital heart disease are surviving into adulthood and some have indications for device therapy. Complex anatomical abnormalities may hinder the operator and require the adaptation of standard implantation techniques. We present the first report of successful biventricular ICD implantation in a patient with mesocardia, congenitally corrected transposition of the great arteries, pulmonary atresia, and a left superior vena cava draining into the coronary sinus. This case posed challenges in lead placement due to both complex anatomy and the risk of inappropriate device therapies secondary to far-field oversensing.
越来越多的先天性心脏病患者存活至成年,其中一些有植入装置治疗的指征。复杂的解剖异常可能会给手术者带来阻碍,需要对标准植入技术进行调整。我们首次报告了在一名中位心、先天性矫正型大动脉转位、肺动脉闭锁且左上腔静脉引流至冠状窦的患者中成功进行双心室植入式心律转复除颤器(ICD)植入的病例。由于解剖结构复杂以及远场过度感知继发不适当装置治疗的风险,该病例在导线放置方面面临挑战。