Honarbakhsh Shohreh, Suman-Horduna Irina, Mantziari Lilian, Ernst Sabine
Royal Brompton and Harefield NHS Foundation Trust and Imperial College London, United Kingdom.
Indian Pacing Electrophysiol J. 2013 Jun 25;13(3):126-30. doi: 10.1016/s0972-6292(16)30631-3. Print 2013 May.
A 33-year old female with a background of Eisenmenger syndrome secondary to multiple congenital muscular ventricular septal defects (VSD) was admitted with a recent history of frequent intermittent palpitations. It was noted that she had an independent accelerated idioventricular rhythm (AIVR), with rates varying between 85-110bpm, which exhibited a repetitive grouped beating pattern. Although generally perceived as benign, in this case this rhythm was drug refractory, was associated with significant compromise to cardiac filling and output and progressed to haemodynamically intolerable sustained ventricular tachyarrhythmia. Successful ablation was performed at the inferior aspect of the residual VSD, from within the Purkinje network.
一名33岁女性,有继发于多发性先天性肌部室间隔缺损(VSD)的艾森曼格综合征病史,因近期频繁发作间歇性心悸入院。注意到她有独立的加速性室性自主心律(AIVR),心率在85-110次/分之间变化,呈现重复的成组搏动模式。虽然一般认为这种心律是良性的,但在该病例中,这种心律对药物难治,与心脏充盈和输出的显著受损相关,并进展为血流动力学难以耐受的持续性室性快速心律失常。在残余室间隔缺损的下方,从浦肯野网络内成功进行了消融。