Hentati Mourad, Krichene Selma, Kechida Zohra, Chahbani Iheb, Hached Leila, Grati Zineb, Charfeddine Hanene, Kammoun Samir
CHU Hédi Chaker, Sfax, Tunisie.
Tunis Med. 2004 Jun;82(6):542-5.
A case report of 38 year old man who experienced syncope and torsade de pointes is presented with the short coupled variant. The patient had a normal QT interval (QTC: 0.37 seconds) and multiform ventricular premature beats on the resting electrocardiogram. Under antiarrhythmic treatment (intravenous xylocaine), torsades de pointes suddenly appeared and cardiac arrest was followed. After cardioversion, sinus rhythm was restored. A cardiovascular disease was excluded, the echocardiography, the left and right ventricular angiography and coronarography were normal. Three months after, the patient presented at home a sudden cardiac death.
本文报告了一名38岁男性发生晕厥和尖端扭转型室速的病例,为短联律间期变异型。患者静息心电图QT间期正常(校正QT间期:0.37秒),有多形性室性早搏。在抗心律失常治疗(静脉注射利多卡因)过程中,突然出现尖端扭转型室速并继以心脏骤停。经心脏复律后,恢复窦性心律。排除了心血管疾病,超声心动图、左右心室血管造影及冠状动脉造影均正常。三个月后,患者在家中发生心源性猝死。