Mesa A, Kaplan R F
Department of Anesthesiology, University of South Florida College of Medicine, Tampa 33612-4479.
Reg Anesth. 1993 Jan-Feb;18(1):60-2.
A 9-year-old boy with a history of poorly controlled insulin-dependent diabetes mellitus was found at home unresponsive. QT prolongation was diagnosed on inspection of Holter monitoring performed immediately before episodes of ventricular fibrillation.
In spite of medical management with propranolol, esmolol, phenytoin, and diazepam, the patient continued to have episodes of QT prolongation followed by ventricular dysrhythmias that reverted to sinus rhythm only after cardiopulmonary resuscitation and cardioversion.
A series of left stellate ganglion blocks with bupivacaine eradicated the dysrhythmias. The child was then referred to another institution for insertion of an automatic internal cardioverter defibrillator.
This case report emphasizes the effectiveness of left stellate ganglion block with bupivacaine in a child with a variant of long QT syndrome.
一名9岁男孩,患有胰岛素依赖型糖尿病且病情控制不佳,在家中被发现无反应。在心室颤动发作前立即进行的动态心电图监测检查中诊断出QT间期延长。
尽管使用普萘洛尔、艾司洛尔、苯妥英钠和地西泮进行药物治疗,但患者仍持续出现QT间期延长,随后发生室性心律失常,仅在心肺复苏和电复律后才恢复为窦性心律。
一系列用布比卡因进行的左侧星状神经节阻滞消除了心律失常。该患儿随后被转诊至另一机构植入自动体内心脏复律除颤器。
本病例报告强调了用布比卡因进行左侧星状神经节阻滞对一名长QT综合征变异型患儿的有效性。