Trappe H J, Klein H, Schröder E, Siclari F, Förster K, Schlepper M, Lichtlen P R
Abteilung Kardiologie, Thorax-, Herz- und Gefässchirurgie der Medizinischen Hochschule Hannover.
Z Kardiol. 1988 Jun;77(6):389-92.
A 30-year-old woman with an idiopathic long QT-syndrome developed recurrent episodes of torsade de pointes ventricular tachycardia. Therapy with beta blocking agents and exhairesis of the left ganglion stellatum had failed to suppress these life-threatening tachyarrhythmias. After implantation of an AAI pacemaker system these ventricular arrhythmias disappeared. The patient remained without ventricular arrhythmias up to the time of discharge and during a 5 months' follow-up.
一名患有特发性长QT综合征的30岁女性反复发作尖端扭转型室性心动过速。使用β受体阻滞剂治疗以及切除左侧星状神经节均未能抑制这些危及生命的快速心律失常。植入AAI起搏器系统后，这些室性心律失常消失。直至出院时以及5个月的随访期间，患者均未再出现室性心律失常。
