Complete atrioventricular block complicated by QT prolongation triggering repeated torsades de pointes polymorphic ventricular tachycardia

Deepak Natarajan
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Abstract

This case report describes a 30 years old female who presented to the Emergency with multiple blackouts the previous 3 days. In the Emergency a Torsades de pointes (TdP) polymorphic ventricular tachycardia was observed on the cardiac monitor that spontaneously resolved into complete atrioventricular block accompanied by significantly prolonged QT and corrected QT (QTc)intervals. The patient underwent immediate temporary pacing, followed by permanent dual chamber implantation the next day. There were no further episodes of TdP subsequent to pacemaker implantation; the patient was discharged on a beta-blocker. Complete atrioventricular block when accompanied by increased QTc interval can result in lethal ventricular tachyarrhythmia manifesting as pre syncope, syncope, cardiac arrest, or death. Such patients, albeit uncommon, may be managed by permanent pacing and beta blocker therapy.

完全性房室传导阻滞合并QT间期延长,引发反复点扭转和多形性室性心动过速
本病例报告描述了一名30岁女性,她在前3天多次昏厥。在急诊a点扭转(TdP)时,在心脏监护仪上观察到多形性室性心动过速,自发分解为完全房室传导阻滞,并伴有QT间期明显延长和QT间期纠正。患者接受了即时临时起搏,第二天进行了永久性双腔植入。起搏器植入后无TdP进一步发作;病人在服用受体阻滞剂后出院。完全性房室传导阻滞伴QTc间期增加可导致致死性室性心动过速,表现为晕厥前期、晕厥、心脏骤停或死亡。这类患者虽然不常见,但可以通过永久性起搏和受体阻滞剂治疗来管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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