Key result
A 14-year-old boy with catecholaminergic polymorphic ventricular tachycardia who suffered cardiopulmonary arrest recovered fully after treatment with beta-blockers and an implantable cardioverter-defibrillator.
Case Report (n=1)
This case highlights CPVT as a rare but critical cause of sudden cardiac arrest in youth triggered by emotional stress, manageable with beta-blockers and ICD.
Supports beta-blockers and ICD after pediatric CPVT arrest; hypothesis-generating and leaves optimal management open.
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare adrenergically mediated arrhythmogenic disorder classically induced by exercise or emotional stress and found in structurally normal hearts. It is an important cause of cardiac syncope and sudden death in childhood. Catecholaminergic polymorphic ventricular tachycardia is a genetic cardiac channelopathy with known mutations involving genes affecting intracellular calcium regulation. We present a case of a 14-year-old boy who had cardiopulmonary arrest after an emotionally induced episode of CPVT while attempting to invite a girl to the school dance. Review of his presenting cardiac rhythm, induction of concerning ventricular arrhythmias during an exercise stress test, and genetic testing confirmed the diagnosis of CPVT. He recovered fully and was treated with β-blocker therapy and placement of an implantable cardioverter-defibrillator. In this report, we discuss this rare but important entity, including its molecular foundation, clinical presentation, basics of diagnosis, therapeutic options, and implications of genetic testing for family members. We also compare CPVT to other notable cardiomyopathic and channelopathic causes of sudden death in youth including hypertrophic cardiomyopathy, arrhythmogenic right ventricular dysplasia, long QT syndrome, short QT syndrome, and Brugada syndrome.
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Heiner et al. (2011) conducted a case report in Catecholaminergic polymorphic ventricular tachycardia (CPVT) (n=1). Beta-blocker therapy and implantable cardioverter-defibrillator was evaluated. A 14-year-old boy with catecholaminergic polymorphic ventricular tachycardia who suffered cardiopulmonary arrest recovered fully after treatment with beta-blockers and an implantable cardioverter-defibrillator.
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