Catecholaminergic polymorphic ventricular tachycardia

Catecholaminergic polymorphic ventricular tachycardia
Other names	CPVT
Bidirectional ventricular tachycardia in a patient with CPVT
Specialty	Cardiology
Symptoms	Blackouts, sudden cardiac death[1]
Usual onset	Childhood / adolescence
Causes	Genetic
Risk factors	Family history
Diagnostic method	Electrocardiogram (ECG), genetic testing, adrenaline provocation, exercise testing[1]
Differential diagnosis	Long QT syndrome, Brugada syndrome, Andersen-Tawil syndrome, Early repolarization syndrome
Treatment	Avoidance of strenuous exercise, medication, implantable cardioverter defibrillator[2]
Medication	Beta-adrenoceptor blockers, Verapamil, Flecainide[2]
Prognosis	13–20% life threatening arrhythmias over 7–8 years[3]
Frequency	1:10,000[4]

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited genetic disorder that predisposes those affected to potentially life-threatening abnormal heart rhythms or arrhythmias. The arrhythmias seen in CPVT typically occur during exercise or at times of emotional stress, and classically take the form of bidirectional ventricular tachycardia or ventricular fibrillation. Those affected may be asymptomatic, but they may also experience blackouts or even sudden cardiac death.

CPVT is caused by genetic mutations affecting proteins that regulate the concentrations of calcium within cardiac muscle cells. The most commonly identified gene is RYR2, which encodes a protein included in an ion channel known as the ryanodine receptor; this channel releases calcium from a cell's internal calcium store, the sarcoplasmic reticulum, during every heartbeat.

CPVT is often diagnosed from an ECG recorded during an exercise tolerance test, but it may also be diagnosed with a genetic test. The condition is treated with medication including beta-adrenoceptor blockers or flecainide, or with surgical procedures including sympathetic denervation and implantation of a defibrillator. It is thought to affect as many as one in ten thousand people and is estimated to cause 15% of all unexplained sudden cardiac deaths in young people. The condition was first defined in 1978,^[5] and the underlying genetics were described in 2001.^[6]