Permanent junctional reciprocating tachycardia

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Permanent junctional reciprocating tachycardia
Illustration of atrioventricular reentrant tachycardia
Synonyms	PJRT
Pronounce	N/A
Specialty	N/A
Symptoms	Palpitations, dizziness, syncope, shortness of breath
Complications	Heart failure, cardiomyopathy
Onset	Childhood or adolescence
Duration	Chronic
Types	N/A
Causes	Accessory pathway
Risks	Congenital heart disease, genetic predisposition
Diagnosis	Electrocardiogram, Holter monitor, electrophysiological study
Differential diagnosis	Atrioventricular nodal reentrant tachycardia, atrial fibrillation, ventricular tachycardia
Prevention	None
Treatment	Medications, catheter ablation, surgery
Medication	Beta blockers, calcium channel blockers, antiarrhythmic drugs
Prognosis	Good with treatment
Frequency	Rare
Deaths	N/A

A type of supraventricular tachycardia

Permanent junctional reciprocating tachycardia (PJRT) is a rare form of supraventricular tachycardia (SVT) characterized by a reentrant circuit involving an accessory pathway that conducts in a retrograde manner. This condition is typically seen in children but can persist into adulthood. Unlike other forms of SVT, PJRT is often incessant, meaning it occurs continuously or very frequently, which can lead to tachycardia-induced cardiomyopathy.

Pathophysiology

PJRT is caused by the presence of an accessory pathway that connects the atrium and ventricle outside of the normal atrioventricular node conduction system. This accessory pathway conducts electrical impulses from the ventricles back to the atria, creating a reentrant circuit. The pathway in PJRT is typically located in the posteroseptal region of the heart and has decremental conduction properties, meaning its conduction speed decreases with increasing heart rates.

Clinical Presentation

Patients with PJRT often present with symptoms of palpitations, fatigue, and dyspnea. In infants and young children, it may present as congestive heart failure due to the persistent tachycardia. Older children and adults may experience exercise intolerance and palpitations. The incessant nature of the tachycardia can lead to tachycardia-induced cardiomyopathy, which can cause heart failure if not treated.

Diagnosis

The diagnosis of PJRT is typically made using electrocardiography (ECG). The ECG in PJRT shows a narrow complex tachycardia with a long RP interval, which is the time between the onset of the P wave and the preceding R wave. This is due to the retrograde conduction through the accessory pathway. Electrophysiological study can be used to confirm the diagnosis and to locate the accessory pathway.

Management

The management of PJRT involves controlling the heart rate and, if possible, eliminating the accessory pathway. Beta blockers and calcium channel blockers are often used to control the heart rate. Antiarrhythmic drugs such as flecainide or amiodarone may be used in some cases. The definitive treatment for PJRT is radiofrequency catheter ablation of the accessory pathway, which can cure the condition by interrupting the reentrant circuit.

Prognosis

With appropriate treatment, the prognosis for patients with PJRT is generally good. Radiofrequency ablation has a high success rate and can prevent the recurrence of tachycardia. If left untreated, PJRT can lead to heart failure and other complications due to the persistent tachycardia.

See also

• Supraventricular tachycardia
• Atrioventricular reentrant tachycardia
• Accessory pathway
• Electrophysiological study