Permanent junctional reciprocating tachycardia


Permanent junctional reciprocating tachycardia is a rare cardiac arrhythmia. It is a supraventricular tachycardia, and a cause of atrioventricular reentrant tachycardia. PJRT can cause chronic tachycardia that, untreated, leads to cardiomyopathy. The cause is an accessory pathway in the heart which conducts from the ventricles back to the atria. Unlike the accessory pathway in a more common cause of AVRT, Wolff-Parkinson-White syndrome, the accessory pathway in PJRT conducts slowly. This means that the associated tachycardia may be subclinical and only diagnosed at a late stage, after significant damage to the heart has been caused from prolonged and recurrent episodes of AVRT.

Cause

In-between episodes there is normal electrical conduction in the heart. During an episode of AVRT caused by PJRT, the accessory pathway conducts electrical activity from the ventricles directly back to the atria at the end of systole, which triggers the atria to contract, and the current to pass back to the ventricles again via the atrioventricular node ; see diagram.

Symptoms

during exercise or stress may be the presenting symptom. Because the initial symptoms are often mild, there may be significant myocardial damage at the time of diagnosis. It is therefore possible for these patients to present with the symptoms of heart failure, such as shortness of breath, fatigue and oedema.

Diagnosis

There may be no signs outside of an episode. An electrocardiogram undertaken during an episode of AVRT demonstrates typical features of retrograde p-waves in the inferior leads II, III, aVF, and V4–V6 with a long RP′ interval. The P:QRS ratio would be 1:1 and they would be narrow complexes.

Treatment

Termination of an episode of AVRT in PJRT can be achieved with vagal manouvres, antidysrhythmic medications or DC cardioversion. Long-term management is best achieved with catheter ablation.

Prognosis

Cathater ablation is very effective with a low recurrence rate. Despite this, the prevalence of tachycardia-induced cardiomyopathy has been reported to be between 16% and 52%.