Oral
encainide, varying from 75 to 300 mg/day (mean 174 mg/day), was administered to 52 patients with
drug-resistant atrioventricular
reciprocating tachycardia (AVRT) associated with the
Wolff-Parkinson-White syndrome. Electrophysiologic studies were performed before and during
drug treatment.
Encainide resulted in anterograde accessory pathway block in 15 of 37 (41%) and retrograde accessory pathway block in 11 of 46 (24%) patients. In patients with residual accessory pathway conduction,
encainide significantly prolonged the shortest pacing cycle length maintaining anterograde (261 +/- 26 to 404 +/- 85 ms) and retrograde (279 +/- 46 to 436 +/- 87 ms) accessory pathway conduction, as well as the anterograde accessory pathway effective refractory period (271 +/- 32 to 329 +/- 73 ms). AVRT could not be induced during
encainide therapy in 20 of 49 patients (41%). In the remaining patients, AVRT cycle length increased (319 +/- 44 to 426 +/- 90 ms, p less than 0.001) due to prolongation of HV and ventriculoatrial intervals. During follow-up (mean 38.5 months), 30 patients continued to take the
drug and 7 patients with favorable
drug response subsequently elected to undergo surgical accessory pathway ablation (71% overall favorable response).
Encainide was ineffective in 11 patients, was discontinued because of
drug intolerance in 2 patients and exacerbated
ventricular tachycardia in 2 patients. Lack of AVRT inducibility at
encainide electrophysiologic study did not always predict recurrence-free follow-up.
Encainide is an effective and well-tolerated
drug to prevent recurrence of AVRT in patients with
Wolff-Parkinson-White syndrome.