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Eleven patients with recurrent paroxysmal tachycardia (PSVT) underwent electrophysiological studies. In each patient, initial study revealed re-entrant PSVT with antegrade conduction via the normal pathway and retrograde conduction via an extranodal pathway (Kent bundle). A temporary electrode catheter was left at the conclusion of initial study and PSVT induction was performed on subsequent days before and after the following intravenous drugs: ouabain 0.01 mg/kg (OU), propranolol 0.1 mg/kg (PRO), ouabain + propranolol (OU + PRO) and procainamide 750 mg (PA). In all patients, control studies prior to drug administration revealed the ability to induce sustained PSVT. In five patients, OU, PRO, or OU + PRO prevented induction of sustained PSVT by increasing atrioventricular (A-V) nodal refractoriness. In four of the patients, (including one of the above), PA prevented induction of sustained PSVT: in one, by increasing His-Purkinje refractoriness, and in three by increasing refractoriness in the Kent bundle. Oral drug therapy based upon the above studies (8 pts) prevented recurrent sustained PSVT for a mean follow-up period of 9 ± 5 months. In the remaining three patients, all drugs failed to prevent induction of sustained PSVT. These patients were either treated with radiofrequency pacemakers or surgery. In conclusion, drug responses in patients with recurrent PSVT utilizing a Kent bundle are variable. Antiarrhythmic drugs may interfere with circus movements at the A-V node, His-Purkinje system, or Kent bundle. Chronic oral drug therapy based upon responses to electrophysiological studies with multiple drugs prevents recurrent sustained PSVT over a short-term followup period.

Electrophysiological studies with multiple drugs in patients with atrioventricular re-entrant tachycardias utilizing an extranodal pathway.