Contrasting effects of verapamil and procainamide on rate-dependent bundle branch block: pharmacologic evidence for the role of depressed sodium channel responses.

The mechanisms responsible for intermittent bundle branch block are still under debate. The role of the time-dependent behavior of the slow calcium channel has recently been emphasized. To test this hypothesis and ascertain the possible involvement of the fast sodium channel, the effects of the slow calcium channel blocker verapamil and the fast sodium channel blocker procainamide were compared in 10 patients with intermittent bundle branch block. All 10 patients showed bundle branch block during spontaneous sinus rhythm. Maneuvers to slow cardiac rate (that is, carotid sinus massage, Valsalva maneuver) were performed to identify normal conduction as well as phase 4 bundle branch block. Thus, the ranges of diastolic intervals (RR) resulting in phase 3 (tachycardia-dependent) bundle branch block, phase 4 (bradycardia-dependent) bundle branch block and normal conduction were measured in two control studies performed before intravenous administration of verapamil (control 1) and procainamide (control 2) and at the peak effect of both drugs. In the control studies, all 10 patients showed phase 3 bundle branch block, whereas phase 4 bundle branch block occurred in only 4 patients. The ranges of phase 3 bundle branch block, phase 4 bundle branch block and normal conduction were very similar in control studies 1 and 2. The phase 3 bundle branch block range was slightly shortened by verapamil (983 +/- 83.5 ms in control 1; 930 +/- 69.4 ms at the peak effect of verapamil), whereas phase 4 bundle branch block remained unchanged. In contrast, conduction was systematically worsened by procainamide.(ABSTRACT TRUNCATED AT 250 WORDS)

Supernormal conduction in the accessory pathway of patients with overt or concealed ventricular pre-excitation.

It was recently shown that supernormal conduction in the diseased His-Purkinje system is more common than previously thought, and is always associated with prolongation of refractoriness. To assess whether supernormal conduction could also occur in the accessory pathway of patients with ventricular pre-excitation, 21 patients with manifestly prolonged refractoriness in the accessory pathway were studied. Under these conditions, programmed atrial stimulation revealed a phase of supernormal conduction in 16 (76%) of the 21. Therefore, what was believed to be a nonexistent or exceptional physiologic event was shown to be a rather common finding, at least under certain circumstances. Supernormal conduction occurred in all 7 patients with an anterograde refractory period of 480 to 980 ms, and in 5 of 10 patients with a refractory period greater than 1.0 second or with no anterograde conduction. Supernormal conduction could not be demonstrated in four patients with a refractory period less than or equal to 440 ms, but appeared in all four patients after the refractory period was prolonged by a rapid rate of stimulation or administration of ajmaline. The electrophysiologic changes underlying the occurrence of supernormal conduction in the accessory pathway are similar to those previously reported for the bundle branch system. The demonstration of supernormal conduction in the accessory pathway may uncover the presence of concealed ventricular pre-excitation. Supernormal conduction over the accessory pathway may facilitate a rapid ventricular response during atrial fibrillation, even if the refractory period is prolonged.

[Comparative multicenter clinical study of flecainide and amiodarone in the treatment of ventricular arrhythmias associated with chronic Chagas cardiopathy]. / Estudio clínico multicéntrico comparativeo de la flecainida y la amiodarona en el tratamiento de las arritmias ventriculares asociadas a la cardiopatía chagásica cronica.

Eighty one patients with ventricular arrhythmias associated with chronic Chagas disease participated in this multi-clinic study. Treatment with Amiodarone and Flecainide were compared using an open, parallel, randomized experimental design. Inclusion criteria required the selected patients to have 1,200 premature ventricular contractions per 24 hours and/or repetitive ventricular arrhythmias. Patients received 60 days of treatment with either Flecainide at 200 to 400 mg per day or Amiodarone 800 to 400 mg per day. This dosage was adjusted to the therapeutic response. Clinical and laboratory evaluations, electrocardiogram and 24 hour Holters were performed at study days: -7, -1, 8/9, 15/16 and 59/60. The percentage reduction of premature ventricular contractions at days 9, 16 and 60 were: 73.1%, 82.9% and 92.4% with Flecainide and 77.6%, 90.1% and 90.7% with Amiodarone. At the end of the study, Flecainide had induced a 92.5% reduction in couplets and 96.5% reduction in ventricular tachycardia. For the same parameters the percentages following Amiodarone were 95.2% and 92.6% respectively. Treatment was discontinued in three patients in the Flecainide group (two because of prolonged sinus node bradycardia and one because of sustained ventricular tachycardia). In the Amiodarone group, treatment was discontinued also in three patients (one because of sustained ventricular tachycardia and two because of severe photosensitive dermatosis). Although there were some differences in the results form center to center, the conclusions from the overall data indicate a similar, therapeutic effect with both drugs.

Estudio clínico multicéntrico comparativo de la flecainida y la amiodarona en el tratamiento de las arritmias ventriculares asociadas a la cardiopatia chagasica cronica / Flecainide and amiodarone in the treatment of ventricular arrhythmias associated with chagas heart disease

En 81 pacientes con miocarditis crónica chagásica (MCC) y arritmias ventriculares (AV) pertenecientes a 4 centros cardiológicos se evaluó comparativamente la eficacia y seguridad de flecainida (F) y amiodarona (A) utilizando un protocolo abierto, randomizado y paralelo. Fueron incluídos pacientes con un número de extrasístoles ventriculares (EV) no inferior a 1200/24 hs y/o formas repetitivas. Los pacientes fueron tratados durante 60 días con una de las drogas (F: 200 a 400 mg/día; A: 800 a 400 mg/día; dosis ajustada según respuesta) y evaluados clínicamente con exámenes de laboratorio, ECG en reposo y ECG ambulatorios continuos de 24 hs (H) días - 7; - 1; 8/9; 15/16; y 59/60). Los porcentajes de reducción de EV obtenidos a los 9, 16 y 60 días con F fueron 73.1%; 82.9% y 92.4% y con A77.6%; 90.1% y 90.7%. Después de 60 días de tratamiento, la Fredujo las duplas en 92.5% y los episodios de taquicardia ventricular en 96.5% y la A, 95.2% y 92.6%, respectivamente. El tratamiento debió ser interrumpido en 6 pacientes; 3 con F (2 por bradicardia sinusal extrema y 1 por TV iterativa), y 3 con A (1 por TV sostenida y 2 por fotodermatosis severa). Aunque existieron algunas diferencias llamativas en los resultados de los distintos centros, El análisis estadísticos en conjunto sugiere una similar eficacia de F y A en el tratamiento de las AV de la MCC