A randomized, double-blind, placebo-controlled evaluation of the efficacy and safety of intravenously administered dofetilide in patients with Wolff-Parkinson-White syndrome
Ad. Krahn et al., A randomized, double-blind, placebo-controlled evaluation of the efficacy and safety of intravenously administered dofetilide in patients with Wolff-Parkinson-White syndrome, PACE, 24(8), 2001, pp. 1258-1260
Citations number
13
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
\Pharmacological conversion of arrhythmias in Wolff-Parkinson-White (WPW) s
yndrome is often frequently undertaken. Current antiarrhythmic drugs used f
or conversion can be associated with significant side effects and variable
efficacy. Fifteen male patients (mean age 34, range 18-63 years) with WPW s
yndrome and atrial fibrillation or AVRT induced in the electrophysiology la
boratory were enrolled in a prospective, randomized, placebo-con trolled cr
ossover study. Patients were randomized to one of two doses of intravenous
dofetilide or placebo. Patients who failed to respond to this initial infus
ion received a second higher dose infusion of dofetilide. With the initial
infusion, six of ten dofetilide patients converted to sinus rhythm compared
to one of five placebo patients. After a second infusion of dofetilide for
placebo patients and higher dose dofetilide for low dose dofetilide patien
ts, the overall conversion rate was 71% with dofetilide compared with 20% f
or placebo (P = 0.046). Atrial fibrillation converted to sinus rhythm in 82
% of patients who received dofetilide. Intravenous dofetilide was safe and
effective at converting induced atrial fibrillation in patients with WPW sy
ndrome.