A randomized, double-blind, placebo-controlled evaluation of the efficacy and safety of intravenously administered dofetilide in patients with Wolff-Parkinson-White syndrome

Citation
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
Journal title
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
ISSN journal
01478389 → ACNP
Volume
24
Issue
8
Year of publication
2001
Pages
1258 - 1260
Database
ISI
SICI code
0147-8389(200108)24:8<1258:ARDPEO>2.0.ZU;2-F
Abstract
\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.