The aim of this prospective, non-randomized interventional study was to assess electrophysiological effects, efficacy and safety of intravenous
propafenone in termination of
atrioventricular nodal reentrant tachycardia (AVNRT) and orthodromic
atrioventricular reentrant tachycardia (AVRT). This single-center study was carried out at Department of Cardiology, Sestre milosrdnice University Hospital in Zagreb, Croatia, between January 1, 2005 and December 31, 2006. Eligibility requirements were fulfilled by a total of 70 patients with AVNRT (n=37) and AVRT (n=33). The intervention consisted of the electrophysiological study aimed at inducing
tachycardia, followed by
intravenous administration of 2 mg/kg
propafenone in both groups. The main outcome measures were safety and efficacy of 2 mg/kg intravenous
propafenone in
tachycardia termination and re-induction. Out of 37 patients with AVNRT,
propafenone managed to terminate it in 28 (75.7%) patients, while
tachycardia was not inducible in 25 (67.56%) patients. Out of 33 patients with AVRT,
propafenone managed to terminate AVRT in 29 (87.9%) patients, while
tachycardia was not inducible in 22 (66.66%) patients. The overall
propafenone efficacy in
tachycardia termination was 81.42%. No
propafenone-related adverse effects were recorded during the study period.
Propafenone was found to be a safe and effective
anti-arrhythmic drug and can be justifiably administered for AVNRT and AVRT termination. It could be considered as an alternative to
adenosine and
verapamil.