Defibrillation effects of intravenous nifekalant in patients with out-of-hospital ventricular fibrillation

Pacing Clin Electrophysiol. 2005 Jan:28 Suppl 1:S155-7. doi: 10.1111/j.1540-8159.2005.00043.x.

Abstract

Nifekalant (NF), a pure K(+) channel blocker developed in Japan, has been reported to be effective in the treatment of life-threatening ventricular arrhythmias. We studied its efficacy in 18 men and 4 women with out-of-hospital ventricular fibrillation (VF) admitted to our emergency department between August 2001 and March 2004. The number of DC shocks delivered for out-of-hospital VF, serum Na(+) and K(+), arterial blood pH, and base excess were compared in 8 patients treated with NF, 0.3 mg/kg i.v. followed by a continuous intravenous (group N) versus 14 patients treated with lidocaine, 2 mg/kg, i.v. (group C). The two groups were similar with respect to their baseline characteristics. Sinus rhythm returned in 5 of 8 patients in group N versus 2 of 14 patients in group C (P < 0.05). These seven patients were admitted to the intensive care unit, though all died within 1 month. The results of this study suggest that NF may be effective in defibrillation of out-of-hospital VF, though controlled studies are needed to confirm our observations.

MeSH terms

  • Adult
  • Aged
  • Anti-Arrhythmia Agents / administration & dosage*
  • Electric Countershock
  • Emergency Treatment
  • Female
  • Humans
  • Injections, Intravenous
  • Male
  • Middle Aged
  • Pyrimidinones / administration & dosage*
  • Ventricular Fibrillation / drug therapy*
  • Ventricular Fibrillation / therapy

Substances

  • Anti-Arrhythmia Agents
  • Pyrimidinones
  • nifekalant