Why the study?
Does KCB-328, dofetilide, or propafenone improve AF termination and electrophysiological parameters in a pacing-induced canine model of AF?
Does KCB-328, dofetilide, or propafenone improve AF termination and electrophysiological parameters in a pacing-induced canine model of AF?
In a canine model of pacing-induced AF, propafenone showed the greatest success in AF termination, while both propafenone and KCB-328 appeared less proarrhythmic than dofetilide.
May favor propafenone over dofetilide for experimental AF termination; leaves open human translation of KCB-328.
HYPOTHESIS: KCB-328 is a new potassium channel blocker, which prolongs action potential duration with exhibition of minimal reverse use dependence. We tested the efficacy and proarrhythmic potential of KCB-328, dofetilide and propafenone in the pacing induced canine model of atrial fibrillation (AF). METHODS: Mongrel dogs in complete heart block were paced for 1-6 weeks to produce AF, and given KCB-328 or dofetilide. A subset then received propafenone 14+/-3 days after testing the first drug. RESULTS: KCB-328 prolonged right and left atrial (RA and LA) activation times and AF cycle length (CL), terminating AF in 3 of 6 dogs. RA effective refractory period (ERP) and ventricular ERP and QT interval were prolonged. Dofetilide terminated AF in 1/6 dogs, and increased AF CL and ventricular ERP and QT interval. Dofetilide's reverse use dependency on the QT interval was greater than KCB-328. Propafenone prolonged RA and LA activation times and AF CL and terminated AF in 8 of 9 dogs. One death occurred with dofetilide, none with KCB-328 or propafenone. CONCLUSION: The spectrum of effect of the three drugs differed significantly: propafenone showed the greatest success in AF termination, and both propafenone and KCB-328 appeared less proarrhythmic than dofetilide in this model.
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Charu Chandra (2004) studied this question.
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