Key result
In a canine model, APD(90) prolongation with ibutilide was greater in congestive heart failure compared to controls.
Why the study?
Does ibutilide alter action potential duration differently in a canine model of congestive heart failure compared to controls?
Does ibutilide alter action potential duration differently in a canine model of congestive heart failure compared to controls?
Ibutilide causes significantly greater APD90 prolongation and increased ventricular dispersion in a canine model of heart failure compared to controls, suggesting altered electrophysiologic responses in CHF.
Answers are grounded in this paper and cite their sources.
May warrant caution with ibutilide in heart failure; leaves open translation to human electrophysiology.
OBJECTIVE: Despite the frequent use of anti-arrhythmic drugs in the general population, the electrophysiologic effects of these agents have not been elucidated in congestive heart failure (CHF). METHODS: To examine the impact of left ventricular dysfunction on actions of type III anti-arrhythmic drugs, we evaluated the actions of ibutilide in a canine model of pacing-induced dilated cardiomyopathy. Following ablation of the atrioventricular node, effects on action potential duration at 90% (APD(90)) were compared in vivo, between eight CHF animals and seven controls. Monophasic action potential recordings were obtained from right and left ventricular endocardium/epicardium during and after three doses of ibutilide (0. 01, 0.02 and 0.05 mg/kg), at pacing cycle lengths of 300-1000 ms. RESULTS: APD(90) prolongation with ibutilide (0.01 mg/kg) was significantly greater in CHF vs. controls (P=0.0026, ANOVA). However, plasma ibutilide levels at this dose, were not significantly different between the two groups. In CHF, maximal effects were observed at the lowest dose, whereas effects were gradual and dose-dependent in controls. With ibutilide administration (0.01 mg/kg), an increased dispersion of left-right ventricular APD(90) was observed in CHF, but not in controls (P=0.03). A trend was observed, for increased incidence of non-sustained polymorphic ventricular tachycardia in CHF. CONCLUSIONS: In the presence of CHF, the actions of ibutilide are altered significantly. These findings may reflect altered tissue effects, as a consequence of myocardial electrical remodeling in CHF.
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Sumeet S. Chugh (2001) studied Congestive heart failure (pacing-induced dilated cardiomyopathy) (n=15). Ibutilide vs. Controls was evaluated on Action potential duration at 90% (APD(90)) (p=0.0026). In a canine model, APD(90) prolongation with ibutilide was greater in congestive heart failure compared to controls.
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