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Published on: February 26, 2013
Haemodynamic and antiarrhythmic effects of intravenous flecainide acetate in chronic congestive heart failure
Insights
Flecainide acetate effectively suppressed ventricular arrhythmias in heart failure patients. Doubling infusion time ensured safety and good antiarrhythmic efficacy, even at lower plasma concentrations.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Congestive heart failure (CHF) patients often experience ventricular arrhythmias.
- Class Ic antiarrhythmic agents, like flecainide acetate, require careful evaluation in heart failure populations due to potential proarrhythmic effects.
Purpose of the Study:
- To assess the hemodynamic and antiarrhythmic effects of flecainide acetate in patients with heart failure.
- To determine the safety and efficacy of flecainide acetate administration in this patient group.
Main Methods:
- Intravenous administration of flecainide acetate (2 mg/kg) over 60 minutes to 9 patients with CHF and ventricular arrhythmias.
- Monitoring of hemodynamic parameters (cardiac index, pulmonary wedge pressure, pre-ejection period, ejection time) and arrhythmia suppression.
Main Results:
- Significant reduction (90%) in ventricular arrhythmias in 6 out of 9 patients for an average of 6.5 hours.
- Hemodynamic changes included increased pre-ejection period and pulmonary wedge pressure, and decreased cardiac index.
- Parameters normalized upon infusion completion; no significant changes in stroke work index, arterial pressure, or vascular resistance.
Conclusions:
- Flecainide acetate (2 mg/kg) can be safely administered to CHF patients when the infusion time is doubled.
- Good antiarrhythmic efficacy is achievable with this modified administration protocol, even at lower plasma concentrations.
Abstract:
The objective of this study was to evaluate the haemodynamic and antiarrhythmic effects of flecainide acetate in patients with heart failure. Flecainide acetate, a class Ic antiarrhythmic agent, was given intravenously to 9 patients with congestive heart failure and frequent ventricular arrhythmias with nonsustained ventricular tachycardia. The drug (2 mg/kg) was infused slowly over 60 minutes. The maximum plasma level achieved was 218 (range 142-350) ng/ml. Six of the 9 patients experienced a 90% suppression of their arrhythmias for an average of 6.5 (range 2-15) hours. Pre-ejection period control (PEPc, 148.8 +/- 3.6 msec) increased to 157 msec and pre-ejection period/ejection time (PEP/ET) [control 0.449 +/- 0.027] to 0.516 (p less than 0.005), while the ejection time index (ETI) did not change. Cardiac index (control 2.4 +/- 0.36 L/min/m2) decreased by 11% (p less than 0.02), and pulmonary wedge pressure (control 13.4 +/- 2.4mm Hg) increased by 23% (p less than 0.05). Stroke work index, arterial pressure and vascular resistance did not change significantly. The parameters returned to control values on completion of the infusion. Flecainide acetate can be safely administered at the usual dose of 2 mg/kg to patients with congestive heart failure, provided that the infusion time is doubled. Antiarrhythmic efficacy under these conditions is good even at lower plasma concentrations.
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