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Does carvedilol improve long-term hemodynamics in patients with chronic heart failure secondary to ischemic heart disease?
Does carvedilol improve long-term hemodynamics in patients with chronic heart failure secondary to ischemic heart disease?
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Chronic carvedilol therapy for 8 weeks significantly improves left ventricular ejection fraction and stroke volume index in ischemic heart failure, despite a lack of acute hemodynamic improvement.
Summary: Several studies have demonstrated the longterm beneficial effects of β-blockers in the treatment of congestive heart failure. Despite interest in this mode of therapy, clinical application of β-blockers has been limited due to their negative inotropic effect. A subset of the heart failure patients do not show improvements with standard β-blocker therapy. Carvedilol, a new nonselective β-blocking agent with concurrent α-blocking properties, was evaluated in 17 patients with chronic heart failure secondary to ischemic heart disease. All had resting left ventricular ejection fraction ≤45% and were maintained on diuretic therapy. Acute hemodynamic measurements were made after administration of intravenous carvedilol (2.5-7.5 mg) and after chronic therapy for 8 weeks (12.5 to 50 mg b.i.d.). Radionuclide ventriculography, ambulatory intra-arterial blood pressure monitoring, and right heart catheterization were performed before and after 8 weeks of chronic therapy. Twelve patients completed the study (five were withdrawn). Symptomatic and hemodynamic improvements were demonstrated in 11 of the 12 patients after 8 weeks of therapy. Mean ± SD systolic intra-arterial blood pressure (133 ± 20 to 114 ± 17 mm Hg, p < 0.005), heart rate (81 ± 11 to 61 ± 5 beats/min, p < 0.0001), pulmonary artery wedge pressure (19 ± 7 to 12 ± 5 mm Hg, p < 0.001), and systemic vascular resistance (1,748 ± 398 to 1,497 ± 310 dynes/s/cm-5/m2, p < 0.02) decreased and mean ± SD stroke volume index (31 ± 6 to 40 ± 6 ml/m2/beat, p < 0.0005) and left ventricular ejection fraction (25 ± 9% to 32 ± 10%, p < 0.01) increased after 8 weeks of therapy with carvedilol. This contrasts with the acute hemodynamic effects of carvedilol, which showed reductions in heart rate (81 ± 11 to 74 ± 10 beats/min, p < 0.0001), systolic intra-arterial blood pressure (133 ± 20 to 117 ± 22 mm Hg, p < 0.0005), and pulmonary artery wedge pressure (19 ± 7 to 14 ± 6 mm Hg, p < 0.002) 10 min after injection. Systemic vascular resistance, left ventricular ejection fraction, and stroke volume index failed to show any significant improvement. Thus, intravenous carvedilol produces a reduction in filling pressure that is maintained after chronic treatment. This effect is clearly beneficial for chronic heart failure patients and differs from that of standard β-blockers. The discrepancy of hemodynamic changes for acute and chronic long-term responses to carvedilol lends further support to the concept of upregulation of β-adrenoceptors in congestive heart failure.
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DasGupta et al. (1992) studied this question.
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