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Am Heart J ; 108(6): 1461-8, 1984 Dec.
Article in English | MEDLINE | ID: mdl-6507242

ABSTRACT

Ten patients with moderate to severe congestive heart failure (CHF) underwent central and regional hemodynamic measurements at rest and central hemodynamic measurements during exercise before and after the oral administration of nifedipine (0.2 mg/kg). Nifedipine significantly decreased systemic blood pressure, systemic vascular resistance, pulmonary artery pressure, pulmonary vascular resistance, and pulmonary capillary wedge pressure. Stroke volume and cardiac output increased after nifedipine. The measured parameters of left ventricular inotropy did not change significantly for this calcium channel blocker. While blood flow to renal, hepatic, and limb vascular beds increased (p less than 0.05 for renal and limb) after nifedipine, only limb blood flow increased in proportion to the increase in cardiac output, suggesting preferential dilatation of limb vasculature. Although initial-dose nifedipine did not increase exercise duration, it elicited an improvement in exercise hemodynamics by reducing systemic vascular resistance and pulmonary capillary wedge pressure and increasing stroke volume and cardiac output. The calcium channel blocker, nifedipine, can be administered safely in the setting of ventricular failure and appears to favorably alter resting and exercise hemodynamics. A select number of patients with CHF may benefit from its long-term administration.


Subject(s)
Heart Failure/drug therapy , Hemodynamics/drug effects , Nifedipine/therapeutic use , Adult , Aged , Blood Pressure/drug effects , Cardiac Output/drug effects , Exercise Test , Extremities/blood supply , Female , Heart Failure/physiopathology , Heart Rate/drug effects , Humans , Liver Circulation/drug effects , Male , Middle Aged , Myocardial Contraction/drug effects , Nifedipine/pharmacology , Pulmonary Wedge Pressure/drug effects , Regional Blood Flow/drug effects , Renal Circulation/drug effects , Stroke Volume/drug effects , Vascular Resistance/drug effects
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