Acute hemodynamic effects of hydralazine (10mg, intravenous, 8 cases), nifedipine (10mg, oral, 9 cases), prazosin (2mg, oral, 8 cases) and captopril (25mg, oral, 9 cases) were evaluated in patients with chronic refractory congestive heart failure. Heart rate (HR), mean blood pressure (MBP), mean pulmonary artery pressure (MPA), pulmonary capillary wedge pressure (PCW), cardiac index (CI), stroke volume index (SVI), left ventricular stroke work index (LVSWI), systemic vascular resistanse (SVR) and pulmonary vascular resistance (PVR) were evaluated at base-line state and 0.5, 1, 2, 3, 4, 5 and 6 hours after each drug administration.
Hydralazine significantly increased HR, CI, SVI and LVSWI throughout the 6 hours period of evaluation and significantly decreased SVR and PVR. MPA and PCW did not show significant change.
Nifedipine showed no change in HR, MBP and LVSWI. Significant increase was observed in CI and SVI at 2 hours and 0.5 hours after dosing respectively. MPA and PCW showed no change during the period when CI and SVI increased significantly. SVR sig-nificantly decreased for 2 hours after dosing, but PVR showed only slight significant change at the point of 4 hours after loading of nifedipine.
Prazosin had no effect on HR. CI, SVI and LVSWI showed significant increase and MBP, MPA, PCW and SVR showed significant decrease.
Captopril significantly decreased HR, MBP, MPA and PCW for 5 hours after drug administration. SVR decreased significantly for 2 hours but PVR showed no significant change. LVSWI decreased significantly at 4 and 5 hours after dosing, probably because of its hypotensive effect. All four drugs had significant correlation between percent decrease in SVR and maximum percent change in CI, but significant correlation between initial value of SVR and maximum percent change in CI was observed only in captopril.
The above data showed that hydralazine and nifedipine affect predominantly impedance vessels, and prazosin and captopril affect both impedance and capacitance vessels. Hydralazine and captopril seemed more potent than nif edipine and prazosin as vasodilator. Since negative chronotropic and hypotensive effects of captopril were very profound in some cases, initial administration of captopril may require close observation
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