TY - JOUR
T1 - Effect of prazosin on renal function in congestive heart failure
AU - Pierpont, Gordon L.
AU - Franciosa, Joseph A.
AU - Cohn, Jay N.
PY - 1980/9
Y1 - 1980/9
N2 - Prazosin improves hemodynamics promptly in patients with congestive heart failure (CHF), but tolerance to repeated doses may develop rapidly. To determine if the kidneys play a role in this attenuation of effect, we studied renal responses in nine CHF patients treated with prazosin (5 mg three times a day for 3 days) preceded and followed by 3 days of placebo. Prazosin decreased mean arterial blood pressure from 87.0 ± 2.2 (x̄ ± SEM) to 84.0 ± 2.0 mm Hg (p < 0.05) with no change in heart rate (73.1 ± 3.3 bpm on placebo and 73.6 ± 3.5 bpm on prazosin). The change in creatinine clearance from 81.6 ± 8.7 to 96.3 ± 10.4 ml/min with prazosin was not statistically significant, but the slight increase in urine volume from 2.33 ± 0.22 to 2.51 ± 0.23 1/24 hr was (p < 0.01). There were no significant changes in serum sodium, potassium, chloride, CO2, blood urea nitrogen, osmolality or glucose, urinary excretion of sodium or potassium, or sodium balance. The data were analyzed for changes within each period but there were no significant changes from day to day. Plasma renin activity rose from 3.93 ± 0.69 to 4.96 ± 0.84 ng/ml/hr during prazosin (p < 0.02). Significant alterations in renal function are not likely when patients with CHF are treated with prazosin, and any attenuation of effect of prazosin after repeated doses is not likely due to mechanisms involving alterations in renal function. Clinical Pharmacology and Therapeutics (1980) 28, 335–339; doi:
AB - Prazosin improves hemodynamics promptly in patients with congestive heart failure (CHF), but tolerance to repeated doses may develop rapidly. To determine if the kidneys play a role in this attenuation of effect, we studied renal responses in nine CHF patients treated with prazosin (5 mg three times a day for 3 days) preceded and followed by 3 days of placebo. Prazosin decreased mean arterial blood pressure from 87.0 ± 2.2 (x̄ ± SEM) to 84.0 ± 2.0 mm Hg (p < 0.05) with no change in heart rate (73.1 ± 3.3 bpm on placebo and 73.6 ± 3.5 bpm on prazosin). The change in creatinine clearance from 81.6 ± 8.7 to 96.3 ± 10.4 ml/min with prazosin was not statistically significant, but the slight increase in urine volume from 2.33 ± 0.22 to 2.51 ± 0.23 1/24 hr was (p < 0.01). There were no significant changes in serum sodium, potassium, chloride, CO2, blood urea nitrogen, osmolality or glucose, urinary excretion of sodium or potassium, or sodium balance. The data were analyzed for changes within each period but there were no significant changes from day to day. Plasma renin activity rose from 3.93 ± 0.69 to 4.96 ± 0.84 ng/ml/hr during prazosin (p < 0.02). Significant alterations in renal function are not likely when patients with CHF are treated with prazosin, and any attenuation of effect of prazosin after repeated doses is not likely due to mechanisms involving alterations in renal function. Clinical Pharmacology and Therapeutics (1980) 28, 335–339; doi:
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U2 - 10.1038/clpt.1980.170
DO - 10.1038/clpt.1980.170
M3 - Article
C2 - 7408392
AN - SCOPUS:0018967050
SN - 0009-9236
VL - 28
SP - 335
EP - 339
JO - Clinical Pharmacology & Therapeutics
JF - Clinical Pharmacology & Therapeutics
IS - 3
ER -