Circulation, Vol 81, 970-977, Copyright © 1990 by American Heart Association
WJ Elliott, RR Weber, KS Nelson, CM Oliner, MT Fumo, DD Gretler, GR McCray and MB Murphy
The renal and hemodynamic effects of intravenously administered fenoldopam
mesylate, a novel dopamine-1 receptor agonist, were compared with those of
sodium nitroprusside in 28 patients (18 male; 26 black, two white; average
age, 49 +/- 3 years) with an average blood pressure of 219/137 mm Hg, most
of whom presented with acute target organ damage. Fenoldopam and
nitroprusside lowered blood pressure safely to an average pressure of
176/105 mm Hg; highly significant dose-response relations were found for
the 13 patients receiving fenoldopam and the 15 receiving nitroprusside.
Volume and sodium, potassium, and creatinine concentrations were measured
in freely voided urine specimens both before and during intravenous
therapy. In the fenoldopam- treated patients, there were significant
increases in urinary flow (92 +/- 21 to 168 +/- 37 ml/hr, p less than
0.003), sodium excretion (227 +/- 73 to 335 +/- 90 mu eq/min, p less than
0.001), and creatinine clearance (70 +/- 11 to 93 +/- 13 ml/hr, p less than
0.003). In the nitroprusside-treated group, however, all these parameters
decreased, but not significantly. For direct comparison of the two agents,
the increments in urinary flow rate (+76 +/- 20 vs. -16 +/- 15 ml/hr,
fenoldopam vs. nitroprusside), sodium excretion (+109 +/- 28 vs. -39 +/- 28
mu eq/min), and creatinine clearance (+23 +/- 6 vs. -11 +/- 7 ml/min) were
significantly greater (p less than 0.001 for each) in the
fenoldopam-treated group. Significant differences were also obtained when
these parameters were calculated as percentage increase over baseline.
Fenoldopam and nitroprusside are effective therapies for severe,
accelerated, or malignant hypertension, but fenoldopam had additional
salutary renal effects in these patients.
ARTICLES
Renal and hemodynamic effects of intravenous fenoldopam versus nitroprusside in severe hypertension
Committee on Clinical Pharmacology, University of Chicago, IL 60637.
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