EFFECTS OF LOW-DOSE DOPAMINE INFUSION ON CARDIOVASCULAR AND RENAL FUNCTIONS, CEREBRAL BLOOD-FLOW, AND PLASMA-CATECHOLAMINE LEVELS IN SICK PRETERM NEONATES

Citation
I. Seri et al., EFFECTS OF LOW-DOSE DOPAMINE INFUSION ON CARDIOVASCULAR AND RENAL FUNCTIONS, CEREBRAL BLOOD-FLOW, AND PLASMA-CATECHOLAMINE LEVELS IN SICK PRETERM NEONATES, Pediatric research, 34(6), 1993, pp. 742-749
Citations number
40
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
00313998
Volume
34
Issue
6
Year of publication
1993
Pages
742 - 749
Database
ISI
SICI code
0031-3998(1993)34:6<742:EOLDIO>2.0.ZU;2-H
Abstract
Effects of 2 and 4 mug/kg/min dopamine infusion on cardiovascular and renal functions, cerebral blood flow (CBF) and plasma catecholamine le vels were studied in sick preterm neonates during the first four days of life. Preterm infants were found to have an enhanced responsiveness to the pressor effects of dopamine during this period. Comparison of the renal effects of 2 and 4 mug/kg/min dopamine in 61 preterm infants indicate that 2 mug/kg/min dopamine induces maximum diuresis and natr iuresis during the first day of life provided that systemic blood pres sure is within the predicted normal range. Although administration of 4 mug/kg/min dopamine induces further increases in blood pressure and glomerular filtration rate, urine output and sodium excretion remain s imilar to that on 2 mug/kg/min of the drug. These findings demonstrate that the direct tubular effects of dopamine play an important role in the diuretic and natriuretic action of the drug in the one-day old pr eterm infant. In rive preterm neonates, changes in CBF transiently par alleled the dopamine-induced alterations in systemic blood pressure in dicating that autoregulation of CBF is impaired but not completely ine ffective in the one-day old preterm infant. In eight term neonates, in creases in blood pressure had no effect on CBF. Measurements of plasma dopamine and norepinephrine levels in 14 preterm neonates and five ch ildren suggest that decreased metabolism of dopamine may contribute to the enhanced pressor responsiveness to dopamine in sick preterm infan ts. Based on these findings, we propose that dopamine should be starte d at 2 mug/kg/min in the hypotensive and/or oliguric preterm infant, a nd that the dose should be increased in a step-wise manner tailored to the cardiovascular and renal response to the patient.