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

被引:88
作者
SERI, I
RUDAS, G
BORS, Z
KANYICSKA, B
TULASSAY, T
机构
[1] CHILDRENS HOSP MED CTR,JOINT PROGRAM NEONATOL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[3] SEMMELWEIS UNIV MED,SCH MED,DEPT PEDIAT 1,H-1085 BUDAPEST 8,HUNGARY
[4] SEMMELWEIS UNIV MED,SCH MED,DEPT PEDIAT 2,H-1085 BUDAPEST 8,HUNGARY
[5] HUNGARIAN ACAD SCI,INST EXPTL MED,H-1361 BUDAPEST 5,HUNGARY
关键词
D O I
10.1203/00006450-199312000-00009
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Effects of 2 and 4 mug/kg/min dopamine infusion on cardiovascular and renal functions, cerebral blood flow (CBF) and plasma catecholamine levels 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 natriuresis during the first day of life provided that systemic blood pressure 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 similar 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 preterm infant. In rive preterm neonates, changes in CBF transiently paralleled the dopamine-induced alterations in systemic blood pressure indicating that autoregulation of CBF is impaired but not completely ineffective in the one-day old preterm infant. In eight term neonates, increases in blood pressure had no effect on CBF. Measurements of plasma dopamine and norepinephrine levels in 14 preterm neonates and five children suggest that decreased metabolism of dopamine may contribute to the enhanced pressor responsiveness to dopamine in sick preterm infants. Based on these findings, we propose that dopamine should be started at 2 mug/kg/min in the hypotensive and/or oliguric preterm infant, and that the dose should be increased in a step-wise manner tailored to the cardiovascular and renal response to the patient.
引用
收藏
页码:742 / 749
页数:8
相关论文
共 40 条
[1]   DOPAMINE CAUSES INHIBITION OF NA+-K+-ATPASE ACTIVITY IN RAT PROXIMAL CONVOLUTED TUBULE SEGMENTS [J].
APERIA, A ;
BERTORELLO, A ;
SERI, I .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (01) :F39-F45
[2]   MEAN ARTERIAL BLOOD-PRESSURE CHANGES IN PREMATURE-INFANTS AND THOSE AT RISK FOR INTRAVENTRICULAR HEMORRHAGE [J].
BADA, HS ;
KORONES, SB ;
PERRY, EH ;
ARHEART, KL ;
RAY, JD ;
POURCYROUS, M ;
MAGILL, HL ;
RUNYAN, W ;
SOMES, GW ;
CLARK, FC ;
TULLIS, KV .
JOURNAL OF PEDIATRICS, 1990, 117 (04) :607-614
[3]  
BHATTMEHTA V, 1991, EUR J CLIN PHARMACOL, V40, P593
[4]   PERIVENTRICULAR LEUKOMALACIA - ULTRASONIC DIAGNOSIS AND NEUROLOGICAL OUTCOME [J].
CALVERT, SA ;
HOSKINS, EM ;
FONG, KW ;
FORSYTH, SC .
ACTA PAEDIATRICA SCANDINAVICA, 1986, 75 (03) :489-496
[5]   SERIAL MEASUREMENTS OF CEREBRAL BLOOD-FLOW VELOCITY IN PRETERM INFANTS DURING THE 1ST 72 HOURS OF LIFE [J].
CALVERT, SA ;
OHLSSON, A ;
HOSKING, MC ;
ERSKINE, L ;
FONG, K ;
SHENNAN, AT .
ACTA PAEDIATRICA SCANDINAVICA, 1988, 77 (05) :625-631
[6]  
CUEVAS L, 1991, AM J DIS CHILD, V145, P799
[7]   THE CARDIOVASCULAR EFFECTS OF DOPAMINE IN THE SEVERELY ASPHYXIATED NEONATE [J].
DISESSA, TG ;
LEITNER, M ;
TI, CC ;
GLUCK, L ;
COEN, R ;
FRIEDMAN, WF .
JOURNAL OF PEDIATRICS, 1981, 99 (05) :772-776
[8]  
DRISCOLL DJ, 1978, J PEDIATR-US, V92, P309, DOI 10.1016/S0022-3476(78)80033-X
[9]   NONINVASIVE BLOOD-PRESSURE MONITORING IN PRETERM INFANTS RECEIVING INTENSIVE-CARE [J].
EMERY, EF ;
GREENOUGH, A .
EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (02) :136-139
[10]   DOPAMINE INHIBITS NA+-H+ EXCHANGER ACTIVITY IN RENAL BBMV BY STIMULATION OF ADENYLATE-CYCLASE [J].
FELDER, CC ;
CAMPBELL, T ;
ALBRECHT, F ;
JOSE, PA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (02) :F297-F303