Dopamine in lage dosis in de neonatale en pediatrische intensive care: is er nog een indicatie?
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Samenvatting
Dopamine is een endogeen catecholamine, een precursor van noradrenaline. Dopamine in lage dosis (ldd) (< 4µ/kg/min) wordt op intensive-care-afdelingen bij zowel volwassenen, zuigelingen en kinderen veelvuldig gebruikt vanwege het vermeende nierfunctiebeschermende effect. In dit overzichtsartikel wordt de fysiologie van dopamine en dopaminereceptoren van de nier besproken. Bij gezonde volwassenen geeft ldd toegenomen nierdoorbloeding met toename in diurese en natriurese. Bij ernstig zieke volwassenen is het gebruik van ldd controversieel, omdat tot op heden in grote gerandomiseerde trials geen toename is gevonden van de creatinineklaring of de glomerulaire filtratiesnelheid. Ook bij zieke zuigelingen en kinderen op de intensive care wordt ldd gebruikt, zoals blijkt uit een door ons gehouden enquête. Wij verrichtten literatuuronderzoek naar de renale effecten van ldd bij deze leeftijdsgroep en vonden slechts één gerandomiseerde studie, waarin geen statistisch significant effect werd gevonden op de nierfunctie of diurese. Alle andere studies waren niet gerandomiseerd en daaruit kon geen duidelijke conclusie getrokken worden. Mogelijk zijn er effecten van ldd, maar die zijn tot nu toe nog niet aangetoond. Het gebruik van ldd kan vooralsnog niet aangeraden worden, ook gezien de bijwerkingen, tot een gerandomiseerde placebo-gecontroleerde studie uitsluitsel geeft.
Summary
Dopamine is an endogenous catecholamine, an immediate precursor of noradrenaline. Low-dose dopamine (< 4 µ/kg/min)(ldd) has widely been used in intensive care for its supposed renal protective effects in adults, children and neonates as well. In this review we discuss the physiology of renal dopamine and dopamine receptors. In healthy adult volunteers ldd increases renal blood flow and sodium excretion and enhances urine volume. In critically ill adults the use of ldd remains controversial as unequivocal evidence of improvement in renal function, i.e. an increase in creatinine clearance or glomerular filtration rate, has not been published to date. ldd is also commonly used in neonatal and pediatric intensive care units for the same reasons. As indicated by the results of our survey of current use in the Netherlands, almost all units used ldd more or less regularly. We reviewed the literature in this age group, but we found only one randomised controlled trial, in which no statistically significant effect of ldd on renal function and urine volume is reported. All other studies were non-randomised and similarly inconclusive. In view of the adverse effects, the use of ldd in neonatal and paediatric patients should be reconsidered until a placebo-controlled trial yields new evidence.
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