Allegaert K, de Hoon J, Naulaers G, Van De Velde M
Neonatal Intensive Care Unit, Division of Woman and Child, University Hospitals Leuven, Leuven, Belgium.
Acta Anaesthesiol Belg. 2008;59(4):283-8.
Neonatal drug dosing needs to be based on the physiological characteristics of the newborn, the pharmacokinetic parameters of the drug and has to take maturational aspects of drug disposition into account. We would like to provide the reader with some recently published compound-specific observations (paracetamol, ibuprofen, tramadol, propofol) in neonates of relevance for anaesthesiologists. Age-specific dosing regimes of intravenous paracetamol have been evaluated and were well tolerated, independent of the postnatal age. Administration of ibuprofen or acetyl salicylic acid resulted in a transient reduction of 20% of the glomerular filtration rate and should be used cautiously in newborns. Both postmenstrual age and pharmacogenetics (CYP2D6) were covariates of tramadol metabolism in newborns. Tramadol seems to be a potential useful analgesic for term neonates and infants, but has limited indications in (extreme) preterm neonates. Finally, propofol clearance depends on post-menstrual and postnatal age. There is a risk for accumulation in preterms and in the first two weeks of postnatal life.
新生儿用药剂量需要基于新生儿的生理特征、药物的药代动力学参数,并必须考虑药物处置的成熟情况。我们希望为读者提供一些最近发表的、与麻醉医生相关的新生儿特定化合物观察结果(对乙酰氨基酚、布洛芬、曲马多、丙泊酚)。已对静脉注射对乙酰氨基酚的年龄特异性给药方案进行了评估,且耐受性良好,与出生后年龄无关。布洛芬或乙酰水杨酸的给药导致肾小球滤过率短暂降低20%,在新生儿中应谨慎使用。胎龄和药物遗传学(CYP2D6)都是新生儿曲马多代谢的协变量。曲马多似乎是足月儿和婴儿潜在有用的镇痛药,但在(极)早产儿中的适应证有限。最后,丙泊酚清除率取决于胎龄和出生后年龄。早产儿以及出生后生命的前两周存在蓄积风险。