Allegaert K, Cossey V, Langhendries J P, Naulaers G, Vanhole C, Devlieger H, Van Overmeire B
Neonatal Intensive Care Unit, University Hospital Gasthuisberg, Leuven, Belgium.
Biol Neonate. 2004;86(3):207-11. doi: 10.1159/000079618. Epub 2004 Jul 7.
The aim of this study was to assess the effects of intravenous co-administration of ibuprofen-lysine on the pharmacokinetics of amikacin during the first days of life in preterm infants. The pharmacokinetics of amikacin were retrospectively calculated in a cohort of 73 neonates (gestational age <31 weeks) who received either ibuprofen-lysine or placebo following inclusion in the multicentre ibuprofen prophylaxis study. Assuming a one-compartment model with instantaneous input and first-order output, there was no significant difference in the median distribution volume (0.63 vs. 0.59 liters/kg), but the median serum half-life (16.4 vs. 12.4 h) of amikacin was significantly longer (p <0.02), and the clearance (0.36 vs. 0.6 ml/kg/min; p <0.005) of amikacin was significantly lower in infants who received ibuprofen-lysine. We conclude that the time interval between consecutive amikacin administrations should be prolonged, if ibuprofen-lysine is co-administered.
本研究旨在评估静脉联合使用赖氨酸布洛芬对早产儿出生后最初几天内阿米卡星药代动力学的影响。在一项多中心布洛芬预防研究中,对73例(胎龄<31周)接受赖氨酸布洛芬或安慰剂治疗的新生儿队列进行回顾性计算,得出了阿米卡星的药代动力学。假设为具有瞬时输入和一级输出的一室模型,分布容积中位数(0.63 vs. 0.59升/千克)无显著差异,但接受赖氨酸布洛芬治疗的婴儿中,阿米卡星的血清半衰期中位数(16.4 vs. 12.4小时)显著延长(p<0.02),且阿米卡星的清除率(0.36 vs. 0.6毫升/千克/分钟;p<0.005)显著降低。我们得出结论,如果联合使用赖氨酸布洛芬,应延长连续两次阿米卡星给药的时间间隔。