Pharmacokinetics of paracetamol in the neonate and infant after administration of propacetamol chlorhydrate.

E Autret, J P Dutertre, M Breteau, A P Jonville, Y Furet, J Laugier
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引用次数: 71

Abstract

The pharmacokinetic parameters of paracetamol were studied after 15 min intravenous infusion of 15 mg/kg of propacetamol (Prodafalgan) in 5 neonates aged less than 10 days and 7 infants aged between 1 and 12 months. Blood was sampled at 0, 0.5, 2 and 6 h after the first intravenous infusion of propacetamol. The infants aged less than 10 days had higher plasma concentrations of paracetamol, a longer half-life (3.5 vs. 2.1 h) and a lower plasma clearance (0.149 vs. 0.365 l/h/kg) than the older children. Dose simulations were performed on the basis of individual data of each child in order to obtain steady-state plasma concentrations between 4 and 18 mg/l permitting the best antipyretic effect for each child. In infants aged less than 10 days a 15 mg/kg dose of propacetamol four times a day (i.e. 30 mg/kg/day paracetamol) is sufficient, corresponding to the dosage recommended by the French pharmacopoeia. On the other hand, double the dosage, nearer to the American dosage, is necessary for children aged over 10 days.

盐酸丙帕他莫在新生儿和婴儿体内的药代动力学。
对5例10天以下新生儿和7例1 ~ 12月龄婴儿静脉滴注15 mg/kg丙帕他莫(Prodafalgan) 15 min后对扑热息痛的药代动力学参数进行了研究。分别于第一次静脉输注丙帕他莫后0、0.5、2、6 h采血。小于10天的婴儿血浆对乙酰氨基酚浓度较高,半衰期较长(3.5 vs 2.1 h),血浆清除率较低(0.149 vs 0.365 l/h/kg)。剂量模拟是根据每个儿童的个人数据进行的,以便获得4至18mg /l之间的稳态血浆浓度,从而使每个儿童获得最佳的解热效果。对于10天以下的婴儿,每天4次15毫克/公斤的丙帕他莫剂量(即30毫克/公斤/天扑热息痛)就足够了,与法国药典推荐的剂量相对应。另一方面,10天以上的儿童需要双倍的剂量,接近美国的剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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