Pullen J, Driessen M, Stolk L M L, Degraeuwe P L J, van Tiel F H, Neef C, Zimmermann L J I
Department of Clinical Pharmacy and Toxicology, University Hospital of Maastricht, Maastricht, The Netherlands.
Ther Drug Monit. 2007 Jun;29(3):376-80. doi: 10.1097/FTD.0b013e318067de5c.
The pharmacokinetic parameters of amoxicillin were determined in 32 newborn infants aged 10 to 52 days (mean postnatal age, 24.7 +/- 12.4 days) to improve amoxicillin dosing in this age group. Amoxicillin plasma concentrations were determined using reversed-phase high-performance liquid chromatography in surplus plasma samples from routine gentamicin assays. Amoxicillin pharmacokinetic parameters (mean +/- SD) were as follows: first-order elimination constant (K(el)) = 0.27 +/- 0.10 h(-1), volume of distribution corrected for body weight (V/W) = 0.66 +/- 0.27 L/kg, total body clearance corrected for body weight (CL/W) = 0.18 +/- 0.10 Lkg(-1)h(-1), and elimination half-life (t(1/2)) = 3.0 +/- 1.3 hours. Amoxicillin body clearance was approximately twofold greater in our patients compared with published values in younger neonates (mean postnatal age, 0.76 +/- 1.57 days). Simulation studies using the observed amoxicillin pharmacokinetic data suggest an amoxicillin dose of 40 mg/kg administered every 8 hours in infants older than 9 days postnatal age, independent of gestational age and postconceptional age, to achieve satisfactory target plasma amoxicillin concentrations less than 140 mg/L and time above minimum inhibitory concentration of at least 40%. Prospective evaluation of this suggested new dosage regimen is necessary before implementation in the care of ill neonates.
为改善阿莫西林在该年龄组中的给药方案,对32名年龄在10至52天(平均出生后年龄,24.7±12.4天)的新生儿进行了阿莫西林的药代动力学参数测定。使用反相高效液相色谱法测定常规庆大霉素检测剩余血浆样本中的阿莫西林血浆浓度。阿莫西林药代动力学参数(平均值±标准差)如下:一级消除常数(K(el))=0.27±0.10 h(-1),体重校正分布容积(V/W)=0.66±0.27 L/kg,体重校正总体清除率(CL/W)=0.18±0.10 Lkg(-1)h(-1),消除半衰期(t(1/2))=3.0±1.3小时。与已发表的较年轻新生儿(平均出生后年龄,0.76±1.57天)的值相比,我们患者的阿莫西林体内清除率大约高出两倍。使用观察到的阿莫西林药代动力学数据进行的模拟研究表明,对于出生后年龄超过9天的婴儿,无论胎龄和受孕后年龄如何,每8小时给予40 mg/kg的阿莫西林剂量,以达到低于140 mg/L的满意目标血浆阿莫西林浓度,且高于最低抑菌浓度的时间至少为40%。在将这一建议的新给药方案应用于患病新生儿护理之前,有必要进行前瞻性评估。