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KMID : 0869619960130040309
Journal of Korean Society of Hospital Pharmacists
1996 Volume.13 No. 4 p.309 ~ p.315
Amikacin Pharmacokinetics and Proposed Dosing Modification in Korean Neonates
ÀÌÀº°æ/Lee, Eun Kyung
±èÁ¤¼±/ÃÖ°æ¾÷/ÀåÀ±½Ç/¹Ú¿ø¼ø/Kim, Jung Sun/Choi, Kyung Eob/Chang, Yun Sil/Park, Won Soon
Abstract
The pharmacokinetic(PK) parameters of amikacin were evaluated in 28 Korean neonates. The NEOFAX regimen was used to determine the amikacin dose that was administered intravenously over 30 minutes by a syringe pump. The peak and trough levels of amikacin were measured at steady-state and analyzed by fluorescence polarization immunoassay. PK parameters were computed by utilizing one-compartment open model and Kruskal-Wallis test was used for statistical analysis. The calculated volume of distribution(Vd) and half-life(t_(1/2)) in the neonates were 0.52¡¾0.15L/§¸ and 5.6¡¾3.2 hrs, respectively. Linear correlations were found between the postconceptional age(PCA)and clearance(CL=-0.1312+0.0057PCA; r=0.74; P=0.0001), and between PCA and half-life(t_(1/2)=22.38-0.4379PCA; r=-0.90; p=0.0001). Since 78.8% of measured peak levels were subtherapeutic, most neonates required higher amikacin doses. In case of neonates whose gestational age(GA) was 30-36 weeks, the dosing interval was shortened to achieve optimal peak levels.
Based on these PK data we propose using modified NEOFAX regimen, which needs to be confirmed by further prospective study.
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