他唑巴坦/哌拉西林在日本社区获得性肺炎患者中的人群药代动力学

The Japanese journal of antibiotics Pub Date : 2013-08-01
Yukihiro Hamada, Saki Takahashi, Takeshi Hirayama, Keisuke Sunakawa, Masakazu Kuroyama
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引用次数: 0

摘要

他唑巴坦/哌拉西林(TAZ/PIPC;使用非线性混合效应模型VI版分析日本社区获得性肺炎患者的1:8,4.5 g x 3)。单室模型分析PIPC的结果如下:总清除率(CL) = 8.22+(Ccr-71.4) x 0.0561 (L/hr),分布体积(Vd) = 13.7 (L)。TAZ的药代动力学参数为:CL = 8.67 + (Ccr-71.4) × 0.0682 (L/hr), Vd = 14.4 (L)。PIPC药代动力学参数中,CL包含Ccr作为变异因子,而Vd不包含变异因子。由于PIPC以不变的形式排泄到尿液中,其药代动力学因素似乎反映了肾功能状态。在本研究中,社区获得性肺炎患者的Vd值平均为0.26 L/kg,结果表明社区获得性肺炎患者的Vd值比健康成人的Vd值有所增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population pharmacokinetics of tazobactam/piperacillin in Japanese patients with community-acquired pneumonia.

The population pharmacokinetics on tazobactam/piperacillin (TAZ/PIPC; 1:8, 4.5 g x 3) was analyzed in Japanese patients with community-acquired pneumonia using the Nonlinear Mixed Effect Model version VI. Analysis by the one-compartment model yielded the following results for PIPC: total clearance (CL) = 8.22+(Ccr-71.4) x 0.0561 (L/hr), distribution volume (Vd) = 13.7 (L). The pharmacokinetic parameters for TAZ were: CL = 8.67 + (Ccr-71.4) x 0.0682 (L/hr), Vd = 14.4 (L). Of the pharmacokinetic parameters of PIPC, CL included Ccr as a variation factor, whereas the Vd included no variation factor. Because PIPC is excreted into the urine in the unchanged form, its pharmacokinetic factors seem to reflect the renal function status. In this study of patients with community-acquired pneumonia, the mean Vd per body weight was 0.26 L/kg, and the results suggested an increase of the Vd in patients with community-acquired pneumonia as compared with the value in healthy adults.

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