[MIC测定浓度范围差异对%T>MIC实现概率的影响-美罗培南对铜绿假单胞菌的分析]。

Zenzo Nagasawa, Yukari Nakashima, Yumiko Fukutomi, Nozomi Uki, Koji Kusaba, Fumio Nagumo, Shoichiro Ohta, Eizaburo Sueoka, Hiroshi Miyamoto
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引用次数: 0

摘要

我们试图通过蒙特卡罗模拟方法分析613株铜绿假单胞菌MEPM的MIC测量浓度范围的差异对%T>MIC实现概率的影响。的分析,我们的成就30%和50%的概率计算MEPM % T >麦克风MEPM卷管理:250毫克,500毫克和1000毫克,管理时间:0.5 h,和3 h,政府频率:2倍,3倍,和肾排泄功能:正常的,轻微的,温和,和高异常的3种类型麦克风浓度测量1级)= 256µg / ml: 13水平,2)= 32µg / ml: 7的水平,和3)= 16µg / ml: 5水平。结果,我们发现了以下发现:1. 在正常肾脏排泄能力的给药方面,250mg与500mg和1000mg相比,由于MIC测量浓度范围的不同而存在差异。2. 推荐给药量为MEPM 500 mg时,由于MIC测量浓度范围的不同,实现概率差异较小。随着肾排泄从正常到轻度、中度到高度异常的变化,MIC测量浓度范围的差异对实现概率的差异逐渐减小。有了这些结果,可以对5个水平的测量浓度进行PK/PD分析。使用自动化微生物分析仪的设施不仅可以提供MIC报告,还可以通过PK/PD分析提供抗菌药物的适当给药方法信息,具有重要意义。
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[Influences of %T>MIC achievement probability due to the difference of the MIC measurement concentration range-analysis of meropenem for Pseudomonas aeruginosa-].

We attempted to analyze any influences to %T>MIC achievement probability due to the difference of the MIC measurement concentration range of MEPM for 613 strains of Pseudomonas aeruginosa by the Monte Carlo simulation method. As for the analysis, we calculated the achievement probability of 30% and 50% for MEPM %T>MIC by the administration volume of MEPM: 250 mg, 500 mg, and 1,000 mg, the administration time: 0.5 h, and 3 h, the administration frequency: 2 times, and 3 times, and the renal excretion capability: Normal, Slight, Moderate, and High abnormal with the 3 types of MIC concentration measurement level 1) <=0.06~>=256 µg/ml: 13 levels, 2) <=0.5~>=32 µg/ml: 7 levels, and 3) <=1~>=16 µg/ml: 5 levels. As the result, we found the following findings; 1. In terms of the administration of normal renal excretion capability, 250 mg, in comparison with 500 mg and 1,000 mg, indicated the differential due to the difference of MIC measurement concentration range. 2. The administration volume of MEPM 500 mg which has been recommended shown the less differential of the achievement probability due to the difference of MIC measurement concentration range. As the renal excretion was shifted through Normal to Slight to Moderate to High abnormal, the differential of the achievement probability due to the difference of MIC measurement concentration range was gradually decreased. With these results, PK/PD analysis is possible for the 5 levels measurement concentration. It is significant that the facility using the automated microbiology analyzer can provide not only the MIC report, but also the information on the appropriate administration method for antibacterial drug by PK/PD analysis.

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