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Rational dosing of antibiotics: the use of plasma concentrations versus tissue concentrations

机译:合理剂量的抗生素:使用血浆浓度与组织浓度

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At the moment, the most common pharmacokinetic/pharmacodynamic (PK/PD) approaches for anti-infective agents, such as time above MIC, C-max/MIC and AUC(24)/MIC, rely on plasma concentration as the PK input value and minimum inhibitory concentration (MIC) as the PD input value. However, only the free tissue concentrations of antibiotics at the target site are responsible for the therapeutic effect. Using plasma concentrations frequently overestimates the target site concentrations and therefore clinical efficacy. Microdialysis is a new technique that allows direct measurement of unbound tissue concentrations. Furthermore, a better PD approach, bacterial time-kill curves, can offer more detailed information about the antibacterial activity as a function of time and antibiotic concentration than MICs. (C) 2002 Elsevier Science B.V. and International Society for Chemotherapy. All rights reserved. [References: 23]
机译:目前,最常用的抗感染药的药代动力学/药效学(PK / PD)方法(例如高于MIC,C-max / MIC和AUC(24)/ MIC的时间)依赖于血浆浓度作为PK输入值最小抑菌浓度(MIC)作为PD输入值。但是,仅靶部位处的抗生素的游离组织浓度负责治疗效果。使用血浆浓度经常会高估目标部位的浓度,因此会高估临床疗效。微透析是一种新技术,可以直接测量未结合的组织浓度。此外,与MIC相比,更好的PD方法(细菌杀灭时间曲线)可以提供有关抗菌活性随时间和抗生素浓度变化的更详细的信息。 (C)2002 Elsevier Science B.V.和国际化学疗法学会。版权所有。 [参考:23]

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