Wicha S G, Huisinga W, Kloft C
Department of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universitaet Berlin, Berlin, Germany.
Institute of Mathematics, University of Potsdam, Potsdam-Golm, Germany.
CPT Pharmacometrics Syst Pharmacol. 2017 Aug;6(8):512-522. doi: 10.1002/psp4.12197. Epub 2017 Jul 13.
Broad-spectrum antibiotic combination therapy is frequently applied due to increasing resistance development of infective pathogens. The objective of the present study was to evaluate two common empiric broad-spectrum combination therapies consisting of either linezolid (LZD) or vancomycin (VAN) combined with meropenem (MER) against Staphylococcus aureus (S. aureus) as the most frequent causative pathogen of severe infections. A semimechanistic pharmacokinetic-pharmacodynamic (PK-PD) model mimicking a simplified bacterial life-cycle of S. aureus was developed upon time-kill curve data to describe the effects of LZD, VAN, and MER alone and in dual combinations. The PK-PD model was successfully (i) evaluated with external data from two clinical S. aureus isolates and further drug combinations and (ii) challenged to predict common clinical PK-PD indices and breakpoints. Finally, clinical trial simulations were performed that revealed that the combination of VAN-MER might be favorable over LZD-MER due to an unfavorable antagonistic interaction between LZD and MER.
由于感染性病原体的耐药性不断增加,广谱抗生素联合治疗经常被应用。本研究的目的是评估两种常见的经验性广谱联合治疗方案,即利奈唑胺(LZD)或万古霉素(VAN)与美罗培南(MER)联合使用,针对金黄色葡萄球菌(S. aureus)这种严重感染最常见的病原体。基于时间杀灭曲线数据,建立了一个模拟金黄色葡萄球菌简化细菌生命周期的半机制药代动力学-药效学(PK-PD)模型,以描述LZD、VAN和MER单独及联合使用时的效果。该PK-PD模型成功地(i)用来自两种临床金黄色葡萄球菌分离株和其他药物组合的外部数据进行了评估,(ii)用于预测常见的临床PK-PD指标和断点。最后,进行了临床试验模拟,结果显示,由于LZD和MER之间存在不利的拮抗相互作用,VAN-MER组合可能比LZD-MER组合更有利。