Texas Tech University Health Sciences Center, 1300 Coulter, Suite 203, Amarillo, TX 79106, USA.
Expert Rev Anti Infect Ther. 2010 Jan;8(1):95-106. doi: 10.1586/eri.09.123.
Vancomycin is a commonly used antimicrobial in patients with methicillin-resistant Staphylococcus aureus (MRSA) infections. Increasing vancomycin MIC values in MRSA clinical isolates makes the optimization of vancomycin dosing pivotal to its continued use. Unfortunately, limited data exist regarding the optimal pharmacokinetic-pharmacodynamic (PK-PD) goal to improve bacterial killing and clinical outcomes with vancomycin. The hallmark study in this area suggests that achieving an AUC to MIC ratio of over 400 improves the likelihood of achieving these outcomes. Challenges in the implementation of PK-PD-based dosing for vancomycin include current methodologies utilized in microbiology laboratories, as well as intra- and interpatient pharmacokinetic variability. Individualized dosing based on MIC and specific patient factors is important to achieve optimal outcomes from vancomycin therapy.
万古霉素是耐甲氧西林金黄色葡萄球菌 (MRSA) 感染患者常用的抗菌药物。MRSA 临床分离株中万古霉素 MIC 值的增加使得优化万古霉素剂量对于其持续使用至关重要。不幸的是,关于优化药代动力学-药效学 (PK-PD) 目标以提高万古霉素杀菌效果和临床结局的数据有限。该领域的标志性研究表明,达到 AUC/MIC 比值超过 400 可提高实现这些结局的可能性。万古霉素基于 PK-PD 的给药实施面临的挑战包括微生物学实验室目前使用的方法,以及患者内在和个体间的药代动力学变异性。基于 MIC 和特定患者因素的个体化给药对于实现万古霉素治疗的最佳结局非常重要。