Prediction of Vancomycin Pharmacodynamics in Children With Invasive Methicillin-Resistant Staphylococcus aureus Infections: A Monte Carlo Simulation

被引:42
作者
Frymoyer, Adam [1 ]
Hersh, Adam L. [2 ,3 ]
Coralic, Zlatan [4 ]
Benet, Leslie Z. [5 ]
Guglielmo, B. Joseph [4 ]
机构
[1] Univ Calif San Francisco, Div Clin Pharmacol, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pediat, Div Pediat Infect Dis, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pediat, Div Gen Pediat, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Clin Pharm, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
关键词
vancomycin; methicillin-resistant Staphylococcus aureus; pediatrics; pharmacokinetics/pharmacodynamics; Monte Carlo simulation; REGULATOR AGR GROUP; EFFICACY; PHARMACOKINETICS;
D O I
10.1016/j.clinthera.2010.03.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Due to the emergence of community-associated strains, the prevalence of invasive methicillin-resistant Staphylococcus aureus (MRSA) infections has increased substantially in pediatric patients. A vancomycin AUC(0-24)/MIC index >400 best predicts treatment outcomes for invasive MRSA infection in adults. Data on whether recommended vancomycin doses in children achieve this break point are lacking. Objective: This study aimed to assess the likelihood that currently recommended vancomycin doses in children achieve AUC(0-24)/MIC >400. Methods: Vancomycin AUC(0-24)/MIC predictions were conducted across a range of dosages (40-70 mg/kg/d) using a Monte Carlo simulation (n = 5000). AUC(0-24) was calculated as daily dose divided by vancomycin clearance, and daily dose was fixed for a given simulation. Three literature-reported estimates in children were used to define vancomycin clearance and its variance. For the MIC distribution of MRSA isolates, susceptibility data were obtained from the University of California, San Francisco Children's Hospital, San Francisco, California (n = 180; 40% <= 0.5 mg/L; 59% = 1 mg/L; and 1% = 2 mg/L). Results: Using the recommended empiric dosage of 40 mg/kg/d, 58% to 66% of children were predicted to achieve AUC(0-24)/MIC >400. Increasing the vancomycin dosage to 60 mg/kg/d substantially increased the likelihood (88%-98%) of achieving this pharmacodynamic target. On sensitivity analysis, a dosage of 40 mg/kg/d was more strongly influenced by small changes in MIC compared with 60 mg/kg/d. Conclusions: Recommended empiric vancomycin dosing in children (40 mg/kg/d) was not predicted to consistently achieve the pharmacodynamic target of AUC(0-24)/MIC >400 for invasive MRSA infections. A vancomycin dosage of 60 mg/kg/d was predicted to optimize achievement of this target in children. (Clin Ther. 2010;32:534-542) (C) 2010 Excerpta Medica Inc.
引用
收藏
页码:534 / 542
页数:9
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