• Kathryn J Eagye, Joseph L Kuti, Christina A Sutherland, Henry Christensen, and David P Nicolau.
• Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut 06102, USA.
• Clin Ther. 2009 Nov 1;31(11):2678-88.

BackgroundTreatment of infections caused by gram-negative bacilli is increasingly challenging because of emerging resistance. Current surveillance data are informative, but may not discern differences by infection site and clinical setting, and do not incorporate pharmacodynamic (PD) characteristics when determining susceptibility.ObjectivesThis study explored the differences in infection site and clinical setting and evaluated dose-optimization strategies using PD principles. The stud focused only on systemic isolates, and targeted a cohort of 40 hospitals in the United States with a nationwide geographic distribution.MethodsNonduplicate, nonurine isolates of Escherichia coli (n = 937) and Pseudomonas aeruginosa (n = 1044) collected from adult patients at 40 US hospitals underwent MIC testing by broth microdilution to 15 agents. Results were analyzed by infection site and unit type (ward or intensive care unit [ICU]). PD modeling employing Monte Carlo simulation was used to predict the microbiologic success of varying dosing strategies.ResultsE coli were highly susceptible except to fluoroquinolones; 6.8% were multidrug resistant (MDR) and were more likely in ICUs (risk ratio [RR], 2.5; 95% CI, 1.6-4.0). P aeruginosa displayed ConclusionsThese data suggest that susceptibility of E coli to commonly used antibiotics remains high (>90% for most drug classes), with the important exception of the fluoroquinolones; however, susceptibility of P aeruginosa is low enough to warrant concern. Attention to the source of the organism and the patient's location in an ICU or a ward-combined with knowledge of local epidemiology and PD principles--should prove valuable in empiric agent selection. Additionally, reassessment of breakpoints employing PD principles is recommended, particularly for fluoroquinolones and piperacillin/tazobactam.Copyright 2009 Excerpta Medica Inc. All rights reserved.

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