Pharmacodynamics of an 800-mg dose of telithromycin in patients with community-acquired pneumonia caused by extracellular pathogens

被引:31
作者
Lodise, TP
Preston, S
Bhargava, V
Bryskier, A
Nusrat, R
Chapel, S
Rangaraju, M
Drusano, GL [1 ]
机构
[1] New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
[2] Albany Med Coll, Albany Coll Pharm, Albany, NY 12208 USA
[3] Albany Med Coll, Div Clin Pharmacol, Albany, NY 12208 USA
[4] Albany Med Coll, Clin Res Inst, Albany, NY 12208 USA
[5] Aventis Pharmaceut, Bridgewater, NJ 08807 USA
关键词
telithromycin; pharmacokinetics; pharmacodynamics;
D O I
10.1016/j.diagmicrobio.2004.12.005
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The pharmacodynamics of telithromycin, a new ketolide antibacterial, was examined in 115 patients with community-acquired pneumonia (CAP). Patients received telithromycin 800 mg qd for 7-10 days. Pharmacokinetic parameters were determined, and exposure was linked to microbiological outcome using logistic regression analysis. A breakpoint for increased probability of microbiological eradication was developed and was found to be the ratio of area under the concentration-time curve (AUC) to minimum inhibitory concentration (MIC) of 3.375. The final logistic regression model of microbiological outcome included body weight and AUC/MIC ratio breakpoint. This model was found in analyses of the entire population and when Streptococcus pneumoniae and Haemophihis influence were examined separately. The AUC/MIC ratio target attainment rate is expected to be > 99.9% for S. pneumoniae and Moraxella catarrhalis and 93.1% for H. influenzae. This study demonstrated a relationship between telithromycin drug exposure and microbiological outcome. Telithromycin is expected to achieve the drug exposure breakpoint for the majority of isolates causing CAP. (c) 2005 Published by Elsevier Inc.
引用
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页码:45 / 52
页数:8
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