Relationship between fluoroquinolone area under the curve:minimum inhibitory concentration ratio and the probability of eradication of the infecting pathogen, in patients with nosocomial pneumonia
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作者:
Drusano, GL
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Drusano, GL
Preston, SL
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Preston, SL
Fowler, C
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Fowler, C
Corrado, M
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Corrado, M
Weisinger, B
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Weisinger, B
Kahn, J
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机构:New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
Kahn, J
机构:
[1] New York State Dept Hlth, Ordway Res Inst, Albany, NY 12208 USA
[2] Robert Wood Johnson Pharmaceut Res & Dev, Lambertville, NJ USA
Our objective was to prospectively determine the factors influencing the probability of a good microbiological or clinical outcome in patients with nosocomial pneumonia treated with a fluoroquinolone. Levofloxacin was administered as an infusion of 500 mg/h for 1.5 h (total dose, 750 mg). For patients with Pseudomonas aeruginosa or methicillin-resistant Staphylococcus aureus, a second drug was added (ceftazidime or piperacillin/tazobactam for P. aeruginosa and vancomycin for methicillin-resistant S. aureus). Population pharmacokinetic studies of 58 patients demonstrated that this population handled the drug differently from populations of volunteers. Multivariate logistic regression analysis (n = 47 patients) demonstrated that only the age of the patient and the achievement of an area under the curve:minimum inhibitory concentration ratio of greater than or equal to87 had a significant effect on eradication of the pathogen (P<.001). Achieving the breakpoint made the patient 4 times more likely to achieve eradication. The effect was greatest in patients >= 67 years old.
机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Chow, AT
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Fowler, C
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RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Fowler, C
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Williams, RR
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RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Williams, RR
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Morgan, N
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RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Morgan, N
;
Kaminski, S
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RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Kaminski, S
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Natarajan, J
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Chow, AT
;
Fowler, C
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Fowler, C
;
Williams, RR
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Williams, RR
;
Morgan, N
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Morgan, N
;
Kaminski, S
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA
Kaminski, S
;
Natarajan, J
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机构:
RW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USARW Johnson Pharmaceut Res Inst, Dept Clin Drug Metab, Raritan, NJ 08869 USA