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Clinical Investigations: COPD |

Pharmacodynamics of Levofloxacin in Patients With Acute Exacerbation of Chronic Bronchitis*

Mario Cazzola, MD, FCCP; Maria Gabriella Matera, MD, PhD; Giovanna Donnarumma, MD; Maria Antonietta Tufano, MD; Alessandro Sanduzzi, MD; Federico Marchetti, BSc; Francesco Blasi, MD
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*From the Department of Pneumology (Dr. Cazzola), Unit of Pneumology and Allergology, A. Cardarelli Hospital, Naples; Department Experimental Medicine, Units of Pharmacology (Dr. Matera) and Microbiology (Drs. Donnarumma and Tufano), Second University, Naples; Department of Cardiovascular and Respiratory Sciences (Dr. Sanduzzi), Unit of Pneumology, University Federico II, Naples; Medical Department (Mr. Marchetti), GlaxoSmithKline S.p.A., Verona; and Institute of Respiratory Medicine (Dr. Blasi), Polyclinic Hospital, Institute of Care and Research, University of Milan, Milan, Italy.

Correspondence to: Mario Cazzola, MD, FCCP, Via del Parco Margherita 24, 80121 Napoli, Italy; e-mail mcazzola@qubisoft.it



Chest. 2005;128(4):2093-2098. doi:10.1378/chest.128.4.2093
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Study objectives: Levofloxacin is a fluoroquinolone antimicrobial agent for which pharmacodynamic relationships between the maximum serum antibiotic concentration (Cmax)/minimum inhibitory concentration (MIC) ratio and/or the area under the serum concentration-time curve during a 24-h dosing period (AUC0–24)/MIC ratio and clinical and/or microbiological outcomes have been developed. In this study we examined the relationship between the in vitro bacterial susceptibility to levofloxacin, the achieved levofloxacin serum and sputum concentrations, and the in vivo bacterial eradication in patients with acute exacerbations of chronic bronchitis.

Patients and interventions: Thirty patients received levofloxacin, 500 mg/d po for 7 days. Samples of venous blood and sputum for the determination of levofloxacin concentrations were collected on day 1 immediately prior to dosing, and then at 1, 4, 8, 12, and 24 h.

Results: The mean peak concentration in serum (6.5 mg/L) was found 1 h after administration, and at 4 h after administration in sputum (5.1 mg/L). Levofloxacin was always detectable 24 h after administration from both samples. Successful treatment occurred in 90% (27 of 30 patients) when assessed both clinically and bacteriologically. Treatment was successful in eight patients when the AUC0–24/MIC ratio was > 40 for serum, and in nine patients when it was > 30 for sputum. Treatment was also successful in seven patients when the Cmax/MIC ratio was > 5.01 for serum, and in nine patients when the Cmax/MIC ratio was > 4.01 for sputum. Treatment was successful in 90% (27 of 30 patients) when the AUC0–24/MIC ratio was > 125 for serum and > 100 for sputum, and when Cmax/MIC was > 10.01 for serum and > 8.01 for sputum following the first dose.

Conclusions: The pharmacodynamics values that we have obtained in sputum with levofloxacin may be used as predictors of therapy outcomes.

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