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Plasma and lung concentrations of ceftazidime administered in continuous infusion to critically ill patients with severe nosocomial pneumonia
Authors:Emmanuel?Boselli  author-information"  >  author-information__contact u-icon-before"  >  mailto:emmanuel.boselli@chu-lyon.fr"   title="  emmanuel.boselli@chu-lyon.fr"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Dominique?Breilh,Thomas?Rimmelé,Jean-Charles?Poupelin,Marie-Claude?Saux,Dominique?Chassard,Bernard?Allaouchiche
Affiliation:(1) Department of Anesthesiology and Intensive Care, Hôtel-Dieu, 1 Place de l"rsquo"Hôpital, 69288 Lyon cedex 02, France;(2) Clinical Pharmacokinetic Laboratory, Haut-Lévêque Hospital, University of Bordeaux II, Bordeaux, France;(3) Department of Anesthesiology and Intensive Care, Edouard Herriot Hospital, Lyon, France
Abstract:Objective To determine the steady-state plasma and epithelial lining fluid (ELF) concentrations of ceftazidime administered in continuous infusion to critically ill patients with severe nosocomial pneumonia.Design Prospective, open-label study.Setting An intensive care unit and research ward in a university hospital.Patients A total of 15 adult patients with severe nosocomial bacterial pneumonia on mechanical ventilation were enrolled.Interventions All subjects received a 30 min intravenous infusion of 2 g ceftazidime followed by a continuous infusion of 4 g over 24 h. The concentrations of ceftazidime in plasma and ELF were determined at steady-state after 2 days of therapy by high performance liquid chromatography.Measurements and main results The mean ±SD steady-state plasma and ELF concentrations of 4 g ceftazidime in continuous infusion were 39.6±15.2 µg/mL and 8.2±4.8 µg/mL, respectively, showing a mean ±SD percentage penetration of ceftazidime into ELF of 20.6±8.9%.Conclusion The administration of 4 g ceftazidime in continuous infusion in critically ill patients with severe nosocomial pneumonia provides concentrations in excess of the minimal inhibitory concentration of many susceptible organisms over the course of therapy both in serum and ELF. However, for some pathogens such as P. aeruginosa, higher doses of ceftazidime should be administered, or another agent should be used in combination.
Keywords:Ceftazidime  Lung diffusion  Continuous infusion  Intensive care  Nosocomial pneumonia  Ventilator-associated pneumonia
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