Intravenous versus nebulized ceftazidime in ventilated piglets with and without experimental bronchopneumonia: Comparative effects of helium and nitrogen
dc.contributor.author | Tonnellier, Marc | |
dc.contributor.author | Ferrari, Fabio | |
dc.contributor.author | Goldstein, Ivan | |
dc.contributor.author | Sartorius, Alfonso | |
dc.contributor.author | Marquette, Charles-Hugo | |
dc.contributor.author | Rouby, Jean-Jacques | |
dc.contributor.institution | University of Paris VI | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | University of Lille | |
dc.contributor.institution | Hopital de la Pitie-Salpetriere | |
dc.date.accessioned | 2014-05-27T11:21:19Z | |
dc.date.available | 2014-05-27T11:21:19Z | |
dc.date.issued | 2005-05-01 | |
dc.description.abstract | Background: Lung deposition of intravenous cephalosporins is low. The lung deposition of equivalent doses of ceftazidime administered either intravenously or by ultrasonic nebulization using either nitrogen-oxygen or helium-oxygen as the carrying gas of the aerosol was compared in ventilated piglets with and without experimental bronchopneumonia. Methods: Five piglets with noninfected lungs and 5 piglets with Pseudomonas aeruginosa experimental bronchopneumonia received 33 mg/kg ceftazidime intravenously. Ten piglets with noninfected lungs and 10 others with experimental P. aeruginosa bronchopneumonia received 50 mg/kg ceftazidime by ultrasonic nebulization. In each group, the ventilator was operated in half of the animals with a 65%/35% helium-oxygen or nitrogen-oxygen mixture. Animals were killed, and multiple lung specimens were sampled for measuring ceftazidime lung tissue concentrations by high-performance liquid chromatography. Results: As compared with intravenous administration, nebulization of ceftazidime significantly increased lung tissue concentrations (17 ± 13 vs. 383 ± 84 μg/g in noninfected piglets and 10 ± 3 vs. 129 ± 108 μg/g in piglets with experimental bronchopneumonia; P < 0.001). The use of a 65%/35% helium-oxygen mixture induced a 33% additional increase in lung tissue concentrations in noninfected piglets (576 ± 141 μg/g; P < 0.001) and no significant change in infected piglets (111 ± 104 μg/g). Conclusion: Nebulization of ceftazidime induced a 5- to 30-fold increase in lung tissue concentrations as compared with intravenous administration. Using a helium-oxygen mixture as the carrying gas of the aerosol induced a substantial additional increase in lung deposition in noninfected piglets but not in piglets with experimental bronchopneumonia. © 2005 American Society of Anesthesiologists, Inc. Lippincott Williams & Wilkins, Inc. | en |
dc.description.affiliation | Reanimation Chir. Pierre Viars Departement d' Anesthesie Hop. de la Pitie-Salpetriere, Botucatu | |
dc.description.affiliation | Departement d' Anesthésie Hopital de la Pitie-Salpetriere University of Paris VI, Paris | |
dc.description.affiliation | Department of Anesthesiology Fac. Med. Univ. Estadual J. D. M. F., Botucatu | |
dc.description.affiliation | Department of Pneumology University of Lille | |
dc.description.affiliation | Reanimation Chir. Pierre Viars Hopital de la Pitie-Salpetriere, 47-83 boulevard de l'hôpital, 75013 Paris | |
dc.format.extent | 995-1000 | |
dc.identifier | http://dx.doi.org/10.1097/00000542-200505000-00019 | |
dc.identifier.citation | Anesthesiology, v. 102, n. 5, p. 995-1000, 2005. | |
dc.identifier.doi | 10.1097/00000542-200505000-00019 | |
dc.identifier.issn | 0003-3022 | |
dc.identifier.scopus | 2-s2.0-17844393121 | |
dc.identifier.uri | http://hdl.handle.net/11449/68212 | |
dc.language.iso | eng | |
dc.relation.ispartof | Anesthesiology | |
dc.relation.ispartofjcr | 6.523 | |
dc.relation.ispartofsjr | 2,123 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Scopus | |
dc.subject | ceftazidime | |
dc.subject | cephalosporin derivative | |
dc.subject | drug carrier | |
dc.subject | helium | |
dc.subject | nitrogen | |
dc.subject | oxygen | |
dc.subject | aerosol | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | artificial ventilation | |
dc.subject | bronchopneumonia | |
dc.subject | controlled study | |
dc.subject | drug administration route | |
dc.subject | drug delivery system | |
dc.subject | drug distribution | |
dc.subject | drug penetration | |
dc.subject | drug tissue level | |
dc.subject | experimental model | |
dc.subject | high performance liquid chromatography | |
dc.subject | nebulization | |
dc.subject | nonhuman | |
dc.subject | particle size | |
dc.subject | priority journal | |
dc.subject | Pseudomonas aeruginosa | |
dc.subject | swine | |
dc.subject | tissue distribution | |
dc.subject | ultrasound | |
dc.subject | Administration, Inhalation | |
dc.subject | Animals | |
dc.subject | Blood Gas Analysis | |
dc.subject | Bronchopneumonia | |
dc.subject | Ceftazidime | |
dc.subject | Cephalosporins | |
dc.subject | Escherichia coli Infections | |
dc.subject | Helium | |
dc.subject | Injections, Intravenous | |
dc.subject | Lung | |
dc.subject | Nebulizers and Vaporizers | |
dc.subject | Oxygen | |
dc.subject | Particle Size | |
dc.subject | Respiration, Artificial | |
dc.subject | Respiratory Mechanics | |
dc.subject | Swine | |
dc.subject | Ultrasonics | |
dc.title | Intravenous versus nebulized ceftazidime in ventilated piglets with and without experimental bronchopneumonia: Comparative effects of helium and nitrogen | en |
dc.type | Artigo | |
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