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pubmed-article:19854590pubmed:abstractTextThe aims of this multicentre open-label study was to evaluate the pharmacokinetics of linezolid in patients with burn injury above 20 % BSA and to compare them with healthy volunteers, matched in age, sex and weight. After a single 600 mg IV dose of linezolid, multiple blood and urine samples were taken from subjects, in order to determine linezolid concentrations, using a HPLC assay. C(max) and volume of distribution at steady state were not different between the two groups. Values describing clearance were altered in burns, leading to a reduction by half in AUC in these patients (42.5 versus 98.1 mghL(-1)). The enhancement of clearance was due to which of non renal clearance (323+/-191 versus 80.4+/-27.5 mLmin(-1)). We conclude that pharmacokinetics of linezolid are altered in burn patients, in a magnitude sufficient that linezolid concentration may be subtherapeutic in some patients and we suggest that the dosage interval may need to be decreased in this patient population.lld:pubmed
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pubmed-article:19854590pubmed:authorpubmed-author:BretPPlld:pubmed
pubmed-article:19854590pubmed:authorpubmed-author:Le FlochRRlld:pubmed
pubmed-article:19854590pubmed:authorpubmed-author:LoveringA MAMlld:pubmed
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pubmed-article:19854590pubmed:authorpubmed-author:HovsepianLLlld:pubmed
pubmed-article:19854590pubmed:copyrightInfoCopyright 2009 Elsevier Masson SAS. All rights reserved.lld:pubmed
pubmed-article:19854590pubmed:issnTypeElectroniclld:pubmed
pubmed-article:19854590pubmed:volume58lld:pubmed
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pubmed-article:19854590pubmed:paginatione27-31lld:pubmed
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pubmed-article:19854590pubmed:year2010lld:pubmed
pubmed-article:19854590pubmed:articleTitle[Pharmacokinetic evaluation of linezolid in patients with major thermal injuries].lld:pubmed
pubmed-article:19854590pubmed:affiliationCentre de traitement des brûlés, CHU de Nantes, 44093 Nantes cedex 1, France. ronan.lefloch@chu-nantes.frlld:pubmed
pubmed-article:19854590pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19854590pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:19854590pubmed:publicationTypeControlled Clinical Triallld:pubmed
pubmed-article:19854590pubmed:publicationTypeMulticenter Studylld:pubmed