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dc.contributor.authorSoraluce Olañeta, Amaia
dc.contributor.authorBarrasa González, Helena
dc.contributor.authorAsín-Prieto, Eduardo
dc.contributor.authorSánchez Izquierdo, José Ángel
dc.contributor.authorMaynar, Javier
dc.contributor.authorIsla Ruiz, Arantxazu ORCID
dc.contributor.authorRodríguez Gascón, Alicia
dc.date.accessioned2024-02-08T07:55:44Z
dc.date.available2024-02-08T07:55:44Z
dc.date.issued2020-01-09
dc.identifier.citationPharmaceutics 12(1) : (2020) // Article ID 54es_ES
dc.identifier.issn1999-4923
dc.identifier.urihttp://hdl.handle.net/10810/64856
dc.description.abstractAntimicrobial treatment in critically ill patients remains challenging. The aim of this study was to develop a population pharmacokinetic model for linezolid in critically ill patients and to evaluate the adequacy of current dosing recommendation (600 mg/12 h). Forty inpatients were included, 23 of whom were subjected to continuous renal replacement therapies (CRRT). Blood and effluent samples were drawn after linezolid administration at defined time points, and linezolid levels were measured. A population pharmacokinetic model was developed, using NONMEM 7.3. The percentage of patients that achieved the pharmacokinetic/pharmacodynamic (PK/PD) targets was calculated (AUC24/MIC > 80 and 100% T>MIC). A two‐compartment model best described the pharmacokinetics of linezolid. Elimination was conditioned by the creatinine clearance and by the extra‐corporeal clearance if the patient was subjected to CRRT. For most patients, the standard dose of linezolid did not cover infections caused by pathogens with MIC ≥es_ES
dc.description.sponsorshipThis research was funded by Pfizer (012 ASPIRE EUMRSA _ Pharmacokinetic pharmacodynamic study of linezolid in critically ill septic patients undergoing continuous hemodiafiltration) and by the University of the Basque Country UPV/EHU (PPG17/65 and GIU17/32).
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectlinezolides_ES
dc.subjectpopulation pharmacokinetics
dc.subjectcritically ill
dc.subjectcontinuous renal replacement therapies
dc.subjectpharmacokinetic/pharmacodynamics
dc.subjectcontinuous infusion
dc.titleNovel Population Pharmacokinetic Model for Linezolid in Critically Ill Patients and Evaluation of the Adequacy of the Current Dosing Recommendationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
dc.relation.publisherversionhttps://www.mdpi.com/1999-4923/12/1/54
dc.identifier.doi10.3390/pharmaceutics12010054
dc.departamentoesFarmacia y ciencias de los alimentoses_ES
dc.departamentoeuFarmazia eta elikagaien zientziakes_ES


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© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).