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dc.contributor.authorValero, Ana
dc.contributor.authorIsla Ruiz, Arantxazu ORCID
dc.contributor.authorRodríguez Gascón, Alicia
dc.contributor.authorCalvo, Begoña
dc.contributor.authorCanut, Andrés
dc.contributor.authorSolinis Aspiazu, María Ángeles
dc.date.accessioned2024-01-17T17:46:35Z
dc.date.available2024-01-17T17:46:35Z
dc.date.issued2018-10-11
dc.identifier.citationEnfermedades Infecciosas y Microbiología Clínica 37(6) : 380-386 (2019)es_ES
dc.identifier.issn0213-005X
dc.identifier.urihttp://hdl.handle.net/10810/64069
dc.description.abstractIntroduction: To evaluate the changes in the susceptibility of Pseudomonas aeruginosa overtime (2000–2017) against antimicrobials used in an intensive care unit of a Spanish tertiaryhospital, and to compare them with the antimicrobial activity considering theoretical pharmacoki-netic/pharmacodynamic (PK/PD) criteria. The influence of the method for handling duplicate isolatesto quantify susceptibility rates was also evaluated.Methods: The susceptibility was studied considering the Clinical and Laboratory Standards Institute (CLSI)breakpoints. Monte Carlo simulations were conducted to calculate the cumulative fraction of response(CFR). Linear regression analysis was applied to determine the trends in susceptibility and in the CFR.Results: A significant decrease in the susceptibility to gentamicin and imipenem was observed, and morerecently the highest percentages of susceptible strains were found for amikacin, cephalosporins andpiperacillin/tazobactam (>80%). The probability of success of an empiric treatment or CFR for most of theevaluated antimicrobials was lower than 70% during the last two-year period. Only meropenem providedhigh probabilities (>90%) to achieve the PK/PD target. Cephalosporins provided moderate probabilities(>80%) although for ceftazidime, the highest dose (2 g/8 h) was required. Moreover, a significant decreasein the CFR trend for ciprofloxacin, imipenem and levofloxacin was observed.Conclusions: Both susceptibility rates and CFR values have to be considered together to optimize theantimicrobial dose regimen for clinical making-decisions. They are complementary tools and, theyshould be used jointly in surveillance programmes. In fact, susceptibility data are not always usefulto detect changes in the CFR. No relevant differences were observed among the methods for handlingrepeated isolates.es_ES
dc.description.sponsorshipThis work was supported by the UPV/EHU (PPG17/65,GIU17/032). A Valero thanks Universia Foundation for her grant.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titlePharmacokinetic/pharmacodynamic analysis as a tool for surveillance of the activity of antimicrobials against Pseudomonas aeruginosa strains isolated in critically ill patientses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2018 Elsevier under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)es_ES
dc.relation.publisherversionhttps://www.elsevier.es/es-revista-enfermedades-infecciosas-microbiologia-clinica-28-avance-resumen-pharmacokinetic-pharmacodynamic-analysis-as-tool-for-S0213005X18302970es_ES
dc.identifier.doi10.1016/j.eimc.2018.10.013
dc.departamentoesFarmacia y ciencias de los alimentoses_ES
dc.departamentoeuFarmazia eta elikagaien zientziakes_ES


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© 2018 Elsevier under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Except where otherwise noted, this item's license is described as © 2018 Elsevier under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)