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               <dc:title>Impact of ceftolozane/tazobactam concentrations in continuous infusion against extensively drug-resistant Pseudomonas aeruginosa isolates in a hollow-fiber infection model</dc:title>
               <dc:creator>Montero, María M.</dc:creator>
               <dc:creator>Domene-Ochoa, Sandra</dc:creator>
               <dc:creator>López-Causapé, Carla</dc:creator>
               <dc:creator>Luque, Sonia</dc:creator>
               <dc:creator>Sorlí, Luisa</dc:creator>
               <dc:creator>Campillo, Núria</dc:creator>
               <dc:creator>Padilla León, Eduardo</dc:creator>
               <dc:creator>Prim, Núria</dc:creator>
               <dc:creator>Ferrer-Alapont, Lorena</dc:creator>
               <dc:creator>Angulo-Brunet, Ariadna</dc:creator>
               <dc:creator>Grau, Santiago</dc:creator>
               <dc:creator>Oliver, Antonio</dc:creator>
               <dc:creator>Horcajada, Juan Pablo</dc:creator>
               <dc:creator>Universitat Autònoma de Barcelona</dc:creator>
               <dc:subject>Antimicrobials</dc:subject>
               <dc:subject>Bacteria</dc:subject>
               <dc:description>Ceftolozane/tazobactam (C/T) has emerged as a potential agent for the treatment of extensively drug-resistant (XDR) Pseudomonas aeruginosa infections. As it is a time-dependent antimicrobial, prolonged infusion may help achieve pharmacokinetic/pharmacodynamic (PK/PD) targets. To compare alternative steady-state concentrations (Css) of C/T in continuous infusion (CI) against three XDR P. aeruginosa ST175 isolates with C/T minimum inhibitory concentration (MIC) values of 2 to 16 mg/L in a hollow-fiber infection model (HFIM). Duplicate 10-day HFIM assays were performed to evaluate Css of C/T in CI: one compared 20 and 45 mg/L against the C/T-susceptible isolate while the other compared 45 and 80 mg/L against the two C/T-non-susceptible isolates. C/T resistance emerged when C/T-susceptible isolate was treated with C/T in CI at a Css of 20 mg/L; which showed a deletion in the gene encoding AmpC β-lactamase. The higher dosing regimen (80 mg/L) showed a slight advantage in effectiveness. The higher dosing regimen has the greatest bactericidal effect, regardless of C/T MIC. Exposure to the suboptimal Css of 20 mg/L led to the emergence of C/T resistance in the susceptible isolate. Antimicrobial regimens should be optimized through C/T levels monitoring and dose adjustments to improve clinical management.</dc:description>
               <dc:date>2024-11-04T06:40:39Z</dc:date>
               <dc:date>2024-11-04T06:40:39Z</dc:date>
               <dc:date>2021</dc:date>
               <dc:type>Article</dc:type>
               <dc:identifier>http://hdl.handle.net/2072/471328</dc:identifier>
               <dc:relation>Ministerio de Economía y Competitividad PI16/00669</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI17/00251</dc:relation>
               <dc:relation>Scientific reports ; Vol. 11 (november 2021)</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
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