<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-07-22T09:50:31Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/23320" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/23320</identifier><datestamp>2024-11-29T07:32:42Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16967</setSpec><setSpec>col_20.500.12105_16983</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Montero, Maria M</subfield>
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      <subfield code="a">Domene-Ochoa, Sandra</subfield>
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      <subfield code="a">López-Causapé, Carla</subfield>
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      <subfield code="a">Luque, Sonia</subfield>
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      <subfield code="a">Sorli, Luisa</subfield>
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      <subfield code="a">Campillo, Nuria</subfield>
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      <subfield code="a">Padilla, Eduardo</subfield>
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      <subfield code="a">Prim, Nuria</subfield>
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      <subfield code="a">Ferrer-Alapont, Lorena</subfield>
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      <subfield code="a">Angulo-Brunet, Ariadna</subfield>
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      <subfield code="a">Grau, Santiago</subfield>
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      <subfield code="a">Oliver, Antonio</subfield>
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      <subfield code="a">Horcajada, Juan P</subfield>
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      <subfield code="c">2021-11-12</subfield>
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      <subfield code="a">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 beta-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.</subfield>
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      <subfield code="a">Montero MM, Domene-Ochoa S, Lopez-Causape C, Luque S, Sorli L, Campillo N, et al. Impact of ceftolozane/tazobactam concentrations in continuous infusion against extensively drug-resistant Pseudomonas aeruginosa isolates in a hollow-fiber infection model. Sci Rep. 2021 Nov 12;11(1):22178.</subfield>
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      <subfield code="a">10.1038/s41598-021-01784-4</subfield>
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      <subfield code="a">Scientific Reports</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.13003/19634</subfield>
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      <subfield code="a">Impact of ceftolozane/tazobactam concentrations in continuous infusion against extensively drug-resistant Pseudomonas aeruginosa isolates in a hollow-fiber infection model</subfield>
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