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    <subfield code="a">10.37201/req/007.2023</subfield>
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    <subfield code="2">sideral</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">García-Fernández, Sergio</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Activity of imipenem/relebactam against Enterobacterales and Pseudomonas aeruginosa in Spain. SMART 2016-2020</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2023</subfield>
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    <subfield code="a">Objectives. To determine susceptibility to the novel β-lactam/β-lactamase inhibitor combination imipenem/relebactam in clinical isolates recovered from intra-abdominal (IAI), urinary (UTI), respiratory (RTI) and bloodstream (BSI) infections in the SMART (Study for Monitoring Antimicrobial Resistance Trends) study in SPAIN during 2016 – 2020. Methods. Broth microdilution MICs for imipenem/relebactam and comparators were determined by a central laboratory against isolates of Enterobacterales and Pseudomonas aeruginosa. MICs were interpreted using EUCAST-2021 breakpoints. Results. In total, 5,210 Enterobacterales and 1,418 P. aeruginosa clinical isolates were analyzed. Imipenem/relebactam inhibited 98.8% of Enterobacterales. Distinguishing by source of infection susceptibility was 99.1% in BSI, 99.2% in IAI, 97.9% in RTI, and 99.2% in UTI. Of intensive care unit isolates (ICU) 97.4% were susceptible and of non-ICU isolates 99.2% were susceptible. In Enterobacterales, activity against Class A, Class B and Class D carbapenemases was 96.2%, 15.4% and 73.2%, respectively. In P. aeruginosa, imipenem/relebactam was active in 92.2% of isolates. By source of infection it was 94.8% in BSI, 92.9% in IAI, 91.7% in RTI, and 93.1% in UTI. An 88.7% of ICU isolates and 93.6% of non-ICU isolates were susceptible to imipenem/relebactam. Imipenem/relebactam remained active against P. aeruginosa ceftazidime-resistant (76.3%), cefepime-resistant (73.6%), imipenem-resistant (71.5%) and piperacillin-resistant (78.7%) isolates. Of all multidrug-resistant or difficult-to-treat resistance P. aeruginosa isolates, 75.1% and 46.2%, respectively, were susceptible to imipenem/relebactam. Conclusions. Imipenem/relebactam showed high rates of susceptibility in Enterobacterales and P. aeruginosa isolates from different sources of infection as well as depending on patients’ location (ICU or non-ICU scenarios).</subfield>
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    <subfield code="a">PHARMACOLOGY &amp; PHARMACY</subfield>
    <subfield code="b">231 / 354 = 0.653</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="b">130 / 161 = 0.807</subfield>
    <subfield code="c">2023</subfield>
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    <subfield code="a">Pharmacology</subfield>
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    <subfield code="a">Microbiology (medical)</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Calvo, Jorge</subfield>
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    <subfield code="a">Cercenado, Emilia</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Suárez-Barrenechea, Ana Isabel</subfield>
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    <subfield code="a">Fernández-Billón, María</subfield>
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    <subfield code="a">Castillo, Francisco Javier</subfield>
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    <subfield code="a">Gálvez-Benítez, Lydia</subfield>
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    <subfield code="a">Tubau, Fe</subfield>
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    <subfield code="a">Figueroa Cerón, Ruth Esther</subfield>
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    <subfield code="a">González Romo, Fernando</subfield>
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    <subfield code="a">Fariñas, María Carmen</subfield>
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    <subfield code="a">Gómez, María</subfield>
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    <subfield code="a">Cantón, Rafael</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">36, 3 (2023), 302-309</subfield>
    <subfield code="p">Rev. esp. quimioter.</subfield>
    <subfield code="t">Revista española de quimioterapia</subfield>
    <subfield code="x">0214-3429</subfield>
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