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In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019

Cefiderocol was evaluated by broth microdilution versus 1,050 highly antimicrobial-resistant Pseudomonas aeruginosa clinical isolates from the CANWARD study (2007 to 2019). Overall, 98.3% of isolates remained cefiderocol susceptible (MIC, ≤4 μg/mL), including 97.4% of extensively drug-resistant (XDR...

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Autores principales: Karlowsky, James A., Walkty, Andrew J., Baxter, Melanie R., Adam, Heather J., Lagacé-Wiens, Philippe R. S., Schweizer, Frank, Bay, Denice, Lynch, Joseph P., Mulvey, Michael R., Zhanel, George G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430561/
https://www.ncbi.nlm.nih.gov/pubmed/35758747
http://dx.doi.org/10.1128/spectrum.01724-22
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author Karlowsky, James A.
Walkty, Andrew J.
Baxter, Melanie R.
Adam, Heather J.
Lagacé-Wiens, Philippe R. S.
Schweizer, Frank
Bay, Denice
Lynch, Joseph P.
Mulvey, Michael R.
Zhanel, George G.
author_facet Karlowsky, James A.
Walkty, Andrew J.
Baxter, Melanie R.
Adam, Heather J.
Lagacé-Wiens, Philippe R. S.
Schweizer, Frank
Bay, Denice
Lynch, Joseph P.
Mulvey, Michael R.
Zhanel, George G.
author_sort Karlowsky, James A.
collection PubMed
description Cefiderocol was evaluated by broth microdilution versus 1,050 highly antimicrobial-resistant Pseudomonas aeruginosa clinical isolates from the CANWARD study (2007 to 2019). Overall, 98.3% of isolates remained cefiderocol susceptible (MIC, ≤4 μg/mL), including 97.4% of extensively drug-resistant (XDR) (n = 235) and 97.9% of multidrug-resistant (MDR) (n = 771) isolates. Most isolates testing not susceptible to ceftolozane-tazobactam, ceftazidime-avibactam, and imipenem-relebactam remained susceptible to cefiderocol. In vitro data suggest that cefiderocol may be a treatment option for infections caused by MDR and XDR P. aeruginosa. IMPORTANCE After testing cefiderocol against a large collection of clinical isolates of highly antimicrobial-resistant Pseudomonas aeruginosa, we report that cefiderocol is active versus 97.4% of extensively drug-resistant (XDR) and 97.9% of multidrug-resistant (MDR) (n = 771) isolates. These data show that cefiderocol may be a treatment option for infections caused by MDR and XDR P. aeruginosa.
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spelling pubmed-94305612022-09-01 In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019 Karlowsky, James A. Walkty, Andrew J. Baxter, Melanie R. Adam, Heather J. Lagacé-Wiens, Philippe R. S. Schweizer, Frank Bay, Denice Lynch, Joseph P. Mulvey, Michael R. Zhanel, George G. Microbiol Spectr Observation Cefiderocol was evaluated by broth microdilution versus 1,050 highly antimicrobial-resistant Pseudomonas aeruginosa clinical isolates from the CANWARD study (2007 to 2019). Overall, 98.3% of isolates remained cefiderocol susceptible (MIC, ≤4 μg/mL), including 97.4% of extensively drug-resistant (XDR) (n = 235) and 97.9% of multidrug-resistant (MDR) (n = 771) isolates. Most isolates testing not susceptible to ceftolozane-tazobactam, ceftazidime-avibactam, and imipenem-relebactam remained susceptible to cefiderocol. In vitro data suggest that cefiderocol may be a treatment option for infections caused by MDR and XDR P. aeruginosa. IMPORTANCE After testing cefiderocol against a large collection of clinical isolates of highly antimicrobial-resistant Pseudomonas aeruginosa, we report that cefiderocol is active versus 97.4% of extensively drug-resistant (XDR) and 97.9% of multidrug-resistant (MDR) (n = 771) isolates. These data show that cefiderocol may be a treatment option for infections caused by MDR and XDR P. aeruginosa. American Society for Microbiology 2022-06-27 /pmc/articles/PMC9430561/ /pubmed/35758747 http://dx.doi.org/10.1128/spectrum.01724-22 Text en Copyright © 2022 Karlowsky et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Observation
Karlowsky, James A.
Walkty, Andrew J.
Baxter, Melanie R.
Adam, Heather J.
Lagacé-Wiens, Philippe R. S.
Schweizer, Frank
Bay, Denice
Lynch, Joseph P.
Mulvey, Michael R.
Zhanel, George G.
In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title_full In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title_fullStr In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title_full_unstemmed In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title_short In Vitro Activity of Cefiderocol against Extensively Drug-Resistant Pseudomonas aeruginosa: CANWARD, 2007 to 2019
title_sort in vitro activity of cefiderocol against extensively drug-resistant pseudomonas aeruginosa: canward, 2007 to 2019
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430561/
https://www.ncbi.nlm.nih.gov/pubmed/35758747
http://dx.doi.org/10.1128/spectrum.01724-22
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