In vitro activity of ceftolozane-tazobactam and ceftazidime-avibactam against Pseudomonas aeruginosa isolated from patients with cystic fibrosis

Pseudomonas aeruginosa is a commonly isolated pathogen in adults with cystic fibrosis (CF). Antimicrobial resistance is an escalating problem due to chronic colonization and frequent antimicrobial exposure. Ceftolozane-tazobactam (C/T) and ceftazidime-avibactam (CZA) exhibit promising activity again...

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Veröffentlicht in:Diagnostic microbiology and infectious disease 2021-02, Vol.99 (2), p.115204-115204, Article 115204
Hauptverfasser: Nolan, Patrick J., Jain, Raksha, Cohen, Leah, Finklea, James D., Smith, Tiffeny T.
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Sprache:eng
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Zusammenfassung:Pseudomonas aeruginosa is a commonly isolated pathogen in adults with cystic fibrosis (CF). Antimicrobial resistance is an escalating problem due to chronic colonization and frequent antimicrobial exposure. Ceftolozane-tazobactam (C/T) and ceftazidime-avibactam (CZA) exhibit promising activity against antimicrobial resistant organisms, including P. aeruginosa. A retrospective review was conducted comparing the in vitro activities of C/T and CZA against 42 P. aeruginosa isolates from the respiratory tract of 32 adults with CF. The first isolate per patient per year that underwent susceptibility testing for C/T, CZA, and colistin was included. C/T was more susceptible than CZA (60% versus 43%). Thirty-eight (90%) isolates were considered highly drug resistant and demonstrated higher C/T susceptibilities compared to CZA (55% versus 45%). These results suggest using C/T while awaiting susceptibilities when standard antipseudomonal agents cannot be used. •P. aeruginosa is commonly isolated in lungs of adults with cystic fibrosis.•Ceftolozane-tazobactam and ceftazidime-avibactam are antipseudomonal agents.•Direct comparison of agents in vitro respiratory cultures against P. aeruginosa.•Susceptibility to ceftolozane-tazobactam was higher against P. aeruginosa.•The MIC50 for C/T was 2-fold lower than CZA.
ISSN:0732-8893
1879-0070
DOI:10.1016/j.diagmicrobio.2020.115204