Journal article
Susceptibility trends of ceftolozane/tazobactam and comparators when tested against U.S. gram-negative bacterial surveillance isolates (2012-2018)
Diagnostic microbiology and infectious disease, Vol.100(1), pp.115302-115302
05/2021
DOI: 10.1016/j.diagmicrobio.2020.115302
PMID: 33516987
Abstract
Ceftolozane/tazobactam is an antipseudomonal cephalosporin combined with a β-lactamase inhibitor. Ceftolozane/tazobactam has been approved in >60 countries for treating complicated urinary tract infections, acute pyelonephritis, complicated intra-abdominal infections (with metronidazole), and hospital-acquired pneumonia, including ventilator-associated pneumonia in adults. We analyzed susceptibilities for 35,882 gram-negative isolates collected from patients in 35 US medical centers from 2012 to 2018. The rate of multi-drug resistant Enterobacterales was stable (9.5%-10.1%), while the P. aeruginosa multi-drug resistance rate increased from 15.5% in 2012 to 22.9% in 2018. The carbapenem-resistant Enterobacterales rates varied from 0.9% to 2.2% and extended-spectrum β-lactamase phenotypes increased from 10.5% to 16.8%. The most active drugs against P. aeruginosa were ceftolozane/tazobactam (95.8%-97.5% susceptible) and amikacin (93.9%-98.0%); against Enterobacterales, amikacin (97.9%-98.8%), meropenem (97.7%-98.8%), and ceftolozane/tazobactam (93.3%-95.6%) were the most active. These data suggest that ceftolozane/tazobactam has effective in vitro activity against organisms causing serious gram-negative infections.
Details
- Title: Subtitle
- Susceptibility trends of ceftolozane/tazobactam and comparators when tested against U.S. gram-negative bacterial surveillance isolates (2012-2018)
- Creators
- Dee Shortridge - JMI LaboratoriesCecilia G Carvalhaes - JMI LaboratoriesJennifer M Streit - JMI LaboratoriesRobert K Flamm - JMI Laboratories
- Resource Type
- Journal article
- Publication Details
- Diagnostic microbiology and infectious disease, Vol.100(1), pp.115302-115302
- DOI
- 10.1016/j.diagmicrobio.2020.115302
- PMID
- 33516987
- ISSN
- 0732-8893
- eISSN
- 1879-0070
- Grant note
- DOI: 10.13039/100004334, name: Merck
- Language
- English
- Date published
- 05/2021
- Academic Unit
- Pathology
- Record Identifier
- 9984183991602771
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