Activity of ceftolozane-tazobactam and comparators when tested against Gram-negative isolates collected from paediatric patients in the USA and Europe between 2012 and 2016 as part of a global surveillance programme.


Journal

International journal of antimicrobial agents
ISSN: 1872-7913
Titre abrégé: Int J Antimicrob Agents
Pays: Netherlands
ID NLM: 9111860

Informations de publication

Date de publication:
May 2019
Historique:
received: 22 10 2018
revised: 15 01 2019
accepted: 27 01 2019
pubmed: 5 2 2019
medline: 9 8 2019
entrez: 5 2 2019
Statut: ppublish

Résumé

Ceftolozane-tazobactam is a combination of an antipseudomonal cephalosporin and a β-lactamase inhibitor. Ceftolozane-tazobactam was approved by the US Food and Drug Administration in 2014 and by the European Medicines Agency in 2015 for use in adults to treat complicated urinary tract infections, acute pyelonephritis, and complicated intra-abdominal infections with metronidazole. Studies for paediatric indications are planned. The Programme to Assess Ceftolozane-Tazobactam Susceptibility monitors the resistance of ceftolozane-tazobactam to Gram-negative isolates worldwide. In total, 6240 Gram-negative isolates were collected between 2012 and 2016 from paediatric patients (<18 years old) in 31 US hospitals (4207 isolates) and 48 European hospitals (2033 isolates), and tested for susceptibility (S) to ceftolozane-tazobactam by broth microdilution. Other antibiotics tested included amikacin, colistin and meropenem. The most common infection type in hospitalized paediatric patients was pneumonia (n=2018), followed by urinary tract infection (n=1569) and bloodstream infection (n=1236). In total, 4316 Enterobacteriaceae and 1765 non-enterics were isolated. The most common species were Escherichia coli (n=1919), Pseudomonas aeruginosa (n=1236) and Klebsiella pneumoniae (n=709). In all regions, the three most active antimicrobials against paediatric Enterobacteriaceae isolates were amikacin (99.0%S), meropenem (98.9%S) and ceftolozane-tazobactam (94.6%S). For all P. aeruginosa, colistin (98.9%S) and ceftolozane-tazobactam (97.4%S) were the most active. In conclusion, for all Enterobacteriaceae, ceftolozane-tazobactam was the most potent cephalosporin tested, with only meropenem and colistin having higher susceptibility rates. For P. aeruginosa, ceftolozane-tazobactam was the most potent β-lactam and had a similar susceptibility rate to colistin.

Identifiants

pubmed: 30716448
pii: S0924-8579(19)30022-6
doi: 10.1016/j.ijantimicag.2019.01.015
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cephalosporins 0
beta-Lactamase Inhibitors 0
ceftolozane, tazobactam drug combination 0
Tazobactam SE10G96M8W

Types de publication

Journal Article

Langues

eng

Pagination

637-643

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Dee Shortridge (D)

JMI Laboratories, North Liberty, IA, USA. Electronic address: dee-shortridge@jmilabs.com.

Leonard R Duncan (LR)

JMI Laboratories, North Liberty, IA, USA.

Michael A Pfaller (MA)

JMI Laboratories, North Liberty, IA, USA.

Robert K Flamm (RK)

JMI Laboratories, North Liberty, IA, USA.

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Classifications MeSH