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Which non-carbapenem antibiotics are active against extended-spectrum ß-lactamase-producing Enterobacteriaceae?
Bouxom, Hélène; Fournier, Damien; Bouiller, Kevin; Hocquet, Didier; Bertrand, Xavier.
Affiliation
  • Bouxom H; Hygiène Hospitalière, Centre Hospitalier Régional Universitaire, Besançon, France.
  • Fournier D; Bactériologie, Centre Hospitalier Régional Universitaire, Besançon, France; UMR 6249 Chrono-environnement, Université de Bourgogne-Franche-Comté, Besançon, France.
  • Bouiller K; UMR 6249 Chrono-environnement, Université de Bourgogne-Franche-Comté, Besançon, France; Maladies infectieuses et tropicales, Centre Hospitalier Régional Universitaire, Besançon, France.
  • Hocquet D; Hygiène Hospitalière, Centre Hospitalier Régional Universitaire, Besançon, France; UMR 6249 Chrono-environnement, Université de Bourgogne-Franche-Comté, Besançon, France; Centre de ressources biologiques-Filière microbiologique de Besançon, Centre Hospitalier Régional Universitaire, Besançon, France
  • Bertrand X; Hygiène Hospitalière, Centre Hospitalier Régional Universitaire, Besançon, France; UMR 6249 Chrono-environnement, Université de Bourgogne-Franche-Comté, Besançon, France. Electronic address: xbertrand@chu-besancon.fr.
Int J Antimicrob Agents ; 52(1): 100-103, 2018 Jul.
Article in En | MEDLINE | ID: mdl-29580930
ABSTRACT
In this study, the activity of 18 non-carbapenem antibiotics was evaluated against 100 extended-spectrum ß-lactamase (ESBL)-producing Escherichia coli (ESBL-Ec) and 50 ESBL-producing Klebsiella pneumoniae (ESBL-Kp) isolated from urinary tract infections and bacteraemia in 2016. Minimum inhibitory concentrations (MICs) were determined using reference methods and the susceptibility profiles were defined according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) 2017 recommendations. All of the ESBL-Ec isolates were susceptible to ceftazidime/avibactam and a great majority of them were susceptible to fosfomycin (98%), piperacillin/tazobactam (97%), amikacin (97%) and nitrofurantoin (96%). Mecillinam, cefoxitin and ceftolozane/tazobactam remained active against 92%, 83% and 78% of the ESBL-Ec isolates, respectively. Moreover, 100%, 94% and 90% of the ESBL-Kp tested were susceptible to ceftazidime/avibactam, amikacin and mecillinam, respectively. This study showed that there are non-carbapenem options (including orally administrable drugs) for the treatment of all of the situations of ESBL-Ec or ESBL-Kp infections, with ceftazidime/avibactam being the most efficient alternative.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Lactamases / Enterobacteriaceae / Anti-Bacterial Agents Type of study: Guideline Limits: Humans Language: En Journal: Int J Antimicrob Agents Year: 2018 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Lactamases / Enterobacteriaceae / Anti-Bacterial Agents Type of study: Guideline Limits: Humans Language: En Journal: Int J Antimicrob Agents Year: 2018 Document type: Article Affiliation country:
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