| Literature DB >> 33573148 |
Alexandre Bleibtreu1, Laurent Dortet2,3, Remy A Bonnin2,3, Benjamin Wyplosz4, Sophie-Caroline Sacleux5, Liliana Mihaila2, Hervé Dupont6, Helga Junot7, Vincent Bunel8, Nathalie Grall9,10, Keyvan Razazi11, Clara Duran12, Pierre Tattevin13, Aurélien Dinh12, On Behalf Of The Cefiderocol French Study Group.
Abstract
Cefiderocol is a novel siderophore cephalosporin, which has proven in vitro activity against carbapenem-resistant (CR) Gram-negative pathogens and stability towards all carbapenemases. The aim of this study was to describe the first cases of prescriptions and the efficacy of cefiderocol for compassionate use in the 2 months following its access in France. We performed a national retrospective study of all patients who received at least one dose of cefiderocol from 2 November 2018 to 5 November 2019. We collected clinical characteristics and outcome through a standard questionnaire. Bacterial isolates from 12 patients were centralized and analyzed in the French National Reference Center for Antimicrobial Resistance, and sequenced using Illumina technology. Finally, 13 patients from 7 French university hospitals were included in the study. The main type of infection treated by cefiderocol was respiratory tract infections (RTI, n = 10). The targeted bacteria were Pseudomonas aeruginosa (n = 12), including carbapenemase-producing P. aeruginosa (n = 9), Acinetobacter baumannii (n = 2), Klebsiella pneumoniae (n = 1), and Enterobacter hormaechei (n = 1). Overall, of the 12 patients whose samples were analyzed, 5 P. aeruginosa strains were not susceptible to cefiderocol (4 categorized as resistant and 1 as intermediate) according to Clinical and Laboratory Standards Institute (CLSI) breakpoints. If considering susceptible strains, the cure rate was 6/7, while being 0/5 among not-susceptible strains. This study underlines the necessity to test strains in adequate conditions.Entities:
Keywords: Pseudomonas aeruginosa; bacterial resistance; carbapenem; cefiderocol; respiratory tract infection
Year: 2021 PMID: 33573148 PMCID: PMC7911443 DOI: 10.3390/microorganisms9020282
Source DB: PubMed Journal: Microorganisms ISSN: 2076-2607