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In vitro activity of imipenem/relebactam against Gram-negative clinical isolates in two Spanish tertiary hospitals

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REVISTA ESPANOLA DE QUIMIOTERAPIA
卷 34, 期 6, 页码 668-671

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SOCIEDAD ESPANOLA QUIMIOTERAPIA
DOI: 10.37201/req/102.2021

关键词

Imipenem-relebactam; Pseudomonas aeruginosa; Carbapenemresistant; Enterobacterales; Klebsiella pneumoniae carbapenemase; oxacillinase 48; Extended-spectrum beta-lactamase

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The study found that the IMI/REL combination has high activity against bacteria carrying KPC enzymes, while there was no change in activity against P. aeruginosa and A. baumannii strains carrying VIM enzyme. In P. aeruginosa strains without carbapenemase, the MIC for IMI/REL was reduced.
Objetive. The aim of this study was to analyze the activity of the imipenem-relebactam combination (IMI/REL) against a collection of multidrug-resist Enterobacterales, Pseudomonas aeruginosa and Acinetobacter baumannii clinical isolates. Material and methods. The study was conducted in two tertiary hospitals in Spain and included 192 clinical isolates of these 3 genera (139 resistant and 53 susceptible to IMI). The MICs for IMI with and without REL (at a fixed concentration of 4 mg/L) were determined by a standard broth microdilution method according to international recommendations. Results. All IMI-susceptible E. coli strains were also susceptible to IMI/REL. Enterobacterales resistant to IMI due to the production of carbapenemases, the MIC50 and MIC90 decreased from 64/256 with IMI to 8/64 mg/L with IMI/REL. This high activity was principally detected among isolates with KPC enzymes. Enterobacterales with class B carbapenemases, P. aeruginosa carrying VIM carbapenemase and A. baumannii strains showed no changes on IMI MIC50 or MIC90 after adding REL. Among P. aeruginosa strains without carbapenemase the MIC for IMI/REL was reduced between 1 to 5 dilutions. Conclusions. IMI/REL showed high activity against the strains that carry Klebsiella pneumoniae carbapenemase (KPC) and against carbapenem-resistant P. aeruginosa unrelated to the VIM enzyme, mainly AmpC beta lactamase associated with impermeability. Against strains carrying oxacillinase 48 (OXA-48) associated with extended-spectrum beta-lactamase (ESBL), IMI/REL presented activity only slightly better than IMI and had no beneficial effect superior to IMI against A. baumannii.

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