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Clavulanate combinations with mecillinam, cefixime or cefpodoxime against ESBL-producing Enterobacterales frequently associated with blaOXA-1 in a paediatric population with febrile urinary tract infections.

Authors :
Birgy, André
Madhi, Fouad
Jung, Camille
Levy, Corinne
Cointe, Aurélie
Bidet, Philippe
Hobson, Claire Amaris
Bechet, Stéphane
Sobral, Elsa
Vuthien, Hoang
Ferroni, Agnès
Aberrane, Saïd
Cuzon, Gaëlle
Beraud, Laetitia
Gajdos, Vincent
Launay, Elise
Pinquier, Didier
Haas, Hervé
Desmarest, Marie
Dommergues, Marie-Aliette
Source :
Journal of Antimicrobial Chemotherapy (JAC). Nov2021, Vol. 76 Issue 11, p2839-2846. 8p.
Publication Year :
2021

Abstract

<bold>Objectives: </bold>Oral treatment of febrile urinary tract infections (FUTIs) can be impaired by MDR Enterobacterales often combining ESBL and inhibitor-resistant genes. We studied the impact of β-lactamases and Enterobacterales' genotypes on the cefixime, cefpodoxime and mecillinam ± amoxicillin/clavulanate MICs.<bold>Materials and Methods: </bold>In this multicentric study, we included 251 previously whole-genome-sequenced ESBL-producing Enterobacterales, isolated in French children with FUTIs. The MICs of cefixime, cefpodoxime, mecillinam alone and combined with amoxicillin/clavulanate were determined and analysed with respect to genomic data. We focused especially on the isolates' ST and their type of β-lactamases. Clinical outcomes of patients who received cefixime + amoxicillin/clavulanate were also analysed.<bold>Results: </bold>All isolates were cefixime and cefpodoxime resistant. Disparities depending on blaCTX-M variants were observed for cefixime. The addition of amoxicillin/clavulanate restored susceptibility for cefixime and cefpodoxime in 97.2% (MIC50/90 of 0.38/0.75 mg/L) and 55.4% (MIC50/90 of 1/2 mg/L) of isolates, respectively, whatever the ST, the blaCTX-M variants or the association with inhibitor-resistant β-lactamases (34.2%). All isolates were susceptible to mecillinam + amoxicillin/clavulanate with MIC50/90 of 0.19/0.25 mg/L, respectively. Neither therapeutic failure nor any subsequent positive control urine culture were reported for patients who received cefixime + amoxicillin/clavulanate as an oral relay therapy (n = 54).<bold>Conclusions: </bold>Despite the frequent association of ESBL genes with inhibitor-resistant β-lactamases, the cefixime + amoxicillin/clavulanate MICs remain low. The in vivo efficacy of this combination was satisfying even when first-line treatment was ineffective. Considering the MIC distributions and pharmacokinetic parameters, mecillinam + amoxicillin/clavulanate should also be an alternative to consider when treating FUTIs in children. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03057453
Volume :
76
Issue :
11
Database :
Academic Search Index
Journal :
Journal of Antimicrobial Chemotherapy (JAC)
Publication Type :
Academic Journal
Accession number :
153717311
Full Text :
https://doi.org/10.1093/jac/dkab289