In vivo efficacy & resistance prevention of cefiderocol in combination with ceftazidime/avibactam, ampicillin/sulbactam or meropenem using human-simulated regimens versus Acinetobacter baumannii.
J Antimicrob Chemother
; 78(4): 983-990, 2023 04 03.
Article
em En
| MEDLINE
| ID: mdl-36775993
OBJECTIVE: Evaluate the in vivo efficacy and resistance prevention of cefiderocol in combination with ceftazidime/avibactam, ampicillin/sulbactam and meropenem using human-simulated regimens (HSR) in the murine infection model. METHODS: In total, 15 clinical A. baumannii were assessed: cefiderocol MICs, 2 mg/L (previously developed resistance on therapy), nâ=â3; 8 mg/L, nâ=â2; ≥32 mg/L, nâ=â10 (including VEB and PER-harbouring isolates). Mice received inactive control, cefiderocol, cefiderocolâ+âceftazidime/avibactam (C-CZA), cefiderocolâ+âampicillin/sulbactam (C-SAM) or cefiderocolâ+âmeropenem (C-MEM) HSRs. The mean change in log10 cfu/thigh compared with starting inoculum was assessed. Resistance development on treatment was a >4-fold increase in MIC relative control animals. In vitro activities of combinations were assessed by disc stacking. RESULTS: Against cefiderocol-non-susceptible isolates, combinations produced significant kill with C-CZA -3.75â±â0.37 reduction in log10 cfu/thigh, C-SAM produced -3.55â±â0.50 and C-MEM produced -2.18â±â1.75 relative to baseline. Elevated MICs in cefiderocol treated animals occurred in three out of three isolates with MICs of 2 mg/L. Of these isolates, one developed elevated MICs with C-MEM compared with none treated with C-CZA or C-SAM. Disc stacking with C-CZA or C-SAM returned all isolates to at least the CLSI intermediate breakpoint, which may correlate with in vivo efficacy. CONCLUSIONS: Against cefiderocol-non-susceptible isolates, cefiderocolâ+âceftazidime/avibactam or ampicillin/sulbactam HSR produced in vivo kill against all 12 cefiderocol-non-susceptible isolates. Cefiderocol with ceftazidime/avibactam or ampicillin/sulbactam prevented the development of resistance during treatment against cefiderocol-high-end-susceptible isolates with a propensity for resistance on therapy. These data support the clinical evaluation of cefiderocol with ceftazidime/avibactam or ampicillin/sulbactam against A. baumannii, including multi-drug-resistant isolates.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Ceftazidima
/
Acinetobacter baumannii
Limite:
Animals
/
Humans
Idioma:
En
Revista:
J Antimicrob Chemother
Ano de publicação:
2023
Tipo de documento:
Article
País de afiliação:
Estados Unidos