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. 2022 Oct 18;66(10):e0075122.
doi: 10.1128/aac.00751-22. Epub 2022 Sep 14.

Ceftazidime-Avibactam plus Aztreonam for the Treatment of Infections by VIM-Type-Producing Gram-Negative Bacteria

Affiliations

Ceftazidime-Avibactam plus Aztreonam for the Treatment of Infections by VIM-Type-Producing Gram-Negative Bacteria

Abiu Sempere et al. Antimicrob Agents Chemother. .

Abstract

This is a retrospective single-center study of 24 patients who received ceftazidime-avibactam plus aztreonam (CZA/ATM) for the treatment of VIM-type-producing Gram-negative bacillus (GNB) infections. The bacteria isolated were Enterobacterales in 22 patients and Pseudomonas aeruginosa in 2. Sixteen out of 19 isolates showed synergistic activity. Two patients presented clinical failure at day 14, and the 30-day mortality was 17% (4/24). CZA/ATM could be considered an alternative therapy for VIM-type-producing GNB infections.

Keywords: MBL; VIM; aztreonam; ceftazidime-avibactam; metallo-β-lactamase.

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Conflict of interest statement

The authors declare a conflict of interest. I. Los-Arcos has received honoraria for speaking at educational events from MSD and Pfizer and has received travel support from Gilead, Merck and Novartis for scientific purposes. D. Rodriguez-Pardo declares no conflicts of interest in relation to this work. Regarding other activities outside this study, D. Rodriguez-Pardo declares having received honoraria from Pfizer, Angellini, MSD and Astellas as payment for lectures, consultancy tasks and travel/accommodation for scientific purposes. X. Nuvials has received honoraria from MSD, Pfizer, Gilead and Shionogi as payment for speaking at educational events and consultancy tasks. B. Almirante has received honoraria for speaking at educational events from MSD, Pfizer, Gilead Sciences, Shionogi and Angellini and has received research funding from Gilead Sciences, MSD and Pfizer. L. Escolà-Vergé declares no conflicts of interest in relation to this work. Regarding other activities, L. Escolà-Vergé has received travel/accommodation support from Pfizer and MSD for scientific purposes.

The authors declare a conflict of interest. I. Los-Arcos has received honoraria for speaking at educational events from MSD and Pfizer and has received travel support from Gilead, Merck and Novartis for scientific purposes. D. Rodriguez-Pardo declares no conflicts of interest in relation to this work. Regarding other activities outside this study, D. Rodriguez-Pardo declares having received honoraria from Pfizer, Angellini, MSD and Astellas as payment for lectures, consultancy tasks and travel/accommodation for scientific purposes. X.Nuvials has received honoraria from MSD, Pfizer, Gilead and Shionogi as payment for speaking at educational events and consultancy tasks. B. Almirante has received honoraria for speaking at educational events from MSD, Pfizer, Gilead Sciences, Shionogi and Angellini and has received research funding from Gilead Sciences, MSD and Pfizer. L. Escolà-Vergé declares no conflicts of interest in relation to this work. Regarding other activities, L. Escolà-Vergé has received travel/accommodation support from Pfizer and MSD for scientific purposes.

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