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DOI 10.1016/j.diagmicrobio.2024.116235

Медицинская библиотека · Diagnostic microbiology and infectious disease · 2024

In vitro activity of ceftazidime-avibactam against gram-negative bacteria in patients with bacteremia and skin and soft-tissue infections in Colombia 2019-2021.

Lemos-Luengas Elkin Vladimir, Rentería-Valoyes Sixta, Muñoz Diana Marcela Almario, Gonzalez Cinthya Katherine Galindo, Guerrón-Gómez Gabriela, Ramos-Castaneda Jorge Andres

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Аннотация

OBJECTIVES

Ceftazidime-avibactam (CAZ-AVI) is an option for infections caused by MDR gram-negative bacilli. In this study, we aimed to analyze the in vitro antimicrobial activity of CAZ-AVI and other antimicrobial agents against gram-negative bacilli that were collected in Colombia between 2019 and 2021 from patients with bacteremia and skin and soft-tissue infections (SSTIs).

METHODS

A total of 600 Enterobacterales and 259 P. aeruginosa strains were analyzed. The phenotypic resistance of isolates, particularly non-susceptibility to meropenem, multidrug-resistant (MDR) isolates, and difficult-to-treat (DTR) P. aeruginosa, was evaluated according to CLSI breakpoints.

RESULTS

Enterobacterales had the most susceptibility to CAZ-AVI (96.5 %) and tigecycline (95 %). Tigecycline and CAZ-AVI were the antimicrobial agents with the most in vitro activity against carbapenem-resistant Enterobacterales (CRE). CAZ-AVI was the antimicrobial treatment with the most activity against P. aeruginosa.

CONCLUSIONS

Tigecycline and CAZ-AVI were the antimicrobial agents with the most activity against CRE and MDR Enterobacterales. For P. aeruginosa, CAZ-AVI was the antimicrobial treatment with the most in vitro activity.

Для цитирования: Lemos-Luengas Elkin Vladimir, Rentería-Valoyes Sixta, Muñoz Diana Marcela Almario, Gonzalez Cinthya Katherine Galindo, Guerrón-Gómez Gabriela, Ramos-Castaneda Jorge Andres. In vitro activity of ceftazidime-avibactam against gram-negative bacteria in patients with bacteremia and skin and soft-tissue infections in Colombia 2019-2021.. Diagnostic microbiology and infectious disease. 2024. DOI: 10.1016/j.diagmicrobio.2024.116235.

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