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Activity of aztreonam-avibactam against Enterobacterales resistant to recently approved beta-lactamase inhibitor combinations collected in Europe, Latin America, and the Asia-Pacific Region (2020-2022).
Sader, Helio S; Carvalhaes, Cecilia G; Kimbrough, John H; Mendes, Rodrigo E; Castanheira, Mariana.
Afiliación
  • Sader HS; JMI Laboratories/Element Materials Technology, North Liberty, IA, USA. Electronic address: helio.sader@element.com.
  • Carvalhaes CG; JMI Laboratories/Element Materials Technology, North Liberty, IA, USA.
  • Kimbrough JH; JMI Laboratories/Element Materials Technology, North Liberty, IA, USA.
  • Mendes RE; JMI Laboratories/Element Materials Technology, North Liberty, IA, USA.
  • Castanheira M; JMI Laboratories/Element Materials Technology, North Liberty, IA, USA.
Int J Antimicrob Agents ; 63(4): 107113, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38354826
ABSTRACT

BACKGROUND:

Aztreonam-avibactam is under clinical development for treatment of infections caused by carbapenem-resistant Enterobacterales (CRE), especially those resistant to recently approved ß-lactamase inhibitor combinations (BLICs).

OBJECTIVES:

To evaluate a large collection of CRE isolates, including those non-susceptible to ceftazidime-avibactam, meropenem-vaborbactam, and/or imipenem-relebactam.

METHODS:

Overall, 24 580 Enterobacterales isolates were consecutively collected (1/patient) in 2020-2022 from 64 medical centres located in Western Europe (W-EU), Eastern Europe (E-EU), Latin America (LATAM), and the Asia-Pacific region (APAC). Of those, 1016 (4.1%) were CRE. Isolates were susceptibility tested by broth microdilution. CRE isolates were screened for carbapenemase genes by whole genome sequencing.

RESULTS:

Aztreonam-avibactam inhibited 99.6% of CREs at ≤8 mg/L. Ceftazidime-avibactam, meropenem-vaborbactam, and imipenem-relebactam were active against 64.6%, 57.4%, and 50.7% of CRE isolates, respectively; most of the non-susceptible isolates carried metallo-beta-lactamases. Aztreonam-avibactam was active against ≥98.9% of isolates non-susceptible to these BLICs. The activity of these BLICs varied by region, with highest susceptibility rates observed in W-EU (76.9% for ceftazidime-avibactam, 72.5% for meropenem-vaborbactam, 63.8% for imipenem-relebactam) and the lowest susceptibility rates identified in the APAC region (39.9% for ceftazidime-avibactam, 37.8% for meropenem-vaborbactam, and 27.5% for imipenem-relebactam). The most common carbapenemase types overall were KPC (44.6% of CREs), NDM (29.9%), and OXA-48-like (16.0%). KPC predominated in LATAM (64.1% of CREs in the region) and W-EU (61.1%). MBL occurrence was highest in APAC (59.5% of CREs in the region), followed by LATAM (34.0%), E-EU (28.9%), and W-EU (23.6%).

CONCLUSIONS:

Aztreonam-avibactam demonstrated potent activity against CRE isolates resistant to ceftazidime-avibactam, meropenem-vaborbactam, and/or imipenem-relebactam independent of the carbapenemase produced.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Borónicos / Aztreonam / Inhibidores de beta-Lactamasas Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Int J Antimicrob Agents Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Borónicos / Aztreonam / Inhibidores de beta-Lactamasas Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Int J Antimicrob Agents Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos