Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Dec;44(12):927-938.
doi: 10.1002/phar.4629. Epub 2024 Nov 27.

Aztreonam-avibactam: The dynamic duo against multidrug-resistant gram-negative pathogens

Affiliations
Review

Aztreonam-avibactam: The dynamic duo against multidrug-resistant gram-negative pathogens

Mohammed Al Musawa et al. Pharmacotherapy. 2024 Dec.

Abstract

Antimicrobial resistance poses a significant public health challenge, particularly with the rise of gram-negative hospital-acquired infections resistant to carbapenems. Aztreonam-avibactam (ATM-AVI) is a promising new combination therapy designed to combat multidrug-resistant (MDR) gram-negative bacteria, including those producing metallo-β-lactamases (MBLs). Aztreonam, a monobactam antibiotic, is resistant to hydrolysis by MBLs but can be degraded by other β-lactamases. Avibactam, a novel non-β-lactam β-lactamase inhibitor, effectively neutralizes extended-spectrum β-lactamases (ESBLs) and AmpC β-lactamases, restoring aztreonam's efficacy against resistant pathogens. This review covers the chemistry, mechanisms of action, spectrum of activity, pharmacokinetics, pharmacodynamics, and clinical efficacy of ATM-AVI. ATM-AVI combination has shown efficacy against a wide range of resistant Enterobacterales and other gram-negative bacteria in both in vitro and clinical studies. Pharmacokinetic and pharmacodynamic analyses demonstrate that ATM-AVI maintains effective drug concentrations in the body, with dose adjustments recommended for patients with renal impairment. Clinical trials, including the REVISIT and ASSEMBLE studies, have demonstrated the safety and efficacy of ATM-AVI in treating complicated intra-abdominal infections (cIAI), urinary tract infections (UTIs), and hospital-acquired pneumonia (HAP) caused by MDR gram-negative pathogens. The European Medicines Agency (EMA) has approved ATM-AVI for these indications, and further research is ongoing to optimize dosing regimens and expand its clinical use. This combination represents a critical advancement in the fight against antimicrobial resistance, offering a new therapeutic option for treating severe infections caused by MDR gram-negative, including MBL-producing, bacteria.

Keywords: Enterobacterales; antimicrobial resistance; avibactam; aztreonam; carbapenemase; gram‐negative bacteria; metallo‐β‐lactamase; monobactam.

PubMed Disclaimer

Conflict of interest statement

Michael J. Rybak has received grant support, consulted, or has participated on a speaker bureau for AbbVie, Innoviva, Melinta, Merck, and Shionogi. All other authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Aztreonam chemical structure.
FIGURE 2
FIGURE 2
Avibactam chemical structure.

Similar articles

Cited by

References

    1. Centers for Disease Control and Prevention (U.S.) . Antibiotic resistance threats in the United States, 2019. Centers for Disease Control and Prevention (U.S.); 2019. doi:10.15620/cdc:82532 - DOI
    1. COVID‐19: U.S . Impact on antimicrobial resistance, special report 2022. National Center for emerging and zoonotic. Infect Dis. 2022. doi:10.15620/cdc:117915 - DOI
    1. Global Antimicrobial Resistance and Use Surveillance System (GLASS) Report 2022. World Health Organization; 2022. Licence: CC BY‐NC‐SA 3.0 IGO.
    1. Bush K. Past and present perspectives on β‐lactamases. Antimicrob Agents Chemother. 2018;62(10):e01076. doi:10.1128/AAC.01076-18 - DOI - PMC - PubMed
    1. Bush K, Bradford PA. Interplay between β‐lactamases and new β‐lactamase inhibitors. Nat Rev Microbiol. 2019;17(5):295‐306. doi:10.1038/s41579-019-0159-8 - DOI - PubMed

MeSH terms