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Clinical data from studies involving novel antibiotics to treat multidrug-resistant Gram-negative bacterial infections

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ELSEVIER
DOI: 10.1016/j.ijantimicag.2022.106633

Keywords

Antibiotic resistance; beta-lactam-beta-lactamase inhibitor; Clinical trial; Gram-negative bacteria

Funding

  1. Pfizer

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Multidrug-resistant Gram-negative bacteria pose a critical threat to healthcare. New antibiotics and combination therapies, including ceftazidime-avibactam, meropenem-vaborbactam, and ceftolozane-tazobactam, have shown effectiveness in treating these infections.
Multidrug-resistant (MDR) Gram-negative bacteria (GNB) pose a critical threat to global healthcare, worsening outcomes and increasing mortality among infected patients. Carbapenemase- and extended-spectrum beta-lactamase-producing Enterobacterales, as well as carbapenemase-producing Pseudomonas and Acinetobacter spp., are common MDR pathogens. New antibiotics and combinations have been developed to address this threat. Clinical trial findings support several combinations, notably ceftazidime-avibactam (CZA, a cephalosporin-beta-lactamase inhibitor combination), which is effective in treating complicated urinary tract infections (cUTI), complicated intra-abdominal infections and hospital-acquired and ventilator-associated pneumonia caused by GNBs. Other clinically effective combinations include meropenem-vaborbactam (MVB), ceftolozane-tazobactam (C/T) and imipenem-relebactam (I-R). Cefiderocol is a recent siderophore beta-lactam antibiotic that is useful against cUTIs caused by carbapenem-resistant Enterobacterales (CRE) and is stable against many beta-lactamases. Carbapenem-resistant Enterobacterales are a genetically heterogeneous group that vary in different world regions and are a substantial cause of infections, among which Klebsiella pneumoniae are the most common. Susceptible CRE infections can be treated with fluoroquinolones, aminoglycosides or fosfomycin, but alternatives include CZA, MVB, I-R, cefiderocol, tigecycline and eravacycline. Multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa are increasingly common pathogens producing a range of different carbapenemases, and infections are challenging to treat, often requiring novel antibiotics or combinations. Currently, no single agent can treat all MDR-GNB infections, but new beta-lactam-beta-lactamase inhibitor combinations are often effective for different infection sites and, when used appropriately, have the potential to improve outcomes. This article reviews clinical studies investigating novel beta-lactam approaches for treatment of MDR-GNB infections. (c) 2022 Published by Elsevier Ltd.

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