Sulbactam-durlobactam: a β-lactam/β-lactamase inhibitor combination targeting Acinetobacter baumannii .
Sarah M McLeodJohn P O'DonnellNavaneeth NarayananJohn P MillsKeith S KayePublished in: Future microbiology (2024)
Sulbactam-durlobactam is a pathogen-targeted β-lactam/β-lactamase inhibitor combination that has been approved by the US FDA for the treatment of hospital-acquired and ventilator-associated bacterial pneumonia caused by susceptible isolates of Acinetobacter baumannii-calcoaceticus complex (ABC) in patients 18 years of age and older. Sulbactam is a penicillin derivative with antibacterial activity against Acinetobacter but is prone to hydrolysis by β-lactamases encoded by contemporary isolates. Durlobactam is a diazabicyclooctane β-lactamase inhibitor with activity against Ambler classes A, C and D serine β-lactamases that restores sulbactam activity both in vitro and in vivo against multidrug-resistant ABC. Sulbactam-durlobactam is a promising alternative therapy for the treatment of serious Acinetobacter infections, which can have high rates of mortality.
Keyphrases
- acinetobacter baumannii
- multidrug resistant
- gram negative
- drug resistant
- klebsiella pneumoniae
- pseudomonas aeruginosa
- escherichia coli
- end stage renal disease
- prognostic factors
- cystic fibrosis
- combination therapy
- genetic diversity
- coronary artery disease
- cardiovascular disease
- peritoneal dialysis
- type diabetes
- community dwelling
- patient reported
- candida albicans