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

dc.contributor.authorKanj S.S.
dc.contributor.authorBassetti M.
dc.contributor.authorKiratisin P.
dc.contributor.authorRodrigues C.
dc.contributor.authorVillegas M.V.
dc.contributor.authorYu Y.
dc.contributor.authorvan Duin D.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-20T05:26:35Z
dc.date.available2023-06-20T05:26:35Z
dc.date.issued2022-09-01
dc.description.abstractMultidrug-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 β-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-β-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 β-lactam antibiotic that is useful against cUTIs caused by carbapenem-resistant Enterobacterales (CRE) and is stable against many β-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 β-lactam–β-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 β-lactam approaches for treatment of MDR-GNB infections.
dc.identifier.citationInternational Journal of Antimicrobial Agents Vol.60 No.3 (2022)
dc.identifier.doi10.1016/j.ijantimicag.2022.106633
dc.identifier.eissn18727913
dc.identifier.issn09248579
dc.identifier.pmid35787918
dc.identifier.scopus2-s2.0-85136560271
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/87256
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleClinical data from studies involving novel antibiotics to treat multidrug-resistant Gram-negative bacterial infections
dc.typeReview
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85136560271&origin=inward
oaire.citation.issue3
oaire.citation.titleInternational Journal of Antimicrobial Agents
oaire.citation.volume60
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationSir Run Run Shaw Hospital
oairecerif.author.affiliationIRCCS San Martino Polyclinic Hospital
oairecerif.author.affiliationUniversidad El Bosque
oairecerif.author.affiliationAmerican University of Beirut Medical Center
oairecerif.author.affiliationUniversità degli Studi di Genova
oairecerif.author.affiliationP.D. Hinduja National Hospital and Medical Research Centre
oairecerif.author.affiliationUNC School of Medicine
oairecerif.author.affiliationKey Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province

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