Treatment Options for Carbapenem-resistant Gram-negative Bacterial Infections
- PMID: 31724043
- PMCID: PMC6853760
- DOI: 10.1093/cid/ciz830
Treatment Options for Carbapenem-resistant Gram-negative Bacterial Infections
Abstract
Antimicrobial resistance has become one of the greatest threats to public health, with rising resistance to carbapenems being a particular concern due to the lack of effective and safe alternative treatment options. Carbapenem-resistant gram-negative bacteria of clinical relevance include the Enterobacteriaceae, Pseudomonas aeruginosa, Acinetobacter baumannii, and more recently, Stenotrophomonas maltophilia. Colistin and tigecycline have been used as first-line agents for the treatment of infections caused by these pathogens; however, there are uncertainties regarding their efficacy even when used in combination with other agents. More recently, several new agents with activity against certain carbapenem-resistant pathogens have been approved for clinical use or are reaching late-stage clinical development. They include ceftazidime-avibactam, ceftolozane-tazobactam, meropenem-vaborbactam, imipenem-cilastatin-relebactam, plazomicin, eravacycline, and cefiderocol. In addition, fosfomycin has been redeveloped in a new intravenous formulation. Data regarding the clinical efficacy of these new agents specific to infections caused by carbapenem-resistant pathogens are slowly emerging and appear to generally favor newer agents over previous best available therapy. As more treatment options become widely available for carbapenem-resistant gram-negative infections, the role of antimicrobial stewardship will become crucial in ensuring appropriate and rationale use of these new agents.
Keywords: antimicrobial stewardship; carbapenemase; multidrug resistance; rapid diagnostics.
© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.
References
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- World Health Organization. Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics 2017. Available at: https://www.who.int/medicines/publications/WHO-PPL-Short_Summary_25Feb-E.... Accessed 1 February 2019.
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