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Therapy of Infections due to Carbapenem-Resistant Gram-Negative Pathogens

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초록

The prevalence of carbapenem-resistant gram-negative bacterial pathogens (CRGNs) has increased dramatically during the last10 years, but the optimal treatment for CRGN infections is not well established due to the relative scarcity of robust clinicaldata. The polymyxins remain the most consistently active agents against CRGNs in vitro. Tigecycline, based on its in vitro antibacterialspectrum, could also be considered as a therapeutic option in the treatment of infections caused by certain CRGNs. Other agents, including aminoglycosides, rifampin, trimethoprim-sulfamethoxazole, fosfomycin and fluoroquinolones, could beconsidered as monotherapy or combination therapy against CRGNs in appropriate contexts, as combination therapy with twoor more in vitro active drugs appears to be more effective than monotherapy based on some clinical data. Several promisingnew agents are in late-stage clinical development, including ceftolozane-tazobactam, ceftazidime-avibactam and plazomicin. Given the shortage of adequate treatment options, containment of CRGNs should be pursued through implementation of adequateinfection prevention procedures and antimicrobial stewardship to reduce the disease burden and prevent future outbreaksof CRGNs.

Abstract

The prevalence of carbapenem-resistant gram-negative bacterial pathogens (CRGNs) has increased dramatically during the last10 years, but the optimal treatment for CRGN infections is not well established due to the relative scarcity of robust clinicaldata. The polymyxins remain the most consistently active agents against CRGNs in vitro. Tigecycline, based on its in vitro antibacterialspectrum, could also be considered as a therapeutic option in the treatment of infections caused by certain CRGNs. Other agents, including aminoglycosides, rifampin, trimethoprim-sulfamethoxazole, fosfomycin and fluoroquinolones, could beconsidered as monotherapy or combination therapy against CRGNs in appropriate contexts, as combination therapy with twoor more in vitro active drugs appears to be more effective than monotherapy based on some clinical data. Several promisingnew agents are in late-stage clinical development, including ceftolozane-tazobactam, ceftazidime-avibactam and plazomicin. Given the shortage of adequate treatment options, containment of CRGNs should be pursued through implementation of adequateinfection prevention procedures and antimicrobial stewardship to reduce the disease burden and prevent future outbreaksof CRGNs.

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