Novel Beta-Lactamase Inhibitors: Unlocking Their Potential in Therapy

被引:122
作者
Wong, Darren [1 ]
van Duin, David [2 ]
机构
[1] USC, Keck Sch Med, Div Infect Dis, Los Angeles, CA USA
[2] Univ N Carolina, Div Infect Dis, Chapel Hill, NC 27599 USA
关键词
IN-VITRO ACTIVITY; INCLUDING ACUTE PYELONEPHRITIS; URINARY-TRACT-INFECTIONS; EPITHELIAL LINING FLUID; CEFTAZIDIME-AVIBACTAM; PSEUDOMONAS-AERUGINOSA; IMIPENEM-CILASTATIN; ANAEROBIC-BACTERIA; PLUS METRONIDAZOLE; DOUBLE-BLIND;
D O I
10.1007/s40265-017-0725-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Carbapenem-resistant Enterobacteriaceae are amongst the most feared pathogens due to severely limited treatment options. In response to this threat, three novel blactamase inhibitors have been developed in an attempt to reinvigorate and sustain our current antimicrobial therapies. Avibactam, vaborbactam, and relebactam are inhibitor agents with high affinity to Ambler class A and C blactamases and favorable outcomes in current clinical trials. However, although they do possess key similarities, these agents have unique differences which may have important clinical implications. The microbiologic spectrum, pharmacokinetics, and key clinical trials for each of these novel agents are reviewed. A proposed role in therapy and potential novel combinations are examined.
引用
收藏
页码:615 / 628
页数:14
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