阿维巴坦
头孢他啶/阿维巴坦
阿兹屈南
鲍曼不动杆菌
碳青霉烯
医学
β-内酰胺酶抑制剂
微生物学
耐碳青霉烯类肠杆菌科
美罗培南
抗菌剂
头孢菌素
肠杆菌科
抗生素耐药性
亚胺培南
抗生素
生物
头孢他啶
铜绿假单胞菌
细菌
大肠杆菌
生物化学
遗传学
基因
作者
Ilias Karaiskos,Irene Galani,Maria Souli,Helen Giamarellou
标识
DOI:10.1080/17425255.2019.1563071
摘要
Introduction: The burden of antimicrobial resistance among Gram-negative bacteria is increasing and growing into a major threat of public health. Treatment options for carbapenem-resistant Enterobacteriaceae are limited and resistance rates to existing compounds are mounting. The pipeline includes only a small number of novel anti-infective agents in development or in the market with promising results against multidrug-resistant (MDR) Gram-negative.Areas covered: Herein the authors present the modern available knowledge regarding novel β-lactam-β-lactamase inhibitors, i.e. mechanisms of action, in vitro activity, current PK/PDs, clinical trials and clinical efficacy against MDR and XDR Gram-negatives, as well as toxicity issues.Expert opinion: Ceftazidime-avibactam and meropenem-vaborbactam are promising therapeutic options as both are active against Enterobacteriaceae producing ESBL, AmpC, and KPC, whereas only avibactam inhibits certain class D β-lactamases, mainly OXA-48. New drugs active against Gram-negative MDR isolates including imipenem/cilastatin with relebactam and avibactam combined with aztreonam or ceftaroline are in different stages of development. However, the disadvantage to be seriously considered by the clinician is that β-lactam/β-lactamase inhibitors are ineffective against metallo-β-lactamases (with the exception of aztreonam-avibactam) as well as Acinetobacter baumannii.
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