医学
鲍曼不动杆菌
头孢吡肟
舒巴坦钠
多重耐药
抗菌剂
重症监护医学
抗生素
药理学
抗生素耐药性
微生物学
铜绿假单胞菌
细菌
生物
亚胺培南
遗传学
作者
Radhika Arya,Breanna S. Goldner,Andrew F. Shorr
标识
DOI:10.1097/qco.0000000000000885
摘要
Purpose of review To review novel antiinfective agents in development for multidrug-resistant (MDR) Gram-negative bacterial infections. Recent findings Four novel agents are in various phases of development (tebipenem, durlobactam-sulbactam, cefepime-taniborbactam, and xeruborbactam). Tebpipenem is an oral carbapenem with a recently completed phase III trial for complicated urinary tract infections while durlobactam-sulbactam represents a potential alternative for drug-resistant Acinetobacter baumannii . Cefepime-taniborbactam possesses in-vitro potency against a range of troubling pathogens and we await further information on a recently completed study on complicated urinary tract infection. Finally, xeruborbactam is an ultrabroad beta-lactamase inhibitor that can be paired with a range of intravenous and oral agents. It exhibits enhanced in-vitro activity against many MDR pathogens, including those resistant to newer, broader spectrum options. Data in humans with xeruborbactam are limited. Summary Each of the newer options reviewed possesses a unique range of in-vitro activity against select, challenging pathogens with some narrowly tailored and other broader in activity. Several have both oral and intravenous formulations. Two agents have presented data from recent phase III trials, whereas two are not as advanced in their clinical programs.
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