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Activity of Cefepime-Zidebactam against Multidrug-Resistant (MDR) Gram-Negative Pathogens

机译:头孢吡肟-齐德巴坦对多药耐药革兰氏阴性病原菌的活性

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This study compared the activity of cefepime + zidebactam (FEP-ZID) and selected currently available antibacterial agents against a panel of multidrug-resistant (MDR) clinical isolates chosen to provide an extreme challenge for antibacterial activity. FEP–ZID had a very broad and potent in vitro spectrum of activity, and was highly active against many MDR isolates of Enterobacterales , Pseudomonas aeruginosa , and Acinetobacter baumannii . Notably, it inhibited isolates producing carbapenemases of Ambler classes A, B, and D, and P. aeruginosa isolates with multiple resistance mechanisms including combinations of upregulated efflux, diminished or non-functional OprD porins, and AmpC overproduction. Its clinical role will be determined initially by the breakpoints assigned to it, comparison studies with other investigational β-lactamase inhibitor combinations, and ultimately by the developing body of therapeutic outcome data.
机译:这项研究比较了头孢吡肟+齐达巴坦(FEP-ZID)的活性,并选择了目前可用的抗菌剂与一组耐多药耐药性(MDR)临床分离株进行比较,这些菌株对抗菌活性提出了严峻挑战。 FEP-ZID在体外具有非常广泛和有效的活性谱,对肠杆菌,铜绿假单胞菌和鲍曼不动杆菌的许多MDR分离物具有很高的活性。值得注意的是,它抑制了产生Ambler类A,B和D碳青霉烯酶的分离株,以及具有多种抗性机制的铜绿假单胞菌分离株,包括上调外排,OprD孔蛋白减少或无功能,以及AmpC过量生产。它的临床作用将首先由为其指定的断点,与其他研究性β-内酰胺酶抑制剂组合的比较研究以及最终由治疗结果数据的发展而决定。

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