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Multidrug-resistant Gram-negative bacterial infections: Are you ready for the challenge?

机译:多药耐药革兰氏阴性细菌感染:您准备好应对挑战了吗?

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摘要

Paralleling the developments in Gram-positive bacteria, infections caused by multidrug-resistant (MDR) Gramnegative bacilli have become a growing challenge. The most important resistance problems are encountered in Enterobacteriaceae, Pseudomonas aeruginosa and Acinetobacter spp., with increasing trends observed for all major anti- Gram-negative agents (beta-lactams, fluoroquinolones and aminoglycosides). A matter of major concern is the emergence of new beta-lactamases capable of degrading the expanded-spectrum cephalosporins and/or carbapenems, such as the extended-spectrum beta-lactamases (ESBLs) and the carbapenemases (ie. KPC, NDM and other metallo-β; -lactamases). This paper reviews the evidence in the published literature of the pharmacokinetic/pharmacodynamic profile, clinical efficacy of new antimicrobial agents, against MDR- Gram-negative pathogens, such us: i-new carbapenems (doripenem, biapenem, panipenem, tonopenem, FSI-1686); ii-new cephalosporins (ceftaroline, ceftobiprole); iii-tigecycline; and iv- β- lactamases inhibitors (BLI-489, Ro 48-1220, ME 1071, aviactam [NXL104]).
机译:与革兰氏阳性细菌的发展平行,由多重耐药性(MDR)革兰氏阴性杆菌引起的感染已成为日益严峻的挑战。在肠杆菌科,铜绿假单胞菌和不动杆菌属中遇到最重要的耐药性问题,所有主要的抗革兰氏阴性药物(β-内酰胺类,氟喹诺酮类和氨基糖苷类)的趋势都在增加。一个主要令人关注的问题是出现了能够降解广谱头孢菌素和/或碳青霉烯类的新的β-内酰胺酶,例如超广谱β-内酰胺酶(ESBLs)和碳青霉烯酶(即KPC,NDM和其他金属酶)。 -β;-内酰胺酶)。本文综述了已发表的文献中有关MDR-革兰氏阴性病原体的药代动力学/药效学概况,新型抗菌剂的临床疗效的证据,例如:i-新型碳青霉烯类(多利培南,比阿培南,帕尼培南,tonopenem,FSI-1686 ); ii-新的头孢菌素(头孢洛林,头孢比普罗); iii-替加环素;和iv-β-内酰胺酶抑制剂(BLI-489,Ro 48-1220,ME 1071,aviactam [NXL104])。

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