Suppr超能文献

多重耐药革兰氏阴性菌感染:你准备好应对挑战了吗?

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

作者信息

Curcio Daniel

机构信息

Hospital Municipal Chivilcoy, Infectología Institucional SRL, Santo Tomé 5239 4 to 22, (1419) Capital Federal, Buenos Aires, Argentina.

出版信息

Curr Clin Pharmacol. 2014 Feb;9(1):27-38. doi: 10.2174/15748847113089990062.

Abstract

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]).

摘要

与革兰氏阳性菌的发展情况相平行,耐多药(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了最重要的耐药问题,所有主要的抗革兰氏阴性菌药物(β-内酰胺类、氟喹诺酮类和氨基糖苷类)的耐药趋势都在增加。一个主要令人担忧的问题是出现了能够降解广谱头孢菌素和/或碳青霉烯类的新型β-内酰胺酶,如超广谱β-内酰胺酶(ESBLs)和碳青霉烯酶(即KPC、NDM和其他金属β-内酰胺酶)。本文综述了已发表文献中有关新型抗菌药物针对耐多药革兰氏阴性病原体的药代动力学/药效学特征及临床疗效的证据,这些病原体包括:i-新型碳青霉烯类(多尼培南、比阿培南、帕尼培南、替诺培南、FSI-1686);ii-新型头孢菌素(头孢洛林、头孢托罗);iii-替加环素;以及iv-β-内酰胺酶抑制剂(BLI-489、Ro 48-1220、ME 1071、阿维巴坦[NXL104])。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验