Suppr超能文献

对来自美国医疗中心(2011 - 2014年)的头孢他啶不敏感的柠檬酸杆菌属、肠杆菌属、粘质沙雷氏菌和铜绿假单胞菌进行测试时,头孢他啶 - 阿维巴坦的活性。

Ceftazidime-avibactam activity when tested against ceftazidime-nonsusceptible Citrobacter spp., Enterobacter spp., Serratia marcescens, and Pseudomonas aeruginosa from Unites States medical centers (2011-2014).

作者信息

Sader Helio S, Castanheira Mariana, Farrell David J, Flamm Robert K, Jones Ronald N

机构信息

JMI Laboratories, North Liberty, IA, USA.

JMI Laboratories, North Liberty, IA, USA.

出版信息

Diagn Microbiol Infect Dis. 2015 Dec;83(4):389-94. doi: 10.1016/j.diagmicrobio.2015.06.008. Epub 2015 Jun 17.

Abstract

A total of 6910 Enterobacteriaceae with inducible AmpC β-lactamases and 5328 Pseudomonas aeruginosa were collected from 71 US hospitals in 2011-2014 and were susceptibility tested using the reference broth microdilution method. Ceftazidime-avibactam demonstrated potent in vitro activity against all 3 Enterobacteriaceae genus groups evaluated, with MIC(50)/MIC(90) values of 0.12/0.5 μg/mL for Enterobacter spp. and Serratia marcescens and 0.12/0.25 μg/mL for Citrobacter spp. (99.8-99.9% susceptibility rates at ≤8 μg/mL). Furthermore, 99.3% of ceftazidime-nonsusceptible Enterobacteriaceae isolates (1015 of 1022) were susceptible to ceftazidime-avibactam (MIC(50)/MIC(90) of 0.25-0.5/1-2 μg/mL), whereas susceptibility rates for cefepime ranged from 45.9% (Citrobacter spp.) to 80.0% (S. marcescens). Ceftazidime-avibactam was also very active against P. aeruginosa (MIC(50)/MIC(90), 2/4 μg/mL; 96.8% inhibited at ≤8 μg/mL). P. aeruginosa susceptibility rates to other antipseudomonal β-lactams ranged from 79.6% for piperacillin-tazobactam to 84.5% for cefepime. Ceftazidime-avibactam inhibited 67.4% of isolates at ≤8 μg/mL (MIC(50)/MIC(90), 8/32 μg/mL) that were nonsusceptible to ceftazidime, cefepime, piperacillin-tazobactam, and meropenem.

摘要

2011年至2014年期间,从美国71家医院收集了总共6910株产诱导型AmpCβ-内酰胺酶的肠杆菌科细菌和5328株铜绿假单胞菌,并采用参考肉汤微量稀释法进行药敏试验。头孢他啶-阿维巴坦对所有评估的3个肠杆菌科属组均显示出强大的体外活性,对于肠杆菌属和粘质沙雷氏菌,其MIC(50)/MIC(90)值为0.12/0.5μg/mL,对于柠檬酸杆菌属为0.12/0.25μg/mL(在≤8μg/mL时的药敏率为99.8 - 99.9%)。此外,99.3%的对头孢他啶不敏感的肠杆菌科分离株(1022株中的1015株)对头孢他啶-阿维巴坦敏感(MIC(50)/MIC(90)为0.25 - 0.5/1 - 2μg/mL),而头孢吡肟的药敏率范围为45.9%(柠檬酸杆菌属)至80.0%(粘质沙雷氏菌)。头孢他啶-阿维巴坦对铜绿假单胞菌也具有很高活性(MIC(50)/MIC(90),2/4μg/mL;在≤8μg/mL时96.8%被抑制)。铜绿假单胞菌对其他抗假单胞菌β-内酰胺类药物的药敏率范围为哌拉西林-他唑巴坦的79.6%至头孢吡肟的84.5%。头孢他啶-阿维巴坦在≤8μg/mL(MIC(50)/MIC(90),8/32μg/mL)时抑制了67.4%对头孢他啶、头孢吡肟、哌拉西林-他唑巴坦和美罗培南不敏感的分离株。

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