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环丙沙星与选定的β-内酰胺类药物及氨基糖苷类药物对多重耐药铜绿假单胞菌的体外协同研究。

In vitro synergy studies with ciprofloxacin and selected beta-lactam agents and aminoglycosides against multidrug-resistant Pseudomonas aeruginosa.

作者信息

Meyer R D, Liu S

机构信息

Department of Medicine, Cedars-Sinai Medical Center/UCLA School of Medicine.

出版信息

Diagn Microbiol Infect Dis. 1988 Nov;11(3):151-7. doi: 10.1016/0732-8893(88)90017-x.

Abstract

In order to determine the effect of combining ciprofloxacin with beta-lactam and aminoglycoside agents against multidrug-resistant P. aeruginosa, ciprofloxacin was tested in vitro with the checkerboard broth microdilution technique with various current beta-lactam and aminoglycoside agents. In both inhibitory and bactericidal testing, the combination of ciprofloxacin with a beta-lactam agent (ceftazidime, piperacillin, mezlocillin, azlocillin, or imipenem) was more likely to show a synergistic effect or additive effect and lack of antagonism (96.5% of all inhibitory and cidal tests) than was a combination of ciprofloxacin with an aminoglycoside [(amikacin, tobramycin, or gentamicin), 90% of all inhibitory and cidal tests]. Finding of antagonism in some testing, especially with aminoglycosides, indicates that results are unpredictable. These results may influence selection of agents for selection in clinical situations.

摘要

为了确定环丙沙星与β-内酰胺类和氨基糖苷类药物联合使用对多重耐药铜绿假单胞菌的作用,采用棋盘肉汤微量稀释技术,将环丙沙星与各种目前使用的β-内酰胺类和氨基糖苷类药物进行体外试验。在抑菌和杀菌试验中,环丙沙星与β-内酰胺类药物(头孢他啶、哌拉西林、美洛西林、阿洛西林或亚胺培南)联合使用比环丙沙星与氨基糖苷类药物(阿米卡星、妥布霉素或庆大霉素)联合使用更有可能显示协同作用或相加作用且无拮抗作用(在所有抑菌和杀菌试验中分别占96.5%和90%)。在某些试验中发现有拮抗作用,尤其是与氨基糖苷类药物联合时,表明结果不可预测。这些结果可能会影响临床情况下药物的选择。

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