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阿米卡星或庆大霉素与三种新型广谱头孢菌素联合使用对耐头孢噻吩肠杆菌科细菌的体外杀菌活性增强。

Enhanced in vitro bactericidal activity of amikacin or gentamicin combined with three new extended-spectrum cephalosporins against cephalothin-resistant members of the family Enterobacteriaceae.

作者信息

Bayer A S, Eisenstadt R, Morrison J O

出版信息

Antimicrob Agents Chemother. 1984 Jun;25(6):725-8. doi: 10.1128/AAC.25.6.725.

Abstract

The in vitro bactericidal interactions of three new extended-spectrum cephalosporins (ceftriaxone, ceftizoxime, or ceftazidime) in combination with gentamicin or amikacin were compared against 40 recent nosocomial bloodstream Enterobacteriaceae isolates by the timed-kill curve technique. All of the study strains were cephalothin resistant, and 56% were resistant to cefamandole. Combinations of aminoglycosides plus ceftriaxone or ceftizoxime exhibited an enhanced bactericidal effect with the highest frequency (approximately 85 to 90%), whereas gentamicin-ceftazidime combinations demonstrated the lowest frequency (for 60% of assays, P less than 0.0005 against the nonceftazidime regimens). The enhanced bactericidal effects occurred within readily achievable drug levels in serum for all of the single antibiotic constituents. No bactericidal antagonism was observed. There was no discernible relationship between the relative in vitro susceptibilities of the 40 study isolates to ceftazidime and the potential for gentamicin-ceftazidime combinations to demonstrate enhanced bactericidal activity. In 14 of the 40 study strains (35%) all six drug combinations tested demonstrated an enhanced bactericidal effect. In nearly 50% of bactericidal interactions which resulted in enhanced bactericidal effect at 24 h, such enhanced killing was clearly demonstrable by 4 h of incubation. These results delineate a frequent and rapid enhancement of in vitro bactericidal activity between three new extended-spectra cephalosporins and aminoglycosides against nosocomial members of the family Enterobacteriaeceae.

摘要

采用定时杀菌曲线技术,比较了三种新型广谱头孢菌素(头孢曲松、头孢唑肟或头孢他啶)与庆大霉素或阿米卡星联合应用对40株近期医院血流感染肠杆菌科细菌分离株的体外杀菌相互作用。所有研究菌株均对头孢噻吩耐药,56%对头孢孟多耐药。氨基糖苷类与头孢曲松或头孢唑肟联合应用表现出增强杀菌作用的频率最高(约85%至90%),而庆大霉素-头孢他啶联合应用表现出增强杀菌作用的频率最低(在60%的试验中,与非头孢他啶方案相比,P<0.0005)。所有单一抗生素成分在血清中易于达到的药物水平下均出现增强的杀菌作用。未观察到杀菌拮抗作用。40株研究分离株对头孢他啶的相对体外敏感性与庆大霉素-头孢他啶联合应用显示增强杀菌活性的可能性之间没有明显关系。在40株研究菌株中的14株(35%)中,所有六种测试的药物联合应用均表现出增强的杀菌作用。在24小时时导致杀菌作用增强的近50%的杀菌相互作用中,在孵育4小时时这种增强的杀灭作用就明显可辨。这些结果表明,三种新型广谱头孢菌素与氨基糖苷类对医院内肠杆菌科细菌成员的体外杀菌活性经常且迅速增强。

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