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通过肉汤微量稀释法和纸片扩散药敏试验对阿莫西林克拉维酸进行体外评估:回归分析、暂定解释标准和质量控制限度。

In vitro evaluation of Augmentin by broth microdilution and disk diffusion susceptibility testing: regression analysis, tentative interpretive criteria, and quality control limits.

作者信息

Fuchs P C, Barry A L, Thornsberry C, Gavan T L, Jones R N

出版信息

Antimicrob Agents Chemother. 1983 Jul;24(1):31-8. doi: 10.1128/AAC.24.1.31.

Abstract

Augmentin (Beecham Laboratories, Bristol, Tenn.), a combination drug consisting of two parts amoxicillin to one part clavulanic acid and a potent beta-lactamase inhibitor, was evaluated in vitro in comparison with ampicillin or amoxicillin or both for its inhibitory and bactericidal activities against selected clinical isolates. Regression analysis was performed and tentative disk diffusion susceptibility breakpoints were determined. A multicenter performance study of the disk diffusion test was conducted with three quality control organisms to determine tentative quality control limits. All methicillin-susceptible staphylococci and Haemophilus influenzae isolates were susceptible to Augmentin, although the minimal inhibitory concentrations for beta-lactamase-producing strains of both groups were, on the average, fourfold higher than those for enzyme-negative strains. Among the Enterobacteriaceae, Augmentin exhibited significantly greater activity than did ampicillin against Klebsiella pneumoniae, Citrobacter diversus, Proteus vulgaris, and about one-third of the Escherichia coli strains tested. Bactericidal activity usually occurred at the minimal inhibitory concentration. There was a slight inoculum concentration effect on the Augmentin minimal inhibitory concentrations. On the basis of regression and error rate-bounded analyses, the suggested interpretive disk diffusion susceptibility breakpoints for Augmentin are: susceptible, greater than or equal to 18 mm; resistant, less than or equal to 13 mm (gram-negative bacilli); and susceptible, greater than or equal to 20 mm (staphylococci and H. influenzae). The use of a beta-lactamase-producing organism, such as E. coli Beecham 1532, is recommended for quality assurance of Augmentin susceptibility testing.

摘要

奥格门汀(田纳西州布里斯托尔比彻姆实验室生产)是一种复合药物,其成分为两部分阿莫西林与一部分克拉维酸,是一种强效β-内酰胺酶抑制剂。对其进行了体外评估,与氨苄西林或阿莫西林或两者相比,观察其对选定临床分离株的抑制和杀菌活性。进行了回归分析并确定了初步的纸片扩散药敏试验断点。使用三种质量控制菌株进行了纸片扩散试验的多中心性能研究,以确定初步的质量控制限度。所有对甲氧西林敏感的葡萄球菌和流感嗜血杆菌分离株对奥格门汀敏感,尽管两组中产β-内酰胺酶菌株的最低抑菌浓度平均比酶阴性菌株高四倍。在肠杆菌科细菌中,奥格门汀对肺炎克雷伯菌、奇异柠檬酸杆菌、普通变形杆菌以及约三分之一受试大肠杆菌菌株的活性明显高于氨苄西林。杀菌活性通常在最低抑菌浓度时出现。接种物浓度对奥格门汀的最低抑菌浓度有轻微影响。根据回归分析和误差率限定分析,奥格门汀建议的解释性纸片扩散药敏试验断点为:敏感,大于或等于18毫米;耐药,小于或等于13毫米(革兰氏阴性杆菌);敏感,大于或等于20毫米(葡萄球菌和流感嗜血杆菌)。建议使用产β-内酰胺酶的菌株,如比彻姆大肠杆菌1532,用于奥格门汀药敏试验的质量保证。

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