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新型β-内酰胺类药物与氨基糖苷类药物对铜绿假单胞菌临床分离株的体外活性比较。

Comparison of the in vitro activity of new beta-lactams and aminoglycosides against clinical isolates of Pseudomonas aeruginosa.

作者信息

Patzer J, Gieburowska R, Dzierzanowska D

出版信息

Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1982 Oct;253(1):110-20.

PMID:6817544
Abstract

In vitro susceptibility of 338 clinical isolates of Pseudomonas aeruginosa to twelve antipseudomonal antibiotics were determined. Correlation between antibiotic resistance and serotypes was also performed. It was shown that the newer beta-lactams cefsulodin, piperacillin, azlocillin and mezlocillin had high biological activity against carbenicillin-resistant strains of P. aeruginosa. The most active aminoglycosides against gentamicin-resistant strains of P. aeruginosa were amikacin and netilmicin. Carbenicillin-resistant strains were most frequently observed among serotypes 4, 11 and NT group, and gentamicin-resistant strains among serotypes 3, 11 and NT group.

摘要

测定了338株铜绿假单胞菌临床分离株对12种抗假单胞菌抗生素的体外敏感性。还进行了抗生素耐药性与血清型之间的相关性分析。结果表明,新型β-内酰胺类抗生素头孢磺啶、哌拉西林、阿洛西林和美洛西林对耐羧苄西林的铜绿假单胞菌菌株具有较高的生物活性。对耐庆大霉素的铜绿假单胞菌菌株最具活性的氨基糖苷类抗生素是阿米卡星和奈替米星。耐羧苄西林菌株在血清型4、11和NT组中最常见,耐庆大霉素菌株在血清型3、11和NT组中最常见。

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