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E试验、琼脂稀释法和肉汤微量稀释法检测幽门螺杆菌菌株对20种抗菌药物敏感性的比较评估

Comparative evaluation of the E test, agar dilution, and broth microdilution for testing susceptibilities of Helicobacter pylori strains to 20 antimicrobial agents.

作者信息

Piccolomini R, Di Bonaventura G, Catamo G, Carbone F, Neri M

机构信息

Department of Biomedical Sciences, G. D'Annunzio University, Chieti, Italy.

出版信息

J Clin Microbiol. 1997 Jul;35(7):1842-6. doi: 10.1128/jcm.35.7.1842-1846.1997.

Abstract

The Epsilometer test (E test; AB Biodisk, Solna, Sweden), a new quantitative technique for the determination of antimicrobial susceptibility, was compared to reference methods (agar dilution and broth microdilution) for the antimicrobial susceptibility testing of Helicobacter pylori. Seventy-one H. pylori strains isolated from patients with duodenal ulcers were tested against 20 antimicrobial agents. The E test and the agar dilution method were carried out on Mueller-Hinton agar; the broth microdilution method was performed with Mueller-Hinton broth. The E-test results showed excellent correlation with the agar dilution results, with 91.3 and 98.8% agreement within 1 and 2 log2 dilution steps, respectively, in a total of 1,350 tests. The correlation between the E-test results and the broth microdilution results was slightly higher, with 91.6 and 99.1% agreement within 1 and 2 log2 dilution steps, respectively, in a total of 1,317 tests. There were six major errors and two very major errors by the metronidazole E test compared to the results obtained by reference methods. Excellent agreement between E-test, agar dilution, and broth microdilution results was found for resistance to erythromycin (8%), clarithromycin (6%), and tetracycline (6%). Our results confirm that the E test is comparable to standardized methods for susceptibility testing. Therefore, the E test is a reliable and alternative method for testing H. pylori susceptibility to a wide range of antimicrobial agents in clinical practice.

摘要

E试验(Etest;AB Biodisk公司,瑞典索尔纳)是一种用于测定抗菌药物敏感性的新定量技术,本研究将其与参考方法(琼脂稀释法和肉汤微量稀释法)用于幽门螺杆菌的抗菌药物敏感性测试进行了比较。对从十二指肠溃疡患者中分离出的71株幽门螺杆菌菌株进行了20种抗菌药物的测试。E试验和琼脂稀释法在Mueller-Hinton琼脂上进行;肉汤微量稀释法用Mueller-Hinton肉汤进行。E试验结果与琼脂稀释结果显示出极好的相关性,在总共1350次测试中,在1和2个log2稀释步骤内的一致性分别为91.3%和98.8%。E试验结果与肉汤微量稀释结果之间的相关性略高,在总共1317次测试中,在1和2个log2稀释步骤内的一致性分别为91.6%和99.1%。与参考方法获得的结果相比,甲硝唑E试验有6个主要错误和2个非常主要的错误。对于红霉素(8%)、克拉霉素(6%)和四环素(6%)的耐药性,E试验、琼脂稀释法和肉汤微量稀释法的结果显示出极好的一致性。我们的结果证实,E试验与标准化的药敏试验方法具有可比性。因此,E试验是临床实践中检测幽门螺杆菌对多种抗菌药物敏感性的一种可靠且可替代的方法。

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