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首页> 外文期刊>Journal of Clinical Microbiology >Suggested modifications for disk diffusion susceptibility testing criteria for levofloxacin and sparfloxacin following tests with a predictor panel of ciprofloxacin-resistant clinical isolates.
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Suggested modifications for disk diffusion susceptibility testing criteria for levofloxacin and sparfloxacin following tests with a predictor panel of ciprofloxacin-resistant clinical isolates.

机译:建议用耐环丙沙星临床分离株的预测指标进行试验后,对左氧氟沙星和司帕沙星的纸片扩散敏感性测试标准进行修改。

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摘要

A predictor panel of 300 clinical bacterial isolates (200 resistant to ciprofloxacin) was used to compare 5-micrograms disk diffusion test results with the MICs of ofloxacin (control), levofloxacin, and sparfloxacin. Regression analysis demonstrated high correlations between the methods for all three fluoroquinolones (r > or = 0.95). In order to minimize disk diffusion testing errors among the fluoroquinolone-resistant strains, the following modifications to previously proposed or published interpretive criteria were suggested: for levofloxacin, susceptible at > or = 17 mm (< or = 2 micrograms/ml) and resistant at < or = 13 mm (> or = 8 micrograms/ml); for sparfloxacin, susceptible at > or = 20 mm (< or = 1 microgram/ml) and resistant at < or = 16 mm (> or = 4 micrograms/ml). The study control drug, ofloxacin, did not appear to possess a significant error rate (5% minor error) when fluoroquinolone-resistant strains were tested, and no modifications were proposed. Under these proposed interpretive criteria, the absolute categorical agreements between standardized susceptibility testing methods for levofloxacin and sparfloxacin results were 91.3 and 94.0%, respectively (< or = 0.3% major errors and nil very major errors).
机译:使用300个临床细菌分离株(200个对环丙沙星耐药)的预测指标组将5微克圆片扩散测试结果与氧氟沙星(对照),左氧氟沙星和司帕沙星的MIC进行比较。回归分析表明,所有三种氟喹诺酮类药物的方法之间具有高度相关性(r>或= 0.95)。为了使耐氟喹诺酮菌株之间的磁盘扩散测试错误最小化,建议对先前提出或公布的解释性标准进行以下修改:对于左氧氟沙星,易感性≥17 mm(≤2微克/ ml),抗性≥15 mm <或= 13毫米(>或= 8微克/毫升);对司帕沙星而言,对>或= 20毫米(<或= 1微克/毫升)敏感,对<或= 16毫米(>或= 4微克/毫升)耐药。当测试氟喹诺酮耐药菌株时,研究对照药物氧氟沙星似乎没有显着的错误率(5%较小的错误),并且未提出修饰方案。在这些拟议的解释标准下,左氧氟沙星和司帕沙星结果的标准化药敏试验方法之间的绝对分类一致性分别为91.3%和94.0%(重大误差<或= 0.3%,无极重大误差)。

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