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首页> 外文期刊>Journal of Clinical Microbiology >New vancomycin disk diffusion breakpoints for enterococci. The National Committee for Clinical Laboratory Standards Working Group on Enterococci.
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New vancomycin disk diffusion breakpoints for enterococci. The National Committee for Clinical Laboratory Standards Working Group on Enterococci.

机译:肠球菌的新万古霉素圆盘扩散断点。全国临床实验室标准委员会肠球菌工作组。

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Since 1988, when the first vancomycin-resistant enterococcus was described, several descriptions of failures of disk diffusion breakpoints to detect low-level vancomycin resistance (MICs, 8 to 32 micrograms/ml) have been published. A four-laboratory collaborative study was undertaken to establish more accurate breakpoints for the disk test. Mueller-Hinton agar was used to perform dilution testing (in three laboratories) and disk diffusion testing (in all laboratories). Results were determined at 18, 24, and 48 h, and zones of inhibition were read using both transmitted and reflected light. One hundred organisms (35 Enterococcus faecalis, 55 E. faecium, and 10 E. gallinarum or E. casseliflavus isolates) were selected to represent vancomycin-susceptible and -resistant phenotypes. Interlaboratory agreement of agar dilution MICs was better at 24 h (91 to 94% within +/- 1 dilution) than at 18 h (76% within +/- 1 dilution). Therefore, 24-h agar dilution MIC results were used as the reference. For disk diffusion, it was critical to note the presence of a haze or colonies inside the zone when interpreting the test, since this correlated better with the results of the agar dilution test. The presence of a haze or inner colonies was best detected by reading the zones with transmitted light and incubating the plates for a full 24 h. When plotted against 24-h agar dilution MICs, breakpoints of /= 17 mm (susceptible) resulted in 58 minor errors (14.5% of total values) and 5 very major errors (2.2% of resistant values or 1.3% of total values). No major errors were seen. Results of repeat testing using a common lot of Mueller-Hinton agar showed 52 minor errors (13.3%) and 4 major errors (4.2% of susceptible values of 1.0% pf total values) but no very major errors. It is recommended that any haze or colonies within the zone be taken into account when determining zones of inhibition and that an MIC test be performed for strains with intermediate zones if vancomycin is being considered for treatment.
机译:自1988年以来,当描述了第一个耐万古霉素的肠球菌时,已经发表了一些关于磁盘扩散断点无法检测低水平万古霉素耐药性(MIC,8至32微克/毫升)的描述。进行了四个实验室的合作研究,以为磁盘测试建立更准确的断点。使用Mueller-Hinton琼脂进行稀释测试(在三个实验室中)和圆盘扩散测试(在所有实验室中)。在第18、24和48小时确定结果,并使用透射光和反射光读取抑制区域。选择了一百种生物体(35粪肠球菌,55粪肠球菌和10鸡肠球菌或casseliflavus分离株)来代表对万古霉素敏感和耐药的表型。琼脂稀释MIC的实验室间一致性在24 h时(+/- 1稀释内为91%至94%)要好于18 h(+/- 1稀释内76%)。因此,将24小时琼脂稀释MIC结果用作参考。对于盘片扩散,在解释测试时,必须注意该区域内是否存在混浊或菌落,因为这与琼脂稀释测试的结果更好地相关。通过用透射光读取区域并孵育平板整整24小时,可以最好地检测到是否存在混浊或内部菌落。当针对24小时琼脂稀释MIC绘图时,断点≤14 mm(抗性),15至16 mm(中等)和> / = 17 mm(易感),导致58个小错误(占总值的14.5%)和5个非常重大的错误(电阻值的2.2%或总值的1.3%)。没有发现重大错误。使用常用的Mueller-Hinton琼脂进行重复测试的结果显示52个较小的错误(13.3%)和4个较大的错误(4.2%的敏感度值占1.0%pf总值),但没有很大的错误。建议在确定抑制区域时考虑该区域内的任何雾度或菌落,如果正在考虑使用万古霉素进行治疗,则建议对具有中间区域的菌株进行MIC测试。

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