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首页> 外文期刊>Journal of Clinical Microbiology >Multicenter Evaluation of Ethambutol Susceptibility Testing of Mycobacterium tuberculosis by Agar Proportion and Radiometric Methods
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Multicenter Evaluation of Ethambutol Susceptibility Testing of Mycobacterium tuberculosis by Agar Proportion and Radiometric Methods

机译:琼脂比例和放射法对结核分枝杆菌乙胺丁醇药敏试验的多中心评价

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摘要

Reproducibility of ethambutol (EMB) susceptibility test results for Mycobacterium tuberculosis has always been difficult for a variety of reasons, including the narrow range between the critical breakpoint for EMB resistance and the MIC for susceptible strains, borderline results obtained with the BACTEC 460TB method, the presence of microcolonies determined using the agar proportion (AP) method, and a lack of agreement between these two testing methods. To assess the frequency of these problems, M. tuberculosis drug susceptibility data were collected in a multicenter study involving four laboratories. Resistant, borderline, and susceptible isolates were shared among the laboratories to measure interlaboratory test agreement. Half of isolates determined by BACTEC 460TB to be resistant were determined to be susceptible by the AP method. Isolates determined to be resistant to EMB by both BACTEC 460TB and AP methods were almost always resistant to isoniazid. Results from isolates tested by the BACTEC 460TB method with an EMB concentration of 3.75 μg/ml in addition to the standard 2.5 μg/ml did not show improved agreement by the AP method. While these results do not indicate that the AP method is more accurate than the BACTEC 460TB method, laboratories should not report EMB monoresistance based on BACTEC 460TB results alone. Monoresistance to EMB should only be reported following confirmation by the AP method. Microcolonies could not be confirmed as resistant by the BACTEC 460TB method or by repeat testing with the AP method and do not appear to be indicative of resistance.
机译:乙胺丁醇(EMB)结核分枝杆菌敏感性测试结果的可重复性一直很困难,原因有多种,包括EMB耐药性的临界断裂点和易感菌株的MIC之间的范围狭窄,获得了临界结果使用BACTEC 460TB方法时,使用琼脂比例(AP)方法确定存在微菌落,并且这两种测试方法之间缺乏一致性。为了评估这些问题的发生频率, M。一项涉及四个实验室的多中心研究收集了结核药物敏感性数据。实验室之间共享抗性,临界和易感菌株,以测量实验室间的测试协议。通过BACTEC 460TB确定为抗药性的一半分离株通过AP方法确定为易感。通过BACTEC 460TB和AP方法确定为对EMB耐药的分离株几乎始终对异烟肼具有耐药性。通过BACTEC 460TB方法分离的EMB浓度为3.75μg/ ml,标准品为2.5μg/ ml的分离物的结果,未通过AP方法显示出更好的一致性。尽管这些结果并不表明AP方法比BACTEC 460TB方法更准确,但实验室不应仅根据BACTEC 460TB结果报告EMB单抗。仅在通过AP方法确认后才报告对EMB的单抗。不能通过BACTEC 460TB方法或通过AP方法进行重复测试确认小菌落具有抗性,并且似乎不能指示抗性。

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