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首页> 外文期刊>Journal of Clinical Microbiology >Direct detection of Mycobacterium tuberculosis complex in respiratory specimens by a target-amplified test system.
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Direct detection of Mycobacterium tuberculosis complex in respiratory specimens by a target-amplified test system.

机译:通过目标扩增测试系统直接检测呼吸道标本中的结核分枝杆菌复合物。

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A total of 938 respiratory specimens (633 sputa, 249 bronchial and tracheal aspirates, and 56 bronchoalveolar lavages) from 589 patients were tested for direct detection of Mycobacterium tuberculosis complex by the Gen-Probe amplified Mycobacterium tuberculosis direct test (MTD), and the results were compared with those of the conventional methods of fluorescence microscopy and cultivation (solid and radiometric media). One series of specimens (n = 515) was decontaminated with N-acetyl-L-cysteine (NALC)-NaOH: the other one (n = 423) was decontaminated with sodium dodecyl (lauryl) sulfate (SDS)-NaOH. Of the specimens decontaminated with NALC, 39 were MTD and culture positive, 455 were MTD and culture negative, 18 were MTD positive and culture negative, and 3 were MTD negative and culture positive, indicating a sensitivity of 92.9% and a specificity of 96.2% for the MTD. Of the specimens decontaminated with SDS, 35 were MTD and culture positive, 372 were MTD and culture negative, 15 were MTD positive and culture negative, and 1 was MTD negative and culture positive, indicating a sensitivity of 97.2% and a specificity of 96.1% for the MTD. After resolution of discrepant results by review of the patients' clinical data, the sensitivity of the MTD was 93.9%, the specificity was 97.6%, the positive predictive value was 80.7%, and the negative predictive value was 99.3% for the NALC series; the corresponding values were 97.4, 96.9, 76.0, and 99.7%, respectively, for the SDS series. In conclusion, the MTD is a highly sensitive and specific technique for detecting M. tuberculosis complex within hours in both smear-positive and smear-negative respiratory specimens.
机译:通过Gen-Probe扩增结核分枝杆菌直接试验(MTD)对来自589名患者的总共938个呼吸道标本(633痰液,249支气管和气管抽吸物以及56支支气管肺泡灌洗液)进行了直接检测,以检测结核分枝杆菌复合物。将其与荧光显微镜和培养的常规方法(固体和辐射介质)进行了比较。用N-乙酰基-L-半胱氨酸(NALC)-NaOH对一系列标本(n = 515)进行去污:用十二烷基(十二烷基)硫酸钠(SDS)-NaOH对另一组标本(n = 423)进行去污。在用NALC净化的标本中,MTD和培养阳性的标本为39个,MTD和培养阴性的标本为455个,MTD阳性和培养阴性的标本为18个,MTD阴性和培养阳性的标本为3个,灵敏度为92.9%,特异性为96.2%对于MTD。在用SDS消毒的标本中,MTD和培养阳性的样本为35个,MTD和培养阴性的样本为372个,MTD阳性和培养阴性的样本为15个,MTD阴性和培养阳性的样本为1个,灵敏度为97.2%,特异性为96.1%对于MTD。通过回顾患者的临床数据解决差异性结果后,对于NALC系列,MTD的敏感性为93.9%,特异性为97.6%,阳性预测值为80.7%,阴性预测值为99.3%; SDS系列的相应值分别为97.4、96.9、76.0和99.7%。总之,MTD是在涂片阳性和涂片阴性呼吸道标本中数小时内检测结核分枝杆菌复合体的高度灵敏和特异的技术。

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