首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Note: Clinical Evaluation of the Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test for Rapid Detection of Mycobacterium tuberculosis in Select Nonrespiratory Specimens
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Note: Clinical Evaluation of the Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test for Rapid Detection of Mycobacterium tuberculosis in Select Nonrespiratory Specimens

机译:注意:Gen-Probe结核分枝杆菌直接检测法在非呼吸性标本中快速检测结核分枝杆菌的临床评估

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摘要

The performance of the Amplified Mycobacterium Tuberculosis Direct Test (MTD; Gen-Probe, Inc., San Diego, Calif.) for rapid diagnosis of extrapulmonary tuberculosis was evaluated by testing 178 nonrespiratory specimens from 158 patients. Criteria for specimen inclusion were (i) a positive smear for acid-fast bacilli (n = 54) and (ii) the source if the smear was negative (tissue biopsies and aspirates and abscess material were tested; n = 124). Results were compared to those of mycobacterial culture; clinical history was reviewed when MTD and culture results disagreed. Forty-eight specimens (27.0%) were positive for mycobacteria, including 23 Mycobacterium tuberculosis complex specimens; of which 21 were smear positive. Twenty-five specimens were MTD positive; 20 of these grew M. tuberculosis complex. All of the five MTD-positive, M. tuberculosis complex culture-negative specimens were considered truly positive, based on review of the medical record. Of the three MTD-negative, M. tuberculosis complex culture-positive specimens, two contained inhibitory substances; one of the two was smear positive. Excluding the latter specimen from analysis, after chart review, the sensitivity, specificity, and positive and negative predictive values of the MTD were 92.6, 100, 100, and 98.7%, respectively, by specimen and 89.5, 100, 100, and 98.6% by patient. Given the few smear-negative samples from patients with extrapulmonary tuberculosis in our study, additional similar studies that include more smear-negative, M. tuberculosis complex culture-positive specimens to confirm our data are desirable.
机译:通过测试158例患者的178例非呼吸性标本,评估了扩增的结核分枝杆菌直接试验(MTD; Gen-Probe,Inc。,圣地亚哥,加利福尼亚)对肺外结核的快速诊断的性能。标本纳入的标准是(i)耐酸杆菌涂片阳性(n = 54),以及(ii)如果涂片阴性则来源(测试组织活检,抽吸物和脓肿材料; n = 124)。将结果与分枝杆菌培养的结果进行比较;当MTD和培养结果不一致时,回顾临床历史。结核分枝杆菌阳性的标本为48份(占27.0%),其中结核分枝杆菌的标本为23份。其中21例涂片阳性。 25个标本为MTD阳性;这些中有20个生长着结核分枝杆菌复合体。根据对病历的回顾,所有五个MTD阳性,结核分枝杆菌复杂培养阴性样本均被视为真正阳性。在三个MTD阴性,结核分枝杆菌复杂培养阳性样本中,两个含有抑制性物质。两者之一为涂片阳性。从分析中排除后一个样本后,在图表审查后,MTD的敏感性,特异性以及阳性和阴性预测值分别为92.6、100、100和98.7%(按样本),分别为89.5、100、100和98.6%。由病人。考虑到我们研究中肺外结核患者的涂片阴性样品很少,因此需要更多类似的研究,包括更多涂片阴性,结核分枝杆菌复杂培养阳性样品来证实我们的数据。

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