首页> 外文期刊>Journal of Clinical Microbiology >Molecular Detection and Identification of Mycobacterium tuberculosis Complex and Four Clinically Important Nontuberculous Mycobacterial Species in Smear-Negative Clinical Samples by the GenoType Mycobacteria Direct Test
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Molecular Detection and Identification of Mycobacterium tuberculosis Complex and Four Clinically Important Nontuberculous Mycobacterial Species in Smear-Negative Clinical Samples by the GenoType Mycobacteria Direct Test

机译:通过基因分型分枝杆菌直接测试对涂片阴性临床样品中结核分枝杆菌复合物和四种临床上重要的非结核分枝杆菌分子进行分子检测和鉴定

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Although the sensitivity and specificity of nucleic acid amplification assays are high with smear-positive samples, the sensitivity with smear-negative and extrapulmonary samples for the diagnosis of tuberculosis in suspicious tuberculosis cases still remains to be investigated. This study evaluates the performance of the GenoType Mycobacteria Direct (GTMD) test for rapid molecular detection and identification of the Mycobacterium tuberculosis complex and four clinically important nontuberculous mycobacteria (M. avium, M. intracellulare, M. kansasii, and M. malmoense) in smear-negative samples. A total of 1,570 samples (1,103 bronchial aspiration, 127 sputum, and 340 extrapulmonary samples) were analyzed. When we evaluated the performance criteria in combination with a positive culture result and/or the clinical outcome of the patients, the overall sensitivity, specificity, and positive and negative predictive values were found to be 62.4, 99.5, 95.9, and 93.9%, respectively, whereas they were 63.2, 99.4, 95.7, and 92.8%, respectively, for pulmonary samples and 52.9, 100, 100, and 97.6%, respectively, for extrapulmonary samples. Among the culture-positive samples which had Mycobacterium species detectable by the GTMD test, three samples were identified to be M. intracellulare and one sample was identified to be M. avium. However, five M. intracellulare samples and an M. kansasii sample could not be identified by the molecular test and were found to be negative. The GTMD test has been a reliable, practical, and easy tool for rapid diagnosis of smear-negative pulmonary and extrapulmonary tuberculosis so that effective precautions may be taken and appropriate treatment may be initiated. However, the low sensitivity level should be considered in the differentiation of suspected tuberculosis and some other clinical condition until the culture result is found to be negative and a true picture of the clinical outcome is obtained.
机译:尽管涂片阳性样品的核酸扩增检测灵敏度和特异性很高,但涂片阴性和肺外样品对可疑结核病例诊断结核的敏感性仍有待研究。这项研究评估了GenoType分枝杆菌直选(GTMD)测试在结核分枝杆菌复合物和四种临床上重要的非结核分枝杆菌(鸟分枝杆菌,胞内分枝杆菌,堪萨西分枝和马尔默分枝杆菌)的快速分子检测和鉴定中的性能。涂片阴性样品。共分析了1,570个样本(1,103个支气管抽吸,127个痰液和340个肺外样本)。当我们结合阳性培养结果和/或患者的临床结果评估性能标准时,发现总体敏感性,特异性以及阳性和阴性预测值分别为62.4%,99.5%,95.9和93.9% ,而肺部样本分别为63.2、99.4、95.7和92.8%,肺外样本分别为52.9、100、100和97.6%。在具有通过GTMD测试可检测到的分枝杆菌菌种的培养阳性样品中,有3个样品被鉴定为胞内分枝杆菌,一个样品被鉴定为鸟分枝杆菌。但是,通过分子测试无法鉴定出五个胞内分枝杆菌样品和堪萨斯分枝杆菌样品,并且它们均为阴性。 GTMD测试已经成为快速诊断涂片阴性的肺结核和肺外结核的可靠,实用和简便的工具,因此可以采取有效的预防措施并开始适当的治疗。但是,在鉴别可疑结核病和其他一些临床状况时应考虑低敏感性水平,直到发现培养结果为阴性并获得临床结果的真实照片为止。

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