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BDProbeTec系统用于直接检测呼吸道标本中结核分枝杆菌复合群的性能特征。

Performance characteristics of the BDProbeTec system for direct detection of Mycobacterium tuberculosis complex in respiratory specimens.

作者信息

Pfyffer G E, Funke-Kissling P, Rundler E, Weber R

机构信息

Swiss National Center for Mycobacteria, Department of Medical Microbiology, University of Zurich, CH-8028 Zurich, Switzerland.

出版信息

J Clin Microbiol. 1999 Jan;37(1):137-40. doi: 10.1128/JCM.37.1.137-140.1999.

Abstract

Strand displacement amplification (SDA) technology has been established in a fully automated system known as BDProbeTec. Target sequences of the insertion sequence IS6110 and the 16S rRNA gene are simultaneously amplified, which thus allows the detection of Mycobacterium tuberculosis complex and, as an additional option, of most Mycobacterium species. Detection occurs via a chemiluminescent microwell assay that employs the simultaneous hybridization and capture of SDA products with a biotinylated capture probe and an alkaline phosphatase detector probe. We have evaluated the performance of the BDProbeTec system in detecting M. tuberculosis complex by testing 799 respiratory specimens and comparing the results to those obtained by conventional diagnostic techniques, i.e. , microscopy and culture (solid and radiometric media). M. tuberculosis was cultivated from 41 specimens, of which 28 (68.4%) were smear positive and 13 (31.6%) were smear negative. The overall sensitivity of the SDA assay was 97.6% (for smear-positive specimens, 100%; for smear-negative specimens, 92.3%), and specificity was 95. 0%. After resolution of the discrepancies by studying the patients' clinical data, sensitivity and specificity were 97.9 and 96.5%, respectively, and positive and negative predictive values were 63.9 and 99.9%, respectively. These preliminary data demonstrate that the BDProbeTec system has promising performance characteristics with respiratory specimens and that it allows the detection of M. tuberculosis complex within hours.

摘要

链置换扩增(SDA)技术已被应用于一种名为BDProbeTec的全自动系统中。插入序列IS6110和16S rRNA基因的靶序列可同时被扩增,从而能够检测结核分枝杆菌复合群,此外还可检测大多数分枝杆菌菌种。检测通过化学发光微孔测定法进行,该方法利用生物素化捕获探针和碱性磷酸酶检测探针同时杂交并捕获SDA产物。我们通过检测799份呼吸道标本,并将结果与传统诊断技术(即显微镜检查和培养(固体和放射性培养基))所得结果进行比较,评估了BDProbeTec系统检测结核分枝杆菌复合群的性能。从41份标本中培养出结核分枝杆菌,其中28份(68.4%)涂片阳性,13份(31.6%)涂片阴性。SDA检测的总体敏感性为97.6%(涂片阳性标本为100%;涂片阴性标本为92.3%),特异性为95.0%。通过研究患者的临床数据解决差异后,敏感性和特异性分别为97.9%和96.5%,阳性和阴性预测值分别为63.9%和99.9%。这些初步数据表明,BDProbeTec系统在检测呼吸道标本方面具有良好的性能特征,并且能够在数小时内检测出结核分枝杆菌复合群。

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