Performance assessment of the Capilia TB assay and the BD ProbeTec ET system for rapid culture confirmation of Mycobacterium tuberculosis

被引:42
作者
Wang, Jann-Yuan
Lee, Li-Na
Lai, Hsin-Chih [2 ]
Hsu, Hsiao-Leng
Jan, I-Shiow
Yu, Chong-Jen
Hsueh, Po-Ren [1 ]
Yang, Pan-Chyr
机构
[1] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Taipei 100, Taiwan
关键词
M; tuberculosis; culture confirmation; nontuberculous mycobacteria; Capilia TB assay; CTB assay;
D O I
10.1016/j.diagmicrobio.2007.06.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Because of the increasing numbers of nontuberculous mycobacterial isolates from clinical specimens, rapid and accurate methods for culture confinriation of Mycobacterium tuberculosis are urgently needed. The study evaluated the performance of the Capilia TB immunochromatographic assay (TAUNS, Numazu, Japan) for culture confirmation of M. tuberculosis using 242 culture-positive liquid media in 2 mycobacterial laboratories from November 2005 to February 2006. Among the 242 samples, 183 were also tested with the BD ProbeTec ET (CTB) assay (Becton Dickinson, Sparks, MD). The results of both assays were compared to the culture results and to each other. The overall sensitivity and specificity of the Capilia TB assay were 98.6% and 97.9%, respectively, and for the CTB assay were 97.3% and 97.1%, respectively. The positive and negative predictive values for the Capilia TB assay were 98.6% and 97.9%, respectively, and for the CTB assay were 98.2% and 95.8%, respectively. Among the 183 samples tested with both assays, 8 had discrepant results, including Capilia-TB-false-positive in 2, CTB-false-positive in another 2, CTB-false-negative in 2, Capilia TB-false-negative in 1, and both assays with false-negative results in the remaining one. This study demonstrated that the Capilia TB assay has a similar diagnostic value with the CTB assay. In addition, with the immunochromatographic method, it is less time-consuming and does not require other laboratory equipment. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:395 / 399
页数:5
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