Diagnostic accuracy of the microscopic observation drug susceptibility assay: a pilot study from India

被引:0
|
作者
Michael, J. S. [1 ]
Daley, P. [2 ]
Kalaiselvan, S. [1 ]
Latha, A. [2 ]
Vijayakumar, J. [2 ]
Mathai, D. [2 ]
John, K. R. [3 ]
Pai, M. [4 ]
机构
[1] Christian Med Coll & Hosp, Dept Microbiol, Vellore 632004, Tamil Nadu, India
[2] Christian Med Coll & Hosp, Dept Med, Vellore 632004, Tamil Nadu, India
[3] Christian Med Coll & Hosp, Dept Community Hlth, Vellore 632004, Tamil Nadu, India
[4] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
关键词
tuberculosis; MODS; diagnostic accuracy; MYCOBACTERIUM-TUBERCULOSIS; RESISTANT TUBERCULOSIS; CORD FORMATION; SPUTUM; TB; DECONTAMINATION; IDENTIFICATION; DIGESTION; CULTURE;
D O I
暂无
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
SETTING: The microscopic observation drug susceptibility (MODS) assay is a rapid, sensitive, low-cost liquid culture technique. OBJECTIVE: To establish the accuracy of MODS for the detection of active pulmonary tuberculosis (TB), and to document the costs and challenges of setting up this assay in a low-income setting. DESIGN: Prospective blinded pilot study of 200 adult TB suspects at a tertiary referral hospital in India. Reference standard included culture (Lowenstein-Jensen and automated liquid culture) and clinical diagnosis. RESULTS: Patients were mostly male (n = 122, 61.1%) and out-patients (n = 184, 92.0%), with a mean age of 40.4 years (standard deviation 16.2). Seventeen (8.5%) were human immunodeficiency virus infected and 47 (23.5%) were reference culture-positive. Compared to reference culture, MODS was 78.9% sensitive (95%CI 62.2-90.0) and 96.7% specific (95%CI 92.0-98.8). Clinical assessment suggested that MODS was false-negative in 3/8 reference culture-positive MODS-negatives and true-positive in 4/6 reference culture-negative MODS-positives. MODS was faster than solid (P < 0.001) and liquid culture (P = 0.088), and cheaper than both. CONCLUSION: MODS may be a good alternative to automated liquid culture, but there were several challenges in setting up the assay. Prior training and validation, setup costs and inability to rule out cross-contamination need to be taken into account before the test can be established.
引用
收藏
页码:482 / 488
页数:7
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