Prospective evaluation of thin-layer agar colour test in routine diagnosis of multidrug-resistant TB
BACKGROUND This study evaluated the diagnostic performance of the thin-layer agar MDR/XDR-TB Colour Test (CT), a Mycobacterium tuberculosis complex (MTBC) detection and direct drug susceptibility testing (DST) method with routine sputum, bronchoalveolar lavage and pleural fluid specimen. METHODS In...
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Published in | The international journal of tuberculosis and lung disease Vol. 28; no. 8; pp. 387 - 394 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
France
International Union Against Tuberculosis and Lung Disease
01.08.2024
International Union against Tuberculosis and Lung Disease (IUATLD) |
Subjects | |
Online Access | Get full text |
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Summary: | BACKGROUND This study evaluated the diagnostic performance of the thin-layer agar MDR/XDR-TB Colour Test (CT), a Mycobacterium tuberculosis complex (MTBC) detection and direct drug susceptibility testing (DST) method with routine sputum,
bronchoalveolar lavage and pleural fluid specimen. METHODS In a prospective study, the time and rate of MTBC detection were compared between CT, Löwenstein-Jensen, and MGIT media. Times until DST result, sensitivities, and specificities
were evaluated between CT and MGIT 960 indirect DST. RESULTS The cultivation of 177 pulmonary specimens resulted in 83 MTBC-positive cultures. The sensitivity of CT for MTBC detection was 81.3% with a median time of 20 days compared to
13 days and 93.5% for MGIT. The sensitivity of CT for DST results was 100% for isoniazid and levofloxacin and 94.7% for rifampicin. The specificities for isoniazid and rifampicin DST were 97.3% and 98.0% for levofloxacin. The median time until a DST result was significantly shorter with CT
than the BACTEC MGIT 960 system, 20 and 27 days, respectively, independent of the specimen type used. CONCLUSIONS The CT is a highly accurate and fast initial diagnostic test for high-incidence settings and could also be used as a first
culture and direct DST in peripheral settings. |
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Bibliography: | 1027-3719(20240801)28:8L.387;1- (R) Medicine - General ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ISSN: | 1027-3719 1815-7920 1815-7920 |
DOI: | 10.5588/ijtld.23.0536 |