z-logo
Premium
The value of microscopic‐observation drug susceptibility assay in the diagnosis of tuberculosis and detection of multidrug resistance
Author(s) -
Sertel Şelale Denİz,
Uzun Meltem
Publication year - 2018
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/apm.12783
Subject(s) - sputum , tuberculosis , mycobacterium tuberculosis complex , medicine , multiple drug resistance , drug resistance , microbiology and biotechnology , mycobacterium tuberculosis , biology , pathology
Inexpensive, rapid, and reliable tests for detecting the presence and drug susceptibility of Mycobacterium tuberculosis complex ( MTBC ) are urgently needed to control the transmission of tuberculosis. In this study, we aimed to assess the accuracy and speed of the microscopic‐observation drug susceptibility ( MODS ) assay in the identification of MTBC and detection of multidrug resistance. Sputum samples from patients suspected to have tuberculosis were simultaneously tested with MODS and conventional culture [Löwenstein‐Jensen ( LJ ) culture, BACTEC MGIT ™ 960 ( MGIT ) system], and drug susceptibility testing ( MGIT system) methods. A total of 331 sputum samples were analyzed. Sensitivity and specificity of MODS assay for detection of MTBC strains were 96% and 98.8%, respectively. MODS assay detected multidrug resistant MTBC isolates with 92.3% sensitivity and 96.6% specificity. Median time to culture positivity was similar for MGIT (8 days) and MODS culture (8 days), but was significantly longer with LJ culture (20 days) (p < 0.0001 for both comparisons). Median time to availability of the susceptibility results was significantly (p < 0.0001) shorter with MODS assay (8 days) than MGIT system (20 days). In conclusion, MODS is an inexpensive and rapid test with good performance characteristics for direct diagnosis of tuberculosis and detection of multidrug resistance.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here