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DOI 10.1016/j.diagmicrobio.2008.02.015

Медицинская библиотека · Diagnostic microbiology and infectious disease · 2008

Performance of the BACTEC MGIT 960 compared with solid media for detection of Mycobacterium in Bangkok, Thailand.

Srisuwanvilai La-Ong, Monkongdee Patama, Podewils Laura Jean, Ngamlert Keerataya, Pobkeeree Vallerut, Puripokai Panitchaya, Kanjanamongkolsiri Photjanart, Subhachaturas Wonchat, Akarasewi Pasakorn, Wells Charles D, Tappero Jordan W, Varma Jay K

Сравнительное исследованиеОценочное исследованиеСтатьяПеревод в очереди

Аннотация

Controlled trials have demonstrated that liquid media culture (LMC) is superior to solid media culture for diagnosis of Mycobacterium tuberculosis (MTB), but there is limited evidence about its performance in resource-limited settings. We evaluated the performance of LMC in a demonstration project in Bangkok, Thailand. Sputum specimens from persons with suspected or clinically diagnosed tuberculosis were inoculated in parallel on solid (Lowenstein-Jensen [LJ]) and liquid (mycobacterial growth indicator tube [MGIT 960]) media. Biochemical tests identified isolates as MTB or nontuberculosis mycobacteria (NTM). Of 2566 specimens received from October 2004 to September 2006, 1355 (53%) were culture positive by MGIT compared with 1013 (39%) by LJ. Median time to growth for MGIT was significantly less than LJ: 11 versus 27 days. Of 1417 isolates detected by at least 1 media, 1255 (86%) were identified as MTB and 162 (11%) NTM. MGIT improved speed and sensitivity of MTB isolation and drug susceptibility testing, regardless of HIV status.

Для цитирования: Srisuwanvilai La-Ong, Monkongdee Patama, Podewils Laura Jean, Ngamlert Keerataya, Pobkeeree Vallerut, Puripokai Panitchaya, Kanjanamongkolsiri Photjanart, Subhachaturas Wonchat, Akarasewi Pasakorn, Wells Charles D, Tappero Jordan W, Varma Jay K. Performance of the BACTEC MGIT 960 compared with solid media for detection of Mycobacterium in Bangkok, Thailand.. Diagnostic microbiology and infectious disease. 2008. DOI: 10.1016/j.diagmicrobio.2008.02.015.

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