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Research ArticleOriginal Article
Open Access

Evaluation of direct detection of Mycobacterium tuberculosis in clinical samples using the BD ProbeTec ET system

Nada A. Abdel-Aziz, Khaled M. Al-Harbi, MohamedMofeed F. Morsy, Khaled A. Turkistani and Faisal N. Kurdi
Saudi Medical Journal February 2011, 32 (2) 123-127;
Nada A. Abdel-Aziz
Department of Microbiology and Immunology, Sohag Faculty of Medicine, Sohag, Egypt. Tel. +966 503558083. Fax: +966 (1) 4827621. E-mail: [email protected]
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Khaled M. Al-Harbi
Department of Microbiology and Immunology, Sohag Faculty of Medicine, Sohag, Egypt. Tel. +966 503558083. Fax: +966 (1) 4827621. E-mail: [email protected]
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MohamedMofeed F. Morsy
Department of Microbiology and Immunology, Sohag Faculty of Medicine, Sohag, Egypt. Tel. +966 503558083. Fax: +966 (1) 4827621. E-mail: [email protected]
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Khaled A. Turkistani
Department of Microbiology and Immunology, Sohag Faculty of Medicine, Sohag, Egypt. Tel. +966 503558083. Fax: +966 (1) 4827621. E-mail: [email protected]
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Faisal N. Kurdi
Department of Microbiology and Immunology, Sohag Faculty of Medicine, Sohag, Egypt. Tel. +966 503558083. Fax: +966 (1) 4827621. E-mail: [email protected]
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Abstract

OBJECTIVE: To evaluate the performance of the semi-automated BD ProbeTec ET system for the direct detection of Mycobacterium tuberculosis complex (MTBC) in comparison with microscopy, and culture for respiratory and non-respiratory specimens.

METHODS: The study was conducted in the Maternity and Children's Hospital, Madina, Saudi Arabia from October 2008 to October 2009. A single center prospective study of 70 suspected tuberculosis samples were subjected to microscopy, culture (solid and liquid), and the DB ProbeTec ET system.

RESULTS: A total of 70 specimens were studied; 47 respiratory, and 23 non-respiratory. Twelve (92.3%) ProbeTec positive results were obtained from 13 MTBC isolates from culture, while one specimen was BD ProbeTec ET positive, but yielded no growth on culture. Two samples gave anomalous results (false negative and positive results). The evaluated system showed sensitivity of 92.3%, specificity of 98%, positive predictive value of 92.3%, and negative predictive value of 98% for all specimens, while 88% sensitivity, 100% specificity, 100% positive predictive value, and 97.3% negative predictive value in cases of respiratory specimens, and 100% sensitivity, 93.3% specificity, 80% positive predictive value, and 100% negative predictive value in cases of non-respiratory specimens.

CONCLUSION: The ProbeTec ET is a rapid and specific method for direct detection of MTBC in clinical specimens compared with the gold standard of culture, especially in patients with smear-negative non-respiratory specimens.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (CC BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 32 (2)
Saudi Medical Journal
Vol. 32, Issue 2
1 Feb 2011
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Evaluation of direct detection of Mycobacterium tuberculosis in clinical samples using the BD ProbeTec ET system
Nada A. Abdel-Aziz, Khaled M. Al-Harbi, MohamedMofeed F. Morsy, Khaled A. Turkistani, Faisal N. Kurdi
Saudi Medical Journal Feb 2011, 32 (2) 123-127;

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Evaluation of direct detection of Mycobacterium tuberculosis in clinical samples using the BD ProbeTec ET system
Nada A. Abdel-Aziz, Khaled M. Al-Harbi, MohamedMofeed F. Morsy, Khaled A. Turkistani, Faisal N. Kurdi
Saudi Medical Journal Feb 2011, 32 (2) 123-127;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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