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Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam

BACKGROUND: To control multidrug resistant tuberculosis (MDR-TB), the drug susceptibility profile is needed to guide therapy. Classical drug susceptibility testing (DST) may take up to 2 to 4 months. The GenoType(® )MTBDRplus test is a commercially available line-probe assay that rapidly detects Myc...

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Autores principales: Huyen, Mai NT, Tiemersma, Edine W, Lan, Nguyen TN, Cobelens, Frank GJ, Dung, Nguyen H, Sy, Dinh N, Buu, Tran N, Kremer, Kristin, Hang, Pham T, Caws, Maxine, O'Brien, Richard, van Soolingen, Dick
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901356/
https://www.ncbi.nlm.nih.gov/pubmed/20525271
http://dx.doi.org/10.1186/1471-2334-10-149
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author Huyen, Mai NT
Tiemersma, Edine W
Lan, Nguyen TN
Cobelens, Frank GJ
Dung, Nguyen H
Sy, Dinh N
Buu, Tran N
Kremer, Kristin
Hang, Pham T
Caws, Maxine
O'Brien, Richard
van Soolingen, Dick
author_facet Huyen, Mai NT
Tiemersma, Edine W
Lan, Nguyen TN
Cobelens, Frank GJ
Dung, Nguyen H
Sy, Dinh N
Buu, Tran N
Kremer, Kristin
Hang, Pham T
Caws, Maxine
O'Brien, Richard
van Soolingen, Dick
author_sort Huyen, Mai NT
collection PubMed
description BACKGROUND: To control multidrug resistant tuberculosis (MDR-TB), the drug susceptibility profile is needed to guide therapy. Classical drug susceptibility testing (DST) may take up to 2 to 4 months. The GenoType(® )MTBDRplus test is a commercially available line-probe assay that rapidly detects Mycobacterium tuberculosis (MTB) complex, as well as the most common mutations associated with rifampin and isoniazid resistance. We assessed sensitivity and specificity of the assay by using a geographically representative set of MTB isolates from the South of Vietnam. METHODS: We re-cultured 111 MTB isolates that were MDR, rifampin-resistant or pan-susceptible according to conventional DST and tested these with the GenoType(® )MTBDRplus test. RESULTS: By conventional DST, 55 strains were classified as MDR-TB, four strains were rifampicin mono-resistant and 52 strains were susceptible to all first-line drugs. The sensitivity of the GenoType(® )MTBDRplus was 93.1% for rifampicin, 92.6% for isoniazid and 88.9% for the combination of both; its specificity was 100%. The positive predictive value of the GenoType(® )MTBDRplus test for MDR-TB was 100% and the negative predictive value 90.3%. CONCLUSIONS: We found a high specificity and positive predictive value of the GenoType(® )MTBDRplus test for MDR-TB which merits its use in the MDR-TB treatment program in Vietnam.
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spelling pubmed-29013562010-07-10 Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam Huyen, Mai NT Tiemersma, Edine W Lan, Nguyen TN Cobelens, Frank GJ Dung, Nguyen H Sy, Dinh N Buu, Tran N Kremer, Kristin Hang, Pham T Caws, Maxine O'Brien, Richard van Soolingen, Dick BMC Infect Dis Research Article BACKGROUND: To control multidrug resistant tuberculosis (MDR-TB), the drug susceptibility profile is needed to guide therapy. Classical drug susceptibility testing (DST) may take up to 2 to 4 months. The GenoType(® )MTBDRplus test is a commercially available line-probe assay that rapidly detects Mycobacterium tuberculosis (MTB) complex, as well as the most common mutations associated with rifampin and isoniazid resistance. We assessed sensitivity and specificity of the assay by using a geographically representative set of MTB isolates from the South of Vietnam. METHODS: We re-cultured 111 MTB isolates that were MDR, rifampin-resistant or pan-susceptible according to conventional DST and tested these with the GenoType(® )MTBDRplus test. RESULTS: By conventional DST, 55 strains were classified as MDR-TB, four strains were rifampicin mono-resistant and 52 strains were susceptible to all first-line drugs. The sensitivity of the GenoType(® )MTBDRplus was 93.1% for rifampicin, 92.6% for isoniazid and 88.9% for the combination of both; its specificity was 100%. The positive predictive value of the GenoType(® )MTBDRplus test for MDR-TB was 100% and the negative predictive value 90.3%. CONCLUSIONS: We found a high specificity and positive predictive value of the GenoType(® )MTBDRplus test for MDR-TB which merits its use in the MDR-TB treatment program in Vietnam. BioMed Central 2010-06-03 /pmc/articles/PMC2901356/ /pubmed/20525271 http://dx.doi.org/10.1186/1471-2334-10-149 Text en Copyright ©2010 Huyen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Huyen, Mai NT
Tiemersma, Edine W
Lan, Nguyen TN
Cobelens, Frank GJ
Dung, Nguyen H
Sy, Dinh N
Buu, Tran N
Kremer, Kristin
Hang, Pham T
Caws, Maxine
O'Brien, Richard
van Soolingen, Dick
Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title_full Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title_fullStr Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title_full_unstemmed Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title_short Validation of the GenoType(® )MTBDRplus assay for diagnosis of multidrug resistant tuberculosis in South Vietnam
title_sort validation of the genotype(® )mtbdrplus assay for diagnosis of multidrug resistant tuberculosis in south vietnam
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901356/
https://www.ncbi.nlm.nih.gov/pubmed/20525271
http://dx.doi.org/10.1186/1471-2334-10-149
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