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Association between tuberculin skin test result and clinical presentation of tuberculosis disease
BACKGROUND: The tuberculin skin test (TST) is used to test for latent tuberculosis (TB) infection and support the diagnosis of active TB. However, little is known about the relationship between the TST result and the clinical presentation of TB disease. METHODS: We analyzed US TB surveillance data,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851915/ https://www.ncbi.nlm.nih.gov/pubmed/24093965 http://dx.doi.org/10.1186/1471-2334-13-460 |
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author | Auld, Sara C Click, Eleanor S Heilig, Charles M Miramontes, Roque Cain, Kevin P Bisson, Gregory P Mac Kenzie, William R |
author_facet | Auld, Sara C Click, Eleanor S Heilig, Charles M Miramontes, Roque Cain, Kevin P Bisson, Gregory P Mac Kenzie, William R |
author_sort | Auld, Sara C |
collection | PubMed |
description | BACKGROUND: The tuberculin skin test (TST) is used to test for latent tuberculosis (TB) infection and support the diagnosis of active TB. However, little is known about the relationship between the TST result and the clinical presentation of TB disease. METHODS: We analyzed US TB surveillance data, 1993–2010, and used multinomial logistic regression to calculate the association between TST result (0–4 mm [negative], 5–9 mm, 10–14 mm, and ≥ 15 mm) and clinical presentation of disease (miliary, combined pulmonary and extrapulmonary, extrapulmonary only, non-cavitary pulmonary, and cavitary pulmonary). For persons with pulmonary disease, multivariate logistic regression was used to calculate the odds of having acid-fast bacilli (AFB) positive sputum. RESULTS: There were 64,238 persons with culture-confirmed TB included in the analysis, which was stratified by HIV status and birthplace (US- vs. foreign-born). Persons with a TST ≥ 15 mm were less likely to have miliary or combined pulmonary and extrapulmonary disease, but more likely to have cavitary pulmonary disease than non-cavitary pulmonary disease. Persons with non-cavitary pulmonary disease with a negative TST were significantly more likely to have AFB positive sputum. CONCLUSIONS: Clinical presentation of TB disease differed according to TST result and persons with a negative TST were more likely to have disseminated disease (i.e., miliary or combined pulmonary and extrapulmonary). Further study of the TST result may improve our understanding of the host-pathogen relationship in TB disease. |
format | Online Article Text |
id | pubmed-3851915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38519152013-12-06 Association between tuberculin skin test result and clinical presentation of tuberculosis disease Auld, Sara C Click, Eleanor S Heilig, Charles M Miramontes, Roque Cain, Kevin P Bisson, Gregory P Mac Kenzie, William R BMC Infect Dis Research Article BACKGROUND: The tuberculin skin test (TST) is used to test for latent tuberculosis (TB) infection and support the diagnosis of active TB. However, little is known about the relationship between the TST result and the clinical presentation of TB disease. METHODS: We analyzed US TB surveillance data, 1993–2010, and used multinomial logistic regression to calculate the association between TST result (0–4 mm [negative], 5–9 mm, 10–14 mm, and ≥ 15 mm) and clinical presentation of disease (miliary, combined pulmonary and extrapulmonary, extrapulmonary only, non-cavitary pulmonary, and cavitary pulmonary). For persons with pulmonary disease, multivariate logistic regression was used to calculate the odds of having acid-fast bacilli (AFB) positive sputum. RESULTS: There were 64,238 persons with culture-confirmed TB included in the analysis, which was stratified by HIV status and birthplace (US- vs. foreign-born). Persons with a TST ≥ 15 mm were less likely to have miliary or combined pulmonary and extrapulmonary disease, but more likely to have cavitary pulmonary disease than non-cavitary pulmonary disease. Persons with non-cavitary pulmonary disease with a negative TST were significantly more likely to have AFB positive sputum. CONCLUSIONS: Clinical presentation of TB disease differed according to TST result and persons with a negative TST were more likely to have disseminated disease (i.e., miliary or combined pulmonary and extrapulmonary). Further study of the TST result may improve our understanding of the host-pathogen relationship in TB disease. BioMed Central 2013-10-04 /pmc/articles/PMC3851915/ /pubmed/24093965 http://dx.doi.org/10.1186/1471-2334-13-460 Text en Copyright © 2013 Auld 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 Auld, Sara C Click, Eleanor S Heilig, Charles M Miramontes, Roque Cain, Kevin P Bisson, Gregory P Mac Kenzie, William R Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title | Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title_full | Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title_fullStr | Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title_full_unstemmed | Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title_short | Association between tuberculin skin test result and clinical presentation of tuberculosis disease |
title_sort | association between tuberculin skin test result and clinical presentation of tuberculosis disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851915/ https://www.ncbi.nlm.nih.gov/pubmed/24093965 http://dx.doi.org/10.1186/1471-2334-13-460 |
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