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Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil

BACKGROUND: To compare epidemiological data between recurrent cases after cure (RC), distinguishing relapse from reinfection, after dropout (RD) and new cases (NC) in an ambulatory setting in a TB-endemic country. METHODS: Records of patients who started treatment for pulmonary TB between 2004 and 2...

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Autores principales: Unis, Gisela, Ribeiro, Andrezza Wolowski, Esteves, Leonardo Souza, Spies, Fernanda Sá, Picon, Pedro Dornelles, Costa, Elis Regina Dalla, Rossetti, Maria Lucia Rosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215011/
https://www.ncbi.nlm.nih.gov/pubmed/25338623
http://dx.doi.org/10.1186/s12879-014-0548-6
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author Unis, Gisela
Ribeiro, Andrezza Wolowski
Esteves, Leonardo Souza
Spies, Fernanda Sá
Picon, Pedro Dornelles
Costa, Elis Regina Dalla
Rossetti, Maria Lucia Rosa
author_facet Unis, Gisela
Ribeiro, Andrezza Wolowski
Esteves, Leonardo Souza
Spies, Fernanda Sá
Picon, Pedro Dornelles
Costa, Elis Regina Dalla
Rossetti, Maria Lucia Rosa
author_sort Unis, Gisela
collection PubMed
description BACKGROUND: To compare epidemiological data between recurrent cases after cure (RC), distinguishing relapse from reinfection, after dropout (RD) and new cases (NC) in an ambulatory setting in a TB-endemic country. METHODS: Records of patients who started treatment for pulmonary TB between 2004 and 2010 in a TB clinic were reviewed. Epidemiological data were analyzed. Spoligotyping and MIRU patterns were used to determine relapse or reinfection in 13 RC available. RESULTS: Of the eligible group (1449), 1060 were NC (73.2%), among the recurrent cases, 203 (14%) were RC and 186 (12.8%) were RD. Of RC, 171 (84.2%) occurred later than 6 months after a previous episode, 13 had available DNA, in 4 (30.7%) the disease was attributed to reinfection and in 9 (69.3%), to relapse. Comparing RC to NC, HIV (p < 0.0001) was independent risk factor for RC. When RC and RD were compared, alcohol abuse (p = 0.001) and treatment noncompliance (p = 0.006) were more frequent in RD. CONCLUSIONS: HIV is the sole more important associated factor for RC. This finding points the need to improve the approach to manage TB in order to decrease the chance for exposure especially in vulnerable people with increased risk of developing disease and to improve DOTS strategy to deal with factors associated to treatment noncompliance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0548-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-42150112014-11-01 Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil Unis, Gisela Ribeiro, Andrezza Wolowski Esteves, Leonardo Souza Spies, Fernanda Sá Picon, Pedro Dornelles Costa, Elis Regina Dalla Rossetti, Maria Lucia Rosa BMC Infect Dis Research Article BACKGROUND: To compare epidemiological data between recurrent cases after cure (RC), distinguishing relapse from reinfection, after dropout (RD) and new cases (NC) in an ambulatory setting in a TB-endemic country. METHODS: Records of patients who started treatment for pulmonary TB between 2004 and 2010 in a TB clinic were reviewed. Epidemiological data were analyzed. Spoligotyping and MIRU patterns were used to determine relapse or reinfection in 13 RC available. RESULTS: Of the eligible group (1449), 1060 were NC (73.2%), among the recurrent cases, 203 (14%) were RC and 186 (12.8%) were RD. Of RC, 171 (84.2%) occurred later than 6 months after a previous episode, 13 had available DNA, in 4 (30.7%) the disease was attributed to reinfection and in 9 (69.3%), to relapse. Comparing RC to NC, HIV (p < 0.0001) was independent risk factor for RC. When RC and RD were compared, alcohol abuse (p = 0.001) and treatment noncompliance (p = 0.006) were more frequent in RD. CONCLUSIONS: HIV is the sole more important associated factor for RC. This finding points the need to improve the approach to manage TB in order to decrease the chance for exposure especially in vulnerable people with increased risk of developing disease and to improve DOTS strategy to deal with factors associated to treatment noncompliance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0548-6) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-24 /pmc/articles/PMC4215011/ /pubmed/25338623 http://dx.doi.org/10.1186/s12879-014-0548-6 Text en © Unis et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Unis, Gisela
Ribeiro, Andrezza Wolowski
Esteves, Leonardo Souza
Spies, Fernanda Sá
Picon, Pedro Dornelles
Costa, Elis Regina Dalla
Rossetti, Maria Lucia Rosa
Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title_full Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title_fullStr Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title_full_unstemmed Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title_short Tuberculosis recurrence in a high incidence setting for HIV and tuberculosis in Brazil
title_sort tuberculosis recurrence in a high incidence setting for hiv and tuberculosis in brazil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215011/
https://www.ncbi.nlm.nih.gov/pubmed/25338623
http://dx.doi.org/10.1186/s12879-014-0548-6
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