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Disease Transmission by Patients With Subclinical Tuberculosis

BACKGROUND: Subclinical tuberculosis has been increasingly recognized as a separate state in the spectrum of the disease. However, evidence on the transmissibility of subclinical tuberculosis is still inconclusive. METHODS: We re-analyzed the data from the 2007 combined tuberculosis prevalence and t...

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Autores principales: Nguyen, Hai Viet, Tiemersma, Edine, Nguyen, Nhung Viet, Nguyen, Hoa Binh, Cobelens, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249982/
https://www.ncbi.nlm.nih.gov/pubmed/36660850
http://dx.doi.org/10.1093/cid/ciad027
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author Nguyen, Hai Viet
Tiemersma, Edine
Nguyen, Nhung Viet
Nguyen, Hoa Binh
Cobelens, Frank
author_facet Nguyen, Hai Viet
Tiemersma, Edine
Nguyen, Nhung Viet
Nguyen, Hoa Binh
Cobelens, Frank
author_sort Nguyen, Hai Viet
collection PubMed
description BACKGROUND: Subclinical tuberculosis has been increasingly recognized as a separate state in the spectrum of the disease. However, evidence on the transmissibility of subclinical tuberculosis is still inconclusive. METHODS: We re-analyzed the data from the 2007 combined tuberculosis prevalence and tuberculin surveys in Vietnam. Poisson regression with robust standard errors was conducted to assess the effect of clinical presentation of individuals with tuberculosis in the household on tuberculin skin test (TST) positivity among children aged 6–14 years who participated in the tuberculin survey, adjusting for child's age, smear status of the index patient, and other covariates. RESULTS: In the multivariate analysis, we found significantly increased risks for TST positivity in children living with patients with clinical, smear-positive tuberculosis, compared with those living with individuals without tuberculosis (adjusted risk ratio [aRR]: 3.04; 95% confidence interval [CI]: 2.00–4.63) and with those living with patients with subclinical tuberculosis, adjusting for index smear status (aRR: 2.26; 95% CI: 1.03–4.96). Among children aged 6–10 years, those living with patients with clinical, smear-positive tuberculosis and those living with patients with subclinical, smear-positive tuberculosis had similarly increased risks of TST positivity compared with those living with individuals without tuberculosis (aRRs [95% CI] of 3.56 [1.91–6.62] and 3.11 [1.44–6.72], respectively). CONCLUSIONS: Our findings support the hypothesis that smear-positive subclinical tuberculosis contributes to Mycobacterium tuberculosis transmission. To eliminate tuberculosis in 2035, control strategies need to address subclinical presentations of the disease.
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spelling pubmed-102499822023-06-09 Disease Transmission by Patients With Subclinical Tuberculosis Nguyen, Hai Viet Tiemersma, Edine Nguyen, Nhung Viet Nguyen, Hoa Binh Cobelens, Frank Clin Infect Dis Major Article BACKGROUND: Subclinical tuberculosis has been increasingly recognized as a separate state in the spectrum of the disease. However, evidence on the transmissibility of subclinical tuberculosis is still inconclusive. METHODS: We re-analyzed the data from the 2007 combined tuberculosis prevalence and tuberculin surveys in Vietnam. Poisson regression with robust standard errors was conducted to assess the effect of clinical presentation of individuals with tuberculosis in the household on tuberculin skin test (TST) positivity among children aged 6–14 years who participated in the tuberculin survey, adjusting for child's age, smear status of the index patient, and other covariates. RESULTS: In the multivariate analysis, we found significantly increased risks for TST positivity in children living with patients with clinical, smear-positive tuberculosis, compared with those living with individuals without tuberculosis (adjusted risk ratio [aRR]: 3.04; 95% confidence interval [CI]: 2.00–4.63) and with those living with patients with subclinical tuberculosis, adjusting for index smear status (aRR: 2.26; 95% CI: 1.03–4.96). Among children aged 6–10 years, those living with patients with clinical, smear-positive tuberculosis and those living with patients with subclinical, smear-positive tuberculosis had similarly increased risks of TST positivity compared with those living with individuals without tuberculosis (aRRs [95% CI] of 3.56 [1.91–6.62] and 3.11 [1.44–6.72], respectively). CONCLUSIONS: Our findings support the hypothesis that smear-positive subclinical tuberculosis contributes to Mycobacterium tuberculosis transmission. To eliminate tuberculosis in 2035, control strategies need to address subclinical presentations of the disease. Oxford University Press 2023-01-20 /pmc/articles/PMC10249982/ /pubmed/36660850 http://dx.doi.org/10.1093/cid/ciad027 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Nguyen, Hai Viet
Tiemersma, Edine
Nguyen, Nhung Viet
Nguyen, Hoa Binh
Cobelens, Frank
Disease Transmission by Patients With Subclinical Tuberculosis
title Disease Transmission by Patients With Subclinical Tuberculosis
title_full Disease Transmission by Patients With Subclinical Tuberculosis
title_fullStr Disease Transmission by Patients With Subclinical Tuberculosis
title_full_unstemmed Disease Transmission by Patients With Subclinical Tuberculosis
title_short Disease Transmission by Patients With Subclinical Tuberculosis
title_sort disease transmission by patients with subclinical tuberculosis
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249982/
https://www.ncbi.nlm.nih.gov/pubmed/36660850
http://dx.doi.org/10.1093/cid/ciad027
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