ArticleBMJ public health2025
Role of tuberculosis symptoms in transmission risk to cell contacts in prisons.
Article in BMJ public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Longitudinal Symptom Transitions Predict Incident Tuberculosis Risk in Serial Active Case Finding.The Journal of infectious diseases · 2026Article
- Comparison of phylogenetic metrics of transmission between symptomatic and asymptomatic tuberculosis in individuals who were incarcerated in Brazil in 2008-24: a retrospective genomic epidemiology study.The Lancet. Microbe · 2026Article
- Reported Tuberculosis Symptoms: An Inadequate Classifier of Disease State.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026Article
- Factors associated with tuberculosis symptom reporting among persons deprived of liberty in Brazil during active case finding: a cross-sectional study.BMJ public health · 2026Article
- Tuberculosis in prisons: an integrated prevention and care cascade for a persistent structural epidemic.Frontiers in public health · 2026Review
- Using Imaris to rigorously track PET-defined sites of lung inflammation inAmerican journal of diagnostic imaging · 2026Article
- Longitudinal symptom transitions predict incident tuberculosis risk among persons deprived of liberty in Brazil.medRxiv : the preprint server for health sciences · 2025Article
- Comparison of phylogenetic metrics of transmission in symptomatic and asymptomatic tuberculosis.medRxiv : the preprint server for health sciences · 2025Article
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10 authors.
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Abstract
Background: Understanding determinants of Methods: Between 2020 and 2022, we systematically screened persons deprived of liberty (PDL) from three prisons in Brazil for tuberculosis (TB) by symptom assessment and sputum testing with Xpert MTB/RIF Ultra. We performed QuantiFERON-TB Gold Plus (QFT) testing among cell contacts of individuals with TB and in cells with no TB case identified. We evaluated the relationship between TB exposure (symptomatic, asymptomatic and none) and QFT positivity using Bayesian generalised linear mixed models. Results: We screened 7641 PDL for TB and identified 290 cases, yielding a prevalence of 3.8% (290/7641). After applying the exclusion criteria, 686 participants were included for the QFT analysis: 132 contacts of 42 individuals with symptomatic TB, 224 exposed to 52 individuals with asymptomatic TB and 330 with no recent cell exposure. The odds of QFT positivity were higher in symptomatic (adjusted OR (aOR) 2.50, 95% credible interval (CrI) 1.51 to 4.16) and asymptomatic (aOR 1.61, 95% CrI 1.06 to 2.45) exposure groups than in those unexposed. QFT positivity in contacts of symptomatic and asymptomatic TB did not differ (aOR 1.56, 95% CrI 0.92 to 2.63). These associations may be underestimated because of infections acquired outside cell assignments. Conclusions: Approximately two-thirds of individuals with TB lacked symptoms, and their contacts and symptomatic TB contacts had similarly increased risk of QFT positivity compared with individuals without recent cell exposure. These findings indicate that symptom-based screening misses many TB cases. Effective TB control requires systematic screening irrespective of symptoms to interrupt transmission and accelerate diagnosis in high-burden settings.
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