Undetected Transmission: The Impact of Tuberculosis on Migrant Youth in Scotland
Overview
This retrospective observational study evaluated tuberculosis burden, screening uptake, treatment initiation, and time to treatment among migrant and asylum-seeking children and adolescents attending a targeted screening service in Scotland. Screening uptake and treatment initiation were high, although some participants experienced prolonged intervals before treatment.
Background
TB remains a major global public health challenge. Migrant, refugee, and asylum-seeking populations may experience risks related to exposures before migration, conditions during migration journeys, and barriers to healthcare after arrival. Scotland is a low-incidence setting where targeted screening is recommended for higher-risk populations, but implementation varies. Evidence on screening outcomes and subsequent care pathways among migrant children and adolescents remains limited.
Data Highlights
Individuals assessed: 131
Individuals screened: 117 (89.3%)
Median age: 16 years
Participants from high-TB-burden countries: 59 (45.0%)
LTBI cases: 13 (11.1% of those screened)
Active TB cases: 2 (1.7%)
Overall TB positivity: 15 of 117 (12.8%)
Treatment initiated by data collection: 14 of 15 cases (93.3%)
Median time to treatment initiation: 35 days
LTBI treatment initiated after more than 90 days: 3 of 13 cases
Key Findings
Targeted screening achieved 89.3% uptake and identified both latent and active TB.
Thirteen participants had LTBI, and 2 had active pulmonary or disseminated TB.
Twelve of the 15 TB-positive participants originated from high-incidence countries, whereas 3 originated from medium- or low-incidence countries.
Treatment had been initiated in 14 of 15 cases at the time of data collection and was subsequently initiated in the remaining case.
Five of 13 participants with LTBI began treatment within 28 days, while 3 began treatment after more than 90 days.
No evaluated variable was significantly associated with LTBI positivity after correction for multiple testing, and the small number of cases limited statistical power.
Fourteen individuals declined screening or were not screened for operational reasons, leaving their TB status unknown.
Clinical Implications
Targeted screening was feasible and identified a substantial burden of latent and active TB in this single-service cohort. Cases among participants from medium- or low-incidence countries suggest that country of origin alone may not capture individual risk. Migration-related exposures and experiences may warrant consideration alongside country-of-origin incidence, while culturally appropriate communication, interpreters, reminder systems, and integration with broader migrant health assessments may help strengthen continuity of care.
Conclusion
Migrant and asylum-seeking children and adolescents attending this targeted service had high screening uptake and treatment engagement, but clinically important latent and active TB was identified and treatment-initiation intervals varied. Larger multisite studies are needed to confirm the findings, evaluate wider applicability, and determine how migration-related exposures and patient- and system-level factors affect TB risk and care pathways.
Related Resources & Content
Silent Spread: Tuberculosis Burden and Care Pathway Delays Among Migrant and Asylum-Seeking Children and Adolescents in Scotland — Lucas S, Montgomery L, Sculthorpe N, Mackay W, McKay L. International Journal of Infectious Diseases. 2026;171:108930. doi:10.1016/j.ijid.2026.108930.
Global Tuberculosis Report 2024 — World Health Organization. Geneva: WHO; 2024.
Roadmap Towards Ending TB in Children and Adolescents — World Health Organization. 3rd ed. Geneva: WHO; 2023.
Tuberculosis Annual Report 2023 — Public Health Scotland. Edinburgh: Public Health Scotland; 2024.
Tuberculosis (NG33) — National Institute for Health and Care Excellence. London: NICE; 2023.
Refugee and Asylum-Seeking Children and Young People: Guidance for Paediatricians — Royal College of Paediatrics and Child Health. London: RCPCH; 2022.