Evidence map›Paper›PMID 35338849›Full record

ArticleThe Lancet. Public health2022

Effectiveness of nationwide programmatic testing and treatment for latent tuberculosis infection in migrants in England: a retrospective, population-based cohort study.

Luis C Berrocal-Almanza, Ross J Harris, Simon M Collin, Morris C Muzyamba, Olivia D Conroy, Adil Mirza, Anne-Marie O'Connell, Lynn Altass, Sarah R Anderson, H Lucy Thomas and 6 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  6. Expert perspectives on tuberculosis screening procedures for migrants.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Luis C Berrocal-AlmanzaNational Institute for Health Research Health Protection Research Unit in Respiratory Infections, National Heart and Lung Institute, Imperial College London, London, UK.
Ross J HarrisStatistics, Modelling and Economics Department, UK Health Security Agency, London, UK.
Simon M CollinHealthcare Associated Infection, Fungal, Antimicrobial Resistance, Antimicrobial Usage and Sepsis Division, UK Health Security Agency, London, UK.
Morris C MuzyambaTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Olivia D ConroyTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Adil MirzaTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Anne-Marie O'ConnellInformatics and Surveillance Systems, Data Operations Division, UK Health Security Agency, London, UK.
Lynn AltassPrevention Programme, Medical Directorate NHS England and NHS Improvement, London, UK.
Sarah R AndersonTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
H Lucy ThomasTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Colin CampbellTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Dominik ZennerNational Institute for Health Research Health Protection Research Unit in Respiratory Infections, National Heart and Lung Institute, Imperial College London, London, UK; Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Nick PhinTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK; Clinical and Protecting Health Directorate, Public Health Scotland, Edinburgh, UK.
Onn Min KonNational Institute for Health Research Health Protection Research Unit in Respiratory Infections, National Heart and Lung Institute, Imperial College London, London, UK; St Mary's Hospital, Imperial Healthcare NHS Trust, London, UK.
E Grace SmithTuberculosis Unit, Clinical and Emerging Infection Division, UK Health Security Agency, London, UK.
Ajit LalvaniNational Institute for Health Research Health Protection Research Unit in Respiratory Infections, National Heart and Lung Institute, Imperial College London, London, UK; Tuberculosis Research Centre, National Heart and Lung Institute, Imperial College London, London, UK. Electronic address: a.lalvani@imperial.ac.uk.
UK Health Security AgencyImperial College London · GBNHS England

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn low-incidence countries, tuberculosis mainly affects migrants, mostly resulting from reactivation of latent tuberculosis infection (LTBI) acquired in high-incidence countries before migration. A nationwide primary care-based LTBI testing and treatment programme for migrants from high-incidence countries was therefore established in high tuberculosis incidence areas in England. We aimed to assess the effectiveness of this programme.

methodsWe did a retrospective, population-based cohort study of migrants who registered in primary care between Jan 1, 2011, and Dec 31, 2018, in 55 high-burden areas with programmatic LTBI testing and treatment. Eligible individuals were aged 16-35 years, born in a high-incidence country, and had entered England in the past 5 years. Individuals who tested interferon-γ release assay (IGRA)-negative were advised about symptoms of tuberculosis, whereas those who tested IGRA-positive were clinically assessed to rule out active tuberculosis and offered preventive therapy. The primary outcome was incident tuberculosis notified to the national Enhanced Tuberculosis Surveillance system.

findingsOur cohort comprised 368 097 eligible individuals who had registered in primary care, of whom 37 268 (10·1%) were tested by the programme. 1446 incident cases of tuberculosis were identified: 166 cases in individuals who had IGRA testing (incidence 204 cases [95% CI 176-238] per 100 000 person-years) and 1280 in individuals without IGRA testing (82 cases [77-86] per 100 000 person-years). Overall, in our primary analysis including all diagnosed tuberculosis cases, a time-varying association was identified between LTBI testing and treatment and lower risk of incident tuberculosis (hazard ratio [HR] 0·76 [95% CI 0·63-0·91]) when compared with no testing. In stratified analysis by follow-up period, the intervention was associated with higher risk of tuberculosis diagnosis during the first 6 months of follow-up (9·93 [7·63-12·9) and a lower risk after 6 months (0·57 [0·41-0·79]). IGRA-positive individuals had higher risk of tuberculosis diagnosis than IGRA-negative individuals (31·9 [20·4-49·8]). Of 37 268 migrants who were tested, 6640 (17·8%) were IGRA-positive, of whom 1740 (26·2%) started preventive treatment. LTBI treatment lowered the risk of tuberculosis: of 135 incident cases in the IGRA-positive cohort, seven cases were diagnosed in the treated group (1·87 cases [95% CI 0·89-3·93] per 1000 person-years) and 128 cases were diagnosed in the untreated group (10·9 cases [9·16-12·9] per 1000 person-years; HR 0·14 [95% CI 0·06-0·32]).

interpretationA low proportion of eligible migrants were tested by the programme and a small proportion of those testing positive started treatment. Despite this, programmatic LTBI testing and treatment of individuals migrating to a low-incidence region is effective at diagnosing active tuberculosis earlier and lowers the long-term risk of progression to tuberculosis. Increasing programme participation and treatment rates for those testing positive could substantially impact national tuberculosis incidence.

fundingNational Institute for Health Research Health Protection Research Unit in Respiratory Infections.

Indexed as

Latent TuberculosisTransients and MigrantsAdolescentAdultCohort StudiesEnglandHumansRetrospective StudiesYoung Adult

Identifiers

PMID35338849
PMCPMC8967722
OpenAlexW4220683208

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.