Evidence map›Paper›PMID 21996699›Full record

ReviewThe Journal of infectious diseases2011

Diagnosing latent tuberculosis in high-risk individuals: rising to the challenge in high-burden areas.

Victoria O Kasprowicz, Gavin Churchyard, Stephen D Lawn, S Bertel Squire, Ajit Lalvani

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of infectious diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
  5. Review
  6. Article
  7. Review
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  13. Frontiers in immunology · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. ATS Core Curriculum 2014: part I. Adult pulmonary medicine.Annals of the American Thoracic Society · 2014
    Article
  18. Article
  19. The microbiome: stress, health and disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 3 countries.

Victoria O KasprowiczRagon Institute of MGH, MIT, and Harvard, Harvard Medical School, Boston, Massachusetts, USA.
Gavin Churchyard
Stephen D Lawn
S Bertel Squire
Ajit Lalvani
Aurum Institute · ZAImperial College London · GBLiverpool School of Tropical Medicine · GBLondon School of Hygiene & Tropical Medicine · GBRagon Institute of MGH, MIT and Harvard · US

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROBERT A. PARKER · 2004 to 2026
$94.4M
NIAID NIH HHS P30 AI060354Wellcome Trust
6 · The paper itself

Abstract

A key challenge to greater progress in tuberculosis (TB) control is the reservoir of latent TB infection (LTBI), which represents a huge long-lived reservoir of potential TB disease. In parts of Africa, as many as 50% of 15-year-olds and 77%-89% of adults have evidence of LTBI. A second key challenge to TB control is the human immunodeficiency virus (HIV)-associated TB epidemic, and Africa alone accounts for one-quarter of the global burden of HIV-associated TB. HIV co-infection promotes both reactivation TB from LTBI and rapidly progressive primary TB following recent exposure to Mycobacterium tuberculosis. Preventing active TB and tackling latent infection in addition to the Directly Observed Treatment, Short-Course (DOTS) strategy could improve TB control in high-burden settings, especially where there is a high prevalence of HIV co-infection. Current strategies include intensified case finding (ICF), TB infection control, antiretroviral therapy (ART), and isoniazid preventive therapy (IPT). Although ART has been widely rolled out, ICF and IPT have not. A key factor limiting the rollout and effectiveness of IPT and ICF is the limitations of existing tools to both diagnose LTBI and identify those persons most at risk of progressing to active TB. In this review, we examine the obstacles and consider current progress toward the development of new tools to address this pressing global problem.

Indexed as

AfricaHIV InfectionsHumansInterferon-gamma Release TestsLatent TuberculosisPredictive Value of Tests

Identifiers

PMID21996699
PMCPMC3192547
OpenAlexW2166397573

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.