Evidence map›Paper›PMID 42638666›Full record

ReviewFrontiers in tuberculosis2024

Ending tuberculosis: challenges and opportunities.

Beth Gilmour, Kefyalew Addis Alene

Abstract readReview
In one paragraph

Review in Frontiers in tuberculosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  4. Article
  5. Article
  6. Review
  7. Review
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  9. Review
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  12. Frontiers in immunology · 2025
    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

2 authors.

Beth GilmourSchool of Population Health, Faculty of Health Sciences, Curtin University, Perth, WA, Australia.
Kefyalew Addis AleneGeospatial and Tuberculosis Team, The Kids Research Institute, Perth, WA, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite impacting mankind since ancient times, tuberculosis (TB) persists as the leading cause of death from an infectious disease. TB can remain latent and further research is required to understand activation risk and the risks vs. the benefits of treating latent infection. Drug resistance poses an escalating threat to treating active disease and achieving cure. Recent advances in molecular and epidemiological techniques facilitate early diagnosis, drug susceptibility testing and an opportunity to better understand transmission dynamics. Research is ongoing to develop safe, efficacious tolerable drug regimens and the challenges of antibiotic resistance have led to a resurgent interest in therapeutic alternatives. Vaccine development is challenged by the pathogen's genetic diversity, the heterogeneity of host susceptibility and the extreme complexities that occur across the interactions between TB and its host. Across all stages of TB pathogenesis, developments in artificial intelligence, geographic information systems, digital health technologies, renewable energy solutions and nano medicine are providing opportunities to improve TB control. Resource constraints however often challenge the opportunity to access these new technologies by those most in need. The societal inequalities in accessing new technologies further compound socio-economic and health related TB determinants Addressing these complex determinants which include malnutrition, HIV infection, diabetes, substance abuse, poor environmental conditions and multi-factorial barriers to health care access, will require political will, sufficient funding, and a holistic multisectoral response.

Indexed as

challengeseliminationopportunitiesSDGtuberculosis

Identifiers

PMID42638666
PMCPMC13495007

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.