Cited by 32Tuberculosis Research and EpidemiologyHIV, TB, and STIs EpidemiologyMathematical and Theoretical Epidemiology and Ecology Models

The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.

Is IPT more effective in high-burden settings? Modelling the effect of tuberculosis incidence on IPT impact

Open access
Ragonnet, R., Trauer, J. M., McBryde, E. S., Houben, R. M. G. J., Denholm, J. T., Handel, A., Sumner, T.·2017·The International Journal of Tuberculosis and Lung Disease

Abstract

SETTING: Isoniazid preventive therapy (IPT) is effective for preventing active tuberculosis (TB), although its mechanism of action is poorly understood and the optimal disease burden for IPT use has not been defined. OBJECTIVE: To describe the relationship between TB incidence and IPT effectiveness. METHODS: We constructed a model of TB transmission dynamics to investigate IPT effectiveness under various epidemiological settings. The model structure was intended to be highly adaptable to uncertainty in both input parameters and the mechanism of action of IPT. To determine the optimal setting for IPT use, we identified the lowest number needed to treat (NNT) with IPT to prevent one case of active TB. RESULTS: We found that the NNT as a function of TB incidence shows a 'U-shape', whereby IPT impact is greatest at an intermediate incidence and attenuated at both lower and higher incidence levels. This U-shape was observed over a broad range of parameter values; the optimal TB incidence was between 500 and 900 cases per 100 000 per year. CONCLUSIONS: TB burden is a critical factor to consider when making decisions about communitywide implementation of IPT. We believe that the total disease burden should not preclude programmatic application of IPT.

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Crossref · 10.5588/ijtld.16.0297

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Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Some countries are exploring alternative drugs or combination therapies for IPT.

    “However, some countries are now exploring alternative drugs or combination therapies for IPT [209–211].”

    From Current update on malaria in pregnancy: a systematic review (2025) · cites this paper as [209]

    The Discussion mentions specific regimens for multidrug-resistant latent TB only as a hypothetical extension of the model; it does not say that countries are exploring alternative drugs or combination therapies for IPT. Searches for alternative drugs, combination therapies, and country-level exploration found no passage addressing that claim. (LLM, conf=0.72)

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Research works printed but not linked: 7

  1. [23]World Health Organization. Guidelines on the management of latent tuberculosis infection. WHO/HTM/TB/2015.01 Geneva, Switzerland: WHO, 2015. 25973515
  2. [1]Caminero J A, Pena M J, Campos-Herrero M I, Exogenous reinfection with tuberculosis on a European island with a moderate incidence of disease. Am J Respir Crit Care Med 2001; 163: 717– 720. 11254530
  3. [2]van Rie A, Warren R, Richardson M, Exogenous reinfection as a cause of recurrent tuberculosis after curative treatment. N Engl J Med 1999; 341: 1174– 1179. 10519895
  4. [4]Smieja M J, Marchetti C A, Cook D J, Smaill F M. Isoniazid for preventing tuberculosis in non-HIV infected persons. Cochrane Database Syst Rev 2000: (2): CD001363. 10796642 PMC6532737
  5. [10]Vynnycky E, Fine P E. The natural history of tuberculosis: the implications of age-dependent risks of disease and the role of reinfection. Epidemiol Infect 1997; 119: 183– 201. 9363017 PMC2808840
  6. [11]Sloot R, Schim van der Loeff M F, Kouw P M, Borgdorff M W. Risk of tuberculosis after recent exposure. A 10-year follow-up study of contacts in Amsterdam. Am J Respir Crit Care Med 2014; 190: 1044– 1052. 25265362
  7. [18]Houben R M, Glynn J R, Mallard K, Human immunodeficiency virus increases the risk of tuberculosis due to recent re-infection in individuals with latent infection. Int J Tuberc Lung Dis 2010; 14: 909– 915. 20550777 PMC3276831

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Metadata

Authors
Ragonnet, R., Trauer, J. M., McBryde, E. S., Houben, R. M. G. J., Denholm, J. T., Handel, A., & Sumner, T.
Affiliations
  • The Royal Melbourne Hospital (AU)
  • London School of Hygiene & Tropical Medicine (GB)
  • University of Georgia (US)
Corresponding author
Ragonnet, R.
Venue
The International Journal of Tuberculosis and Lung Disease
Published
2017-01-01
Volume
21
Issue
1
Pages
60-66
ISSN
1027-3719 (ISSN-L)
OpenAlex
W2561955155
Cited by
31
References
34
Citations by year
2026: 1 · 2025: 2 · 2024: 1 · 2023: 5 · 2022: 4 · 2021: 1 · 2020: 4 · 2019: 6 · 2018: 7
FWCI
4.00
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • The International Journal of Tuberculosis and Lung Disease (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
  • ResearchOnline at James Cook University (James Cook University) (submittedVersion)
  • Minerva Access (University of Melbourne) (submittedVersion, cc-by)
Funders
Bill and Melinda Gates Foundation (OPP1084276)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Tuberculosis Research and Epidemiology
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › HIV, TB, and STIs Epidemiology
  • Physical Sciences › Mathematics › Applied Mathematics › Mathematical and Theoretical Epidemiology and Ecology Models
Keywords
isoniazid preventive therapy, tuberculosis incidence, tuberculosis transmission dynamics, number needed to treat, disease burden, U-shaped relationship, tuberculosis prevention
MeSH terms
Antitubercular Agents, Humans, Isoniazid, Sensitivity and Specificity, Tuberculosis, World Health Organization, Incidence

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