Cost-effectiveness and health impact of screening and treatment of Mycobacterium tuberculosis infection among formerly incarcerated individuals in Brazil: a Markov modelling study.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 19 12 2023
revised: 23 04 2024
accepted: 22 05 2024
medline: 17 8 2024
pubmed: 17 8 2024
entrez: 16 8 2024
Statut: ppublish

Résumé

Individuals who were formerly incarcerated have high tuberculosis incidence, but are generally not considered among the risk groups eligible for tuberculosis prevention. We investigated the potential health impact and cost-effectiveness of Mycobacterium tuberculosis infection screening and tuberculosis preventive treatment (TPT) for individuals who were formerly incarcerated in Brazil. Using published evidence for Brazil, we constructed a Markov state transition model estimating tuberculosis-related health outcomes and costs among individuals who were formerly incarcerated, by simulating transitions between health states over time. The analysis compared tuberculosis infection screening and TPT, to no screening, considering a combination of M tuberculosis infection tests and TPT regimens. We quantified health effects as reductions in tuberculosis cases, tuberculosis deaths, and disability-adjusted life-years (DALYs). We assessed costs from a tuberculosis programme perspective. We report intervention cost-effectiveness as the incremental costs per DALY averted, and tested how results changed across subgroups of the target population. Compared with no intervention, an intervention incorporating tuberculin skin testing and treatment with 3 months of isoniazid and rifapentine would avert 31 (95% uncertainty interval 14-56) lifetime tuberculosis cases and 4·1 (1·4-5·8) lifetime tuberculosis deaths per 1000 individuals, and cost US$242 per DALY averted. All test and regimen combinations were cost-effective compared with no screening. Younger age, longer incarceration, and more recent prison release were each associated with significantly greater health benefits and more favourable cost-effectiveness ratios, although the intervention was cost-effective for all subgroups examined. M tuberculosis infection screening and TPT for individuals who were formerly incarcerated appears cost-effective, and would provide valuable health gains. National Institutes of Health. For the Portuguese translation of the abstract see Supplementary Materials section.

Sections du résumé

BACKGROUND BACKGROUND
Individuals who were formerly incarcerated have high tuberculosis incidence, but are generally not considered among the risk groups eligible for tuberculosis prevention. We investigated the potential health impact and cost-effectiveness of Mycobacterium tuberculosis infection screening and tuberculosis preventive treatment (TPT) for individuals who were formerly incarcerated in Brazil.
METHODS METHODS
Using published evidence for Brazil, we constructed a Markov state transition model estimating tuberculosis-related health outcomes and costs among individuals who were formerly incarcerated, by simulating transitions between health states over time. The analysis compared tuberculosis infection screening and TPT, to no screening, considering a combination of M tuberculosis infection tests and TPT regimens. We quantified health effects as reductions in tuberculosis cases, tuberculosis deaths, and disability-adjusted life-years (DALYs). We assessed costs from a tuberculosis programme perspective. We report intervention cost-effectiveness as the incremental costs per DALY averted, and tested how results changed across subgroups of the target population.
FINDINGS RESULTS
Compared with no intervention, an intervention incorporating tuberculin skin testing and treatment with 3 months of isoniazid and rifapentine would avert 31 (95% uncertainty interval 14-56) lifetime tuberculosis cases and 4·1 (1·4-5·8) lifetime tuberculosis deaths per 1000 individuals, and cost US$242 per DALY averted. All test and regimen combinations were cost-effective compared with no screening. Younger age, longer incarceration, and more recent prison release were each associated with significantly greater health benefits and more favourable cost-effectiveness ratios, although the intervention was cost-effective for all subgroups examined.
INTERPRETATION CONCLUSIONS
M tuberculosis infection screening and TPT for individuals who were formerly incarcerated appears cost-effective, and would provide valuable health gains.
FUNDING BACKGROUND
National Institutes of Health.
TRANSLATION UNASSIGNED
For the Portuguese translation of the abstract see Supplementary Materials section.

Identifiants

pubmed: 39151980
pii: S2214-109X(24)00221-3
doi: 10.1016/S2214-109X(24)00221-3
pii:
doi:

Substances chimiques

Antitubercular Agents 0
Rifampin VJT6J7R4TR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1446-e1455

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests.

Auteurs

Ana van Lieshout Titan (A)

Department of Global Health and Population, Harvard T H Chan School of Public Health, Boston, MA, USA; Delft Institute of Applied Mathematics, Delft University of Technology, Delft, Netherlands. Electronic address: anavanlieshouttitan23@gmail.com.

Fayette Klaassen (F)

Department of Global Health and Population, Harvard T H Chan School of Public Health, Boston, MA, USA.

Daniele Maria Pelissari (DM)

National Tuberculosis Programme, Ministry of Health, Brasilia, Brazil.

José Nildo de Barros Silva (JN)

National Tuberculosis Programme, Ministry of Health, Brasilia, Brazil.

Kleydson Alves (K)

National Tuberculosis Programme, Ministry of Health, Brasilia, Brazil.

Layana Costa Alves (LC)

National Tuberculosis Programme, Ministry of Health, Brasilia, Brazil; Collective Health Institute, Federal University of Bahia, Salvador, Bahia, Brazil.

Mauro Sanchez (M)

Health and Environment Surveillance Secretariat, Ministry of Health, Brasilia, Brazil.

Patricia Bartholomay (P)

Health and Environment Surveillance Secretariat, Ministry of Health, Brasilia, Brazil.

Fernanda Dockhorn Costa Johansen (FDC)

National Tuberculosis Programme, Ministry of Health, Brasilia, Brazil.

Julio Croda (J)

Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil; Fiocruz Mato Grosso do Sul, Fundação Oswaldo Cruz, Campo Grande, Brazil.

Jason R Andrews (JR)

Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, USA.

Marcia C Castro (MC)

Department of Global Health and Population, Harvard T H Chan School of Public Health, Boston, MA, USA.

Ted Cohen (T)

Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.

Cornelis Vuik (C)

Delft Institute of Applied Mathematics, Delft University of Technology, Delft, Netherlands.

Nicolas A Menzies (NA)

Department of Global Health and Population, Harvard T H Chan School of Public Health, Boston, MA, USA; Center for Health Decision Science, Harvard T H Chan School of Public Health, Boston, MA, USA.

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Classifications MeSH