Evidence map›Paper›PMID 41206134›Full record

ArticleBMJ global health2025

Cost-effectiveness of modified fully oral 9-month treatment regimens for rifampicin-resistant tuberculosis in Belarus, Georgia, Kazakhstan and the Republic of Moldova.

Kasim Allel, Tom Palmer, Gerard Joseph Abou Jaoude, Oleksandr Korotych, Askar Yedilbayev, Valentina Vilc, Andrei Corloteanu, Mariana Macari, Cula Evghenia, Dumitru Laticevschi and 18 more

Abstract read
In one paragraph

Article in BMJ global health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

28 authors.

Kasim AllelNuffield Department of Population Health, University of Oxford, Oxford, Oxfordshire, UK.
Tom PalmerInstitute for Global Health, University College London, London, UK t.palmer@ucl.ac.uk.ORCID 0000-0002-9526-0045
Gerard Joseph Abou JaoudeInstitute for Global Health, University College London, London, UK.ORCID 0000-0001-6022-3036
Oleksandr KorotychWorld Health Organization Regional Office for Europe, Copenhagen, Denmark.
Askar YedilbayevWorld Health Organization Regional Office for Europe, Copenhagen, Denmark.
Valentina VilcInstitute of Phthisiopneumology, Chisinau, Moldova (the Republic of).
Andrei CorloteanuInstitute of Phthisiopneumology, Chisinau, Moldova (the Republic of).
Mariana MacariInstitute of Phthisiopneumology, Chisinau, Moldova (the Republic of).
Cula EvgheniaInstitute of Phthisiopneumology, Chisinau, Moldova (the Republic of).
Dumitru LaticevschiThe Global Fund to Fight AIDS Tuberculosis and Malaria, Grand-Saconnex, Genève, Switzerland.
Ismailov Shakhimurat-ShaimovichNational Scientific Center of Phthisiopulmonology of the Republic of Kazakhstan, Almaty, Kazakhstan.
Rakisheva Anar-SaduakasovnaNational Scientific Center of Phthisiopulmonology of the Republic of Kazakhstan, Almaty, Kazakhstan.
Tulepova Gulzhan-ElbrusovnaNational Scientific Center of Phthisiopulmonology of the Republic of Kazakhstan, Almaty, Kazakhstan.
Daria Anatolievna-RyazanetNational Scientific Center of Phthisiopulmonology of the Republic of Kazakhstan, Almaty, Kazakhstan.
Aimbekova Shahrizada-YergalymovnaNational Scientific Center of Phthisiopulmonology of the Republic of Kazakhstan, Almaty, Kazakhstan.
Natalia YatskevichRepublican Scientific and Practical Center for Pulmonology and Tuberculosis, Minsk, Belarus.
Alena SkrahinaRepublican Scientific and Practical Center for Pulmonology and Tuberculosis, Minsk, Belarus.
Dmitry ZhurkinRepublican Scientific and Practical Center for Pulmonology and Tuberculosis, Minsk, Belarus.
Zaza AvalianiNational Center for Tuberculosis and Lung, Tbilisi, Georgia.
Nana KiriaNational Center for Tuberculosis and Lung, Tbilisi, Georgia.
Nino LomtadzeNational Center for Tuberculosis and Lung, Tbilisi, Georgia.
Nino KiriaNational Center for Tuberculosis and Lung, Tbilisi, Georgia.
Teona AvalianiNational Center for Tuberculosis and Lung, Tbilisi, Georgia.
Irma KhonelidzeNational Center for Disease Control and Public Health, Tbilisi, Georgia.
Maka DaneliaNational Center for Disease Control and Public Health, Tbilisi, Georgia.
Corina MaximThe Global Fund to Fight AIDS Tuberculosis and Malaria, Grand-Saconnex, Genève, Switzerland.
Hassan Haghparast-BidgoliInstitute for Global Health, University College London, London, UK.
Jolene SkordisInstitute for Global Health, University College London, London, UK.

Funding

Emory-Georgia TB Research Training ProgramD43TW007124 · FIC · EMORY UNIVERSITY · PI HENRY M BLUMBERG, Nestani Tukvadze · 2004 to 2026
$4.6M
FIC NIH HHS D43 TW007124World Health Organization 001
6 · The paper itself

Abstract

introductionPrior to 2020, treatment options for multidrug-resistant tuberculosis (MDR-TB) were limited and typically involved long treatment durations and high financial burdens. In the eastern European and central Asian (EECA) region, traditional inpatient tuberculosis (TB) care models, alongside high MDR-TB rates, escalate nosocomial transmission risks and treatment costs. Modified, fully oral, shorter treatment regimens (mSTR) implemented in the WHO European Region under operational research conditions offered a potential reduction in the burden of MDR-TB treatment for both patients and health systems.

methodsWe conducted the first regional evaluation of the cost-effectiveness of the novel mSTR treatment regimen compared with the standard of care (SOC) in Belarus, Georgia, Kazakhstan and Republic of Moldova. We used cohort data on mSTR efficacy and WHO data on SOC in patients with MDR-TB. We used a Markov model, with treatment costs calculated from the provider perspective. Outcomes were measured in quality-adjusted life years (QALYs), with incremental cost-effectiveness ratios (ICER) calculated per QALY gained in each country. An annual 3% discount rate was used for both costs and outcomes. We performed univariate and probabilistic sensitivity analysis (PSA) to assess the robustness of our cost-effectiveness calculations under varying assumptions. Finally, we estimated potential cost savings if mSTR was implemented nationally and we evaluated the incremental net monetary benefit (iNMB) and willingness-to-pay (WTP) thresholds based on Wood

resultsWe estimated that mSTR can reduce TB treatment costs by between 23% and 47% and drug costs by 39% to 74%, compared with SOC in the countries studied. mSTR resulted in cost savings of between $3596 and $8174 per patient and offered additional health gains of between 0.56 to 2.69 QALYs per patient. mSTR remained cost-effective (iNMB>0) compared with SOC in 78%, 85%, 91% and 92% of PSA simulations in Belarus, Georgia, Kazakhstan and Republic of Moldova, respectively, when compared with their country-level WTP threshold. Implementing mSTR in up to 80% of MDR/rifampicin-resistant TB patients may result in cost savings of $20.5, 2.5, 0.7 and 0.2 million in Kazakhstan, Belarus, Republic of Moldova and Georgia; equivalent to 17%, 3%, 4% and 1% of their national TB budgets, respectively.

conclusionsCompared with SOC, mSTR is a more cost-effective treatment option for MDR/RR-TB, which should be considered by policymakers in the EECA region. Using insights from current implementations to scale up, plan operational changes and reallocate savings from mSTR could greatly enhance TB services and patient care.

Indexed as

Antitubercular AgentsRifampinTuberculosis, Multidrug-ResistantAdministration, OralAdultCost-Benefit AnalysisFemaleGeorgia (Republic)HumansKazakhstanMaleMiddle AgedMoldovaQuality-Adjusted Life YearsRepublic of BelarusAntitubercular AgentsRifampinHealth economicsTuberculosis

Identifiers

PMID41206134
PMCPMC12603705

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Registered trials

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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.