Evidence map›Paper›PMID 41222884›Full record

ArticlePharmacoEconomics2026

Health-Service Costs for the Treatment of Multidrug-Resistant/Rifampicin-Resistant Tuberculosis in South African Children: Application of a Real-World Dataset.

Thomas Wilkinson, Arne von Delft, Anneke C Hesseling, Edina Sinanovic, H Simon Schaaf, James A Seddon

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Article in PharmacoEconomics, 2026. 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
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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

6 authors.

Thomas WilkinsonHealth Economics Unit, School of Public Health, University of Cape Town, Cape Town, South Africa. tommy.d.wilkinson@gmail.com.ORCID http://orcid.org/0000-0003-0806-2196
Arne von DelftCentre for Integrated Data and Epidemiological Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Anneke C HesselingDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, Cape Town, South Africa.
Edina SinanovicHealth Economics Unit, School of Public Health, University of Cape Town, Cape Town, South Africa.
H Simon SchaafDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, Cape Town, South Africa.
James A SeddonDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, Cape Town, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with multidrug-resistant (MDR)/rifampicin-resistant (RR) tuberculosis (TB) are an important but neglected group in cost-effectiveness research. Digital health information systems enable new approaches to health-service cost analysis. The Provincial Health Data Centre (PHDC) in the Western Cape, South Africa, collates disparate health system data including hospital inpatient and outpatient data, medications, laboratory tests, and primary health care utilisation.

methodsA health-service cost analysis used anonymised, integrated PHDC data for children treated for MDR/RR-TB between 2018 and 2021. Health-service utilisation was costed using local unit prices, and total per-patient costs were summarised by key patient and disease characteristics (age, sex, resistance profile, site of disease, and HIV status) and reported in 2021 USD. A log-linear regression model identified cost drivers, and alternative parametric distributions were fitted to total costs to assess distributional fit.

resultsThere was significant total cost variation across the 271 children in the data sample (median US$7576; interquartile range 2725-22,986). Regression analysis indicates younger age, extrapulmonary disease site, living with HIV, and treatment duration had significant impact on costs; impact of resistance profile was significant but subject to modelling assumptions. The distribution of total per-patient costs fitted a gamma distribution (α = 0.93, β = 14,496).

conclusionTreatment for MDR/RR-TB in children remains costly for health systems. Utilising routinely collected, real-world data from an established health information system enables accurate and representative insights to overall costs and major cost drivers. Costs were highly skewed, with a small proportion of patients incurring very high costs. This cost analysis can assist in decision making and programme development at local and international levels and as an input to secondary analysis.

Indexed as

Antitubercular AgentsHealth Care CostsRifampinTuberculosis, Multidrug-ResistantAdolescentChildChild, PreschoolCost-Benefit AnalysisFemaleHumansInfantMaleSouth AfricaAntitubercular AgentsRifampin

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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.