Evidence map›Paper›PMID 39348389›Full record

ArticlePLoS computational biology2024

A new approach to Health Benefits Package design: an application of the Thanzi La Onse model in Malawi.

Margherita Molaro, Sakshi Mohan, Bingling She, Martin Chalkley, Tim Colbourn, Joseph H Collins, Emilia Connolly, Matthew M Graham, Eva Janoušková, Ines Li Lin and 10 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

20 authors.

Margherita MolaroMRC Centre for Global Infectious Disease Analysis, Jameel Institute, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0002-1841-4274
Sakshi MohanCentre for Health Economics, University of York, York, United Kingdom.ORCID 0000-0002-1268-1769
Bingling SheMRC Centre for Global Infectious Disease Analysis, Jameel Institute, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0001-5976-8987
Martin ChalkleyCentre for Health Economics, University of York, York, United Kingdom.ORCID 0000-0002-1091-8259
Tim ColbournInstitute for Global Health, University College London, London, United Kingdom.ORCID 0000-0002-6917-6552
Joseph H CollinsInstitute for Global Health, University College London, London, United Kingdom.ORCID 0000-0003-4801-7218
Emilia ConnollyLondon School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-1671-3190
Matthew M GrahamCentre for Advanced Research Computing, University College London, London, United Kingdom.ORCID 0000-0001-9104-7960
Eva JanouškováInstitute for Global Health, University College London, London, United Kingdom.ORCID 0000-0002-4104-0119
Ines Li LinInstitute for Global Health, University College London, London, United Kingdom.ORCID 0000-0002-1945-3208
Gerald ManthaluDepartment of Planning and Policy Development, Ministry of Health and Population, Lilongwe, Malawi.ORCID 0000-0002-3501-8601
Emmanuel MnjoweKamuzu University of Health Sciences, Blantyre, Malawi.ORCID 0009-0006-4624-9727
Dominic NkhomaKamuzu University of Health Sciences, Blantyre, Malawi.ORCID 0000-0001-6125-6630
Pakwanja D TweaDepartment of Planning and Policy Development, Ministry of Health and Population, Lilongwe, Malawi.
Andrew N PhillipsInstitute for Global Health, University College London, London, United Kingdom.ORCID 0000-0003-2384-4807
Paul RevillCentre for Health Economics, University of York, York, United Kingdom.ORCID 0000-0001-8632-0600
Asif U TamuriCentre for Advanced Research Computing, University College London, London, United Kingdom.ORCID 0000-0001-6633-3789
Joseph Mfutso-BengoKamuzu University of Health Sciences, Blantyre, Malawi.
Tara D MangalMRC Centre for Global Infectious Disease Analysis, Jameel Institute, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0001-9222-8632
Timothy B HallettMRC Centre for Global Infectious Disease Analysis, Jameel Institute, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0002-9681-0424

Funding

Medical Research Council MR/P028004/1Wellcome Trust
6 · The paper itself

Abstract

An efficient allocation of limited resources in low-income settings offers the opportunity to improve population-health outcomes given the available health system capacity. Efforts to achieve this are often framed through the lens of "health benefits packages" (HBPs), which seek to establish which services the public healthcare system should include in its provision. Analytic approaches widely used to weigh evidence in support of different interventions and inform the broader HBP deliberative process however have limitations. In this work, we propose the individual-based Thanzi La Onse (TLO) model as a uniquely-tailored tool to assist in the evaluation of Malawi-specific HBPs while addressing these limitations. By mechanistically modelling-and calibrating to extensive, country-specific data-the incidence of disease, health-seeking behaviour, and the capacity of the healthcare system to meet the demand for care under realistic constraints on human resources for health available, we were able to simulate the health gains achievable under a number of plausible HBP strategies for the country. We found that the HBP emerging from a linear constrained optimisation analysis (LCOA) achieved the largest health gain-∼8% reduction in disability adjusted life years (DALYs) between 2023 and 2042 compared to the benchmark scenario-by concentrating resources on high-impact treatments. This HBP however incurred a relative excess in DALYs in the first few years of its implementation. Other feasible approaches to prioritisation were assessed, including service prioritisation based on patient characteristics, rather than service type. Unlike the LCOA-based HBP, this approach achieved consistent health gains relative to the benchmark scenario on a year- to-year basis, and a 5% reduction in DALYs over the whole period, which suggests an approach based upon patient characteristics might prove beneficial in the future.

Indexed as

Delivery of Health CareComputational BiologyHumansMalawiQuality-Adjusted Life Years

Identifiers

PMID39348389
PMCPMC11567512

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.