Evidence map›Paper›PMID 38388163›Full record

ArticleBMJ global health2024

A model-based approach to estimating the prevalence of disease combinations in South Africa.

Leigh F Johnson, Reshma Kassanjee, Naomi Folb, Sarah Bennett, Andrew Boulle, Naomi S Levitt, Robyn Curran, Kirsty Bobrow, Rifqah A Roomaney, Max O Bachmann and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMJ global health, 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
2.3field-weighted citation impact, top 12% of its field
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, 6 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Leigh F JohnsonCentre for Infectious Disease Epidemiology and Research (CIDER), University of Cape Town, Cape Town, South Africa leigh.johnson@uct.ac.za.ORCID 0000-0002-2717-011X
Reshma KassanjeeCentre for Infectious Disease Epidemiology and Research (CIDER), University of Cape Town, Cape Town, South Africa.
Naomi FolbMedscheme, Cape Town, South Africa.
Sarah BennettMedscheme, Cape Town, South Africa.
Andrew BoulleCentre for Infectious Disease Epidemiology and Research (CIDER), University of Cape Town, Cape Town, South Africa.
Naomi S LevittDepartment of Medicine, University of Cape Town, Cape Town, South Africa.
Robyn CurranKnowledge Translation Unit, University of Cape Town, Cape Town, Western Cape, South Africa.
Kirsty BobrowDepartment of Medicine, University of Cape Town, Cape Town, South Africa.
Rifqah A RoomaneyBurden of Disease Research Unit, South African Medical Research Council, Cape Town, Western Cape, South Africa.ORCID 0000-0003-3267-8484
Max O BachmannNorwich Medical School, University of East Anglia, Faculty of Medicine and Health Sciences, Norwich, UK.ORCID 0000-0003-1770-3506
Lara R FairallKnowledge Translation Unit, University of Cape Town, Cape Town, Western Cape, South Africa.ORCID 0000-0002-7460-4670
University of Cape Town · ZASouth African Medical Research Council · ZAUniversity of East Anglia · GBWestern Cape Department of Health · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of strategies to better detect and manage patients with multiple long-term conditions requires estimates of the most prevalent condition combinations. However, standard meta-analysis tools are not well suited to synthesising heterogeneous multimorbidity data.

methodsWe developed a statistical model to synthesise data on associations between diseases and nationally representative prevalence estimates and applied the model to South Africa. Published and unpublished data were reviewed, and meta-regression analysis was conducted to assess pairwise associations between 10 conditions: arthritis, asthma, chronic obstructive pulmonary disease (COPD), depression, diabetes, HIV, hypertension, ischaemic heart disease (IHD), stroke and tuberculosis. The national prevalence of each condition in individuals aged 15 and older was then independently estimated, and these estimates were integrated with the ORs from the meta-regressions in a statistical model, to estimate the national prevalence of each condition combination.

resultsThe strongest disease associations in South Africa are between COPD and asthma (OR 14.6, 95% CI 10.3 to 19.9), COPD and IHD (OR 9.2, 95% CI 8.3 to 10.2) and IHD and stroke (OR 7.2, 95% CI 5.9 to 8.4). The most prevalent condition combinations in individuals aged 15+ are hypertension and arthritis (7.6%, 95% CI 5.8% to 9.5%), hypertension and diabetes (7.5%, 95% CI 6.4% to 8.6%) and hypertension and HIV (4.8%, 95% CI 3.3% to 6.6%). The average numbers of comorbidities are greatest in the case of COPD (2.3, 95% CI 2.1 to 2.6), stroke (2.1, 95% CI 1.8 to 2.4) and IHD (1.9, 95% CI 1.6 to 2.2).

conclusionSouth Africa has high levels of HIV, hypertension, diabetes and arthritis, by international standards, and these are reflected in the most prevalent condition combinations. However, less prevalent conditions such as COPD, stroke and IHD contribute disproportionately to the multimorbidity burden, with high rates of comorbidity. This modelling approach can be used in other settings to characterise the most important disease combinations and levels of comorbidity.

Indexed as

Models, StatisticalMultimorbidityArthritisAsthmaDiabetes MellitusHIV InfectionsHumansHypertensionPrevalencePulmonary Disease, Chronic ObstructiveSouth AfricaStrokecomorbiditymultimorbiditymultiple long-term conditionsnon-communicable diseasesSouth Africa

Identifiers

PMID38388163
PMCPMC10884267
OpenAlexW4392031121

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.