Evidence map›Paper›PMID 41847324›Full record

ArticleIJTLD open2026

Early interventions reduce multimorbidity and TB disability in Kenya, Uganda, Zambia, and Zimbabwe.

F M Banda, A Bloom, J Chakaya, R Chimzizi, C Chitalu, C Duri, A D Harries, N Kasese-Chanda, I Kathure, F N Kavenga and 15 more

Abstract read
In one paragraph

Article in IJTLD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

25 authors.

F M BandaUniversity Teaching Hospital, Ministry of Health, Lusaka, Zambia.
A BloomPublic Health Specialist, Washington, DC, USA.
J ChakayaDepartment of Medicine, Therapeutics, Dermatology and Psychiatry, Kenyatta University, Nairobi, Kenya.
R ChimziziNational Tuberculosis and Leprosy Programme, Ministry of Health, Lusaka, Zambia.
C ChitaluNational Tuberculosis and Leprosy Programme, Ministry of Health, Lusaka, Zambia.
C DuriDirectorate of Health Services, Harare City Council, Harare, Zimbabwe.
A D HarriesInternational Union Against Tuberculosis and Lung Disease, Paris, France.
N Kasese-ChandaNational Tuberculosis and Leprosy Programme, Ministry of Health, Lusaka, Zambia.
I KathureDivision of National TB, Leprosy and Lung Disease Programme, Ministry of Health, Nairobi, Kenya.
F N KavengaMinistry of Health and Child Care, AIDS and TB Department, Harare, Zimbabwe.
A M V KumarInternational Union Against Tuberculosis and Lung Disease, Paris, France.
H LuzzeNational Tuberculosis and Leprosy Programme, Ministry of Health, Kampala, Uganda.
I MbithiRespiratory Society of Kenya, Nairobi, Kenya.
M MputuUniversity Teaching Hospital, Ministry of Health, Lusaka, Zambia.
A MubangaNational Tuberculosis and Leprosy Programme, Ministry of Health, Lusaka, Zambia.
D MudoolaNational Tuberculosis and Leprosy Programme, Ministry of Health, Kampala, Uganda.
D NairIndependent Researcher, Public Health Specialist, Scottsdale, Arizona.
M NgwenyaMinistry of Health and Child Care, AIDS and TB Department, Harare, Zimbabwe.
S NtambiMulago National Referral Hospital, Kampala, Uganda.
P ThekkurInternational Union Against Tuberculosis and Lung Disease, Paris, France.
C TimireMinistry of Health and Child Care, AIDS and TB Department, Harare, Zimbabwe.
E TweyongyereNational Tuberculosis and Leprosy Programme, Ministry of Health, Kampala, Uganda.
M YaDiulPublic Health Specialist, Washington, DC, USA.
R ZachariahUNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases (TDR), World Health Organization, Geneva, Switzerland.
Kenya, Uganda, Zambia and Zimbabwe TB Disability Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe provided early screening and referrals for multimorbidity and absenteeism and assessed changes in these parameters from TB treatment start to completion in health facilities across Kenya, Uganda, Zambia, and Zimbabwe.

methodsA cohort study in 26 health facilities within national TB programmes.

resultsFollow-up was conducted in 1,146 (77%) of 1,497 patients; assessments took a median time of 30 min (interquartile range: 24-36). Symptom prevalence declined from 96% to 9%. Comorbidities (HIV, diabetes/hyperglycaemia, hypertension/high blood pressure) remained stable, while mental health disorders/probable depression decreased from 7% to 4%. Multimorbidity fell markedly; disability (inability to walk 400 m in 6 min) decreased from 20% to 4%; and those with ≥3 multimorbidity conditions decreased from 20% to 8%. Work/school absenteeism declined from 73% to 10%. Overall, referrals for care exceeded 85%, except for silica exposure (23%), smoking (57%), and recreational drug use (46%). Within-facility referrals were nearly 100%, except for silica exposure and disability (∼35%).

conclusionEarly interventions for multimorbidity led to major reductions in symptoms, risk factors, disability, and absenteeism, advocating for integration of patient-centred care throughout the TB care pathway. This multi-country study provides a promising roadmap for progress towards achieving this goal.

Indexed as

fourth 90patient-centred holistic carereal-time operational researchSORT ITsub-Saharan AfricaTB-associated disabilitytuberculosisuniversal health coverage

Identifiers

PMID41847324
PMCPMC12991729

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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.