Impact of Community-Wide Tuberculosis Active Case Finding and Human Immunodeficiency Virus Testing on Tuberculosis Trends in Malawi.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 07 2023
Historique:
received: 21 10 2022
medline: 6 7 2023
pubmed: 26 4 2023
entrez: 26 4 2023
Statut: ppublish

Résumé

Tuberculosis case-finding interventions are critical to meeting World Health Organization End TB strategy goals. We investigated the impact of community-wide tuberculosis active case finding (ACF) alongside scale-up of human immunodeficiency virus (HIV) testing and care on trends in adult tuberculosis case notification rates (CNRs) in Blantyre, Malawi. Five rounds of ACF for tuberculosis (1-2 weeks of leafleting, door-to-door enquiry for cough and sputum microscopy) were delivered to neighborhoods ("ACF areas") in North-West Blantyre between April 2011 and August 2014. Many of these neighborhoods also had concurrent HIV testing interventions. The remaining neighborhoods in Blantyre City ("non-ACF areas") provided a non-randomized comparator. We analyzed TB CNRs from January 2009 until December 2018. We used interrupted time series analysis to compare tuberculosis CNRs before ACF and after ACF, and between ACF and non-ACF areas. Tuberculosis CNRs increased in Blantyre concurrently with start of ACF for tuberculosis in both ACF and non-ACF areas, with a larger magnitude in ACF areas. Compared to a counterfactual where pre-ACF CNR trends continued during ACF period, we estimated there were an additional 101 (95% confidence interval [CI] 42 to 160) microbiologically confirmed (Bac+) tuberculosis diagnoses per 100 000 person-years in the ACF areas in 3 and a half years of ACF. Compared to a counterfactual where trends in ACF area were the same as trends in non-ACF areas, we estimated an additional 63 (95% CI 38 to 90) Bac + diagnoses per 100 000 person-years in the same period. Tuberculosis ACF was associated with a rapid increase in people diagnosed with tuberculosis in Blantyre.

Sections du résumé

BACKGROUND
Tuberculosis case-finding interventions are critical to meeting World Health Organization End TB strategy goals. We investigated the impact of community-wide tuberculosis active case finding (ACF) alongside scale-up of human immunodeficiency virus (HIV) testing and care on trends in adult tuberculosis case notification rates (CNRs) in Blantyre, Malawi.
METHODS
Five rounds of ACF for tuberculosis (1-2 weeks of leafleting, door-to-door enquiry for cough and sputum microscopy) were delivered to neighborhoods ("ACF areas") in North-West Blantyre between April 2011 and August 2014. Many of these neighborhoods also had concurrent HIV testing interventions. The remaining neighborhoods in Blantyre City ("non-ACF areas") provided a non-randomized comparator. We analyzed TB CNRs from January 2009 until December 2018. We used interrupted time series analysis to compare tuberculosis CNRs before ACF and after ACF, and between ACF and non-ACF areas.
RESULTS
Tuberculosis CNRs increased in Blantyre concurrently with start of ACF for tuberculosis in both ACF and non-ACF areas, with a larger magnitude in ACF areas. Compared to a counterfactual where pre-ACF CNR trends continued during ACF period, we estimated there were an additional 101 (95% confidence interval [CI] 42 to 160) microbiologically confirmed (Bac+) tuberculosis diagnoses per 100 000 person-years in the ACF areas in 3 and a half years of ACF. Compared to a counterfactual where trends in ACF area were the same as trends in non-ACF areas, we estimated an additional 63 (95% CI 38 to 90) Bac + diagnoses per 100 000 person-years in the same period.
CONCLUSIONS
Tuberculosis ACF was associated with a rapid increase in people diagnosed with tuberculosis in Blantyre.

Identifiants

pubmed: 37099318
pii: 7143198
doi: 10.1093/cid/ciad238
pmc: PMC10320183
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

94-100

Subventions

Organisme : Medical Research Council
ID : MR/P022081/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 091769/Z/10/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203905/Z/16/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206575/Z/17/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 200901/Z/16/Z
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. The authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

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Auteurs

Rachael M Burke (RM)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Marriott Nliwasa (M)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.
Helse Nord Tuberculosis Initiative, Kamuzu University of Health Sciences, Blantyre, Malawi.

Peter J Dodd (PJ)

School of Health and Related Research, University of Sheffield, Sheffield, United Kingdom.

Helena R A Feasey (HRA)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

McEwen Khundi (M)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.
(MRC) International Statistics and Epidemiology Group, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Augustine Choko (A)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.

Rebecca Nzawa-Soko (R)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.

James Mpunga (J)

National Tuberculosis Programme, Government of Malawi, Lilongwe, Malawi.

Emily L Webb (EL)

(MRC) International Statistics and Epidemiology Group, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Katherine Fielding (K)

(MRC) International Statistics and Epidemiology Group, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Peter MacPherson (P)

Malawi Liverpool Wellcome Clinical Research Programme, Blantyre, Malawi.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.

Elizabeth L Corbett (EL)

Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

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Classifications MeSH