Cost-effectiveness of sleeping sickness elimination campaigns in five settings of the Democratic Republic of Congo.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
25 02 2022
Historique:
received: 12 04 2021
accepted: 28 01 2022
entrez: 26 2 2022
pubmed: 27 2 2022
medline: 13 4 2022
Statut: epublish

Résumé

Gambiense human African trypanosomiasis (gHAT) is marked for elimination of transmission by 2030, but the disease persists in several low-income countries. We couple transmission and health outcomes models to examine the cost-effectiveness of four gHAT elimination strategies in five settings - spanning low- to high-risk - of the Democratic Republic of Congo. Alongside passive screening in fixed health facilities, the strategies include active screening at average or intensified coverage levels, alone or with vector control with a scale-back algorithm when no cases are reported for three consecutive years. In high or moderate-risk settings, costs of gHAT strategies are primarily driven by active screening and, if used, vector control. Due to the cessation of active screening and vector control, most investments (75-80%) are made by 2030 and vector control might be cost-saving while ensuring elimination of transmission. In low-risk settings, costs are driven by passive screening, and minimum-cost strategies consisting of active screening and passive screening lead to elimination of transmission by 2030 with high probability.

Identifiants

pubmed: 35217656
doi: 10.1038/s41467-022-28598-w
pii: 10.1038/s41467-022-28598-w
pmc: PMC8881616
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1051

Informations de copyright

© 2022. The Author(s).

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Auteurs

Marina Antillon (M)

Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Allschwil, Basel, 4123, Switzerland. marina.antillon@swisstph.ch.
University of Basel, Basel, 4001, Switzerland. marina.antillon@swisstph.ch.

Ching-I Huang (CI)

Zeeman Institute, University of Warwick, Coventry, CV4 7AL, UK.
Mathematics Institute, University of Warwick, Coventry, CV4 7AL, UK.

Ronald E Crump (RE)

Zeeman Institute, University of Warwick, Coventry, CV4 7AL, UK.
Mathematics Institute, University of Warwick, Coventry, CV4 7AL, UK.

Paul E Brown (PE)

Zeeman Institute, University of Warwick, Coventry, CV4 7AL, UK.
Mathematics Institute, University of Warwick, Coventry, CV4 7AL, UK.

Rian Snijders (R)

Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Allschwil, Basel, 4123, Switzerland.
University of Basel, Basel, 4001, Switzerland.
Institute of Tropical Medicine, B-2000 Antwerp, Belgium.

Erick Mwamba Miaka (EM)

Programme National de Lutte contre la Trypanosomiase Humaine Africaine (PNLTHA), Kinshasa, Democratic Republic of Congo.

Matt J Keeling (MJ)

Zeeman Institute, University of Warwick, Coventry, CV4 7AL, UK.
Mathematics Institute, University of Warwick, Coventry, CV4 7AL, UK.
School of Life Sciences, University of Warwick, Coventry, CV4 7AL, UK.

Kat S Rock (KS)

Zeeman Institute, University of Warwick, Coventry, CV4 7AL, UK. k.s.rock@warwick.ac.uk.
Mathematics Institute, University of Warwick, Coventry, CV4 7AL, UK. k.s.rock@warwick.ac.uk.

Fabrizio Tediosi (F)

Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Allschwil, Basel, 4123, Switzerland.
University of Basel, Basel, 4001, Switzerland.

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Classifications MeSH