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Benefit-cost analysis of coordinated strategies for control of rabies in Africa
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4700009
Author(s) Bucher, A.; Dimov, A.; Fink, G.; Chitnis, N.; Bonfoh, B.; Zinsstag, J.
Author(s) at UniBasel Bucher, Alvar
Dimov, Artemiy
Fink, Günther
Chitnis, Nakul
Zinsstag, Jakob
Year 2023
Title Benefit-cost analysis of coordinated strategies for control of rabies in Africa
Journal Nat Commun
Volume 14
Number 1
Pages / Article-Number 5370
Keywords Humans; Animals; Dogs; *Rabies/epidemiology/prevention & control; Cost-Benefit Analysis; Africa/epidemiology; Black People; Mass Vaccination
Mesh terms Animals; Dogs; Humans; Africa, epidemiology; Black People; Cost-Benefit Analysis; Mass Vaccination, methods; Rabies, prevention & control; Dog Diseases, prevention & control; Rabies Vaccines, therapeutic use
Abstract Previous research suggests that dog mass vaccination campaigns can eliminate rabies locally, resulting in large human and animal life gains. Despite these demonstrated benefits, dog vaccination programs remain scarce on the African continent. We conducted a benefit-cost analysis to demonstrate that engaging into vaccination campaigns is the dominant strategy for most countries even in the absence of coordinated action between them. And quantify how coordinated policy measures across countries in Africa could impact rabies incidence and associated costs. We show that coordinated dog mass vaccination between countries and PEP would lead to the elimination of dog rabies in Africa with total welfare gains of USD 9.5 billion (95% CI: 8.1 - 11.4 billion) between 2024 and 2054 (30 years). Coordinated disease control between African countries can lead to more socially and ecologically equitable outcomes by reducing the number of lost human lives to almost zero and possibly eliminating rabies.
ISSN/ISBN 2041-1723 (Electronic)2041-1723
URL https://doi.org/10.1038/s41467-023-41110-2
edoc-URL https://edoc.unibas.ch/95940/
Full Text on edoc Available
Digital Object Identifier DOI 10.1038/s41467-023-41110-2
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/37679314
ISI-Number WOS:001065300300007
Document type (ISI) Journal Article
 
   

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03/05/2024