Maria-Gloria Basáñez
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Neglected Tropical Diseases Modelling Consortium
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Transmission Dynamics and Control of Human Onchocerciasis
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The Detection and Management of Ivermectin Resistance
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Density-dependent Host Choice by Disease Vectors
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Transmission, Control, and Feasibility of Elimination of Human Onchocerciasis in Ghana
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Articles (11)
Background Concerns that annual mass administration of ivermectin, the predominant strategy for onchocerciasis control and elimination, may not lead to elimination of parasite transmission (EoT) in all endemic areas have increased interest in alternative treatment strategies. One such strategy is moxidectin. We performed an updated economic assessment of moxidectin- relative to ivermectin-based strategies. Methods We investigated annual and biannual community-directed treatment with ivermectin (aCDTI, bCDTI) and moxidectin (aCDTM, bCDTM) with minimal or enhanced coverage (65% or 80% of total population taking the drug, respectively) in intervention-naive areas with 30%, 50%, or 70% microfilarial baseline prevalence (representative of hypo-, meso-, and hyperendemic areas). We compared programmatic delivery costs for the number of treatments achieving 90% probability of EoT (EoT90), calculated with the individual-based stochastic transmission model EPIONCHO-IBM. We used the costs for 40 years of program delivery when EoT90 was not reached earlier. The delivery costs do not include drug costs. Results aCDTM and bCDTM achieved EoT90 with lower programmatic delivery costs than aCDTI with 1 exception: aCDTM with minimal coverage did not achieve EoT90 in hyperendemic areas within 40 years. With minimal coverage, bCDTI delivery costs as much or more than aCDTM and bCDTM. With enhanced coverage, programmatic delivery costs for aCDTM and bCDTM were lower than for aCDTI and bCDTI. Conclusions Moxidectin-based strategies could accelerate progress toward EoT and reduce programmatic delivery costs compared with ivermectin-based strategies. The costs of moxidectin to national programs are needed to quantify whether delivery cost reductions will translate into overall program cost reduction.
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2024
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2023
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2023
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2022
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2022
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2022
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2022
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2022
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2022
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2022
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2022
Collaborators (14)
Wilma Stolk
Erasmus University Rotterdam
pierre nouvellet
Professor in Infectious Disease Epidemiology
University of Sussex
Julia Ledien
Imperial College London
Jessica Clark
University of Glasgow
Petr Volf
Charles University
Roy M. Anderson
Imperial College London
T Deirdre Hollingsworth
University of Oxford
Eve Worrall
Reader in Health Economics
Liverpool School of Tropical Medicine
Martin Walker
Lecturer in Epidemiology
Royal Veterinary College
Katie Hampson
Reader
University of Glasgow
Graham Medley
Professor of Infectious Disease Modelling
London School of Hygiene & Tropical Medicine
Zulma M. Cucunubá
Honorary Lecturer
Imperial College London
Joaquin Miguel Prada Jimenez de Cisneros
Senior Lecturer
University of Surrey
Susana Beatriz Adamo
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