An updated economic assessment of moxidectin treatment strategies for onchocerciasis elimination
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Published version
Author(s)
Type
Journal Article
Abstract
Background:
Concerns that annual mass administration of ivermectin, the predominant strategy for onchocerciasis control/elimination, may not lead to elimination of parasite transmission (EoT) in all endemic areas, has 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) implemented with minimal or enhanced coverage (65% or 80% of the total population taking the drug, respectively) in intervention-naïve 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 programme delivery when EoT90 was not reached earlier. Delivery costs do not include the drug costs.
Results:
aCDTM and bCDTM achieved EoT90 with lower programmatic delivery costs than aCDTI with one 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 towards EoT and reduce programmatic delivery costs compared to ivermectin-based strategies. The costs of moxidectin to national programmes are needed to quantify whether delivery cost reductions will translate into overall programme cost reduction.
Concerns that annual mass administration of ivermectin, the predominant strategy for onchocerciasis control/elimination, may not lead to elimination of parasite transmission (EoT) in all endemic areas, has 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) implemented with minimal or enhanced coverage (65% or 80% of the total population taking the drug, respectively) in intervention-naïve 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 programme delivery when EoT90 was not reached earlier. Delivery costs do not include the drug costs.
Results:
aCDTM and bCDTM achieved EoT90 with lower programmatic delivery costs than aCDTI with one 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 towards EoT and reduce programmatic delivery costs compared to ivermectin-based strategies. The costs of moxidectin to national programmes are needed to quantify whether delivery cost reductions will translate into overall programme cost reduction.
Date Issued
2024-05-15
Date Acceptance
2024-01-31
Citation
Clinical Infectious Diseases, 2024, 78 (Supplement 2), pp.S138-S145
ISSN
1058-4838
Publisher
Oxford University Press
Start Page
S138
End Page
S145
Journal / Book Title
Clinical Infectious Diseases
Volume
78
Issue
Supplement 2
Copyright Statement
© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution
License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distri bution, and reproduction in any medium, provided the original work is properly cited.
License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distri bution, and reproduction in any medium, provided the original work is properly cited.
License URL
Identifier
https://academic.oup.com/cid/article/78/Supplement_2/S138/7657831
Publication Status
Published
Date Publish Online
2024-04-25