Efficacy thresholds and target populations for antiviral COVID-19 treatments to save lives and costs: a modelling study.

Efficacy thresholds and target populations for antiviral COVID-19 treatments to save lives and costs: a modelling study.

Publication date: Jul 01, 2024

In 2023 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was declared endemic, yet hospital admissions have persisted and risen within populations at high and moderate risk of developing severe disease, which include those of older age, and those with co-morbidities. Antiviral treatments, currently only available for high-risk individuals, play an important role in preventing severe disease and hospitalisation within this subpopulation. Here, we further explore the public health and economic benefits of extending target populations for treatment, and assess efficacy thresholds for a treatment strategy to be cost-saving. We adapted an individual-based transmission model of SARS-CoV-2, OpenCOVID, which was calibrated and validated to 2020-2023 Swiss, European, and Northern Hemisphere epidemiological data. We used the model to estimate hospitalisations and overall costs for preventatively treating three risk groups for a full range of treatment efficacies and coverages with, besides vaccination and hospital treatments, no other interventions in place. We further calculated efficacy thresholds for strategies to be cost-saving. A global sensitivity analysis was conducted to test the sensitivity of all outcomes for a wide range of treatment properties, emerging variant properties, and vaccination coverages. In a high vaccination coverage setting, we found that a high efficacy antiviral treatment given to all those at high-risk could reduce hospitalisations by up to 40%. When expanding treatment coverage to also include all those at moderate-risk, an additional 50% of hospitalisations could be averted. Targeting both high-risk and moderate-risk groups was found to be cost-saving for a treatment efficacy greater than ∼40%. This threshold was found to be robust regardless of vaccination coverage and emerging variant properties, but highly sensitive to treatment costs. For a sufficiently efficacious antiviral treatment, expanding the target population to include both high-risk and moderate-risk groups should be considered. Equitable treatment costs are found crucial in achieving the best possible public health and health economic outcomes. Botnar Research Centre for Child Health (DZX2165 to MAP), the Swiss National Science Foundation Professorship of MAP (P00P3_203450) and Swiss National Science Foundation NFP 78 Covid-19 2020 (4079P0_198428 to MAP).

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Concepts Keywords
4079p0_198428 SARS-CoV-2
Antiviral Transmission modelling
Eclinicalmedicine Treatment
Swiss

Semantics

Type Source Name
disease MESH COVID-19
disease VO Severe acute respiratory syndrome coronavirus 2
disease MESH morbidities
disease VO vaccination
disease VO vaccination coverage
disease VO population
disease VO USA
disease MESH syndrome
drug DRUGBANK Coenzyme M
disease VO vaccine
drug DRUGBANK Spinosad
disease MESH influenza
disease VO Respiratory syncytial virus
disease MESH emergency
drug DRUGBANK Ritonavir
pathway KEGG Viral replication
disease MESH death
disease VO effective
disease MESH infection
disease IDO host
disease VO vaccine dose
disease IDO intervention
disease VO dose
disease MESH uncertainty
drug DRUGBANK Aspartame
disease VO report
drug DRUGBANK Trestolone
disease VO primary vaccination
disease MESH long COVID
disease VO time
disease MESH burnout
disease VO Optaflu
disease VO effectiveness
disease VO publication
disease VO organization
disease VO immunization
disease IDO facility
disease MESH reinfection
disease IDO symptom
disease VO frequency
disease MESH obesity
disease MESH complications
drug DRUGBANK (S)-Des-Me-Ampa

Original Article

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