A guided twin delayed deep deterministic reinforcement learning for vaccine allocation in human contact networks

This manuscript introduces an innovative approach to optimizing the distribution of a limited vaccine resource within a population modeled as a contact network, aiming to mitigate the spread of infectious diseases. The study develops a novel methodology that combines reinforcement learning and graph neural networks. To understand the dynamics of disease propagation, the study constructs an analytical model that outlines conditions for disease eradication or endemic states. This model supports a series of simulation experiments across various scenarios, demonstrating the proposed method’s superiority over random and centrality-based approaches in reducing the average number of infections per individual during an outbreak. The adaptability of the proposed method is further emphasized by its robust performance across networks of diverse sizes and configurations, highlighting its real-world applicability. The findings of this study have significant implications for public health policy and resource allocation, offering a promising framework for managing infectious disease outbreaks in complex and dynamic environments. • Study uses a network-based model to address heterogeneity in disease transmission. • Develops an analytical model for disease spread and equilibrium states. • Integration of Reinforcement Learning and Graph Neural Networks used for vaccination. • Addresses vaccine supply limitations with a phased, time-dependent allocation model. • Introduces a modified actor loss function regularized with nodes centrality.

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Publication Details

Journal
Applied Soft Computing
Published
2024-10-09
DOI
https://doi.org/10.1016/j.asoc.2024.112322
Citations
4
Primary Topic
COVID-19 epidemiological studies
Type
article
Field-Weighted Citation Impact
1.58
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article

A guided twin delayed deep deterministic reinforcement learning for vaccine allocation in human contact networks

Anwar Mahmoodi, Ehsan Ardjmand, Alireza Fallahtafti, William A. Young et al.
4 citations
Applied Soft Computing
COVID-19 epidemiological studies
1.58
article

A guided twin delayed deep deterministic reinforcement learning for vaccine allocation in human contact networks

Anwar Mahmoodi, Ehsan Ardjmand, Alireza Fallahtafti, William A. Young, Ehsan Yazdani
article en
4 citations

Abstract

This manuscript introduces an innovative approach to optimizing the distribution of a limited vaccine resource within a population modeled as a contact network, aiming to mitigate the spread of infectious diseases. The study develops a novel methodology that combines reinforcement learning and graph neural networks. To understand the dynamics of disease propagation, the study constructs an analytical model that outlines conditions for disease eradication or endemic states. This model supports a series of simulation experiments across various scenarios, demonstrating the proposed method’s superiority over random and centrality-based approaches in reducing the average number of infections per individual during an outbreak. The adaptability of the proposed method is further emphasized by its robust performance across networks of diverse sizes and configurations, highlighting its real-world applicability. The findings of this study have significant implications for public health policy and resource allocation, offering a promising framework for managing infectious disease outbreaks in complex and dynamic environments. • Study uses a network-based model to address heterogeneity in disease transmission. • Develops an analytical model for disease spread and equilibrium states. • Integration of Reinforcement Learning and Graph Neural Networks used for vaccination. • Addresses vaccine supply limitations with a phased, time-dependent allocation model. • Introduces a modified actor loss function regularized with nodes centrality.

Applied Soft ComputingVol. 167
University of Kurdistan (IR), Ohio University (US), Case Western Reserve University (US)
Openalex Percentile: Top 18%
COVID-19 epidemiological studies
1.58
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