Evidence map›Paper›PMID 39109181›Full record

ArticleInfectious Disease Modelling2024

A Bayesian model calibration framework for stochastic compartmental models with both time-varying and time-invariant parameters.

Brandon Robinson, Philippe Bisaillon, Jodi D Edwards, Tetyana Kendzerska, Mohammad Khalil, Dominique Poirel, Abhijit Sarkar

Abstract read
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Article in Infectious Disease Modelling, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Brandon RobinsonDepartment of Civil and Environmental Engineering, Carleton University, Ottawa, ON K1S 5B6, Canada.
Philippe BisaillonDepartment of Civil and Environmental Engineering, Carleton University, Ottawa, ON K1S 5B6, Canada.
Jodi D EdwardsSchool of Epidemiology and Public Health, University of Ottawa and University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Tetyana KendzerskaICES, Ottawa, Ontario, Canada.
Mohammad KhalilQuantitative Modeling & Analysis Department, Sandia National Laboratories, Livermore, CA, USA.
Dominique PoirelDepartment of Mechanical and Aerospace Engineering, Royal Military College of Canada, Kingston, ON, Canada.
Abhijit SarkarDepartment of Civil and Environmental Engineering, Carleton University, Ottawa, ON K1S 5B6, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We consider state and parameter estimation for compartmental models having both time-varying and time-invariant parameters. In this manuscript, we first detail a general Bayesian computational framework as a continuation of our previous work. Subsequently, this framework is specifically tailored to the susceptible-infectious-removed (SIR) model which describes a basic mechanism for the spread of infectious diseases through a system of coupled nonlinear differential equations. The SIR model consists of three states, namely, the susceptible, infectious, and removed compartments. The coupling among these states is controlled by two parameters, the infection rate and the recovery rate. The simplicity of the SIR model and similar compartmental models make them applicable to many classes of infectious diseases. However, the combined assumption of a deterministic model and time-invariance among the model parameters are two significant impediments which critically limit their use for long-term predictions. The tendency of certain model parameters to vary in time due to seasonal trends, non-pharmaceutical interventions, and other random effects necessitates a model that structurally permits the incorporation of such time-varying effects. Complementary to this, is the need for a robust mechanism for the estimation of the parameters of the resulting model from data. To this end, we consider an augmented state vector, which appends the time-varying parameters to the original system states whereby the time evolution of the time-varying parameters are driven by an artificial noise process in a standard manner. Distinguishing between time-varying and time-invariant parameters in this fashion limits the introduction of artificial dynamics into the system, and provides a robust, fully Bayesian approach for estimating the time-invariant system parameters as well as the elements of the process noise covariance matrix. This computational framework is implemented by leveraging the robustness of the Markov chain Monte Carlo algorithm permits the estimation of time-invariant parameters while nested nonlinear filters concurrently perform the joint estimation of the system states and time-varying parameters. We demonstrate performance of the framework by first considering a series of examples using synthetic data, followed by an exposition on public health data collected in the province of Ontario.

Indexed as

Bayesian inferenceStochastic compartmental modelsTime-varying parameter estimation

Identifiers

PMID39109181
PMCPMC11301392

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.