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Bayesian validation framework for dynamic epidemic models
Complex models of infectious diseases are used to understand the transmission dynamics of the disease, project the course of an epidemic, predict the effect of interventions and/or provide information for power calculations of community level intervention studies. However, there have been relatively...
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Published in: | Epidemics 2021-12, Vol.37, p.100514-100514, Article 100514 |
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description | Complex models of infectious diseases are used to understand the transmission dynamics of the disease, project the course of an epidemic, predict the effect of interventions and/or provide information for power calculations of community level intervention studies. However, there have been relatively few opportunities to rigorously evaluate the predictions of such models till now. Indeed, while there is a large literature on calibration (fitting model parameters) and validation (comparing model outputs to data) of complex models based on empirical data, the lack of uniformity in accepted criteria for such procedures for models of infectious diseases has led to simple procedures being prevalent for such steps. However, recently, several community level randomized trials of combination HIV intervention have been planned and/or initiated, and in each case, significant epidemic modeling efforts were conducted during trial planning which were integral to the design of these trials. The existence of these models and the (anticipated) availability of results from the related trials, provide a unique opportunity to evaluate the models and their usefulness in trial design. In this project, we outline a framework for evaluating the predictions of complex epidemiological models and describe experiments that can be used to test their predictions.
•Framework for evaluating predictions of epidemiological models (e.g., HIV transmission models).•Evaluating posterior distribution of the model discrepancy using a Bayesian framework.•Allowing for re-calibration of parameters by updating their priors in a MCMC analysis.•Identifying communities where the model fails by providing a goodness of fit evaluation using posterior tail probability. |
doi_str_mv | 10.1016/j.epidem.2021.100514 |
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•Framework for evaluating predictions of epidemiological models (e.g., HIV transmission models).•Evaluating posterior distribution of the model discrepancy using a Bayesian framework.•Allowing for re-calibration of parameters by updating their priors in a MCMC analysis.•Identifying communities where the model fails by providing a goodness of fit evaluation using posterior tail probability.</description><identifier>ISSN: 1755-4365</identifier><identifier>EISSN: 1878-0067</identifier><identifier>DOI: 10.1016/j.epidem.2021.100514</identifier><identifier>PMID: 34763161</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Bayes Theorem ; Bayesian credible interval ; Communicable Diseases - epidemiology ; Epidemics ; Epidemiological model validation ; HIV transmission model ; Humans ; Markov Chain Monte Carlo</subject><ispartof>Epidemics, 2021-12, Vol.37, p.100514-100514, Article 100514</ispartof><rights>2021 The Authors</rights><rights>Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-d8cd8ce226c33fd7926b8e2c3a276ae518d7695cb38788640f8522d8901d030e3</citedby><cites>FETCH-LOGICAL-c529t-d8cd8ce226c33fd7926b8e2c3a276ae518d7695cb38788640f8522d8901d030e3</cites><orcidid>0000-0001-5055-7075 ; 0000-0001-5271-7247</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S175543652100061X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34763161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dasgupta, Sayan</creatorcontrib><creatorcontrib>Moore, Mia R.</creatorcontrib><creatorcontrib>Dimitrov, Dobromir T.</creatorcontrib><creatorcontrib>Hughes, James P.</creatorcontrib><title>Bayesian validation framework for dynamic epidemic models</title><title>Epidemics</title><addtitle>Epidemics</addtitle><description>Complex models of infectious diseases are used to understand the transmission dynamics of the disease, project the course of an epidemic, predict the effect of interventions and/or provide information for power calculations of community level intervention studies. However, there have been relatively few opportunities to rigorously evaluate the predictions of such models till now. Indeed, while there is a large literature on calibration (fitting model parameters) and validation (comparing model outputs to data) of complex models based on empirical data, the lack of uniformity in accepted criteria for such procedures for models of infectious diseases has led to simple procedures being prevalent for such steps. However, recently, several community level randomized trials of combination HIV intervention have been planned and/or initiated, and in each case, significant epidemic modeling efforts were conducted during trial planning which were integral to the design of these trials. The existence of these models and the (anticipated) availability of results from the related trials, provide a unique opportunity to evaluate the models and their usefulness in trial design. In this project, we outline a framework for evaluating the predictions of complex epidemiological models and describe experiments that can be used to test their predictions.
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subjects | Bayes Theorem Bayesian credible interval Communicable Diseases - epidemiology Epidemics Epidemiological model validation HIV transmission model Humans Markov Chain Monte Carlo |
title | Bayesian validation framework for dynamic epidemic models |
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