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Extended models for nosocomial infection: parameter estimation and model selection
We consider extensions to previous models for patient level nosocomial infection in several ways, provide a specification of the likelihoods for these new models, specify new update steps required for stochastic integration, and provide programs that implement these methods to obtain parameter estim...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145396/ https://www.ncbi.nlm.nih.gov/pubmed/29040678 http://dx.doi.org/10.1093/imammb/dqx010 |
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author | Thomas, Alun Khader, Karim Redd, Andrew Leecaster, Molly Zhang, Yue Jones, Makoto Greene, Tom Samore, Matthew |
author_facet | Thomas, Alun Khader, Karim Redd, Andrew Leecaster, Molly Zhang, Yue Jones, Makoto Greene, Tom Samore, Matthew |
author_sort | Thomas, Alun |
collection | PubMed |
description | We consider extensions to previous models for patient level nosocomial infection in several ways, provide a specification of the likelihoods for these new models, specify new update steps required for stochastic integration, and provide programs that implement these methods to obtain parameter estimates and model choice statistics. Previous susceptible-infected models are extended to allow for a latent period between initial exposure to the pathogen and the patient becoming themselves infectious, and the possibility of decolonization. We allow for multiple facilities, such as acute care hospitals or long-term care facilities and nursing homes, and for multiple units or wards within a facility. Patient transfers between units and facilities are tracked and accounted for in the models so that direct importation of a colonized individual from one facility or unit to another might be inferred. We allow for constant transmission rates, rates that depend on the number of colonized individuals in a unit or facility, or rates that depend on the proportion of colonized individuals. Statistical analysis is done in a Bayesian framework using Markov chain Monte Carlo methods to obtain a sample of parameter values from their joint posterior distribution. Cross validation, deviance information criterion and widely applicable information criterion approaches to model choice fit very naturally into this framework and we have implemented all three. We illustrate our methods by considering model selection issues and parameter estimation for data on methicilin-resistant Staphylococcus aureus surveillance tests over 1 year at a Veterans Administration hospital comprising seven wards. |
format | Online Article Text |
id | pubmed-6145396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61453962019-04-02 Extended models for nosocomial infection: parameter estimation and model selection Thomas, Alun Khader, Karim Redd, Andrew Leecaster, Molly Zhang, Yue Jones, Makoto Greene, Tom Samore, Matthew Math Med Biol Article We consider extensions to previous models for patient level nosocomial infection in several ways, provide a specification of the likelihoods for these new models, specify new update steps required for stochastic integration, and provide programs that implement these methods to obtain parameter estimates and model choice statistics. Previous susceptible-infected models are extended to allow for a latent period between initial exposure to the pathogen and the patient becoming themselves infectious, and the possibility of decolonization. We allow for multiple facilities, such as acute care hospitals or long-term care facilities and nursing homes, and for multiple units or wards within a facility. Patient transfers between units and facilities are tracked and accounted for in the models so that direct importation of a colonized individual from one facility or unit to another might be inferred. We allow for constant transmission rates, rates that depend on the number of colonized individuals in a unit or facility, or rates that depend on the proportion of colonized individuals. Statistical analysis is done in a Bayesian framework using Markov chain Monte Carlo methods to obtain a sample of parameter values from their joint posterior distribution. Cross validation, deviance information criterion and widely applicable information criterion approaches to model choice fit very naturally into this framework and we have implemented all three. We illustrate our methods by considering model selection issues and parameter estimation for data on methicilin-resistant Staphylococcus aureus surveillance tests over 1 year at a Veterans Administration hospital comprising seven wards. Oxford University Press 2018-04 2017-10-12 /pmc/articles/PMC6145396/ /pubmed/29040678 http://dx.doi.org/10.1093/imammb/dqx010 Text en © The authors 2017. Published by Oxford University Press on behalf of the Institute of Mathematics and its Applications. All rights reserved. https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections. |
spellingShingle | Article Thomas, Alun Khader, Karim Redd, Andrew Leecaster, Molly Zhang, Yue Jones, Makoto Greene, Tom Samore, Matthew Extended models for nosocomial infection: parameter estimation and model selection |
title | Extended models for nosocomial infection: parameter estimation and model selection |
title_full | Extended models for nosocomial infection: parameter estimation and model selection |
title_fullStr | Extended models for nosocomial infection: parameter estimation and model selection |
title_full_unstemmed | Extended models for nosocomial infection: parameter estimation and model selection |
title_short | Extended models for nosocomial infection: parameter estimation and model selection |
title_sort | extended models for nosocomial infection: parameter estimation and model selection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145396/ https://www.ncbi.nlm.nih.gov/pubmed/29040678 http://dx.doi.org/10.1093/imammb/dqx010 |
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