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A Bayesian approach to identifying the role of hospital structure and staff interactions in nosocomial transmission of SARS-CoV-2

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A Bayesian approach to identifying the role of hospital structure and staff interactions in nosocomial transmission of SARS-CoV-2. / Bridgen, Jessica R. E.; Lewis, Joseph M.; Todd, Stacy et al.
In: Interface, Vol. 21, No. 212, 20230525, 31.03.2024.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Bridgen JRE, Lewis JM, Todd S, Taegtmeyer M, Read JM, Jewell CP. A Bayesian approach to identifying the role of hospital structure and staff interactions in nosocomial transmission of SARS-CoV-2. Interface. 2024 Mar 31;21(212):20230525. Epub 2024 Mar 6. doi: 10.1098/rsif.2023.0525

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Bibtex

@article{e1702f207d674aafa973e2c2c0ccd162,
title = "A Bayesian approach to identifying the role of hospital structure and staff interactions in nosocomial transmission of SARS-CoV-2",
abstract = "Nosocomial infections threaten patient safety, and were widely reported during the COVID-19 pandemic. Effective hospital infection control requires a detailed understanding of the role of different transmission pathways, yet these are poorly quantified. Using patient and staff data from a large UK hospital, we demonstrate a method to infer unobserved epidemiological event times efficiently and disentangle the infectious pressure dynamics by ward. A stochastic individual-level, continuous-time state-transition model was constructed to model transmission of SARS-CoV-2, incorporating a dynamic staff–patient contact network as time-varying parameters. A Metropolis–Hastings Markov chain Monte Carlo (MCMC) algorithm was used to estimate transmission rate parameters associated with each possible source of infection, and the unobserved infection and recovery times. We found that the total infectious pressure exerted on an individual in a ward varied over time, as did the primary source of transmission. There was marked heterogeneity between wards; each ward experienced unique infectious pressure over time. Hospital infection control should consider the role of between-ward movement of staff as a key infectious source of nosocomial infection for SARS-CoV-2. With further development, this method could be implemented routinely for real-time monitoring of nosocomial transmission and to evaluate interventions.",
keywords = "healthcare-associated infections, Bayesian inference, SARS-CoV-2, epidemiology, nosocomial transmission",
author = "Bridgen, {Jessica R. E.} and Lewis, {Joseph M.} and Stacy Todd and Miriam Taegtmeyer and Read, {Jonathan M.} and Jewell, {Chris P.}",
year = "2024",
month = mar,
day = "31",
doi = "10.1098/rsif.2023.0525",
language = "English",
volume = "21",
journal = "Interface",
issn = "1742-5689",
publisher = "Royal Society of London",
number = "212",

}

RIS

TY - JOUR

T1 - A Bayesian approach to identifying the role of hospital structure and staff interactions in nosocomial transmission of SARS-CoV-2

AU - Bridgen, Jessica R. E.

AU - Lewis, Joseph M.

AU - Todd, Stacy

AU - Taegtmeyer, Miriam

AU - Read, Jonathan M.

AU - Jewell, Chris P.

PY - 2024/3/31

Y1 - 2024/3/31

N2 - Nosocomial infections threaten patient safety, and were widely reported during the COVID-19 pandemic. Effective hospital infection control requires a detailed understanding of the role of different transmission pathways, yet these are poorly quantified. Using patient and staff data from a large UK hospital, we demonstrate a method to infer unobserved epidemiological event times efficiently and disentangle the infectious pressure dynamics by ward. A stochastic individual-level, continuous-time state-transition model was constructed to model transmission of SARS-CoV-2, incorporating a dynamic staff–patient contact network as time-varying parameters. A Metropolis–Hastings Markov chain Monte Carlo (MCMC) algorithm was used to estimate transmission rate parameters associated with each possible source of infection, and the unobserved infection and recovery times. We found that the total infectious pressure exerted on an individual in a ward varied over time, as did the primary source of transmission. There was marked heterogeneity between wards; each ward experienced unique infectious pressure over time. Hospital infection control should consider the role of between-ward movement of staff as a key infectious source of nosocomial infection for SARS-CoV-2. With further development, this method could be implemented routinely for real-time monitoring of nosocomial transmission and to evaluate interventions.

AB - Nosocomial infections threaten patient safety, and were widely reported during the COVID-19 pandemic. Effective hospital infection control requires a detailed understanding of the role of different transmission pathways, yet these are poorly quantified. Using patient and staff data from a large UK hospital, we demonstrate a method to infer unobserved epidemiological event times efficiently and disentangle the infectious pressure dynamics by ward. A stochastic individual-level, continuous-time state-transition model was constructed to model transmission of SARS-CoV-2, incorporating a dynamic staff–patient contact network as time-varying parameters. A Metropolis–Hastings Markov chain Monte Carlo (MCMC) algorithm was used to estimate transmission rate parameters associated with each possible source of infection, and the unobserved infection and recovery times. We found that the total infectious pressure exerted on an individual in a ward varied over time, as did the primary source of transmission. There was marked heterogeneity between wards; each ward experienced unique infectious pressure over time. Hospital infection control should consider the role of between-ward movement of staff as a key infectious source of nosocomial infection for SARS-CoV-2. With further development, this method could be implemented routinely for real-time monitoring of nosocomial transmission and to evaluate interventions.

KW - healthcare-associated infections

KW - Bayesian inference

KW - SARS-CoV-2

KW - epidemiology

KW - nosocomial transmission

U2 - 10.1098/rsif.2023.0525

DO - 10.1098/rsif.2023.0525

M3 - Journal article

VL - 21

JO - Interface

JF - Interface

SN - 1742-5689

IS - 212

M1 - 20230525

ER -