Evidence map›Paper›PMID 35306009›Full record

ArticleMathematical biosciences2022

A hybrid stochastic model and its Bayesian identification for infectious disease screening in a university campus with application to massive COVID-19 screening at the University of Liège.

M Arnst, G Louppe, R Van Hulle, L Gillet, F Bureau, V Denoël

Abstract read
In one paragraph

Article in Mathematical biosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Can infectious modelling be applicable globally - lessons from COVID 19.Current opinion in environmental science & health · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

M ArnstFaculty of Applied Sciences, Université de Liège, 4000 Liège, Belgium. Electronic address: maarten.arnst@uliege.be.
G LouppeFaculty of Applied Sciences, Université de Liège, 4000 Liège, Belgium. Electronic address: g.louppe@uliege.be.
R Van HulleFaculty of Applied Sciences, Université de Liège, 4000 Liège, Belgium. Electronic address: romain.vanhulle@uliege.be.
L GilletImmunology-Vaccinology, FARAH, Université de Liège, 4000 Liège, Belgium. Electronic address: l.gillet@uliege.be.
F BureauLaboratory of Cellular and Molecular Immunology, GIGA Institute, Université de Liège, 4000 Liège, Belgium. Electronic address: fabrice.bureau@uliege.be.
V DenoëlFaculty of Applied Sciences, Université de Liège, 4000 Liège, Belgium. Electronic address: v.denoel@uliege.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amid the COVID-19 pandemic, universities are implementing various prevention and mitigation measures. Identifying and isolating infectious individuals by using screening testing is one such a measure that can contribute to reducing spread. Here, we propose a hybrid stochastic model for infectious disease transmission in a university campus with screening testing and its surrounding community. Based on a compartmental modeling strategy, this hybrid stochastic model represents the evolution of the infectious disease and its transmission using continuous-time stochastic dynamics, and it represents the screening testing as discrete stochastic events. We also develop, in a Bayesian framework, the identification of parameters of this hybrid stochastic model, including transmission rates. These parameters were identified from the screening test data for the university population and observed incidence counts for the surrounding community. We implement the exploration of the Bayesian posterior using a machine-learning simulation-based inference approach. The proposed methodology was applied in a retrospective modeling study of a massive COVID-19 screening conducted at the University of Liège in Fall 2020. The emphasis of the paper is on the development of the hybrid stochastic model to assess the impact of screening testing as a measure to reduce spread. The hybrid stochastic model allows various factors to be represented and examined, such as interplay with the surrounding community, variability of the transmission dynamics, the rate of participation in the screening testing, the test sensitivity, the test frequency, the diagnosis delay, and compliance with isolation. The application in the retrospective modeling study suggests that a high rate of participation and a high test frequency are important factors to reduce spread.

Indexed as

Communicable DiseasesCOVID-19Bayes TheoremHumansPandemicsRetrospective StudiesSARS-CoV-2UniversitiesBayesian inferenceCOVID-19Infectious disease transmissionScreening testingSimulation-based inferenceStochastic dynamics

Identifiers

PMID35306009
PMCPMC8925303

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Registered trials

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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.