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Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity

We present a restricted infection rate inverse binomial-based approach to better predict COVID-19 cases after a family gathering. The traditional inverse binomial (IB) model is inappropriate to match the reality of COVID-19, because the collected data contradicts the model’s requirement that varianc...

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Autores principales: Shanmugam, Ramalingam, Ledlow, Gerald, Singh, Karan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282037/
https://www.ncbi.nlm.nih.gov/pubmed/34264972
http://dx.doi.org/10.1371/journal.pone.0254313
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author Shanmugam, Ramalingam
Ledlow, Gerald
Singh, Karan P.
author_facet Shanmugam, Ramalingam
Ledlow, Gerald
Singh, Karan P.
author_sort Shanmugam, Ramalingam
collection PubMed
description We present a restricted infection rate inverse binomial-based approach to better predict COVID-19 cases after a family gathering. The traditional inverse binomial (IB) model is inappropriate to match the reality of COVID-19, because the collected data contradicts the model’s requirement that variance should be larger than the expected value. Our version of an IB model is more appropriate, as it can accommodate all potential data scenarios in which the variance is smaller, equal, or larger than the mean. This is unlike the usual IB, which accommodates only the scenario in which the variance is more than the mean. Therefore, we propose a refined version of an IB model to be able to accommodate all potential data scenarios. The application of the approach is based on a restricted infectivity rate and methodology on COVID-19 data, which exhibit two clusters of infectivity. Cluster 1 has a smaller number of primary cases and exhibits larger variance than the expected cases with a negative correlation of 28%, implying that the number of secondary cases is lesser when the number of primary cases increases and vice versa. The traditional IB model is appropriate for Cluster 1. The probability of contracting COVID-19 is estimated to be 0.13 among the primary, but is 0.75 among the secondary in Cluster 1, with a wider gap. Cluster 2, with a larger number of primary cases, exhibits smaller variance than the expected cases with a correlation of 79%, implying that the number of primary and secondary cases do increase or decrease together. Cluster 2 disqualifies the traditional IB model and requires its refined version. The probability of contracting COVID-19 is estimated to be 0.74 among the primary, but is 0.72 among the secondary in Cluster 2, with a narrower gap. The advantages of the proposed approach include the model’s ability to estimate the community’s health system memory, as future policies might reduce COVID’s spread. In our approach, the current hazard level to be infected with COVID-19 and the odds of not contracting COVID-19 among the primary in comparison to the secondary groups are estimable and interpretable.
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spelling pubmed-82820372021-07-28 Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity Shanmugam, Ramalingam Ledlow, Gerald Singh, Karan P. PLoS One Research Article We present a restricted infection rate inverse binomial-based approach to better predict COVID-19 cases after a family gathering. The traditional inverse binomial (IB) model is inappropriate to match the reality of COVID-19, because the collected data contradicts the model’s requirement that variance should be larger than the expected value. Our version of an IB model is more appropriate, as it can accommodate all potential data scenarios in which the variance is smaller, equal, or larger than the mean. This is unlike the usual IB, which accommodates only the scenario in which the variance is more than the mean. Therefore, we propose a refined version of an IB model to be able to accommodate all potential data scenarios. The application of the approach is based on a restricted infectivity rate and methodology on COVID-19 data, which exhibit two clusters of infectivity. Cluster 1 has a smaller number of primary cases and exhibits larger variance than the expected cases with a negative correlation of 28%, implying that the number of secondary cases is lesser when the number of primary cases increases and vice versa. The traditional IB model is appropriate for Cluster 1. The probability of contracting COVID-19 is estimated to be 0.13 among the primary, but is 0.75 among the secondary in Cluster 1, with a wider gap. Cluster 2, with a larger number of primary cases, exhibits smaller variance than the expected cases with a correlation of 79%, implying that the number of primary and secondary cases do increase or decrease together. Cluster 2 disqualifies the traditional IB model and requires its refined version. The probability of contracting COVID-19 is estimated to be 0.74 among the primary, but is 0.72 among the secondary in Cluster 2, with a narrower gap. The advantages of the proposed approach include the model’s ability to estimate the community’s health system memory, as future policies might reduce COVID’s spread. In our approach, the current hazard level to be infected with COVID-19 and the odds of not contracting COVID-19 among the primary in comparison to the secondary groups are estimable and interpretable. Public Library of Science 2021-07-15 /pmc/articles/PMC8282037/ /pubmed/34264972 http://dx.doi.org/10.1371/journal.pone.0254313 Text en © 2021 Shanmugam et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shanmugam, Ramalingam
Ledlow, Gerald
Singh, Karan P.
Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title_full Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title_fullStr Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title_full_unstemmed Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title_short Predicting COVID-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
title_sort predicting covid-19 cases with unknown homogeneous or heterogeneous resistance to infectivity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282037/
https://www.ncbi.nlm.nih.gov/pubmed/34264972
http://dx.doi.org/10.1371/journal.pone.0254313
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