scholarly journals Self-Limiting Factors in Pandemics and Multi-Disease Syndemics

2018 ◽  
Author(s):  
David Manheim

AbstractThe potential for an infectious disease outbreak that is much worse than those which have been observed in human history, whether engineered or natural, has been the focus of significant concern in biosecurity. Fundamental dynamics of disease spread make such outbreaks much less likely than they first appear. Here we present a slightly modified formulation of the typical SEIR model that illustrates these dynamics more clearly, and shows the unlikely cases where concern may still be warranted. This is then applied to an extreme version of proposed pandemic risk, multi-disease syndemics, to show that (absent much clearer reasons for concern) the suggested dangers are overstated.The models used in this paper are available here: https://github.com/davidmanheim/Infectious-Disease-Models

2021 ◽  
Vol 3 (2) ◽  
pp. 114-126
Author(s):  
Sudi Mungkasi

We consider a SEIR model for the spread (transmission) of an infectious disease. The model has played an important role due to world pandemic disease spread cases. Our contributions in this paper are three folds. Our first contribution is to provide successive approximation and variational iteration methods to obtain analytical approximate solutions to the SEIR model. Our second contribution is to prove that for solving the SEIR model, the variational iteration and successive approximation methods are identical when we have some particular values of Lagrange multipliers in the variational iteration formulation. Third, we propose a new multistage-analytical method for solving the SEIR model. Computational experiments show that the successive approximation and variational iteration methods are accurate for small size of time domain. In contrast, our proposed multistage-analytical method is successful to solve the SEIR model very accurately for large size of time domain. Furthermore, the order of accuracy of the multistage-analytical method can be made higher simply by taking more number of successive iterations in the multistage evolution.


Biostatistics ◽  
2020 ◽  
Author(s):  
M D Mahsin ◽  
Rob Deardon ◽  
Patrick Brown

Summary Infectious disease models can be of great use for understanding the underlying mechanisms that influence the spread of diseases and predicting future disease progression. Modeling has been increasingly used to evaluate the potential impact of different control measures and to guide public health policy decisions. In recent years, there has been rapid progress in developing spatio-temporal modeling of infectious diseases and an example of such recent developments is the discrete-time individual-level models (ILMs). These models are well developed and provide a common framework for modeling many disease systems; however, they assume the probability of disease transmission between two individuals depends only on their spatial separation and not on their spatial locations. In cases where spatial location itself is important for understanding the spread of emerging infectious diseases and identifying their causes, it would be beneficial to incorporate the effect of spatial location in the model. In this study, we thus generalize the ILMs to a new class of geographically dependent ILMs, to allow for the evaluation of the effect of spatially varying risk factors (e.g., education, social deprivation, environmental), as well as unobserved spatial structure, upon the transmission of infectious disease. Specifically, we consider a conditional autoregressive (CAR) model to capture the effects of unobserved spatially structured latent covariates or measurement error. This results in flexible infectious disease models that can be used for formulating etiological hypotheses and identifying geographical regions of unusually high risk to formulate preventive action. The reliability of these models is investigated on a combination of simulated epidemic data and Alberta seasonal influenza outbreak data ($2009$). This new class of models is fitted to data within a Bayesian statistical framework using Markov chain Monte Carlo methods.


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