conclusions.tex 8.6 KB

123456789101112131415161718192021222324252627282930313233343536373839404142434445464748495051525354555657585960616263646566676869707172737475767778798081828384858687888990919293949596979899100101102103104105106107108109110111112113114115116117118119120121122123124125126127128129130131132133134135
  1. % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
  2. % Author: Phillip Rothenbeck
  3. % Title: Your Thesis
  4. % File: conclusions/conclusions.tex
  5. % Part: conclusions
  6. % Description:
  7. % summary of the content in this chapter
  8. % Version: 01.09.2024
  9. % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
  10. \chapter{Conclusions}
  11. \label{chap:conclusions}
  12. The objective of this thesis is to identify quantifying measures for the
  13. COVID-19 pandemic in Germany and its 16 federal states. We use the SIR model to
  14. describe the dynamics of the disease over time, offering an approximation of the
  15. reality. In this model, the transmission rate $\beta$ and recovery rate $\alpha$
  16. describe the infectiousness and resolution of the disease that the respective
  17. population experience. These rates serve as constant evaluation measures
  18. throughout the entire duration of the pandemic. The time-dependent reproduction
  19. number indicates the number of individuals infected by a single infectious
  20. individual. The SIR model is defined on a system of differential equations that
  21. elucidates the relations between these rates. In order to obtain these values
  22. for Germany, it is necessary to solve the ordinary differential equations (ODEs)
  23. for the data pertaining to the pandemic in each state and in Germany as a whole.
  24. We employ a physics-informed neural network in our approach to solve the ODE's.
  25. The data on which we train is collected by the Robert Koch Institute and made
  26. publicly available on GitHub, where they can be accessed for download. We
  27. preprocess the data to fit have the required format for the PINNs to reconstruct
  28. it, and at the same time predicts the transition rates and the reproduction
  29. number for the given data. Using this we conduct experiments on synthetic data
  30. and on the data for the German states and Germany itself. The results for the
  31. synthetic data demonstrate the efficacy of our data on small datasets.\\
  32. The results of our work regarding the real-world data are divided into two
  33. groups. First we have the constant transmission rates, which provide insight
  34. into the overall trajectory of the pandemic in a given region. A high
  35. transmission rate indicates that, on average, the significant number of
  36. individuals were infected during the pandemic. Conversely, a high recovery rate
  37. indicates that individuals either recovered or died from the disease at a faster
  38. rate. Due to this contradiction in positive or negative meaning in $\alpha$
  39. paired with the uncertainty of a possible dependency on $\beta$ during training,
  40. we want to shift the focus on our results of $\beta$. The states with the
  41. highest transmission rate values are Thuringia, Saxony-Anhalt and
  42. Mecklenburg-Vorpommern. Furthermore, it is evident the six eastern
  43. states exhibit a higher transmission rate than the overall German rate
  44. (see~\Cref{fig:alpha_beta_mean_std}). These results align with the ongoing
  45. narrative of the COVID-19 pandemic in Germany, which has highlighted a perceived
  46. discrepancy in vaccination rates between the eastern and western federal states.
  47. This assertion which can be substantiated by a comparison of the vaccination
  48. ratios $\nu$ of each state and our findings. We find a strong negative
  49. correlation between $\nu$ and $\beta$. The results from our second experiments,
  50. underscore these findings. Here, we approximate the reproduction number $\Rt$
  51. from the data. When $\Rt>1$, the disease spreads rapidly through the population.
  52. Our results indicate a tendency for states with a high $\beta$ to experience
  53. longer periods with $\Rt>1$. Furthermore, we can identify the time point on
  54. which the most impactful events happened during the pandemic in Germany.\\
  55. Although larger events are visible, smaller, less impactful events that are
  56. still visible on the raw data, do not appear in our results. This discrepancy
  57. can be attributed to the less precise reconstruction of the input data. The
  58. predicted version is smooth and does not contain any smaller peaks. To address
  59. these implementational limitations of our method, we intend to conduct
  60. comprehensive hyperparameter search to find the best configuration of our models
  61. to fit the data. Further optimizations can be applied to the epidemiological
  62. model that we employ, for which we present options in the subsequent section.
  63. % -------------------------------------------------------------------
  64. \section{Further Work}
  65. \label{sec:furtherWork}
  66. Our findings demonstrate that with our methods enable the quantification of the
  67. course of the COVID-19 pandemic in Germany using the data provided by the
  68. Robert Koch Institute. Additionally, we present the limitations of our work.
  69. The SIR model is subject to numerous limitations. For instance, it does not
  70. account for individuals, who may be immune due to the vaccination status or
  71. those who are not infectious due to quarantine. In this section, we explore
  72. epidemiological models that illustrate these dynamics observed in real-world
  73. pandemics and recommend further investigation for Germany. First, we examine
  74. extensions of the SIR models, then we focus on agent-based models (ABMs).
  75. % -------------------------------------------------------------------
  76. \subsection{Further Compartmental Models}
  77. As our results demonstrate, the SIR model is capable of approximating the
  78. dynamics of real-world pandemics. However, the model is not without
  79. limitations. As previously stated, the SIR model assumes that recovered
  80. individuals remain immune and does not account for the reduction of exposure of
  81. susceptible individuals through the introduction of non-pharmaceutical
  82. mitigation policies, such as social distancing policies. These shortcomings can
  83. be addressed by incorporating additional compartments and transmission rates
  84. into the model. For example, the SEIRD model incorporates an \emph{Exposed}
  85. group and subdivides the \emph{Removed} group into \emph{Dead} and
  86. \emph{Recovered} compartments. Furthermore, this adds four additional rates to
  87. the model: the contact rate, representing the average number of contacts
  88. between infectious and susceptible people with a high probability of infection;
  89. the manifestation index, indicating the proportion of individuals exposed to
  90. the disease who will become infectious; the incubation rate, measuring the time
  91. required for exposed individuals to become infectious; and the infection
  92. fatality rate, quantifying the fraction of individuals who succumb to the
  93. disease. As Doerre and Doblhammer~\cite{Doerre2022} show for Germany using a
  94. numerical approximation method, for an SIERD model that they specialize to be
  95. age- and gender-specific, that it shows the impact of non-pharmaceutical
  96. mitigation policies. In their work, Cooke and van den Driessche~\cite{Cooke1996}
  97. propose the SEIRS model with two delays. This is model is capable of
  98. approximating diseases, that have an immune period, after which the recovered
  99. individual becomes susceptible again. These are just a few examples of
  100. the numerous modifications of the basic SIR model that can be used to
  101. approximate and consequently quantify a pandemic.
  102. % -------------------------------------------------------------------
  103. \subsection{Agent based models}
  104. While compartmental models, such as the SIR model, look at the population as a
  105. divided group, with each group representing a specific characterization that
  106. all inhabitants of that group share, an \emph{Agent-Based Model} (ABM) sets its
  107. focus on the individual. Each individual, or agent, has specific attributes
  108. that determine its behavior and interactions with other agents during the
  109. simulation. As Gilbert~\cite{Gilbert2010} states, ABMs simulate the behavior of
  110. large groups, with each individual following simple rules. Kerr
  111. \etal~\cite{Kerr2021} put forth a simulation tool, \emph{Covasim}, which they
  112. base on an ABM. The ABM employs local data, including demographic data, disease
  113. incidence data from the region, and contact data for household, schools and
  114. workplaces, to define its simulation for a specific region. In their work,
  115. Maziarz and Zach~\cite{Maziarz2020} address the criticism levied against ABMs
  116. for simplifying the dynamics and lacking the empirical support for the
  117. assumptions it they make. The authors utilize an ABM and the data specific to
  118. Australia to demonstrate the efficacy of ABMs in portraying the dynamics of the
  119. COVID-19 pandemic. They further state that ABMs can serve as serve as a tool
  120. for assessing the impact of non-pharmaceutical mitigation policies. This
  121. illustrates that ABMs play a distinct role in analyzing the COVID-19 pandemic.
  122. As the data situation has evolved, it is imperative to investigate the
  123. potential of utilizing ABMs as a tool to assess the pandemic's course.
  124. % -------------------------------------------------------------------