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Erschienen in: BMC Infectious Diseases 1/2020

Open Access 01.12.2020 | COVID-19 | Research article

The COVID-19 pandemic preparedness simulation tool: CovidSIM

verfasst von: Kristan A. Schneider, Gideon A. Ngwa, Markus Schwehm, Linda Eichner, Martin Eichner

Erschienen in: BMC Infectious Diseases | Ausgabe 1/2020

Abstract

Background

Efficient control and management in the ongoing COVID-19 pandemic needs to carefully balance economical and realizable interventions. Simulation models can play a cardinal role in forecasting possible scenarios to sustain decision support.

Methods

We present a sophisticated extension of a classical SEIR model. The simulation tool CovidSIM Version 1.0 is an openly accessible web interface to interactively conduct simulations of this model. The simulation tool is used to assess the effects of various interventions, assuming parameters that reflect the situation in Austria as an example.

Results

Strict contact reduction including isolation of infected persons in quarantine wards and at home can substantially delay the peak of the epidemic. Home isolation of infected individuals effectively reduces the height of the peak. Contact reduction by social distancing, e.g., by curfews, sanitary behavior, etc. are also effective in delaying the epidemic peak.

Conclusions

Contact-reducing mechanisms are efficient to delay the peak of the epidemic. They might also be effective in decreasing the peak number of infections depending on seasonal fluctuations in the transmissibility of the disease.
Hinweise

Supplementary Information

The online version contains supplementary material available at (doi:https://​doi.​org/​10.​1186/​s12879-020-05566-7).
Kristan A. Schneider, Gideon A. Ngwa and Martin Eichner contributed equally to this work.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
SEIR
Susceptible, exposed, infected, recovered
WHO
World health organisation
COVID-19
Coronavirus disease 2019
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
ICU
Intensive care units
API
Application programming interface

Backgound

The whole world has been shaken by the outbreak of a new corona virus disease outbreak that started in Wuhan province of China in late 2019 [1]. Due to international travel and interconnectivity, the virus has spread worldwide and affected almost every major nation of the world. Though there is limited data on the extent of the spread of the infection in many parts of the world, on March 11, 2020, the WHO has declared the 2019 corona virus disease outbreak, COVID-19, a global pandemic [2]. COVID-19 is caused by a virus known as the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) [3]. The COVID-19 outbreak, has meanwhile caused over 46 million cases and over 1.19 million deaths in over 200 countries (November 3, [4]). Human-to-human transmission can occur via droplets or contaminated surfaces and materials [5].
The symptoms of COVID-19 appear after an incubation period of 2 to 14 days (mean 5-6 days) [6, 7] and can vary in intensity, ranging from asymptomatic infections to pneumonia and subsequent death. Serious upper respiratory tract infections with case fatality rates of 1% to 5% are reported outside of mainland China, whereby the data from the Hubei province in China indicate a figure of 18% [8, 9]. Elderly and people with chronic diseases are considered a high-risk population [10]. It is however estimated that about 80% of infections only lead to mild or moderate symptoms [1113]. The most commonly displayed symptoms are cough, fever and rhinitis [9]. In the absence of a vaccine and an approved treatment, local control of the coronavirus transmission requires a combined and coordinated control effort [4]. In an effort to decelerate the spread of this disease, many countries have taken drastic measures to reduce social contacts, for instance, by closing schools and forbidding social gatherings. Some even go as far as introducing a total system shut down. Such practices are however very costly and have devastating effects not merely on the fabric of society but also on the economy [14].
Efficient control and management can be achieved if new, more economical, and realizable methods are used. Mathematical models can play a cardinal role in forecasting possible scenarios.
This article describes the background of the COVID-19 pandemic preparedness tool, CovidSIM Version 1.0, which was made publicly available in February 2020 (http://​covidsim.​eu). The main purpose of CovidSIM Version 1.0, is to provide a realistic and easy-to-use simulation tool with the capacity to support decision making in public and global health, epidemiology and economy. It can be used to simulate the pandemic under different scenarios. The focus lies on establishing a model with realistic dynamics. The model is first verbally described in Methods, followed by mathematical formulations presented in Supplement file 1 which may be skipped by readers who are predominantly interested in model applications.
The dynamics of the model can be readily employed to derive variables, which are epidemiologically or economically relevant. Some of the derived quantities arise naturally in the model description, whereas others are obviously relevant and easily calculated from the dynamics implemented in CovidSIM version 1.0.

Methods

We model the spread of COVID-19 deterministically, using an extended SEIR model, i.e., a deterministic compartmental model of ordinary differential equations. We first describe the model verbally and provide a concise mathematical description in Supplement file 1. Figure 1 illustrates the model.
A population of size N is divided into susceptible, infected, and recovered individuals. During the course of the infection, individuals pass through (i) the latency period, during which they are not yet infective, (ii) the prodromal period, during which they are already infective, but the infection is still in an early state where it cannot be yet transmitted as easily as in the later period, in which viral load already increased (in this period, individuals do not yet show typical symptoms), and (iii) the final infectious period during which infected individuals may or may not have symptoms. Finally, individuals recover and obtain a full immunity or die. The model follows the time change of the number of individuals being susceptible (S), in the latent period (E), in the prodromal period (P), in the final infectious period (I), and in the final recovered (R) and dead (D) stages.
The classical approach to model the time change of the number of latent, prodromal and infected individuals would be to assume that individuals simply proceed from one stage to the next. This, however, is too simplistic, because it implies that the time-delay would be exponentially distributed, which does not appropriately describe the dynamics. To mitigate this issue, the latent, prodromal, and final infectious periods are divided into several sub-stages. Infected individuals first pass through the latent, then through the prodromal, and through the final infectious period in a stepwise process, which leads to much more realistic delays for people passing on from the latent to the prodromal period, to the final infectious period and finally to the immune stage.
As the model is built for an epidemic which occurs in a large population in a relatively short time period, deaths, which are unrelated to the disease, are ignored. Contacts between individuals are assumed to occur at random. Susceptible individuals acquire infections through contacts with individuals in the prodromal or the final infectious periods at rates βP and βI, respectively. The basic reproduction number R0 is the average number of infections caused by an infected individual in a completely susceptible population, in which no interventions occur, during the entire infectious period, consisting of the prodromal period and the final infectious period. This number summarizes all the infections, which are caused during the entire infectious period. This definition of R0 specifically requires that initially everybody but the infected individuals in the population is susceptible and there are no intervention measures. The basic reproduction number is allowed to fluctuate seasonally.
Infected individuals first become latent carriers. After that, they enter the prodromal period, in which they can infect others even before entering the final infectious period. At the beginning of the final infectious period, it is determined whether the infection proceeds as symptomatic or asymptomatic. A fraction fSick of individuals in the final infectious period develops symptoms. CovidSIM Version 1.0 allows to isolate individuals with symptoms and to restrict this intervention to a time interval. The detected fraction of symptomatic infections is isolated in quarantine wards, but if it is full, they go directly into home isolation. Home isolation only prevents a fraction of contacts, while quarantine wards are assumed to prevent all infectious contacts.
After the final infectious period, symptomatic infections result in death with a given probability. Infected individuals that do not die at the end of the final infectious period become permanently immune.
Furthermore, CovidSIM allows addressing time-dependent interventions to prevent contacts because of social distancing measures.

Derived quantities

In this section, the derived quantities used in CovidSIM are described verbally; a mathematical description is provided in Supplement file 2.
A fraction of infected individuals develops symptoms in the final infectious period, while the rest remains asymptomatic. We first calculate the number of symptomatic infections and then multiply this number with fractions in order to calculate the demand for medical care, hospital capacities, isolation facilities, and intensive care units (ICU), respectively. These derived quantities only provide additional output of CovidSIM, but they do not influence the model dynamics.
The cumulative disease incidence is a measure which is frequently reported. This is given by the number of cases that have occurred since the start of the outbreak. The number of symptomatic infections occurring within a given time interval is obtained by cumulating the fraction of all infections that progress from the prodromal period to the final infectious period and become symptomatic. Infections are cumulated over the appropriate time interval to obtain the daily and weekly numbers of cases, hospitalizations, etc. They are referred to as daily and weekly incidences, respectively.

Implementation of CovidSIM

The web interface of CovidSim Version 1.0 is implemented in Javascript. The source code is available on GitLab under https://​gitlab.​com/​exploratory-systems/​covidsim/​. CovidSIM uses an ODE solver to run the simulation in the browser of the clients, based on a fourth-order Runge-Kutta method with step size control as described in [15]. The original Fortran code was translated into Java code and JavaScriptCore, V8 using the Web Workers API to facilitate a series of simulation requests in parallel on the host computer’s CPUs. The web application is created in typescript with Angular, ngrx, rxjs, and observable-webworker. The user interface uses Angular Material, d3, ng2-dvd3.

Parameter choices

Model parameters as they occur in the web interface are summarized in Table 1 with their corresponding notation in the model description. By default, at the start of the simulation, one infection is introduced in a fully susceptible population of 100 million inhabitants. Furthermore, one infection per day originating from outside the population is assumed. The number of initial infections (1-1,000 infections at the start of the simulation), the size of the population (1-1,000 million) and the number of infections from outside (1-100) per day can be adjusted by the user. Other parameters such as timing and duration of preventative measures such as social distancing can also easily be adjusted by the user.
Table 1
Web interface and model parameters of CovidSIM Version 1.0
Parameter name on the CovidSIM interface
Parameter
Unit
Default value
Population:
   
Population size
N
million
100
Number of initial infections
LInit
individuals
1
Infections from outside of the population
λExt
per day
1
Durations:
   
Latency period average duration
DE=nE/ε
days
4
Number of latency stages
nE
 
16
Prodromal period average duration
DP=nP/φ
days
1
Number of prodromal stages
nP
 
16
Final infectious period average duration
DI=nI/γ
days
10
Number of final infectious stages
nI
 
16
Severity:
   
Infections which will lead to sickness
fSick
%
58
Sick patients seek medical help
fConsult
%
40
Sick patients are hospitalized
fHosp
%
2
Hospitalized cases need intensive care
fICU
%
2
Sick patients die from the disease
fDead
%
2
Contagiousness:
   
Annual average of the basic reproduction number
\(\bar R_{0}\)
 
4
Amplitude of the seasonal fluctuation of R0
a
% of \(\bar R_{0}\)
0
Day when the seasonal R0 reaches its maximum
\(t_{\mathrm {R}_{0_{\max }}}\)
day
0
Relative contagiousness in prodromal period
cP
%
50
Interventions:
   
General contact reduction
pDist(t)
%
50
General contact reduction begin
\(\phantom {\dot {i}\!}t_{\text {Dist}_1}\)
day of
0
General contact reduction duration
\(\phantom {\dot {i}\!}t_{\text {Dist}_2}-t_{\text {Dist}_1}\)
day
0
Probability that a sick patient is isolated
fIso
%
0
Maximum capacity of isolation units
Qmax
abs. number
0
Contact reduction for cases in home isolation
pHome
%
0
Begin of case isolation measures
\(\phantom {\dot {i}\!}t_{\text {Iso}_1}\)
day
0
Duration of case isolation measures
\(\phantom {\dot {i}\!}t_{\text {Iso}_2}-t_{\text {Iso}_1}\)
day
0

Results

To exemplify the dynamics of the COVID-19 pandemic, parameters are adjusted to reflect the situation in the Federal Republic of Austria, one of the first countries in Europe that implemented strict control interventions. Parameter values are listed in Tables 2 and 3, which follow literature values (cf. [9]) or data regularly published by the John Hopkins University (https://​coronavirus.​jhu.​edu/​data).
Table 2
Parameter values used in Figs. 2, 3, 4, 5 and 6. Note, a=0 implies no seasonal variation
 
parameter
value
Population
N
9 million
 
I(0)
15
 
λExt
10/day
Durations
DE=nE/ε
4 days
 
nE
16
 
DP=nP/φ
1 day
 
nP
16
 
DI=nI/γ
10 days
 
nI
16
Severity
fSick
82%
 
fDead
7
Contagiousness
\(\bar R_{0}\)
4
 
a
0% or 43%
 
\(t_{\mathrm {R}_{0_{\max }}}\)
day 290
 
cP
50%
Interventions
\(\phantom {\dot {i}\!}t_{\text {Iso}_1}\)
day 30
 
\(\phantom {\dot {i}\!}t_{\text {Iso}_2}-t_{\text {Iso}_1}\)
365 days
Table 3
Different parameters used in Figs. 2, 3, 4, 5 and 6. The table lists the specific parameter choices for the figures. Parameters which are not modified are marked with ‘-’
 
Figures
parameter
3&4a-c
3&4d-f
5&6a-c
5&6d-f
5&6g-i
pDist(t)
75%
0-80%
75%
0%
0%
0%
fIso
0 or 66%
0%
0%
0-80%
66%
66%
Qmax
200/10,000
-
-
200/10,000
0-200/10,000
200/10,000
pHome
0 or 75%
-
-
0%
0%
0-80%
\(\phantom {\dot {i}\!}t_{\text {Dist}_2}-t_{\text {Dist}_1}\)
30 days
0 days
0-56 days
-
-
-
It was assumed that the first cases were introduced in the middle of February 2020, so that t=0 corresponds to that day of introduction. As a baseline, a constant R0=4 was assumed. To study the effects of seasonal variation in R0, a yearly average \(\bar R_{0}=4\) was assumed with a 43% fluctuation during the year and a peak in late December (\(t_{\mathrm {R}_{0_{\max }}}=200\)). The average latency period DE was assumed to be 4 days, the prodromal period (DP) 1 day, and the infective period 10 days (DI). In the prodromal period, individuals were supposed to be half as contagious as in the final infectious period.
The impact of general contact reductions and case-isolation are depicted in Fig. 2. The various aspects of both interventions are explained below. Seasonal variation has an impact on both the location and the height of the epidemic peak.

No interventions

The case without interventions needs to be understood as a reference scenario. It leads to a peak of infections which occurs approximately 90 days after the first infection.

General contact reduction – social distancing

Assuming a contact-reducing intervention (social distancing) of 30 days, starting at day 30, the measures delay the peak (Figs. 3 and 4). The more efficient the reduction of person-to-person contacts, the longer is the delay.
In the absence of seasonal fluctuations of R0, social distancing leads only to a delay of the epidemic peak but not to a reduction of its height. In particular, the number of deaths throughout the pandemic is independent of such interventions. More severe contact reductions lead to a disproportionally long delay (Fig. 3a-c).
The peak’s height is affected by seasonal fluctuations and becomes lower or higher due to the timing of the fluctuations (Fig. 4a-c). Importantly any delay will – in the absence of any other control measures – ultimately result in a higher number of deaths in the population if the peak is shifted into a season with higher R0.
Assuming a general reduction of 75% of all contacts, the duration of the interventions scale linearly with the shift of the epidemic peak (Fig. 3d-f), yet the height of the peak is unaffected if there is no seasonality. This changes with seasonal fluctuations, where the peak’s height can substantially increase in the flu season, resulting in higher mortality (Fig. 4d-f).
Importantly, effectiveness and duration of general contact-reducing measures show bigger delays in the case of seasonal fluctuations if they are implemented during a time in which R0 is low.

Isolation of symptomatic cases

Isolating cases has a profound effect on the location and the height of the peak. Assuming that no further person-to-person contact reductions take place and that there is a capacity of 200 isolation wards per 10,000 individuals, and a reduction of contacts by 75% in home isolated cases delays the peak substantially (Figs. 5a-c and 6a-c).
The shift in the peak does not scale linearly, but is disproportionally long for high percentages of infections being isolated. Additionally, in the absence of seasonal fluctuations, the peak will decrease profoundly, resulting in reduced mortality (Fig. 5a-c). With seasonal fluctuations in R0, the peak’s shift is more pronounced if R0 originally is seasonally low. However, it starts to increase, if the delay shifts the peak into the season with higher transmissibility (Fig. 6a-c). Notably, it is assumed that the isolation measures are continued until the end of the simulation time. Once these are discontinued, some of the susceptible individuals will get infected.
Assuming that 66% of symptomatic infections are isolated and a reduction of 75% of contacts in home isolation, we studied the effect of the capacity of isolation wards. An increase in the capacity of wards shifts and decreases the peak (Fig. 5d-e). However, the gain of further increasing the wards’ capacities in shifting and decreasing the peak soon become insignificant. Seasonal fluctuations in R0 again complicate the picture. While the shift in the peak is more pronounced if R0 initially is low, the height of the peak increases or decreases, depending on its timing (Fig. 6d-e).
Finally, assuming (a) an isolation capacity of 200 wards per 10,000 individuals and (b) 66% of the symptomatic infections being isolated, and (c) decreasing the contact rate of home isolated individuals, does not significantly delay the peak, but reduces its height (Figs. 5g-i and 6g-i). This is due to the effective reduction of infectious contacts. This effect is hardly affected by seasonal variations in R0 because it has only a minor delaying effect.

Combination

In the absence of seasonal fluctuations, combinations of both isolation mechanisms result in the longest delay and in the best reduction of the peak’s height (75% reduction of contacts in home isolation, a fraction of 66% of symptomatic infections being isolated, isolation ward capacity of 200 places per 10,000 individuals, 75% general reduction of contacts for 30 days starting at day 30). Notably the delaying effect is mainly due to the solation of cases, not to social distancing measures. The height of the epidemic peak is clearly affected by seasonal fluctuations in R0 (compare Fig. 2a-c with d-f). In the absence of seasonal fluctuation, general contact reduction measures have just a shifting effect on the peak (because the intervention is limited in time), whereas the isolation of sick individuals has a shifting and reducing effect on the peak (because the intervention is not limited in time). Seasonal fluctuation affects both the extent of the delay and the height of the peak in a pattern that can better be understood when looking at the seasonal values of R0.

Discussion

The results suggest that temporal social distancing measures will simply shift the epidemic peak essential by the time the interventions are sustained. If there is seasonal variation, the peak can be shifted towards the flu season, which ultimately leads to increased morality. The isolation of sick cases is more efficient to delay the epidemic peak and to lower it. However, such a strategy results in a higher number of cases and thus higher mortality, if the resulting delay shifts the peak into a period with higher transmissibility. A combination of both measures is most efficient in delaying the epidemic peak and keeping the number of infections and COVID-19-related deaths low. However, seasonal fluctuations can again cause higher mortality. Such a combined strategy is, thus, only meaningful if there is confidence to rapidly develop better treatments for symptomatic cases, prophylaxes, or immunizing vaccines, or if more time is necessary to prepare the healthcare systems to face a full pandemic outbreak. It should be mentioned, that the considerations here are purely epidemiologically. Evolutionary considerations should also be taken into account. Namely, it is unclear to what extent the virus can mutate during the pandemic.
Importantly, general social-distancing interventions cannot simply be decided, as they are subject to individual behavioral decisions. The model clearly assumes that social distancing is temporary and the contacts will reach normal levels again as soon as this intervention has been abolished. This, however, seems hardly plausible, as people will most likely stick to contact-avoiding behaviors in the aftermath of such interventions. Yet, there is no guarantee that this kind of interventions can be sustained over extended periods of time. In particular, the achievable reduction in contact behavior depends on the economic situation, the available infrastructure and cultural habits. Also, the effect of home isolation has to be treated with caution, as it assumes that disease-negative individuals do not constrain their contacts. This again seems implausible as many COVID-19-free individuals may also retreat into self-imposed isolation if they experience influenza-like symptoms. Again, the effectiveness of home isolation depends on several factors as the economic status of a society, its hygienic standards, the family size distribution etc.
Notably, our predictions essentially assume a closed population which is exposed to a few infections imported from outside (which do not strongly affect the dynamics once the infection starts to spread in the population). However, in the absence of restrictions in mobility and international travel, a population cannot be considered as independent. Effective social distancing essentially assumes that hardly any infection is imported, thus, in essence that boarders are closed. Nevertheless, CovidSIM is a convenient tool to get robust estimates of the impact of several interventions and thereby facilitates decision-support. However, other confounding factors including ethical, cultural and economic ones need to be considered and the interpretation of predictive results should be discussed with experts in the field of infectious disease modeling.
The numbers of symptomatic infections, hospital or ICU capacities, and mortality are derived quantities that can be deduced in an age-dependent fashion from the model output. However, CovidSIM Version 1.0 does not yet explicitly incorporate age structure, and particularly age-dependent contact behaviour, in the model. Thus, CovidSIM Version 1.0 is more relevant for industrialized nations than for countries in which the demography is strongly dominated by an expanding population, e.g., for many countries in Subsaharan Africa. where adjustments to the model would be necessary. Future extensions of CovidSIM, building upon the basic model described here, will include age structure explicitly.

Concluions

CovidSIM allows predictions on the COVID-19 pandemic under various interventions. The tool will be extended in the future by necessary and meaningful model refinements and additional interventions which are emerging as control measures are being discussed and implemented. All planned extensions will be based on the model described here. By using substages, the model avoids exponentially distributed durations of disease stages that emerge implicitly from the classical SEIR type models.
The CovidSim web interface was employed to explore the impact of different control measures with parameter choices that roughly reflect the situation in the Federal Republic of Austria as an example. The purpose was to illustrate the effects of different control strategies and their combined effects. Any decision based on these results must be taken with caution, especially attempts to optimally control the disease.

Acknowledgements

We want to dedicate this work to all the victims of the SARS-CoV-2 virus. Our grief is with the friends and families of the dreadful disease. The authors like to express their sympathy to all working to find a cure for the virus. The authors gratefully acknowledge the comments of three anonymous reviewers!
Not Applicable.
Not Applicable.

Competing interests

All authors declare no competing interests.
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Metadaten
Titel
The COVID-19 pandemic preparedness simulation tool: CovidSIM
verfasst von
Kristan A. Schneider
Gideon A. Ngwa
Markus Schwehm
Linda Eichner
Martin Eichner
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Schlagwort
COVID-19
Erschienen in
BMC Infectious Diseases / Ausgabe 1/2020
Elektronische ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-020-05566-7

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Worauf kommt es beim Management von Personen mit infektiöser Endokarditis an? Eine Kardiologin und ein Kardiologe fassen die zehn wichtigsten Punkte der neuen ESC-Leitlinie zusammen.

Update Innere Medizin

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