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The goal of this report is to inform interested parties about dynamics of SARS-CoV-2 spread in Orange County, CA and to predict (if feasible) the outbreak epidemic trajectory. Our approach is based on fitting a mechanistic model of SARS-CoV-2 spread to multiple sources of surveillance data. More specifically, we use daily numbers of new cases and deaths, while taking into account changes in the total number of tests reported on each day.
Since we rely on a mechanistic model, it is important to acknowledge limitations of this model. We will try to be transparent about our assumptions in the hope to receive feedback about their realism. So if something does not look right to you, please get in touch with us to help us improve our model.
Our method takes three time series as input: daily new tests, case counts, and deaths. However, we find daily resolution to be too noisy due to delay in testing reports, weekend effect, etc. So we aggregated/binned the three types of counts in 3 day intervals. These aggregated time series are shown below.
We assume that all individuals in Orange County, CA can be split into 6 compartments: S = susceptible individuals, E = infected, but not yet infectious individuals, \(\text{I}_\text{e}\) = individuals at early stages of infection, \(\text{I}_\text{p}\) = individuals at progressed stages of infection (assumed 20% less infectious than individuals at the early infection stage), R = recovered individuals, D = individuals who died due to COVID-19. Possible progressions of an individual through the above compartments are depicted in the diagram below.
Mathematically, we assume that dynamics of the proportions of individuals in each compartment follow a set of ordinary differential equations corresponding to the above diagram. These equations are controlled by the following parameters:
We fit this model to data by assuming that case counts are noisy realizations of the actual number of individuals progressing from \(\text{I}_\text{e}\) compartment to \(\text{I}_\text{p}\) compartment. Similarly we assume that observed deaths are noisy realizations of the actual number of individuals progressing from \(\text{I}_\text{p}\) compartment to \(\text{D}\) compartment. A priori, we assume that death counts are significantly less noisy than case counts. We use a Bayesian estimation framework, which means that all estimated quantities receive credible intervals (e.g., 80% or 95% credible intervals). Width of these credible intervals encode the amount of uncertainty that we have in the estimated quantities.
We report estimated trajectories of latent cumulative deaths, incidence (i.e., total infections and deaths that have occurred by some prespecified time point), and prevalence . These trajectories represent our estimation of accumulation of unobserved/hidden number of infections and deaths in the Orange County population. We also project these three trajectories 4 weeks into the future.
Next we report prior and posterior distributions of key model parameters. Prior distributions represent our beliefs about these parameters before seeing/analyzing data. Posterior distributions encode our updated beliefs after seeing/analyzing data.
We report predictive distribution of observed deaths and positive test rate during the observation interval (blue shaded area with black dots in the plot below). In addition, we show a four week ahead forecast for both quantities. Our forecast assumes that interventions (physical distancing orders, mask recommendations, etc.) stay at the status quo, and that there are 2100 tests in each three day interval in the future. We plan to archive our forecasts and retrospectively measure their predictive ability/skill.
We examine how sensitive our conclusions about \(R_0\) to our prior assumptions by repeating estimation of all model parameters under different priors for this parameter. The priors are listed in the titles of the figures. Although the prior distribution of \(R_0\) does have some effect on its posterior (as it should), the our results and conclusions are not too sensitive to a particular specification of this prior.
R version 4.0.2 (2020-06-22)
Platform: x86_64-w64-mingw32/x64 (64-bit)
Running under: Windows 10 x64 (build 18362)
Matrix products: default
locale:
[1] LC_COLLATE=English_United States.1252
[2] LC_CTYPE=English_United States.1252
[3] LC_MONETARY=English_United States.1252
[4] LC_NUMERIC=C
[5] LC_TIME=English_United States.1252
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] patchwork_1.0.1 scales_1.1.1 tidybayes_2.1.1 forcats_0.5.0
[5] stringr_1.4.0 dplyr_1.0.0 purrr_0.3.4 readr_1.3.1
[9] tidyr_1.1.0 tibble_3.0.3 ggplot2_3.3.2 tidyverse_1.3.0
[13] here_0.1 lubridate_1.7.9 workflowr_1.6.2
loaded via a namespace (and not attached):
[1] matrixStats_0.56.0 fs_1.4.2 RColorBrewer_1.1-2
[4] httr_1.4.1 rprojroot_1.3-2 rstan_2.21.1
[7] tools_4.0.2 backports_1.1.8 utf8_1.1.4
[10] R6_2.4.1 DBI_1.1.0 colorspace_1.4-1
[13] ggdist_2.2.0 withr_2.2.0 gridExtra_2.3
[16] tidyselect_1.1.0 prettyunits_1.1.1 processx_3.4.3
[19] curl_4.3 compiler_4.0.2 git2r_0.27.1
[22] cli_2.0.2 rvest_0.3.5 arrayhelpers_1.1-0
[25] xml2_1.3.2 labeling_0.3 callr_3.4.3
[28] digest_0.6.25 StanHeaders_2.21.0-5 rmarkdown_2.3
[31] pkgconfig_2.0.3 htmltools_0.5.0 dbplyr_1.4.4
[34] rlang_0.4.7 readxl_1.3.1 rstudioapi_0.11
[37] farver_2.0.3 generics_0.0.2 svUnit_1.0.3
[40] jsonlite_1.7.0 distributional_0.1.0 inline_0.3.15
[43] magrittr_1.5 loo_2.3.1 Rcpp_1.0.5
[46] munsell_0.5.0 fansi_0.4.1 lifecycle_0.2.0
[49] stringi_1.4.6 whisker_0.4 yaml_2.2.1
[52] pkgbuild_1.1.0 plyr_1.8.6 grid_4.0.2
[55] blob_1.2.1 parallel_4.0.2 promises_1.1.1
[58] crayon_1.3.4 lattice_0.20-41 haven_2.3.1
[61] hms_0.5.3 knitr_1.29 ps_1.3.3
[64] pillar_1.4.6 codetools_0.2-16 stats4_4.0.2
[67] reprex_0.3.0 glue_1.4.1 evaluate_0.14
[70] V8_3.2.0 RcppParallel_5.0.2 modelr_0.1.8
[73] vctrs_0.3.2 httpuv_1.5.4 cellranger_1.1.0
[76] gtable_0.3.0 assertthat_0.2.1 ckanr_0.4.0
[79] xfun_0.15 broom_0.7.0 coda_0.19-3
[82] later_1.1.0.1 ellipsis_0.3.1