A model for the spread of infectious diseases compatible with case data

Norden E. Huang, Fangli Qiao, Qian Wang, Hong Qian, Ka Kit Tung

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

For epidemics such as COVID-19, with a significant population having asymptomatic, untested infection, model predictions are often not compatible with data reported only for the cases confirmed by laboratory tests. Additionally, most compartmental models have instantaneous recovery from infection, contrary to observation. Tuning such models with observed data to obtain the unknown infection rate is an ill-posed problem. Here, we derive from the first principle an epidemiological model with delay between the newly infected (N) and recovered (R) populations. To overcome the challenge of incompatibility between model and case data, we solve for the ratios of the observed quantities and show that log(N(t)/R(t)) should follow a straight line. This simple prediction tool is accurate in hindcasts verified using data for China and Italy. In traditional epidemiology, an epidemic wanes when much of the population is infected so that 'herd immunity' is achieved. For a highly contagious and deadly disease, herd immunity is not a feasible goal without human intervention or vaccines. Even before the availability of vaccines, the epidemic was suppressed with social measures in China and South Korea with much less than 5% of the population infected. Effects of social behaviour should be and are incorporated in our model.

Original languageEnglish
Article number20210551
JournalProceedings of the Royal Society B: Biological Sciences
Volume477
Issue number2254
DOIs
StatePublished - 1 Oct 2021

Keywords

  • basic reproduction number
  • COVID-19
  • herd immunity
  • SIR and SEIR models
  • vaccination

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