BeyondR0: heterogeneity in secondary infections and probabilistic epidemic forecasting

Author:

Hébert-Dufresne Laurent123,Althouse Benjamin M.456ORCID,Scarpino Samuel V.7891011,Allard Antoine312ORCID

Affiliation:

1. Vermont Complex Systems Center, University of Vermont, Burlington, VT 05405, USA

2. Department of Computer Science, University of Vermont, Burlington, VT 05405, USA

3. Département de physique, de génie physique et d’optique, Université Laval, Québec, Canada G1V 0A6

4. Institute for Disease Modeling, Bellevue, WA 98005, USA

5. Information School, University of Washington, Seattle, WA 98195-2840, USA

6. Department of Biology, New Mexico State University, Las Cruces, NM 88003, USA

7. Network Science Institute, Northeastern University, Boston, MA 02115, USA

8. Department of Marine and Environmental Sciences, Northeastern University, Boston, MA 02115, USA

9. Department of Physics, Northeastern University, Boston, MA 02115, USA

10. Department of Health Sciences, Northeastern University, Boston, MA 02115, USA

11. ISI Foundation, Turin 10126, Italy

12. Centre interdisciplinaire en modélisation mathématique, Université Laval, Québec, Canada G1V 0A6

Abstract

The basic reproductive number,R0, is one of the most common and most commonly misapplied numbers in public health. Often used to compare outbreaks and forecast pandemic risk, this single number belies the complexity that different epidemics can exhibit, even when they have the sameR0. Here, we reformulate and extend a classic result from random network theory to forecast the size of an epidemic using estimates of the distribution of secondary infections, leveraging both its averageR0and the underlying heterogeneity. Importantly, epidemics with lowerR0can be larger if they spread more homogeneously (and are therefore more robust to stochastic fluctuations). We illustrate the potential of this approach using different real epidemics with known estimates forR0, heterogeneity and epidemic size in the absence of significant intervention. Further, we discuss the different ways in which this framework can be implemented in the data-scarce reality of emerging pathogens. Lastly, we demonstrate that without data on the heterogeneity in secondary infections for emerging infectious diseases like COVID-19 the uncertainty in outbreak size ranges dramatically. Taken together, our work highlights the critical need for contact tracing during emerging infectious disease outbreaks and the need to look beyondR0.

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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