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Published on: March 7, 2019
What you saw was what you got? Correcting reported incidence data for testing intensity
Rasmus Kristoffer Pedersen1, Christian Berrig2, Tamás Tekeli3
1Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany; Interdisciplinary Center for Mathematical Modeling of Infectious Disease Dynamics (IMMIDD), University of Münster, Münster, Germany; PandemiX center, Department of Science and Environment, Roskilde University, Roskilde, Denmark.
Abstract:
During the COVID-19 pandemic, non-pharmaceutical interventions were employed to limit the spread of the SARS-CoV-2 virus. In some countries, this included large-scale voluntary testing of non-symptomatic individuals to gauge the prevalence in the general population and to identify asymptomatic and pre-symptomatic infections in order to reduce disease spread. Differences between the intensity of testing means that comparing case-counts across borders may be deceptive. In this work, we use mathematical modeling to investigate the dynamics of both observed and unobserved infections as a function of the rate of voluntary testing. The model indicates that increasing the rate of testing causes the number of observed cases to increase, despite a decrease in prevalence due to testing. For large testing rates, the observed case-counts also decrease. The non-monotonicity of the observed cases explains some discrepancies seen when comparing uncorrected case-counts between countries. One such example was observed during the winter 2020/2021 COVID-19 epidemics in Denmark and Hungary, where reported case-counts were comparable, despite differences in prevalence. We determine a quantitative measure for the ascertainment ratio between observed cases and all infections, allowing for test-intensity correction of case-counts. This measure allows us to correct case-counts for testing intensity during the winter 2021/2022 epidemic of the Omicron variant (BA.1 and BA.2) in Denmark, showing good agreement with results from serology-studies. While the model does not capture the full complexity of epidemic dynamics, it provides a simple way to correct case-counts for differences in testing, simplifying comparison across international borders and testing activities.

