Abstract

The number of new infections per day is a key quantity for effective epidemic management. It can be estimated relatively directly by testing of random population samples. Without such direct epidemiological measurement, other approaches are required to infer whether the number of new cases is likely to be increasing or decreasing: for example, estimating the pathogen‐effective reproduction number, R, using data gathered from the clinical response to the disease. For coronavirus disease 2019 (Covid‐19/SARS‐Cov‐2), such R estimation is heavily dependent on modelling assumptions, because the available clinical case data are opportunistic observational data subject to severe temporal confounding. Given this difficulty, it is useful to retrospectively reconstruct the time course of infections from the least compromised available data, using minimal prior assumptions. A Bayesian inverse problem approach applied to UK data on first‐wave Covid‐19 deaths and the disease duration distribution suggests that fatal infections were in decline before full UK lockdown (24 March 2020), and that fatal infections in Sweden started to decline only a day or two later. An analysis of UK data using the model of Flaxman et al. gives the same result under relaxation of its prior assumptions on R, suggesting an enhanced role for non‐pharmaceutical interventions short of full lockdown in the UK context. Similar patterns appear to have occurred in the subsequent two lockdowns.

Highlights

  • Clinical data on the number of cases of Covid-19 (SARS-CoV-2) are subject to severe temporal confounding, as the rate of testing and criteria for testing have been changing rapidly on the same time scale as the infections, in the early weeks and months of the epidemic

  • The most notable feature of the results is that fatal infections are inferred to be in substantial decline before full lockdown

  • There is an argument for preferring hospital data for inferring community fatal infections, in that the care home epidemic is known to have special features with at least some of the infection not coming from normal community transmission

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Summary

Introduction

Clinical data on the number of cases of Covid-19 (SARS-CoV-2) are subject to severe temporal confounding, as the rate of testing and criteria for testing have been changing rapidly on the same time scale as the infections, in the early weeks and months of the epidemic. Because these are samples of convenience where the ascertainment fraction is changing and unknown, the data can clearly not be used to infer the actual number of infections. Only possible with a delay of some weeks, it is of interest to establish what these relatively high quality data imply about the time course of infections, without strong modelling assumptions

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