A mathematical model to assess the effectiveness of test-trace-isolate-and-quarantine under limited capacities

PLoS One. 2024 Mar 12;19(3):e0299880. doi: 10.1371/journal.pone.0299880. eCollection 2024.

Abstract

Diagnostic testing followed by isolation of identified cases with subsequent tracing and quarantine of close contacts-often referred to as test-trace-isolate-and-quarantine (TTIQ) strategy-is one of the cornerstone measures of infectious disease control. The COVID-19 pandemic has highlighted that an appropriate response to outbreaks of infectious diseases requires a firm understanding of the effectiveness of such containment strategies. To this end, mathematical models provide a promising tool. In this work, we present a delay differential equation model of TTIQ interventions for infectious disease control. Our model incorporates the assumption of limited TTIQ capacities, providing insights into the reduced effectiveness of testing and tracing in high prevalence scenarios. In addition, we account for potential transmission during the early phase of an infection, including presymptomatic transmission, which may be particularly adverse to a TTIQ based control. Our numerical experiments inspired by the early spread of COVID-19 in Germany demonstrate the effectiveness of TTIQ in a scenario where immunity within the population is low and pharmaceutical interventions are absent, which is representative of a typical situation during the (re-)emergence of infectious diseases for which therapeutic drugs or vaccines are not yet available. Stability and sensitivity analyses reveal both disease-dependent and disease-independent factors that impede or enhance the success of TTIQ. Studying the diminishing impact of TTIQ along simulations of an epidemic wave, we highlight consequences for intervention strategies.

MeSH terms

  • COVID-19*
  • Communicable Diseases*
  • Contact Tracing
  • Humans
  • Models, Theoretical
  • Pandemics / prevention & control
  • Quarantine
  • SARS-CoV-2

Grants and funding

The work of JH and MVB was supported by the LOEWE focus Center for Multiscale Modelling in Life Sciences (CMMS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.