TY - JOUR
T1 - A framework for counterfactual analysis, strategy evaluation, and control of epidemics using reproduction number estimates
AU - She, Baike
AU - Smith, Rebecca Lee
AU - Pytlarz, Ian
AU - Sundaram, Shreyas
AU - Paré, Philip E.
N1 - RLS was funded by SHIELD T3 and SHIELD Illinois (https://www.uillinois.edu/shield; no grant number). PEP was partially funded by the National Science Foundation, Division of Electrical, Communications and Cyber Systems (https:// www.nsf.gov/div/index.jsp?div=ECCS), grant NSFECCS #2238388. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Professor Nigel Goldenfeld at the University of California San Diego for taking the time to review our paper and for providing invaluable insights and feedback. We thank the SHIELD: Target, Test, Tell team at the University of Illinois Urbana-Champaign for collecting and providing data, and for helpful discussion for this research. The IRB for this research was ruled exempt by UIUC (protocol #21216). We thank the Institutional Data Analytics + Assessment team at Purdue University for collecting and providing data, and for helpful discussion for this research. The IRB for this research was ruled exempt by Purdue IRB-2020-1683. We thank Humphrey C. H. Leung for plotting several figures based on testing data from Purdue University.
PY - 2024/11
Y1 - 2024/11
N2 - During pandemics, countries, regions, and communities develop various epidemic models to evaluate spread and guide mitigation policies. However, model uncertainties caused by complex transmission behaviors, contact-tracing networks, time-varying parameters, human factors, and limited data present significant challenges to model-based approaches. To address these issues, we propose a novel framework that centers around reproduction number estimates to perform counterfactual analysis, strategy evaluation, and feedback control of epidemics. The framework 1) introduces a mechanism to quantify the impact of the testing-for-isolation intervention strategy on the basic reproduction number. Building on this mechanism, the framework 2) proposes a method to reverse engineer the effective reproduction number under different strengths of the intervention strategy. In addition, based on the method that quantifies the impact of the testing-for-isolation strategy on the basic reproduction number, the framework 3) proposes a closed-loop control algorithm that uses the effective reproduction number both as feedback to indicate the severity of the spread and as the control goal to guide adjustments in the intensity of the intervention.
AB - During pandemics, countries, regions, and communities develop various epidemic models to evaluate spread and guide mitigation policies. However, model uncertainties caused by complex transmission behaviors, contact-tracing networks, time-varying parameters, human factors, and limited data present significant challenges to model-based approaches. To address these issues, we propose a novel framework that centers around reproduction number estimates to perform counterfactual analysis, strategy evaluation, and feedback control of epidemics. The framework 1) introduces a mechanism to quantify the impact of the testing-for-isolation intervention strategy on the basic reproduction number. Building on this mechanism, the framework 2) proposes a method to reverse engineer the effective reproduction number under different strengths of the intervention strategy. In addition, based on the method that quantifies the impact of the testing-for-isolation strategy on the basic reproduction number, the framework 3) proposes a closed-loop control algorithm that uses the effective reproduction number both as feedback to indicate the severity of the spread and as the control goal to guide adjustments in the intensity of the intervention.
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U2 - 10.1371/journal.pcbi.1012569
DO - 10.1371/journal.pcbi.1012569
M3 - Article
C2 - 39565799
AN - SCOPUS:85209878464
SN - 1553-734X
VL - 20
JO - PLoS computational biology
JF - PLoS computational biology
IS - 11
M1 - e1012569
ER -