Utilizing a capture–recapture strategy to accelerate infectious disease surveillance

Monitoring key elements of disease dynamics (e.g., prevalence, case counts) is of great importance in infectious disease prevention and control, as emphasized during the COVID-19 pandemic. To facilitate this effort, we propose a new capture-recapture (CRC) analysis strategy that adjusts for misclassification stemming from the use of easily administered but imperfect diagnostic test kits, such as rapid antigen test-kits or saliva tests. Our method is based on a recently proposed "anchor stream" design, whereby an existing voluntary surveillance data stream is augmented by a smaller and judiciously drawn random sample. It incorporates manufacturer-specified sensitivity and specificity parameters to account for imperfect diagnostic results in one or both data streams. For inference to accompany case count estimation, we improve upon traditional Wald-type confidence intervals by developing an adapted Bayesian credible interval for the CRC estimator that yields favorable frequentist coverage properties. When feasible, the proposed design and analytic strategy provides a more efficient solution than traditional CRC methods or random sampling-based bias-corrected estimation to monitor disease prevalence while accounting for misclassification. We demonstrate the benefits of this approach through simulation studies and a numerical example that underscore its potential utility in practice for economical disease monitoring among a registered closed population.

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Publication Details

Journal
The Annals of Applied Statistics
Published
2024-10-31
DOI
https://doi.org/10.1214/24-aoas1927
Primary Topic
Census and Population Estimation
Type
article
Field-Weighted Citation Impact
0.00

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article

Utilizing a capture–recapture strategy to accelerate infectious disease surveillance

Robert H. Lyles, Yuzi Zhang, Lin Ge, Lance Allyn Waller
The Annals of Applied Statistics
Census and Population Estimation
article

Utilizing a capture–recapture strategy to accelerate infectious disease surveillance

Robert H. Lyles, Yuzi Zhang, Lin Ge, Lance Allyn Waller
article en

Abstract

Monitoring key elements of disease dynamics (e.g., prevalence, case counts) is of great importance in infectious disease prevention and control, as emphasized during the COVID-19 pandemic. To facilitate this effort, we propose a new capture-recapture (CRC) analysis strategy that adjusts for misclassification stemming from the use of easily administered but imperfect diagnostic test kits, such as rapid antigen test-kits or saliva tests. Our method is based on a recently proposed "anchor stream" design, whereby an existing voluntary surveillance data stream is augmented by a smaller and judiciously drawn random sample. It incorporates manufacturer-specified sensitivity and specificity parameters to account for imperfect diagnostic results in one or both data streams. For inference to accompany case count estimation, we improve upon traditional Wald-type confidence intervals by developing an adapted Bayesian credible interval for the CRC estimator that yields favorable frequentist coverage properties. When feasible, the proposed design and analytic strategy provides a more efficient solution than traditional CRC methods or random sampling-based bias-corrected estimation to monitor disease prevalence while accounting for misclassification. We demonstrate the benefits of this approach through simulation studies and a numerical example that underscore its potential utility in practice for economical disease monitoring among a registered closed population.

The Annals of Applied StatisticsVol. 18(4)
Emory University (US)
National Institutes of Health, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Center for Advancing Translational Sciences
Openalex Percentile: Top 80%
Census and Population Estimation
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Utilizing a capture–recapture strategy to accelerate infectious disease surveillance — Robert H. Lyles, Yuzi Zhang, et al. · The Annals of Applied Statistics (2024) | TGRS Research Map | TGRS