Adjusting Incidence Estimates with Laboratory Test Performances: A Pragmatic Maximum Likelihood Estimation-Based Approach

Author:

Weng Yingjie1,Tian Lu2,Boothroyd Derek1,Lee Justin1,Zhang Kenny1,Lu Di1,Lindan Christina P.34,Bollyky Jenna5,Huang Beatrice6,Rutherford George W.34,Maldonado Yvonne7,Desai Manisha12ORCID,

Affiliation:

1. Quantitative Sciences Unit, Department of Medicine, Stanford University, Palo Alto, CA

2. Biomedical Data Science, Department of Medicine, Stanford University, Palo Alto, CA

3. Department of Epidemiology and Biostatistics, University of California, San Francisco, CA

4. Institute for Global Health Sciences, University of California San Francisco, San Francisco, CA

5. Division of Primary Care & Population Health, School of Medicine, Stanford University, Stanford, CA

6. Department of Family and Community Medicine, University of California, San Francisco, CA

7. Division of Pediatric Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA.

Abstract

Understanding the incidence of disease is often crucial for public policy decision-making, as observed during the COVID-19 pandemic. Estimating incidence is challenging, however, when the definition of incidence relies on tests that imperfectly measure disease, as in the case when assays with variable performance are used to detect the SARS-CoV-2 virus. To our knowledge, there are no pragmatic methods to address the bias introduced by the performance of labs in testing for the virus. In the setting of a longitudinal study, we developed a maximum likelihood estimation-based approach to estimate laboratory performance-adjusted incidence using the expectation-maximization algorithm. We constructed confidence intervals (CIs) using both bootstrapped-based and large-sample interval estimator approaches. We evaluated our methods through extensive simulation and applied them to a real-world study (TrackCOVID), where the primary goal was to determine the incidence of and risk factors for SARS-CoV-2 infection in the San Francisco Bay Area from July 2020 to March 2021. Our simulations demonstrated that our method converged rapidly with accurate estimates under a variety of scenarios. Bootstrapped-based CIs were comparable to the large-sample estimator CIs with a reasonable number of incident cases, shown via a simulation scenario based on the real TrackCOVID study. In more extreme simulated scenarios, the coverage of large-sample interval estimation outperformed the bootstrapped-based approach. Results from the application to the TrackCOVID study suggested that assuming perfect laboratory test performance can lead to an inaccurate inference of the incidence. Our flexible, pragmatic method can be extended to a variety of disease and study settings.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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