A Framework for SARS-CoV-2 Testing on a Large University Campus: Statistical Considerations

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Abstract

We consider testing strategies for active SARS-CoV-2 infection for a large university community population, which we define. Components of such a strategy include individuals tested because they self-select or are recommended for testing by a health care provider for their own health care; individuals tested because they belong to a high-risk group where testing serves to disrupt transmission; and, finally, individuals randomly selected for testing from the university community population as part of a proactive community testing , or surveillance, program. The proactive community testing program is predicated on a mobile device application that asks individuals to self-monitor COVID-like symptoms daily. The goals of this report are (i) to provide a framework for estimating prevalence of SARS-CoV-2 infection in the university community wherein proactive community testing is a major component of the overall strategy, (ii) to address the issue of how many tests should be performed as part of the proactive community testing program, and (iii) to consider how effective proactive community testing will be for purposes of detection of new disease clusters.

We argue that a comprehensive prevalence estimate informed by all testing done of the university community is a good metric to obtain a global picture of campus SARS-CoV-2 infection rates at a particular point in time and to monitor the dynamics of infection over time, for example, estimating the population-level reproductive number, R 0 ). Importantly, the prevalence metric can be useful to campus leadership for decision making. One example involves comparing campus prevalence to that in the broader off-campus community. We also show that under some reasonable assumptions, we can obtain valid statements about the comprehensive prevalence by only testing symptomatic persons in the proactive community testing component.

The number of tests performed for individual-level and high-risk group-level needs will depend on the disease dynamics, individual needs, and testing availability. For purposes of this report, we assume that, for these groups of individuals, inferential precision — that is, the accuracy with which we can estimate the true prevalence from testing a random sample of individuals — does not drive decisions on the number of tests.

On the other hand, for proactive community testing, the desired level of inferential precision in a fixed period of time can be used to justify the number of tests to perform in that period. For example, our results show that, if we establish a goal of ruling out with 98% confidence a background prevalence of 2% in a given week, and the actual prevalence is 1% among those eligible for proactive community testing, we would need to test 835 randomly-selected symptomatics (i.e., those presenting with COVID-like symptoms) per week via the proactive community testing program in a campus of 80k individuals. In addition to justifying decisions about the number of tests to perform, inferential precision can formalize the intuition that testing of symptomatic individuals should be prioritized over testing asymptomatic individuals in the proactive community testing program.

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  1. SciScore for 10.1101/2020.07.23.20160788: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    NIH rigor criteria are not applicable to paper type.

    Table 2: Resources

    Software and Algorithms
    SentencesResources
    Finite population counts and sampled counts: Population: where an N indicates population counts, 1/0 indicates positive/negative, and s/a indicates symptomatic or asymptomatic, including among those who are COVID-19 negative.
    Population
    suggested: (Current Population Survey, RRID:SCR_007334)

    Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).


    Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:
    Limitations arise in this framework if sampled individuals do not present for testing, if individuals mis- or under-report their symptoms, e.g., through the mobile app, if persons with symptoms do not present for testing, or if adherence to the mobile app requirement is weak. The sample sizes presented are based on the totals actually tested and those individuals comprising a truly representative sample. As such, there are several opportunities for bias in results here. In addition, we have avoided the issue of defining the criteria for having COVID-like symptoms (i.e., being assigned to Group D.s) versus being asymptomatic (Group D.a), and have only assumed that a crisp definition can be established based on data from the mobile app. Finally, we have not yet accounted for less than 100% test sensitivity in the testing needed for Groups B and C. That can be handled at analysis time.

    Results from TrialIdentifier: No clinical trial numbers were referenced.


    Results from Barzooka: We did not find any issues relating to the usage of bar graphs.


    Results from JetFighter: We did not find any issues relating to colormaps.


    Results from rtransparent:
    • Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
    • No protocol registration statement was detected.

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