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Are fast test results preferable to high test sensitivity in contact-tracing strategies?

Morten Rahbæk Boilesen, Kaare Græsbøll and Jonas L Juul

PLOS Complex Systems, 2026, vol. 3, issue 10, 1-17

Abstract: When an epidemic is spreading in a population, mitigation measures often rely on testing individuals, tracing possible secondary infections, and isolating known or suspected infected individuals. Because more accurate tests often take longer to analyse, and the benefits of contact tracing are strengthened by rapid diagnosis, there exists a trade-off between test sensitivity and test waiting time in test-trace-isolate strategies. Here we ask: How many false negatives can be tolerated in a rapid test so that it reduces transmission better than a slower, more accurate test? How does this change with contact tracing efficiency and test waiting time? We examine these questions using a mathematical branching-process model with adjustable contact tracing efficiency, test turnaround times, test sensitivity, and disease infectiousness profile. For a disease with infectiousness profile similar to that of COVID-19, we find that highly-accurate tests with turnaround times less than 6 days result in greater transmission reduction than less-accurate rapid tests for most parameter choices. If contact tracing is highly effective, however, fast and less reliable test results can be preferable to slower and more accurate tests. On the contrary, if no contact tracing is enforced, our model demonstrates that a self-isolate strategy with no testing yields mitigation at least as good as strategies relying on any tests, even tests with perfect sensitivity and zero turnaround time. Furthermore, we find that if the sensitivity of the rapid test is not static, but correlates with the time-dependent viral load of patients, the rapid test is more often preferable to the slower, more accurate test. We support our numerical contributions with analytical results that clarify the findings and the trade-offs between the key parameters in our model: test sensitivity, turnaround time, and contact tracing efficiency. We analytically demonstrate that, under our model, a rapid test with zero test turnaround time never exceeds a test with perfect sensitivity but non-zero test turnaround time in the absence of contact tracing. Our analysis suggests employing rapid tests to reduce test turnaround times as a viable strategy to reduce transmission when testing infrastructure is under severe stress.Author summary: During disease outbreaks, public health officials might face a decision on whether to use rapid tests that give quick but sometimes inaccurate results, or slower and more precise tests. This choice matters because delays in diagnosis slow down contact tracing, allowing infected and their potential secondary infections to spread illness longer. Here, we use mathematical modeling to examine the trade-off between test speed and test accuracy. We use the mathematical model to simulate epidemic outbreaks with different levels of contact tracing efficiency, test turnaround time and test sensitivity. In each case, we evaluate whether disease mitigation is best with slow-and-accurate tests or fast-and-inaccurate tests. For diseases similar to COVID-19, we find that accurate tests with test turnaround time less than six days generally reduce transmission better than rapid, less reliable tests. However, when contact tracing is highly efficient, faster results become advantageous. We also discover that if test sensitivity is proportional to the viral loads of the infected, rapid tests become more favourable overall. Finally, our analysis shows that when contact tracing isn’t feasible, neither rapid nor accurate testing outperforms simply having people self-isolate without testing infrastructure. Our work can help guide testing strategy decisions when an epidemic is raging, revealing that prioritizing speed can become a viable strategy to reduce transmission when testing infrastructure is under stress.

Date: 2026
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pcsy00:0000134

DOI: 10.1371/journal.pcsy.0000134

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