Contact tracing efficiency, transmission heterogeneity, and accelerating COVID-19 epidemics

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Abstract

Simultaneously controlling COVID-19 epidemics and limiting economic and societal impacts presents a difficult challenge, especially with limited public health budgets. Testing, contact tracing, and isolating/quarantining is a key strategy that has been used to reduce transmission of SARS-CoV-2, the virus that causes COVID-19 and other pathogens. However, manual contact tracing is a time-consuming process and as case numbers increase a smaller fraction of cases’ contacts can be traced, leading to additional virus spread. Delays between symptom onset and being tested (and receiving results), and a low fraction of symptomatic cases being tested and traced can also reduce the impact of contact tracing on transmission. We examined the relationship between increasing cases and delays and the pathogen reproductive number R t , and the implications for infection dynamics using deterministic and stochastic compartmental models of SARS-CoV-2. We found that R t increased sigmoidally with the number of cases due to decreasing contact tracing efficacy. This relationship results in accelerating epidemics because R t initially increases, rather than declines, as infections increase. Shifting contact tracers from locations with high and low case burdens relative to capacity to locations with intermediate case burdens maximizes their impact in reducing R t (but minimizing total infections may be more complicated). Contact tracing efficacy decreased sharply with increasing delays between symptom onset and tracing and with lower fraction of symptomatic infections being tested. Finally, testing and tracing reductions in R t can sometimes greatly delay epidemics due to the highly heterogeneous transmission dynamics of SARS-CoV-2. These results demonstrate the importance of having an expandable or mobile team of contact tracers that can be used to control surges in cases. They also highlight the synergistic value of high capacity, easy access testing and rapid turn-around of testing results, and outreach efforts to encourage symptomatic cases to be tested immediately after symptom onset.

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  1. SciScore for 10.1101/2020.09.04.20188631: (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

    No key resources detected.


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    Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:
    A major caveat must be kept in mind in interpreting these results. A smaller reduction in Rt (e.g. 10%) in one population can prevent more infections (especially over multiple generations of transmission) than a larger (e.g. 20%) reduction in Rt in a second population if Rt in the second location is lower (especially when Rt>1 in the first population), or when there is a larger number of infected individuals in the first population. Thus, transferring contact tracers from a region with a high case burden relative to contact tracing capacity to maximize their efficacy in reducing Rt should only be done if other measures (e.g. social distancing) will be put into place to reduce Rt where case numbers are high. More generally, allocation of contact tracers to maximize the number of cases prevented given an array of tools would require a complex dynamic analysis beyond that examined here. We also found that the efficacy of contact tracing itself, regardless of capacity, was strongly influenced by delays between the onset of symptoms and the beginning of tracing, as well as the fraction of symptomatic infections that were traced. Unless delays were short and the fraction of symptomatic cases that were traced was high, contact tracing had limited effects in reducing Rt. This finding parallels results from other studies demonstrating the large effects of delays in reducing efficacy of isolating infections by testing alone (26). We note that in the model considered here, only symptoma...

    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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