| Literature DB >> 34624516 |
Hali L Hambridge1, Rebecca Kahn2, Jukka-Pekka Onnela3.
Abstract
Objectives Universities have turned to SARS-CoV-2 models to examine campus reopening strategies. While these studies have explored a variety of modeling techniques, none have used empirical data. Methods In this study, we use an empirical proximity network of college freshmen obtained using smartphone Bluetooth to simulate the spread of the virus. We investigate the role of immunization, testing, isolation, mask wearing, and social distancing in the presence of implementation challenges and imperfect compliance. Results We show that frequent testing could drastically reduce the spread of the virus if levels of immunity are low, but its effects are limited if immunity is more ubiquitous. Furthermore, moderate levels of mask wearing and social distancing could lead to additional reductions in cumulative incidence, but their benefit decreases rapidly as immunity and testing frequency increase. However, if immunity from vaccination is imperfect or declines over time, scenarios not studied here, frequent testing and other interventions may play more central roles. Conclusions Our findings suggest that although regular testing and isolation are powerful tools, they have limited benefit if immunity is high or other interventions are widely adopted. If universities can attain even moderate levels of vaccination, masking, and social distancing, they may be able to relax the frequency of testing to once every four weeks. Published by Elsevier Ltd.Entities:
Keywords: Bluetooth; COVID-19; Copenhagen Network Study; Proximity network; Repeat testing; SARS-CoV-2
Mesh:
Year: 2021 PMID: 34624516 PMCID: PMC8492892 DOI: 10.1016/j.ijid.2021.10.008
Source DB: PubMed Journal: Int J Infect Dis ISSN: 1201-9712 Impact factor: 3.623
Parameters for simulation scenarios. The transmission probability, , is per five-minute interaction with an infectious individual. All other epidemic transition parameters are per day, giving an average latent period of three days and an average infectious period of seven and 12 days for asymptomatic and symptomatic cases, respectively. Test sensitivity is time-varying. For distributions, values represent the means and standard deviations, respectively. An overview of the epidemic model is shown in Figure 5. Additional details are presented in the corresponding sections of the supplement.
| probability of transmission per five-minute interaction | ||
| Normal( | probability of external infection per day – high scenario | |
| Normal( | probability of external infection per day – low scenario | |
| probability of asymptomatic infection | ||
| 1 | number of initial infections | |
| transition probability: exposed to asymptomatic infectious | ||
| transition probability: exposed to symptomatic infectious | ||
| transition probability: asymptomatic infectious to recovered | ||
| transition probability: symptomatic infectious to recovered | ||
| sensitivity, time-varying | ||
| specificity | ||
| 1 day | delay between symptom onset and symptomatic testing | |
| Normal( | probability non-compliant with scheduled testing | |
| Normal( | probability non-compliant with symptomatic testing | |
| probability non-infectious present for symptomatic testing | ||
| 1 day | delay between testing and entering isolation | |
| Beta( | isolation compliance | |
| 10 days | isolation period | |
| Normal( | reduction in transmission probability for mask wearing | |
| Normal( | reduction in transmission probability for social distancing | |
| proportion of the population wearing face masks | ||
| proportion of the population social distancing | ||
| proportion of the population immune | ||
Fig. 1Number of students infected over the course of a simulated 16-week semester forand high levels of transmission from the community. Rows show different proportions of the population immunized, as annotated on the right. Columns show scenarios where scheduled testing was conducted every three, seven, 14, and 28 days, respectively, and no scheduled testing. Grey lines denote individual simulations. Blue lines indicate the point-wise average trajectory over all 100 replicates. Vertical red lines and text indicate the average times to reach of the population infected, which were computed by identifying the time required to reach infected for each realization and averaging those times.
Fig. 2Cumulative percentage infected for various proportions of the population social distancing and/or wearing masks for. Cell values indicate the proportion of the population infected by the end of a simulated 16-week semester. Rows show different proportions of the population immunized, as annotated on the right. Columns show scenarios where scheduled testing was conducted every three, seven, 14, and 28 days, respectively, and no scheduled testing.