Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-24T10:49:20.572Z Has data issue: false hasContentIssue false

Comparing multiple infection control measures in a nursing home setting: a simulation study

Published online by Cambridge University Press:  15 March 2024

Haomin Li
Affiliation:
Department of Biostatistics, University of Iowa, Iowa City, IA, USA
Daniel K. Sewell*
Affiliation:
Department of Biostatistics, University of Iowa, Iowa City, IA, USA
Ted Herman
Affiliation:
Department of Computer Science, University of Iowa, Iowa City, IA, USA
Sriram V. Pemmeraju
Affiliation:
Department of Computer Science, University of Iowa, Iowa City, IA, USA
Alberto M. Segre
Affiliation:
Department of Computer Science, University of Iowa, Iowa City, IA, USA
Aaron C. Miller
Affiliation:
Department of Internal Medicine, University of Iowa, Iowa City, IA, USA
Philip M. Polgreen
Affiliation:
Department of Internal Medicine, University of Iowa, Iowa City, IA, USA Departments of Epidemiology, University of Iowa, Iowa City, IA, USA
*
Corresponding author: Daniel K. Sewell; Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective:

Compare the effectiveness of multiple mitigation measures designed to protect nursing home residents from infectious disease outbreaks.

Design:

Agent-based simulation study.

Setting:

Simulation environment of a small nursing home.

Methods:

We collected temporally detailed and spatially fine-grained location information from nursing home healthcare workers (HCWs) using sensor motes. We used these data to power an agent-based simulation of a COVID-19 outbreak using realistic time-varying estimates of infectivity and diagnostic sensitivity. Under varying community prevalence and transmissibility, we compared the mitigating effects of (i) regular screening and isolation, (ii) inter-resident contact restrictions, (iii) reduced HCW presenteeism, and (iv) modified HCW scheduling.

Results:

Across all configurations tested, screening every other day and isolating positive cases decreased the attack rate by an average of 27% to 0.501 on average, while contact restrictions decreased the attack rate by an average of 35%, resulting in an attack rate of only 0.240, approximately half that of screening/isolation. Combining both interventions impressively produced an attack rate of only 0.029. Halving the observed presenteeism rate led to an 18% decrease in the attack rate, but if combined with screening every 6 days, the effect of reducing presenteeism was negligible. Altering work schedules had negligible effects on the attack rate.

Conclusions:

Universal contact restrictions are highly effective for protecting vulnerable nursing home residents, yet adversely affect physical and mental health. In high transmission and/or high community prevalence situations, restricting inter-resident contact to groups of 4 was effective and made highly effective when paired with weekly testing.

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Introduction

Residents of nursing homes and long-term care facilities are at high risk of being severely impacted by infectious disease outbreaks due to both age and comorbidities. 1 Additionally, the relatively dense connections among both residents and healthcare workers (HCWs) can lead to unusually rapid diffusion of infectious pathogens. This has been evident throughout the COVID-19 pandemic, where there have been over 1.6 million cases and 166 thousand deaths among US nursing home residents, as well as over 2,000 deaths among staff/HCWs. 2 Residents’ mortality rate has been over 100 times greater than that of the general population and over 20 times greater than that of the population over 65 years of age. Reference Cronin and Evans3

Current documented strategies aimed at mitigating the risk of COVID-19 to nursing home residents include isolation and contact restrictions, personal protective and hygienic measures, health education and information sharing, monitoring, screening, and entry regulation measures. Reference Usher, Durkin, Gyamfi, Warsini and Jackson4,Reference Stratil, Biallas and Burns5 However, direct evidence connecting such interventions to outcomes is lacking, so high-quality modeling studies are necessary to provide more confidence in the effects of various mitigation measures. Reference Stratil, Biallas and Burns5,Reference Dykgraaf, Matenge and Desborough6

Unlike observational studies, modeling studies have the advantage of avoiding logistical and ethical hurdles when evaluating various strategies and comparing counterfactual scenarios. For example, the impact of varying surveillance strategies has received much attention, Reference Dykgraaf, Matenge and Desborough6Reference Eckardt, Guran and Hennemyre9 and this is also true in modeling studies. Reference Holmdahl, Kahn, Hay, Buckee and Mina10Reference Tsoungui Obama, Adil Mahmoud Yousif and Alawam Nemer14 Rarely have surveillance and isolation been compared against other measures in a nursing home or long-term care facility setting, with the exception of vaccination Reference Vilches, Nourbakhsh and Zhang11 and at least one form contact restriction based on disease status/history Reference Holmdahl, Kahn, Hay, Buckee and Mina10 . These studies’ results varied widely, from very effective when the diagnostic test sensitivity is very high Reference Vilches, Nourbakhsh and Zhang11,Reference Lanièce Delaunay, Saeed and Nguyen13 to potentially counterproductive in other settings such as incarceration facilities with highly seasonal disease incidence. Reference Tsoungui Obama, Adil Mahmoud Yousif and Alawam Nemer14

The goal of this work is to evaluate and compare the efficacy of strategies including (i) screening and isolation, (ii) structured resident contact restrictions, (iii) reduced HCW presenteeism, and (iv) modified HCW scheduling over a wide variety of community prevalence and disease transmissibility parameters. Toward this aim, we used spatially and temporally fine-grained HCW location data obtained from sensor motes in a small nursing home setting to support an agent-based model (ABM) that compares various counterfactual scenarios related to the spread of COVID-19 like respiratory disease.

Methods

Overview

We deployed a sensor mote system of our own design in a 32-room residential care facility in July of 2019. The system consists of rechargeable badges worn by HCWs and line-powered beacons placed in fixed locations to act as geographical markers and data aggregators. Badges periodically broadcast an identifying packet; when a beacon detects such a message, it logs (i) the sender’s id, (ii) the received signal strength index (an observable proxy for physical distance), and (iii) the time the packet was received. Fifteen beacons were placed in hallways, 4 at the nursing station, 2 in the two dining/commons, and 32 in residents’ rooms (all rooms are single occupancy). By fusing beacon data, we can pinpoint when a badge and its associated HCW entered/exited a room.

Because the 32 residents had limited mobility, we were able to reliably infer their location (either their assigned room or one of the common areas) by observing HCW behavior; for example, the data clearly show when HCWs escort residents to the dining rooms for meals or back to their rooms after dinner. For this study, we leveraged 8 hours of data (7:00–15:00) collected from the badges of the 17 HCWs working on July 17, 2019. The data were partially replicated to recreate a full day’s HCW/resident interactions in a manner that reflects the facility’s dining and activity schedule when staffed by 34 HCWs working in shifts.

Contact networks

Using the timestamps and locations of each HCW or resident, we constructed an empirical contact network consisting of nodes representing agents (HCWs or residents) and weighted edges representing the cumulative time the agents spent in the same location for the day. Three alternate contact networks were also constructed from the empirical contact network in a manner consistent with a specified type of infection control intervention:

  1. 1. (Lockdown network) No resident-resident interactions were allowed, that is, all the residents remain in their assigned rooms throughout the day.

  2. 2. (Homogeneous network) Every resident is relocated to a single common area for a prespecified number of social interaction hours each day: pertinent resident/HCW interactions are also remapped accordingly.

  3. 3. (Bubble network) Each resident is randomly assigned to one of N equal sized social “bubbles.” Each bubble is assigned to a distinct common area for a prespecified number of social interaction hours each day: pertinent resident/HCW interactions are also remapped accordingly (see Figure 1 for an example). Note that the homogeneous network is itself a bubble network with N = 1.

    Figure 1. Illustration of how contact networks were constructed from sensor mote data. (a) Empirical contact network based on HCW and inferred resident locations at each time point. (b) No contact between residents was imposed, keeping all residents in their own room (corresponding to lockdown network). (c) Contact between residents was constrained to be between those assigned to the same bubble; residents within same bubbles went to dining hall at same time, as did the HCWs who were in their rooms in empirical network. The bubble network was generated based on this. Note: HCW, healthcare worker.

Simulation

Each of the above contact networks can be used as the basis for an ABM and corresponding simulations. In our simulations, each individual agent (HCW or resident) will be denoted as susceptible, infected, or recovered. Reference Hethcote15 Once the parameters of a simulation are established, a randomly selected on-duty HCW is infected and all other agents are susceptible. We then perform a series of operations on the selected contact network 50 times, once for each simulated day, changing each agent’s status as the simulation demands. Infected agents infect susceptible agents according to a prespecified transmission model. Once infected, some agents will exhibit symptoms, while others will remain asymptomatic: both will progress through a prespecified infection model where the transmissibility varies over time, until they progress to the recovered state after a random-length interval. Because our simulations are short, we do not allow recovered agents to be reinfected. At the end of the simulation, we compare the resident attack rates (percentage of resident agents infected over the course of the simulation) to assess differences between simulation conditions.

For each simulated day:

1. (Permute the contact network) Randomly permute the mapping of HCW identities to HCW nodes; while the pattern of interactions is replayed each day, the HCWs replaying each role changes randomly on a daily basis, thereby ensuring that HCWs were not constrained to interact with the same residents each day.

2. (Reallocate work) For each resident–HCW contact involving an isolated HCW (see steps 3 and 4), reassign the contact to the HCW with the lowest workload among those available at the time of contact.

3. (Testing and mandatory isolation) Selected HCWs and residents are tested on a fixed prespecified schedule, where we assume the test has perfect specificity, but its sensitivity depends on time since infection. Any agent with a positive result is mandatorily isolated for 10 days until recovered according to the infection model.

4. (Self-isolation) Non-isolated infected agents who become symptomatic may self-isolate with a certain probability.

5. (Internal transmission) Susceptible agents may contract the disease during contact with a non-isolated infected agent according to the contact network edge weight (duration of contact) and how long the infected agent has been infected.

6. (Community transmission) Non-isolated susceptible HCWs have a certain probability of becoming infected through external sources based on the community risk value.

7. (External transmission) Each non-isolated resident will have 2 hours of interactions with two visitors (total 4 hours) each week; visitors may be infected, again in accordance with the community risk value, and are not tested prior to visiting.

Model parameters and counterfactuals

The ABM parameters were divided into two groups: disease parameters derived from the existing literature and intervention parameters (Table 1). While the goal of our study was not exclusively focused on COVID-19, we used this as our model disease due to the large body of literature estimating the required parameter values.

Table 1. Agent-based model parameters

To obtain a realistic temporally varying test sensitivity curve, we estimated the severe acute respiratory coronavirus virus 2 (SARS-CoV-2) polymerase chain reaction (PCR) test sensitivity as a function of time since infection by fitting a non-linear logistic regression using natural cubic splines to data collated by Kucirka et al. Reference Kucirka, Lauer, Laeyendecker, Boon and Lessler16

The community risk, that is, community disease prevalence, was fixed at either 0.01, 0.025, 0.05, or 0.1. HCWs are randomly infected from external sources at an incidence rate derived from dividing the community prevalence by the number of days having transmission rate larger than 0.01 (14 days). The probability of visitors being infected is proportional to the prevalence, and the infectiousness is determined by randomly selecting the number of days since becoming infected.

The probability that an infectious individual infected a susceptible contact was derived from assuming an exponential distribution on the time to transmission with rate proportional to the shedding profile in the literature Reference He, Lau and Wu17 and the time in contact. Qualitatively, this led to a transmission rate very small up until a week prior to symptom onset, where it rose to peak at the day prior to symptom onset and then began to steadily decline. The proportionality constant was derived by finding the root of the equation $R_{0} - {\mathbb{E}} \left( transmissions \right)=0$ . The basic reproduction number ${R_0}$ was set to be either 3.15, corresponding to the wild strain of COVID-19, Reference He, Yi and Zhu18 or 5.94, corresponding to the delta strain. Reference Du, Liu and Wang19 Moreover, we also assumed that residents and HCWs would be wearing masks, reducing the ${R_0}$ of the general population by 66%. Reference Chu, Akl and Duda20 Upon becoming infected, an agent is given an incubation period generated from the distribution in the literature, followed by an additional 2 weeks until becoming recovered. Reference Zhang, Litvinova and Wang21

We analyzed the following three testing strategies: all residents and HCWs on the working shift are scheduled for PCR tests (1) every 6 days, (2) every other day, and (3) no testing. We tested all three strategies under restricted contacts within bubbles considering three bubble sizes (N = 1, 4, or 8) and four contact times (t = 0.5, 1, 1.5, or 2 hours/day).

We simulated varying levels of presenteeism among HCWs by considering five self-isolation probabilities (0, 0.180, 0.590, 0.795, and 1) chosen based on observed presenteeism rate of 0.82 among HCWs, Reference Lichtman, Greenblatt, Malenfant and Kuo22 decreasing presenteeism by both ½ and ¼, as well as the extremes of always and never going to work ill.

Work shift arrangements were also evaluated. Assuming two HCW shifts, each shift worked a specific number of consecutive days ranging from 1 to 14 followed by that same number of days off. For example, shift 1 may work 7 days and take 7 days off.

Unless stated otherwise, in each configuration described above, we picked as default settings residents’ contacts restricted to 4 bubbles for 2 hours each day in our simulations, community risk = 0.025, ${R_0}$ = 3.15, HCWs rotated shifts every 6 days, testing every 6 days, and 0.18 self-isolation probability after becoming symptomatic. All total, there were 208 scenarios, and for each, we ran 2,000 simulations.

Results

The results from the nursing home ABM are reported in terms of the attack rate for nursing home residents, that is, the average proportion of the 32 residents infected within the 50-day simulation window.

Figure 2 depicts the effect of different testing strategies. For all three resident contact profiles (homogeneous (A), four bubbles (B), and eight bubbles (C)), the attack rate decreased by 0.32, 0.37, and 0.18, respectively, when going from no testing to testing every 6 days. However, there were much smaller additional reductions in attack rates of 0.11, 0.076, and 0.027, respectively, when moving from testing every 6 days to testing every other day.

Figure 2. The attack rates for residents by different screening strategy. The X axis is the total hours of contact between residents; Y axis is the attack rates. (A) Residents contact each other homogeneously. (B) Residents contact each other within four bubbles. (C) Residents contact each other within eight bubbles.

Figure 3 shows the effect of changing the contact profile on the mean attack rate across different ${R_0}$ (columns) and community prevalence values (rows). While the attack rate reduction from homogeneous contact to the empirical contact patterns was generally dramatic (up to 0.82), the difference between 4 bubbles of 8 residents each and 8 bubbles of 4 residents each depended on the amount of time residents spent with their bubble; for 0.5 hours/day, the reduction in attack rates from 8 to 2 bubbles ranged across our simulation settings from 0.01 to 0.07, while ranging from 0.06 up to 0.36 for 2 hours/day.

Figure 3. The attack rates in nursing home residents by different resident-resident contact profiles. The X axis is the total hours of daily contact between residents; the Y axis is the attack rates among residents. (A–D) R_0 of 3.15. (E–H) R_0 of 5.94. (A, E) A community prevalence of 0.01. (B, F) A prevalence of 0.025. (C, G) A prevalence of 0.05. (D, H) A prevalence of 0.1.

Figure 4 shows the effect of self-isolation on the attack rate. In the absence of screening, changing the self-isolation probability from 0 to 1 greatly reduced the attack rate (reduction of 0.64), while this only minimally reduced the attack rate when screening every 6 days and every other day (reductions of 0.07 and 0.01 respectively). These results match expectations, as screening leads to HCWs who would otherwise engage in presenteeism undergoing mandatory isolation.

Figure 4. The attack rates for residents by different willingness to self-isolate. The X axis is the probability of self-isolation after an individual develops COVID-19 symptoms; Y axis is the attack rates.

Figure 5. The attack rates for residents by different working shift length (ie, number of consecutive days working before the same number of consecutive days off duty). The X axis is the length of working shift; Y axis is the attack rates.

Figure 4 shows the impact of different HCWs’ work shift length. There appears to be complex patterns, but within each testing strategy, the effects appear to be marginal, not exceeding 0.051 for any of the three testing strategies evaluated.

Discussion

Summary

Nursing home residents are older and typically frailer than the general population in high-density contact networks and thus potentially more susceptible to severe illness and mortality from emerging infectious diseases. Non-pharmaceutical interventions can be effective system-level countermeasures to mitigate the risk of severe illness and mortality. This research implements a realistic ABM simulation utilizing fine-grained spatiotemporal information from a sensor mote deployment in a nursing home. We use our simulations to evaluate the effect of four non-pharmaceutical interventions on reducing resident infection rates: (i) screening and isolation, (ii) inter-resident contact restrictions, (iii) reducing HCW presenteeism, and (iv) altering HCW scheduling. By considering all four interventions in the same modeling framework, it becomes easier to meaningfully compare individual or combinations of mitigation measures directly.

Overall, inter-resident contact restrictions were most efficacious, with regular screening and isolation making further substantial gains in reducing the attack rate. Reducing presenteeism was highly effective but only in the absence of regular screening and isolation. Regular screening and isolation alone were insufficient to control transmission; in contrast, restricting inter-resident contacts to bubbles of size four was quite effective alone, although not as effective as the combination of the two strategies.

Effects of bubbling

While the contact patterns impacted the attack rate significantly, this difference depended on the community prevalence and the transmissibility of the disease. Doubling the size of each bubble from 4 to 8 only increased the attack rate by 0.06 for ${R_0}$ = 3.15 and community prevalence of 0.01, whereas this increase climbed up to 0.36 for ${R_0}$ = 5.94 and prevalence of 0.1, suggesting stricter contact restrictions are necessary for highly transmissible diseases with high prevalence.

Fully eliminating contact between residents effectively reduced the attack rate, coming, however, at a very high cost to residents. In a scoping review, Rodrigues et al Reference Rodrigues, Han, Su, Klainin-Yobas and Wu23 found that the social isolation of older adults during the COVID-19 pandemic increased loneliness, worry, stress, anxiety, fear, frustration, boredom, depression, sleep disorders, and suicide ideation. Bubbling can help lower infection rates while diminishing the negative psychosocial effects of isolating during an infectious disease outbreak. Reference Hawkins24 In our study, we found that on average the attack rate from the simulated outbreak was kept below 0.1 when bubbling groups of four residents together for up to 1.5 hours/day in all situations except for when the community prevalence was at 0.1 or when ${R_0}$ = 5.94 with the prevalence ≥0.025; bubbling up to 1 hour/day kept the attack rate below 0.1 unless ${R_0}$ = 5.94 with the ≥0.05. These results suggest that bubbling can be highly effective at reducing transmission while potentially lowering the negative impacts of social isolation on nursing home residents’ mental health.

Effects of presenteeism

The effect of presenteeism, a common issue with HCWs, Reference Challener, Breeher, Frain, Swift, Tosh and O’Horo25 was negated in the presence of regular screening. In the absence of screening, the attack rate was reduced from 0.49 to 0.31 by halving the presenteeism rate from 0.82 to 0.41. These results imply that management should prioritize presenteeism reduction only when there is no regular screening and isolation.

Screening regularity

Our simulations revealed only small improvements when increasing screening rates from every 6 days to every other day. Moreover, the efficacy of screening was highly dependent upon the contact pattern of residents. With homogeneous contact patterns at 1 hour/day, the attack rates for testing every 6 days versus every other day were 0.41 and 0.20, respectively, while for bubbles of size 4, the attack rates were 0.03 and 0.02, respectively. However, in all cases, failing to screen and isolate positives led to much higher attack rates; with the prevalence of 0.025 and ${R_0}$ = 3.15, moving from no testing to testing and isolating every 6 days decreased the attack rate by 35%–79%, depending on the contact pattern and time per day in contact.

Non-effect of work shift alterations

We had hypothesized that the disease characteristics (time to symptom onset, infectiousness profile, etc), testing schedules, and the interaction between the two may lead to different work schedules having an effect on the attack rate. What we observed was a complicated pattern that yielded marginal differences. This seems to imply that a strong knowledge of disease characteristics and transmission is required to know the effect of the work shift schedule on the attack rate, but that even with such knowledge, modifying shift schedules has little impact.

Implications

Bubbling in groups of 4 alongside screening and isolation every 6 days was typically sufficient to maintain a low attack rate in the midst of an epidemic. For ${R_0}$ less than or equal to that of the wild strain SARS-CoV-2, if the community prevalence exceeds 0.05, the time bubbles spend together ought to be restricted to 1 hour per day. For larger ${R_0}$ , when the prevalence exceeds 0.025, the time bubbles spend together ought to be restricted to 0.5 hour per day, and when the prevalence exceeds 0.05, inter-resident contact should be suspended until the community prevalence has reduced.

Limitations

The results from this study should be interpreted in the light of several limitations. First, our ABM was derived from a sensor mote deployment in a single nursing home. This facility’s high-fidelity HCW location/interaction data may not apply to other facilities. Second, due to IRB considerations, we did not obtain patient locations, instead inferring their locations from HCW movements. Third, we focused on a respiratory disease characteristically similar to COVID-19, and our results may not generalize to other dissimilar diseases.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/ice.2024.43.

Acknowledgments

This project was funded by the Centers for Disease Control and Prevention (CDC) MInD-Healthcare (cooperative agreement no. 5 U01 CK000594-03).

Competing interests

All authors report no conflicts of interest relevant to this article.

References

World Health Organization. Infection Prevention and Control Guidance for Long-term Care Facilities in the Context of COVID-19: Interim Guidance, 8 January 2021. World Health Organization; 2021.Google Scholar
Centers for Disease Control and Prevention. COVID-19 Nursing Home Data. Centers for Disease Control and Prevention. https://data.cms.gov/covid-19/covid-19-nursing-home-data. Accessed February 19, 2024.Google Scholar
Cronin, CJ, Evans, WN. Nursing home quality, COVID-19 deaths, and excess mortality. J Health Econ 2022;82:102592102592.10.1016/j.jhealeco.2022.102592CrossRefGoogle ScholarPubMed
Usher, K, Durkin, J, Gyamfi, N, Warsini, S, Jackson, D. Preparedness for viral respiratory infection pandemic in residential aged care facilities: A review of the literature to inform post-COVID-19 response. J Clin Nurs 2024. https://doi-org.proxy.lib.uiowa.edu/10.1111/jocn.15863 Google Scholar
Stratil, JM, Biallas, RL, Burns, J, et al. Non-pharmacological measures implemented in the setting of long-term care facilities to prevent SARS-CoV-2 infections and their consequences: a rapid review. Cochrane Datab Syst Rev 2021;9:CD015085.Google ScholarPubMed
Dykgraaf, SH, Matenge, S, Desborough, J, et al. Protecting nursing homes and long-term care facilities from COVID-19: A rapid review of international evidence. J Am Med Dir Assoc 2021;22:19691988.10.1016/j.jamda.2021.07.027CrossRefGoogle ScholarPubMed
Nunes de Moraes, E, de Gouvêa Viana, L, Resende, LMH, et al. COVID-19 in long-term care facilities for the elderly: Laboratory screening and disease dissemination prevention strategies. Ciencia Saude Coletiva 2020;25:34453458.Google Scholar
Telford, CT, Onwubiko, U, Holland, DP, et al. Preventing COVID-19 outbreaks in long-term care facilities through preemptive testing of residents and staff members—Fulton County, Georgia, March–May 2020. Morb Mortal Week Rep 2020;69:12961296.10.15585/mmwr.mm6937a4CrossRefGoogle ScholarPubMed
Eckardt, P, Guran, R, Hennemyre, J, et al. Hospital affiliated long term care facility COVID-19 containment strategy by using prevalence testing and infection control best practices. Am J Infect Control 2020;48:15521555.10.1016/j.ajic.2020.06.215CrossRefGoogle ScholarPubMed
Holmdahl, I, Kahn, R, Hay, JA, Buckee, CO, Mina, MJ. Estimation of transmission of COVID-19 in simulated nursing homes with frequent testing and immunity-based staffing. JAMA Netw Open 2021;4:e2110071e2110071.10.1001/jamanetworkopen.2021.10071CrossRefGoogle ScholarPubMed
Vilches, TN, Nourbakhsh, S, Zhang, K, et al. Multifaceted strategies for the control of COVID-19 outbreaks in long-term care facilities in Ontario, Canada. Prevent Med 2021;148:106564106564.10.1016/j.ypmed.2021.106564CrossRefGoogle ScholarPubMed
Smith, DRM, Duval, A, Pouwels, KB, et al. Optimizing COVID-19 surveillance in long-term care facilities: a modelling study. BMC Med 2020;18:386386.10.1186/s12916-020-01866-6CrossRefGoogle ScholarPubMed
Lanièce Delaunay, C, Saeed, S, Nguyen, QD. Evaluation of Testing Frequency and Sampling for Severe Acute Respiratory Syndrome Coronavirus 2 Surveillance Strategies in Long-Term Care Facilities. J Am Med Dir Assoc 2020;21:15741576.10.1016/j.jamda.2020.08.022CrossRefGoogle ScholarPubMed
Tsoungui Obama, HCJ, Adil Mahmoud Yousif, N, Alawam Nemer, L, et al. Preventing COVID-19 spread in closed facilities by regular testing of employees—An efficient intervention in long-term care facilities and prisons? PLOS ONE 2021;16:129.10.1371/journal.pone.0249588CrossRefGoogle ScholarPubMed
Hethcote, HW. The Mathematics of Infectious Diseases. SIAM Rev 2000;42:599653.10.1137/S0036144500371907CrossRefGoogle Scholar
Kucirka, LM, Lauer, SA, Laeyendecker, O, Boon, D, Lessler, J. Variation in false-negative rate of reverse transcriptase polymerase chain reaction–based SARS-CoV-2 tests by time since exposure. Ann Intern Med 2020;173:262267.10.7326/M20-1495CrossRefGoogle ScholarPubMed
He, X, Lau, EHY, Wu, P, et al. Author correction: Temporal dynamics in viral shedding and transmissibility of COVID-19. Nat Med 2020;26:14911493.10.1038/s41591-020-1016-zCrossRefGoogle ScholarPubMed
He, W, Yi, GY, Zhu, Y. Estimation of the basic reproduction number, average incubation time, asymptomatic infection rate, and case fatality rate for COVID-19: Meta-analysis and sensitivity analysis. J Med Virol 2020;92:25432550.10.1002/jmv.26041CrossRefGoogle ScholarPubMed
Du, Z, Liu, C, Wang, C, et al. Reproduction numbers of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) variants: a systematic review and meta-analysis. Clin Infect Dis 2022;75:e293e295.10.1093/cid/ciac137CrossRefGoogle ScholarPubMed
Chu, DK, Akl, EA, Duda, S, et al. Physical distancing, face masks, and eye protection to prevent person-to-person transmission of SARS-CoV-2 and COVID-19: a systematic review and meta-analysis. Lancet 2020;395:19731987.10.1016/S0140-6736(20)31142-9CrossRefGoogle ScholarPubMed
Zhang, J, Litvinova, M, Wang, W, et al. Evolving epidemiology and transmission dynamics of coronavirus disease 2019 outside Hubei province, China: a descriptive and modelling study. Lancet Infect Dis 2020;20:793802.10.1016/S1473-3099(20)30230-9CrossRefGoogle Scholar
Lichtman, A, Greenblatt, E, Malenfant, J, Kuo, A. Universal symptom monitoring to address presenteeism in healthcare workers. Am J Infect Control 2021;49:10211023.10.1016/j.ajic.2021.02.009CrossRefGoogle ScholarPubMed
Rodrigues, NG, Han, CQY, Su, Y, Klainin-Yobas, P, Wu, XV. Psychological impacts and online interventions of social isolation amongst older adults during COVID-19 pandemic: A scoping review. J Adv Nurs 2022;78:609644.10.1111/jan.15063CrossRefGoogle ScholarPubMed
Hawkins, M. Quarantine bubbles - when done right - limit coronavirus risk and help fight loneliness. Delaware J Publ Health 2020;6:5051.10.32481/djph.2020.08.013CrossRefGoogle ScholarPubMed
Challener, DW, Breeher, LE, Frain, J, Swift, MD, Tosh, PK, O’Horo, J. Healthcare personnel absenteeism, presenteeism, and staffing challenges during epidemics. Infect Control Hosp Epidemiol 2021;42:388391. doi: 10.1017/ice.2020.453 CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Illustration of how contact networks were constructed from sensor mote data. (a) Empirical contact network based on HCW and inferred resident locations at each time point. (b) No contact between residents was imposed, keeping all residents in their own room (corresponding to lockdown network). (c) Contact between residents was constrained to be between those assigned to the same bubble; residents within same bubbles went to dining hall at same time, as did the HCWs who were in their rooms in empirical network. The bubble network was generated based on this. Note: HCW, healthcare worker.

Figure 1

Table 1. Agent-based model parameters

Figure 2

Figure 2. The attack rates for residents by different screening strategy. The X axis is the total hours of contact between residents; Y axis is the attack rates. (A) Residents contact each other homogeneously. (B) Residents contact each other within four bubbles. (C) Residents contact each other within eight bubbles.

Figure 3

Figure 3. The attack rates in nursing home residents by different resident-resident contact profiles. The X axis is the total hours of daily contact between residents; the Y axis is the attack rates among residents. (A–D) R_0 of 3.15. (E–H) R_0 of 5.94. (A, E) A community prevalence of 0.01. (B, F) A prevalence of 0.025. (C, G) A prevalence of 0.05. (D, H) A prevalence of 0.1.

Figure 4

Figure 4. The attack rates for residents by different willingness to self-isolate. The X axis is the probability of self-isolation after an individual develops COVID-19 symptoms; Y axis is the attack rates.

Figure 5

Figure 5. The attack rates for residents by different working shift length (ie, number of consecutive days working before the same number of consecutive days off duty). The X axis is the length of working shift; Y axis is the attack rates.

Supplementary material: File

Li et al. supplementary material

Li et al. supplementary material
Download Li et al. supplementary material(File)
File 302.1 KB