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      Impact of Population Mask Wearing on Covid-19 Post Lockdown

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      Infectious Microbes & Diseases

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          Abstract

          COVID-19, caused by SARS-CoV-2 is a rapidly spreading global pandemic. Although precise transmission routes and dynamics are unknown, SARS-CoV-2 is thought primarily to spread via contagious respiratory droplets. 1 Unlike with SARS-CoV, maximal viral shedding occurs in the early phase of illness, 1,2 and this is supported by models that suggest 40–80% of transmission events occur from pre- and asymptomatic individuals. 3,4 One widely-discussed strategy to limit transmission of SARS-CoV-2, particularly from presymptomatic individuals, has been population-level wearing of masks. Modelling for pandemic influenza suggests some benefit in reducing total numbers infected with even 50% mask-use. 5 COVID-19 has a higher hospitalization and mortality rate than influenza, 6 and the impacts on these parameters, and critically, at what point in the pandemic trajectory mask-use might exert maximal benefit are completely unknown. We derived a simplified SIR model based on the population of Israel as proof of principle (population 8 million) to investigate the effects of near-universal mask-use on COVID-19 assuming 8 or 16% mask efficacy (see Methods for relevant parameters). We decided to model, in particular, the impact of masks on numbers of critically-ill patients and cumulative mortality, since these are parameters that are likely to have the most severe consequences in the COVID-19 pandemic. Whereas mask use had a relatively minor benefit on critical-care and mortality rates when transmissibility (Reff) was high (Fig. 1A), the reduction on deaths was dramatic as the effective R approached 1 (Fig. 1B), as might be expected after aggressive social-distancing measures such as wide-spread lockdowns. 6 One major concern with COVID-19 is its potential to overwhelm healthcare infrastructures, even in resource-rich settings, with one third of hospitalized patients requiring critical-care. We incorporated this into our model, increasing death rates for when critical-care resources have been exhausted, however, we also modelled the same parameters for scenarios in which critical care capacity was unrestricted (Fig. 1C-D). Our simple model shows that modest efficacy of masks could avert substantial mortality when critical care capacity is limiting, but also derives benefit when it is unrestricted. Importantly, the effects on mortality became hyper-sensitive to mask-wearing as the effective R approaches 1, i.e. near the tipping point of when the infection trajectory is expected to revert to exponential growth, as would be expected after effective lockdown. Figure 1 Mask effectiveness on mortality varies by R eff (A) Number of critically ill patients (red) and total deaths (black) for an epidemic spreading with R of 2.2 (see Methods for parameters) in a simple SIR model, x-axis represents time in days. The different curves are computed for a reduction of infectivity of 0, 8 and 16% by mask-wearing. (B) Same as A, but for an epidemic spreading with R of 1.3. Note that the reduction in infectivity by mask wearing has a larger effect. (C-D) Same as A-B but taking into account decrease in death when beds are unrestricted for critically-ill patients (see Methods). (E-F) Analysis of the data of Ferguson et al (ref 5, Table 4). Assuming a 10% reduction in infectivity, mask wearing may be at least as effective as home confinement at reducing deaths (E) or preventing overwhelming icu beds (F). The different bars (1–5) are different thresholds (“triggers”) for implementing social measures in the Ferguson et al model. In order to understand the generality of the effect of mask wearing upon home confinement removal, we also analysed the potential effects of mask-wearing for data provided by a more comprehensive and realistic model of the COVID-19 infection, which included modelling of different levels of social-distancing measures on infection and likely deaths. 6 When home-confinement is lifted but other social-distancing measures are in place, such as school closure and case isolation, wearing masks can maintain the benefits of home-confinement, both in terms of deaths (Fig. 1E) and critical-care bed use (Fig. 1F). Limitations of our study include the relatively straightforward model we employed, as well as assumptions of high compliance with mask-wearing and their potential efficacy, for which definitive evidence in pandemics is lacking. 7,8 Another recent modelling study of mask use came to similar conclusions as ours despite slightly different input parameters. 9 However, that model mostly considered scenarios where the effective transmissibility of SARS-CoV-2 remained high. Despite the limitations of our study, our model suggests that mask-wearing might exert maximal benefit as nations plan their ‘post-lockdown’ strategies and suggests that mask-wearing should be included in further more sophisticated models of the current pandemic. Since otherwise similar countries are currently devising different mask-wearing scenarios, the current situation offers an unprecedented opportunity to gather evidence on the real-world utility of population mask-wearing for implementation in this and future pandemics. Methods Infection dynamics model (Figure 1a-c) To demonstrate the effect of masks, we used a simple SIR model of the dynamics of infection taking several populations into account: S: susceptible individuals, I: infected, R: resistant, CI: critically ill, D: dead. The goal of the model is not to predict any particular infection in a completely realistic way, but rather to illustrate the impact of reducing infectivity at high versus low Reff values.          Where the Heaviside function is used for changing the death rate when the critically ill number saturates ICU beds. Parameters are defined in the following Table. The model was run using Matlab R2017a (MathsWorks,USA) ODE solver (‘ode23s’). Wearing of masks was implemented in the model as a reduction of infectivity between 8–16%. 5,8,10–15 Total population size was taken as 8x106 In the absence of ICU beds, 86% of the critical care patients die, whereas if ICU beds are not limiting, only 40% of critical care patients would die. The total fraction of critical care patients is 1.8% of the total number of infected cases 6 . Data for (Figure 1E and 1F) was adapted from Ferguson et al 6 (16/3/2020- Table 4) The wearing of masks is assumed to reduce transmissibility by 10%. We, therefore, compared the results of Fergusson et al (Table 4) at different R and for different social-distancing policy measures.

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          Virological assessment of hospitalized patients with COVID-2019

          Coronavirus disease 2019 (COVID-19) is an acute infection of the respiratory tract that emerged in late 20191,2. Initial outbreaks in China involved 13.8% of cases with severe courses, and 6.1% of cases with critical courses3. This severe presentation may result from the virus using a virus receptor that is expressed predominantly in the lung2,4; the same receptor tropism is thought to have determined the pathogenicity-but also aided in the control-of severe acute respiratory syndrome (SARS) in 20035. However, there are reports of cases of COVID-19 in which the patient shows mild upper respiratory tract symptoms, which suggests the potential for pre- or oligosymptomatic transmission6-8. There is an urgent need for information on virus replication, immunity and infectivity in specific sites of the body. Here we report a detailed virological analysis of nine cases of COVID-19 that provides proof of active virus replication in tissues of the upper respiratory tract. Pharyngeal virus shedding was very high during the first week of symptoms, with a peak at 7.11 × 108 RNA copies per throat swab on day 4. Infectious virus was readily isolated from samples derived from the throat or lung, but not from stool samples-in spite of high concentrations of virus RNA. Blood and urine samples never yielded virus. Active replication in the throat was confirmed by the presence of viral replicative RNA intermediates in the throat samples. We consistently detected sequence-distinct virus populations in throat and lung samples from one patient, proving independent replication. The shedding of viral RNA from sputum outlasted the end of symptoms. Seroconversion occurred after 7 days in 50% of patients (and by day 14 in all patients), but was not followed by a rapid decline in viral load. COVID-19 can present as a mild illness of the upper respiratory tract. The confirmation of active virus replication in the upper respiratory tract has implications for the containment of COVID-19.
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            Temporal dynamics in viral shedding and transmissibility of COVID-19

            We report temporal patterns of viral shedding in 94 patients with laboratory-confirmed COVID-19 and modeled COVID-19 infectiousness profiles from a separate sample of 77 infector-infectee transmission pairs. We observed the highest viral load in throat swabs at the time of symptom onset, and inferred that infectiousness peaked on or before symptom onset. We estimated that 44% (95% confidence interval, 25-69%) of secondary cases were infected during the index cases' presymptomatic stage, in settings with substantial household clustering, active case finding and quarantine outside the home. Disease control measures should be adjusted to account for probable substantial presymptomatic transmission.
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              Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV2)

              Estimation of the prevalence and contagiousness of undocumented novel coronavirus (SARS-CoV2) infections is critical for understanding the overall prevalence and pandemic potential of this disease. Here we use observations of reported infection within China, in conjunction with mobility data, a networked dynamic metapopulation model and Bayesian inference, to infer critical epidemiological characteristics associated with SARS-CoV2, including the fraction of undocumented infections and their contagiousness. We estimate 86% of all infections were undocumented (95% CI: [82%–90%]) prior to 23 January 2020 travel restrictions. Per person, the transmission rate of undocumented infections was 55% of documented infections ([46%–62%]), yet, due to their greater numbers, undocumented infections were the infection source for 79% of documented cases. These findings explain the rapid geographic spread of SARS-CoV2 and indicate containment of this virus will be particularly challenging.
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                Author and article information

                Journal
                IM9
                Infectious Microbes & Diseases
                2641-5917
                05 June 2020
                : 10.1097/IM9.0000000000000029
                Affiliations
                [a ]School of Medicine, Tsinghua University, Beijing, China
                [b ]Racah Institute of Physics, the Hebrew University of Jerusalem, Jerusalem, Israel.
                Author notes
                []Corresponding authors: Babak Javid, School of Medicine, Tsinghua University, Beijing, China. E-mail: bjavid@ 123456gmail.com ; Nathalie Q. Balaban, Racah Institute of Physics, the Hebrew University of Jerusalem, Jerusalem, Israel. E-mail: nathalie.balaban@ 123456mail.huji.ac.il .

                Author Contributions: BJ conceived the project, contributed to analysis and wrote the manuscript. NQB conceived the project, designed the model and performed the analysis and contributed to the writing of the manuscript.

                Funding: No specific funding was received for this project.

                Conflicts of interest: The authors declare no conflicts of interest.

                Article
                IMD-20-019
                10.1097/IM9.0000000000000029
                7299124
                6333b5fc-e169-4d24-abee-566fdd5d0b2e
                Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc.

                Thisis an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 10 May 2020
                : 01 June 2020
                : 01 June 2020
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