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      Public Masking: An Urgent Need to Revise Global Policies to Protect against COVID-19

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          Abstract

          Novel severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) is spreading fast around the world, with many uncertainties about routes of transmission, treatment, and prevention. Currently, the United States has the highest number of cases. No drugs or vaccines have yet proven to be effective, and non-vaccine preventative measures are the key in our fight against this transmissible virus with high mortality. The WHO recommends robust control measures to contain community spread of infection worldwide, but the virus is nonetheless spreading within communities, and we have had limited success in breaking the transmission chain. Although new evidence supports tremendous capacity of this virus to spread from asymptomatic individuals, messages about public masking remain conflicting. More clarification from international organizations is needed to optimally support efforts to prevent the spread of SARS-CoV-2. We now know that a significant portion of coronavirus-infected individuals are asymptomatic, or even minimally symptomatic with nonspecific symptoms, 1–3 and can spread the infection. 4,5 In a study from China, nasopharyngeal viral loads from asymptomatic individuals were as high as those from symptomatic patients, suggesting the potential for a major role in community transmission. 6 In an observational study in China, asymptomatic SARS-CoV-2–infected individuals were identified as sources of infection in 79% of confirmed cases. 7 During the Diamond Princess cruise ship investigation, 712 of 3,711 individuals tested positive, whereas 331 (46.5%) of positive cases were asymptomatic at the time of testing. In follow-up, 17.9% of infected cases never developed symptoms. 8 Based on this understanding of virus transmission, public health experts urged mass masking to prevent virus spread. 9 As of the time of this writing (mid-April 2020), the WHO recommends against public masking for asymptomatic individuals, 10 but the science around this topic has been rapidly advancing. Some countries (Austria, Czech Republic, China, Hong Kong, Israel, Italy, Japan, Mongolia, Singapore, South Korea, Taiwan, Turkey, and the United States) have taken varied steps to advocate universal masking as an additional step to reduce community transmission of SARS-CoV-2. The WHO has not endorsed this as a global policy yet, possibly because of lack of supply, limited evidence for effectiveness, potential noncompliance, and/or concerns regarding increased anxiety and stigmatization engendered by masking. Moreover, there is concern that public masking will limit the supply of essential masks for healthcare workers and others at the highest risk of infection. However, a resistance to mass masking seems inconsistent with our knowledge of the rate of asymptomatic infections and the risk of transmission from these individuals. The U.S. CDC has recommended a policy of cloth face covering in public where social distancing is hard to maintain, but this policy has been practiced in many different ways. 11 Following this recommendation, mandatory universal masking for all hospital visitors, patients, and healthcare workers has been proposed 12 and implemented as a robust preventive strategy in many American healthcare facilities including Massachusetts General Hospital, the Johns Hopkins University and Health System, the University of Maryland Medical System, the University of Chicago Medical Center, the University of Illinois Hospital, the University of Rochester Medical Center, the University of California San Francisco, the University of Virginia Heath System, Rochester Regional Health, and St. Luke’s University Health Network. This list is growing fast. Outside of healthcare settings, for many people, the motivation for wearing a mask is primarily for their own protection, which unintentionally leads to protecting their community. We consider both protection of the wearer and of the community to be important, but we believe that source control is most important. In a systematic review before the SARS-CoV-2 pandemic, wearing face masks reduced the odds of contracting acute respiratory infections by 6% among casual community contacts and by 19% among household contacts if both the infected and healthy individuals wore masks. 13 Masks have been shown to be effective in reducing respiratory virus shedding from droplets and aerosols of symptomatic individuals infected with coronavirus, influenza virus, and rhinovirus. 14 There is also laboratory evidence that homemade masks effectively stop droplets from infecting the wearer. 15 Surgical masks are disposable and designed to protect healthcare workers, although surgeons used cloth masks to protect wounds from droplets many years ago. The barrier layer in cloth masks is usually two layers of cotton-woven fabric, compared with two to four layers of nonwoven polypropylene fabric with filtration holes in surgical masks. Effectiveness of cloth masks compared with surgical masks needs further evaluation because some clinical studies have raised concerns regarding their effectiveness. 16 However, the wearing of cloth masks by asymptomatic individuals is justified by evidence that droplets and aerosols get trapped when they hit the weave of the fabric, with potentially better trapping than surgical masks. In any case, cloth masks have been adopted as an alternative when surgical masks are limited in supply. 17 Moreover, cloth masks are cheap, washable, easy to make, and can be used by the general population without imposing extra cost to local governments while they are already overwhelmed by lack of resources. While the SARS-CoV-2 pandemic rages, most nations are not receiving clear and concise instructions about public masking from public health authorities. We call on WHO and country-level public health leaders to urgently consider revising their policies on mass masking to facilitate implementation of appropriate interventions in communities around the world. Considering the close community contact in densely populated areas around the world and documented evidence of SARS-CoV-2 transmission from asymptomatic individuals, it is appropriate to consider masking as a robust tool to limit SARS-CoV-2 transmission. This is highly recommended in public places including public transportation, grocery stores, bakeries, pharmacies, hospitals, rehabilitation units, nursing homes, offices, places of religious worship, workplaces, or even crowded streets. In summary, laboratory data support both surgical and cloth masks, but real-world efficacy of cloth masks needs further evaluation. Cloth masks are affordable globally and might be the only option in some areas with limited resources. Based on our current level of evidence, we highly recommend mass masking around the world during the pandemic. Whereas surgical masks are the preferred recommendation for the general public, cloth masks should be considered as a substitute if supplies are limited or surgical masks are not available.

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          Most cited references13

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          SARS-CoV-2 Viral Load in Upper Respiratory Specimens of Infected Patients

          To the Editor: The 2019 novel coronavirus (SARS-CoV-2) epidemic, which was first reported in December 2019 in Wuhan, China, and has been declared a public health emergency of international concern by the World Health Organization, may progress to a pandemic associated with substantial morbidity and mortality. SARS-CoV-2 is genetically related to SARS-CoV, which caused a global epidemic with 8096 confirmed cases in more than 25 countries in 2002–2003. 1 The epidemic of SARS-CoV was successfully contained through public health interventions, including case detection and isolation. Transmission of SARS-CoV occurred mainly after days of illness 2 and was associated with modest viral loads in the respiratory tract early in the illness, with viral loads peaking approximately 10 days after symptom onset. 3 We monitored SARS-CoV-2 viral loads in upper respiratory specimens obtained from 18 patients (9 men and 9 women; median age, 59 years; range, 26 to 76) in Zhuhai, Guangdong, China, including 4 patients with secondary infections (1 of whom never had symptoms) within two family clusters (Table S1 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). The patient who never had symptoms was a close contact of a patient with a known case and was therefore monitored. A total of 72 nasal swabs (sampled from the mid-turbinate and nasopharynx) (Figure 1A) and 72 throat swabs (Figure 1B) were analyzed, with 1 to 9 sequential samples obtained from each patient. Polyester flock swabs were used for all the patients. From January 7 through January 26, 2020, a total of 14 patients who had recently returned from Wuhan and had fever (≥37.3°C) received a diagnosis of Covid-19 (the illness caused by SARS-CoV-2) by means of reverse-transcriptase–polymerase-chain-reaction assay with primers and probes targeting the N and Orf1b genes of SARS-CoV-2; the assay was developed by the Chinese Center for Disease Control and Prevention. Samples were tested at the Guangdong Provincial Center for Disease Control and Prevention. Thirteen of 14 patients with imported cases had evidence of pneumonia on computed tomography (CT). None of them had visited the Huanan Seafood Wholesale Market in Wuhan within 14 days before symptom onset. Patients E, I, and P required admission to intensive care units, whereas the others had mild-to-moderate illness. Secondary infections were detected in close contacts of Patients E, I, and P. Patient E worked in Wuhan and visited his wife (Patient L), mother (Patient D), and a friend (Patient Z) in Zhuhai on January 17. Symptoms developed in Patients L and D on January 20 and January 22, respectively, with viral RNA detected in their nasal and throat swabs soon after symptom onset. Patient Z reported no clinical symptoms, but his nasal swabs (cycle threshold [Ct] values, 22 to 28) and throat swabs (Ct values, 30 to 32) tested positive on days 7, 10, and 11 after contact. A CT scan of Patient Z that was obtained on February 6 was unremarkable. Patients I and P lived in Wuhan and visited their daughter (Patient H) in Zhuhai on January 11 when their symptoms first developed. Fever developed in Patient H on January 17, with viral RNA detected in nasal and throat swabs on day 1 after symptom onset. We analyzed the viral load in nasal and throat swabs obtained from the 17 symptomatic patients in relation to day of onset of any symptoms (Figure 1C). Higher viral loads (inversely related to Ct value) were detected soon after symptom onset, with higher viral loads detected in the nose than in the throat. Our analysis suggests that the viral nucleic acid shedding pattern of patients infected with SARS-CoV-2 resembles that of patients with influenza 4 and appears different from that seen in patients infected with SARS-CoV. 3 The viral load that was detected in the asymptomatic patient was similar to that in the symptomatic patients, which suggests the transmission potential of asymptomatic or minimally symptomatic patients. These findings are in concordance with reports that transmission may occur early in the course of infection 5 and suggest that case detection and isolation may require strategies different from those required for the control of SARS-CoV. How SARS-CoV-2 viral load correlates with culturable virus needs to be determined. Identification of patients with few or no symptoms and with modest levels of detectable viral RNA in the oropharynx for at least 5 days suggests that we need better data to determine transmission dynamics and inform our screening practices.
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            Presumed Asymptomatic Carrier Transmission of COVID-19

            This study describes possible transmission of novel coronavirus disease 2019 (COVID-19) from an asymptomatic Wuhan resident to 5 family members in Anyang, a Chinese city in the neighboring province of Hubei.
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              Transmission of 2019-nCoV Infection from an Asymptomatic Contact in Germany

              To the Editor: The novel coronavirus (2019-nCoV) from Wuhan is currently causing concern in the medical community as the virus is spreading around the world. 1 Since identification of the virus in late December 2019, the number of cases from China that have been imported into other countries is on the rise, and the epidemiologic picture is changing on a daily basis. We are reporting a case of 2019-nCoV infection acquired outside Asia in which transmission appears to have occurred during the incubation period in the index patient. A 33-year-old otherwise healthy German businessman (Patient 1) became ill with a sore throat, chills, and myalgias on January 24, 2020. The following day, a fever of 39.1°C (102.4°F) developed, along with a productive cough. By the evening of the next day, he started feeling better and went back to work on January 27. Before the onset of symptoms, he had attended meetings with a Chinese business partner at his company near Munich on January 20 and 21. The business partner, a Shanghai resident, had visited Germany between January 19 and 22. During her stay, she had been well with no signs or symptoms of infection but had become ill on her flight back to China, where she tested positive for 2019-nCoV on January 26 (index patient in Figure 1) (see Supplementary Appendix, available at NEJM.org, for details on the timeline of symptom development leading to hospitalization). On January 27, she informed the company about her illness. Contact tracing was started, and the above-mentioned colleague was sent to the Division of Infectious Diseases and Tropical Medicine in Munich for further assessment. At presentation, he was afebrile and well. He reported no previous or chronic illnesses and had no history of foreign travel within 14 days before the onset of symptoms. Two nasopharyngeal swabs and one sputum sample were obtained and were found to be positive for 2019-nCoV on quantitative reverse-transcriptase–polymerase-chain-reaction (qRT-PCR) assay. 2 Follow-up qRT-PCR assay revealed a high viral load of 108 copies per milliliter in his sputum during the following days, with the last available result on January 29. On January 28, three additional employees at the company tested positive for 2019-nCoV (Patients 2 through 4 in Figure 1). Of these patients, only Patient 2 had contact with the index patient; the other two patients had contact only with Patient 1. In accordance with the health authorities, all the patients with confirmed 2019-nCoV infection were admitted to a Munich infectious diseases unit for clinical monitoring and isolation. So far, none of the four confirmed patients show signs of severe clinical illness. This case of 2019-nCoV infection was diagnosed in Germany and transmitted outside Asia. However, it is notable that the infection appears to have been transmitted during the incubation period of the index patient, in whom the illness was brief and nonspecific. 3 The fact that asymptomatic persons are potential sources of 2019-nCoV infection may warrant a reassessment of transmission dynamics of the current outbreak. In this context, the detection of 2019-nCoV and a high sputum viral load in a convalescent patient (Patient 1) arouse concern about prolonged shedding of 2019-nCoV after recovery. Yet, the viability of 2019-nCoV detected on qRT-PCR in this patient remains to be proved by means of viral culture. Despite these concerns, all four patients who were seen in Munich have had mild cases and were hospitalized primarily for public health purposes. Since hospital capacities are limited — in particular, given the concurrent peak of the influenza season in the northern hemisphere — research is needed to determine whether such patients can be treated with appropriate guidance and oversight outside the hospital.
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                Author and article information

                Journal
                Am J Trop Med Hyg
                Am. J. Trop. Med. Hyg
                tpmd
                tropmed
                The American Journal of Tropical Medicine and Hygiene
                The American Society of Tropical Medicine and Hygiene
                0002-9637
                1476-1645
                June 2020
                22 April 2020
                22 April 2020
                : 102
                : 6
                : 1160-1161
                Affiliations
                [1 ]Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland;
                [2 ]Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
                Author notes
                [* ]Address correspondence to Maryam Keshtkar-Jahromi, Johns Hopkins Bayview Medical Center, Mason F. Lord Bldg., Center Tower, 3rd Floor, 5200 Eastern Ave., Baltimore, MD 21224. E-mail: maryam.keshtkar@ 123456jhmi.edu

                Authors’ addresses: Maryam Keshtkar-Jahromi and Mark Sulkowski, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, E-mails: maryam.keshtkar@ 123456jhmi.edu and msulkows@ 123456jhmi.edu . Kourosh Holakouie-Naieni, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran, E-mail: holakouie@ 123456yahoo.com .

                Article
                tpmd200305
                10.4269/ajtmh.20-0305
                7253086
                32323645
                28c576b2-f1eb-4516-9669-82943985a5ec
                © The American Society of Tropical Medicine and Hygiene

                This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 10 April 2020
                : 16 April 2020
                Page count
                Pages: 2
                Categories
                Editorial

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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