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SYSTEMATIC REVIEW article

Front. Med., 12 January 2021
Sec. Infectious Diseases: Pathogenesis and Therapy

Face Mask Use in the Community for Reducing the Spread of COVID-19: A Systematic Review

\nDaniela Coclite&#x;Daniela Coclite1Antonello Napoletano&#x;Antonello Napoletano1Silvia Gianola
Silvia Gianola2*Andrea del MonacoAndrea del Monaco3Daniela D&#x;AngeloDaniela D'Angelo1Alice FauciAlice Fauci1Laura IacorossiLaura Iacorossi1Roberto LatinaRoberto Latina1Giuseppe La TorreGiuseppe La Torre4Claudio M. MastroianniClaudio M. Mastroianni4Cristina RenziCristina Renzi5Greta Castellini&#x;Greta Castellini2Primiano Iannone&#x;Primiano Iannone1
  • 1Centro Eccellenza Clinica, Qualità e Sicurezza delle Cure, Istituto Superiore di Sanità, Rome, Italy
  • 2Unit of Clinical Epidemiology, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy
  • 3Directorate General for Economics, Statistics and Research, Bank of Italy, Rome, Italy
  • 4Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy
  • 5Institute of Epidemiology & Health Care, University College London-UCL, London, United Kingdom

Background: Evidence is needed on the effectiveness of wearing face masks in the community to prevent SARS-CoV-2 transmission.

Methods: Systematic review and meta-analysis to investigate the efficacy and effectiveness of face mask use in a community setting and to predict the effectiveness of wearing a mask. We searched MEDLINE, EMBASE, SCISEARCH, The Cochrane Library, and pre-prints from inception to 22 April 2020 without restriction by language. We rated the certainty of evidence according to Cochrane and GRADE approach.

Findings: Our search identified 35 studies, including three randomized controlled trials (RCTs) (4,017 patients), 10 comparative studies (18,984 patients), 13 predictive models, nine laboratory experimental studies. For reducing infection rates, the estimates of cluster-RCTs were in favor of wearing face masks vs. no mask, but not at statistically significant levels (adjusted OR 0.90, 95% CI 0.78–1.05). Similar findings were reported in observational studies. Mathematical models indicated an important decrease in mortality when the population mask coverage is near-universal, regardless of mask efficacy. In the best-case scenario, when the mask efficacy is at 95%, the R0 can fall to 0.99 from an initial value of 16.90. Levels of mask filtration efficiency were heterogeneous, depending on the materials used (surgical mask: 45–97%). One laboratory study suggested a viral load reduction of 0.25 (95% CI 0.09–0.67) in favor of mask vs. no mask.

Interpretation: The findings of this systematic review and meta-analysis support the use of face masks in a community setting. Robust randomized trials on face mask effectiveness are needed to inform evidence-based policies.

PROSPERO registration: CRD42020184963.

Introduction

Coronavirus disease 2019 (COVID-19) is a new, rapidly emerging infectious disease caused by a novel coronavirus, SARS-CoV-2 (Severe Acute Respiratory Syndrome CoronaVirus-2), which is primarily transmitted via droplets during close unprotected contact with an infector and fomites (1, 2). The virus is genetically similar to the coronaviruses that caused Severe Acute Respiratory Syndrome (SARS) and the Middle East respiratory syndrome (MERS), but SARS-CoV-2 appears to have greater transmissibility and lower pathogenicity than the aforementioned viruses (3). Preliminary estimates of the basic reproduction number (R0) of SARS-CoV-2, as a metric for transmissibility, range from 2.8 to 5.5, in the absence of intense quarantine and social distancing measures (4). COVID-19 has a higher hospitalization and mortality rate than influenza (57) and is spreading in an immune naive population (8). As of 30 November 2020, 61.8 million cases have been infected around the world counting over 1.4 million deaths (9). Moreover, there is increasing evidence that people with mild or no symptoms at the pre-symptomatic and early stages of infection can contribute to the spread of COVID-19 (10).

Since there is no effective treatment nor any vaccine for COVID-19, strategies for reducing the burden of the pandemic are focused on non-pharmaceutical interventions for reducing the spread of the infection, such as social-distancing measures, contact-tracing, quarantine, isolation, and the use of face masks in public (11). Public health policies promoting the use face masks in the community, i.e., in public places, can therefore have an important role in controlling the spread of the SARS-CoV-2 virus and for COVID-19 lockdown exit strategies (12). The published literature on the efficacy, effectiveness and acceptability of different types of face mask in preventing respiratory infections during epidemics is scarce and conflicting. However, face mask use is increasingly recommended and the potential of this intervention is not well-understood (13). National and international health organizations have adopted divergent policies on the subject. Recently, the CDC (Centers for Disease Control and Prevention) and the ECDC (European Center for Disease Prevention and Control) have advocated the use in public places of non-medical face mask (e.g., cloth mask) as a measure for the prevention and/or containment of SARS-CoV-2 infection (10, 14). In areas of significant community-based transmission, where it is difficult to maintain 6-feet social distancing (e.g., grocery stores and pharmacies), CDC recommends wearing cloth face coverings. CDC is additionally advising the use of simple cloth face coverings to slow the spread of the virus and help reduce the transmission of the virus from people who may be infectious without knowing it (14). The World Health Organization (WHO) conditionally recommends face mask use in the community for asymptomatic individuals in severe epidemics or pandemics in order to reduce transmission in the community (15) but it does not recognize its effectiveness in preventing infection (1).

Medical and non-medical face masks are used extensively by the general population in Asian countries, such as China, Singapore, South Korea, and Japan. Face mask wearing practice has been adopted since the 2003 SARS epidemic in addition to many other response measures and practices, including respiratory etiquette and hand hygiene (10). In Europe, as of 1 April 2020, Lithuania, Austria, Czechia, Slovakia, and Bulgaria recommend the use of face masks for persons going out in public (10).

Previous systematic reviews on the effectiveness of face mask use mainly focused on healthcare and household setting including only randomized controlled trials (RCTs) with most of them of low quality (1619). We therefore conducted a systematic review of the existing scientific literature, with randomized trials and observational studies, including modeling and experimental studies, on the effectiveness and efficacy of wearing face masks in the community for reducing the spread of COVID-19 in non-healthcare and non-household setting.

Aim

The aims of this systematic review (SR) were:

(i) to assess the efficacy and effectiveness of using masks in a community setting to reduce the spread of COVID-19 or other similar pandemic (20, 21); and in particular, to evaluate the effects of using vs. not using masks on mortality, infection rate and basic reproduction number (R0).

(ii) to investigate the effect of different filtering capacity of masks used in community settings on the diffusion of the SARS- CoV2.

Methods

The systematic review protocol was registered with the International Prospective Register of Systematic Reviews database (PROSPERO identifier: CRD42020184963). The study protocol and preliminary results are publicly available on https://osf.io/uvjgq. We conducted the systematic review following the preferred reporting items for systematic reviews and meta-analyses, the PRISMA statement (22), and the MOOSE guidelines for conducting meta-analysis of observational studies (23).

Search Strategy

We searched for studies on the electronic databases MEDLINE, EMBASE, SCISEARCH, and The Cochrane Library from inception to April 22, 2020 using index terms related to face mask use in reducing spread of pandemic infection viruses. Gray literature was interrogated in MedRxiv, Rxiv, and bioRxiv databases. We hand searched the reference lists of the included papers. We also incorporated the studies included in any identified relevant systematic reviews. The full search strategy is reported in Supplementary Appendix 1.

Eligibility Criteria

According to our PICOS questions (24), the following eligibility criteria without limit of study design were searched:

i) Population: general population exposed to SARS-COV-2 infection or other similar virus (20, 21);

ii) Intervention and comparators: any type of mask such as non-medical face mask (i.e., cloth, gauze, tissue), medical face mask (i.e., surgical) and N95 respirators vs. no mask;

iii) Outcomes: mortality, respiratory infection rate (number of events) and the R0 of viral respiratory infections; filtering capacity of masks and viral load reduction.

iv) Setting: we defined “community-based setting” people of a group or unit that collectively sharing interests in the society for real life situations (e.g., schools, work, open spaces). Studies assessing the intervention in particular closed cluster setting exposed to higher risk of infection such as healthcare workers or households were excluded.

Study Selection

Two reviewers independently screened the articles based on the titles, abstracts and full texts. The same two review authors independently retrieved and assessed full reports for potentially relevant studies for inclusion and exclusion according to the above criteria using a predefined electronic spreadsheet. In case of disagreement, consensus was achieved by involving a third independent review author. The reviewers' decisions and reasons for exclusion were recorded using appropriate reference management software such as EndNote. The study selection process was reported using the flow diagram of the Preferred-Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) (22).

Data Extraction

Two reviewers independently extracted the study characteristic (e.g., first author, publication year, country, type of virus detected, study design, sample size, settings); for prognostic models, they extracted key characteristics (e.g., factors/predictors, time span, accuracy, and performance) and outcomes to be predicted. Disagreements were solved by consensus. A detailed data extraction form was developed prior to the systematic review being performed. In addition, for prediction modeling studies, the Checklist for critical Appraisal and data extraction for systematic Reviews of prediction Modeling Studies (CHARMS) was utilized (25).

Primary and Secondary Outcomes

The primary outcomes of this systematic review are the following:

- Mortality rate;

- Respiratory infection rate (measured as event frequency), defined as fever ≥37.8°C with at least 1 respiratory symptom (sore throat, cough, sneezing, runny nose, nasal congestion, headache), with or without laboratory confirmation.

- R0 of viral respiratory infections;

The secondary outcomes were filtering capacity of masks and viral load reduction.

Data Analysis

We examined the efficacy and effectiveness of wearing a mask and the models studies available in the literature by study design, setting, and study outcome. The data are summarized in both tabular and narrative formats. As the outcomes were dichotomous, such as respiratory infection, they were analyzed as pooled Risk Ratios (RRs), for unadjusted estimates. Adjusted odds ratios from multivariable regression reported in the studies were pooled as adjusted Odds Ratios (aORs). These are summarized using random effects meta-analysis using the DerSimonian and Laird random effects model (26), with heterogeneity calculated from the Mantel-Haenszel model. Due to the comprehensive definition of community-based setting, when possible, studies were sub-grouped based on study design and identified by appropriate setting to investigate potentially different effects on primary outcomes. If enough studies were present, we performed a sensitivity analysis of the primary outcomes selecting routine conditions for community-based setting excluding conditions at greater risk of gathering. All summary measures were reported with an accompanying 95% confidence interval. Data analyses were performed using RevMan Software.

Assessment of Study Quality

Two independent reviewers appraised the risk of bias. In case of disagreement, a third reviewer was consulted. We used the Cochrane risk of bias tool for randomized controlled trials (27); the Newcastle Ottawa scale for non-randomized studies (28). We planned to use the PROBAST (Prediction model Risk Of Bias Assessment Tool) for Prediction Model Studies (29). However, since we found only quantitative-deterministic models, (statistical) bias was not a suitable measure of model goodness and we analyzed the QUAntitative-Deterministic models Risk of Infeasibility Assessment Checklist (QUADRIAC) according to the appropriate guideline (30). We provided more details in Supplementary Appendix 2.

GRADE—Quality of the Evidence

The Grades of Recommendation, Assessment, Development and Evaluation (GRADE) framework for judging the quality of evidence has been extended to prognosis factor research. Evidence on prognostic models were evaluated by six factors that may decrease quality: (1) phase of investigation; (2) study limitations; (3) inconsistency; (4) indirectness; (5) imprecision; and (6) publication bias; and by two factors that may increase quality: (1) moderate or large effect size; and (2) exposure response gradient (31). Two independent reviewers graded the certainty of the evidence using the GRADE approach. Evidence was presented using GRADE Evidence Profiles developed in the GRADEpro (www.gradepro.org) software.

Results

Study Selection

A total of 684 records resulted from the searches in the electronic databases (MEDLINE, EMBASE, SCISEARCH) and from pre-prints; eleven additional records were identified through citations. After removing duplicates and excluding irrelevant records according to title, abstract and full text reading, 35 studies met our inclusion criteria for the final inclusion. Figure 1 shows the flow diagram of the study selection process.

FIGURE 1
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Figure 1. Flow diagram of study selection process.

Description of the Included Studies

Table 1 reports characteristics of the included studies. Of the 35 included studies, three were cluster-RCTs (32, 33, 35), two cohort studies (38, 41), four were case-control (47, 51, 62, 64), four cross-sectional (34, 46, 49, 60), 13 were quantitative-deterministic predictive models (11, 13, 36, 39, 40, 42, 43, 45, 55, 5759, 63), and nine were laboratory experimental studies (37, 44, 48, 50, 5254, 56, 61).

TABLE 1
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Table 1. General characteristics of the included studies.

Of the 13 epidemiological studies (RCTs and observational studies) included in the review, four were carried out in a university (32, 33) or school setting (49, 60), one on an airplane (64), six during mass gatherings (34, 35, 38, 41, 46, 47), and two in non-specific community settings (51, 62).

As far as the quantitative-deterministic models are concerned, ten studies developed a SIR-based model (11, 13, 36, 39, 40, 42, 5759, 63), two studies developed an agent-based model (43, 55), and one study employed both (45). The whole population was considered in all the studies but one, which was restricted to nursery and primary school children (40). Three out of the 13 modeling studies (40, 43, 45) considered a closed environment; three models (45, 57, 63) contemplated both inward and outward filtering capacity whereas the others did not make such a distinction; furthermore, only two among the reviewed studies have accounted for a proper usage of facial masks (13, 57). It is worth mentioning that five out of the 13 studies that have analyzed a quantitative-deterministic model have also accounted for the intervention timing (11, 13, 42, 45, 59). Four studies across all the reviewed studies were pre-prints (11, 24, 43, 57).

The laboratory experimental studies were highly heterogeneous in terms of setting/participants: four bench test (48, 53, 56, 61), two in vivo studies (52, 54), and three controlled studies (37, 44, 50).

Supplementary Appendix 2 lists included and excluded studies.

Risk of Bias of Epidemiologic Studies and Unfeasibility of Deterministic Models

Focusing on randomized trials, we found high risk of performance and detection bias. However, blinding of participants was not possible due to the nature of the interventions. The included trials were characterized by an overall high quality. Among observational studies the quality ranged from poor to fair for cohort and case-controls studies, whereas it ranged from fair to good for cross-sectional studies. Focusing on mathematical models, we evaluated the unfeasibility of quantitative-deterministic models reporting eight of 13 studies with medium overall risk of infeasibility (two high and three low). Supplementary Appendix 3 lists the risk of bias of epidemiologic studies and unfeasibility of deterministic models.

Outcomes

Although no epidemiologic study on wearing face masks in the community for reducing the spread of COVID-19 has been published, a number of studies gave an indirect estimate of the protective efficacy of masks for other viral respiratory infections from agents similar to SARS-CoV2.

Mortality Rate

Deterministic Models

Four out of 13 quantitative-deterministic models reported data on mortality (13, 36, 45, 59). Among them, only one study (59) has explicitly provided quantitative data in three scenarios based on different initial values of R0; however, the time horizon was not specified. Three studies (13, 36, 45) presented graphs depicting the evolution over time of cumulative deaths. Overall the studies point toward a reduction in mortality when the population mask coverage is near-universal, regardless of mask efficacy.

Table 2 describes the mortality in relation to the initial R0, type of mask, mask filtration efficacy (%) and adherence of population coverage (%). Summary of findings (SOF) are displayed in Table 3.

TABLE 2
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Table 2. Mortality rate in the quantitative-deterministic models.

TABLE 3
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Table 3. Summary of findings.

Respiratory Infection Rate

RCT

The overall findings were similar between adjusted and unadjusted estimates. With very low quality of the evidence (Table 3), in the unadjusted data, three cluster-RCTs (32, 33, 35) have reported a small non-significant reduction in the risk of respiratory infections (Figure 2A, RR 0.97, 95% CI 0.72–1.31, I2 = 62%). The adjusted estimates of two, out of three, cluster-RCTs (32, 33) confirmed the reduction with high consistency, even if not at statistically significant levels (Figure 2B, aOR 0.90, 95% CI 0.78–1.05, I2 = 0%).

FIGURE 2
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Figure 2. (A) Unadjusted forest plot of respiratory infection rate and risk ratios in RCTs. (B) aORs forest plot of respiratory infection rate in RCTs.

Observational Studies

In total, 10 observational studies were identified (34, 38, 41, 46, 47, 49, 51, 60, 62, 64), among which one study reported adjusted data in relation to the outcome of interest (51). Thus, the meta-analysis was reported only for unadjusted estimates. The level of certainty of the evidence in all observational studies was very low (Table 3), with no statistically significant effect; the overall effect was very imprecise across all cross sectional studies (four studies, OR 0.90, 95% CI 0.74–1.10, I2 = 74%) (Figure 3, Comparison 1.3.1) (34, 46, 49, 60), case-control (four studies, OR 0.59, 95% CI 0.34–1.03, I2 = 78%) (Figure 3, Comparison 1.3.2) (47, 51, 62, 64) and prospective cohort studies (two studies, OR 0.55, 95% CI 0.11–2.75, I2 = 97%) (Figure 3, Comparison 1.3.3) (38, 41).

FIGURE 3
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Figure 3. Forest plot of respiratory infection rate in observational studies.

Since we found high heterogeneity, we performed sensitivity analysis excluding aircraft and mass gathering studies to determine the robustness of our original analyses and determine whether special settings might have influenced the overall pooled effect. Focusing on studies set in schools, universities and in the general community, the evidence from cross-sectional studies was not statistically significant (OR 0.74, 95% CI 0.43–1.26, I2 = 76%) (Supplementary Appendix 4, Supplementary Figure 2); whereas case-control studies (OR 0.46, 95% CI 0.34–0.62, I2 = 47%) (Supplementary Appendix 4, Supplementary Figure 2) showed a statistically significant effect in favor of wearing face masks vs. not wearing masks, with a more precise overall estimate.

Deterministic Models

Ten out of 13 studies that deployed mathematical models examined respiratory infection rates (11, 13, 36, 39, 40, 42, 43, 55, 5759, 63). Across them, three studies (39, 43, 55) reported such an outcome as a pure rate; two papers (42, 58) reported results about the respiratory infections rate as the percentage of cumulative cases; one study (59) reported the number of cumulative cases. The remaining studies did not report intelligible results on respiratory infection rate. Across the above-mentioned studies, the ones that reported the use of N95 masks agree that when at least 50% of the population is wearing a mask the respiratory infection rate can be reduced by a percentage ranging from 80% up to 99%.

The use of facial mask results in a reduction of the respiratory infection rate that is at least of 2.0% in the worst case scenario (58) and up to 99% in the best case scenarios (39, 58, 59). No time-horizon is specified, though Supplementary Appendix 5, Supplementary Table 9. The summary of Findings is displayed in Table 3.

Basic Reproduction Number (R0) of Viral Respiratory Infections

Deterministic Models

Seven out of 13 studies that deployed a mathematical model investigated the R0 of viral respiratory infections (11, 39, 40, 42, 55, 57, 58). Across them, four papers reported explicitly the results (40, 42, 51, 57), two papers only reported a graph (11, 39), and the remaining one did not report accessible data (55). Across these studies, the worst-case scenario was reported in the Brienen et al. (39): with mask efficacy at 30% and a 20% population coverage, the R0 reduced from the initial value of 2.0 to just 1.9. On the other hand, the best-case scenario is reported in Chen (40): with mask efficacy at 95%, the R0 can fall to 0.99 from an initial value of 16.90; however, neither population coverage nor time horizon are reported. Supplementary Appendix 5, Supplementary Table 9 show the description of R0 of viral respiratory infections across models. The summary of Findings is displayed in Table 3.

Filtering Capacity of Masks

Among laboratory experimental studies, seven out of nine studies reported the outcome as filtration rate or face mask protection, including goodness-of-fit and filtration efficiency. Outcomes varied according to the materials used.

In adults, generally filtration rate of household materials had high degree of variation, ranging from 49 to 86% for 0.02 μm exhaled particles (44) and from 3 to 60% for particles in the relevant size range (56).

High degree of variation were also present in surgical masks. One study (56) reported a filtration rate of surgical masks comparable to that of masks made of household materials. Other studies reported the best peformance for surgical masks, filtering from 89% (44) to 95.5–97% (52) of small particles. Under a pseudo-steady concentration environment, face mask protection on average was found to be 45%, while under expiratory emissions, protection varied from 33 to 100% for fully sealed face mask (50).

Particularly, in pediatrics, penetration of neutralized polydispersed sodium chloride aerosols varied significantly between brands at the highest flow rates, from 15 to 50% (48).

All types of surgical masks provided a relatively stable reduction of aerosol exposure over time, unaffected by duration of wear or type of activity, but with a high degree of individual variation with reductions ranging from 1.1- to 55-fold (average 6-fold), depending on the design of the mask (53). One study compared all types of masks (N95 personal respirators, surgical and home-made masks): surgical masks provided about twice as much protection as home-made masks, with the difference being slightly more marked among adults. N95 personal respirators provided adults with about 50 times as much protection as home-made masks, and 25 times as much protection as surgical masks (61). The summary of Findings is displayed in Table 3.

Viral Load Reduction

Three experimental laboratory studies were included (37, 44, 54), of which one study having three arms investigating surgical masks, home-made masks (i.e., cotton mask) or no mask; two studies focussed on the comparisons between surgical masks vs. home-made masks or no mask (Supplementary Appendix 5, Supplementary Table 10). According to our PICO, for the SOF GRADE assessment only the comparison between surgical mask vs. no mask reporting outcome data was considered (54). This suggested a viral load reduction of 0.25 (0.09–0.67) in favor of face mask use (risk difference: 324 fewer × 1,000) (Table 3).

Discussion

We found very low-certainty evidence that wearing a face mask is associated with a reduced risk of primary infection in RCTs as well as in observational studies. However, the wide confidence intervals affected the statistical significance of the overall estimate. It was not possible to establish the certainty of evidence about mortality, filtering capacity and R0 whereas viral load was judged to be of very low quality. Our findings indicate (i) a general consensus toward a reduction of deaths, based on prediction modeling studies, when the population mask coverage is near-universal, regardless of mask efficacy; (ii) filtration efficiency depends on the face mask materials, with studies showing high variability. It seems that all types of masks reduce the viral exposure, even though the levels of protection, in terms of reduction of susceptibility to infection in the wearer, are probably lower for some materials (i.e., cloth masks), to the extent that they do not effectively protect against infectious aerosols. Specifically, personal respirators were more efficient than surgical masks, which were more efficient than home-made masks; (iii) in the worst-case scenario with a mask efficacy at 30% and a population coverage at 20%, the R0 reduced from the initial value of 2.0 to just 1.9; whereas in the best-case scenario, when the mask efficacy is 95%, the R0 can fall to 0.99 from an initial value of 16.90, even though no population coverage nor time horizon is reported; (iv) wearing vs. not wearing a mask is associated with a reduction of viral load of RR 0.25 (95% CI 0.09–0.67, based on one experimental laboratory study).

Overall, our findings support the recommendation on using face masks in community settings in a pandemic era: home-made masks, such as those made of teacloths, may confer a significant degree of protection, albeit less strong than surgical masks or N95 personal respirators. Mask efficacy at 95% (N95 personal respirators) seems to be the best scenario, but it is difficult to realize in terms of adherence and costs from a public health perspective. A balanced compromise in the community could be reached with high population coverage using surgical masks (whose mask efficacy is >95%), which is easier to implement. Comparing surgical masks to no mask has shown a viral load reduction of a quarter (risk difference: 324 fewer × 1,000). Surgical masks were more effective than homemade masks in reducing the number of microorganisms expelled. However, high levels of filtration efficiency have been found among surgical and non-surgical masks, with evidence from all experimental laboratory studies emphasizing the importance of high filtration capacity irrespective of the materials used.

Our findings are in line with results from previous systematic reviews, which however had different aims, population and outcomes. For example, examining the infection rate in pandemic influenza transmission Jefferson et al. (65) has shown that wearing masks significantly decreased the spread of SARS (OR = 0.32; 95% CI 0.25–0.40). Similar finding were found in studies on respiratory virus infections including SARS, H1N1, and COVID-19 in all subgroups, including non-health care worker or non-household contacts (66). One review, investigating the optimum use of different personal protective equipment (face masks, respirators, and eye protection) in community and health-care settings, reported a large reduction in the risk of infection in favor of face mask use (OR 0.15; 95% CI 0.07 to 0.34, RD −14.3%; −15.9 to −10.7; low certainty), with stronger associations with N95 or similar respirators, compared with disposable surgical masks or similar masks (67). Anyway, this is the first systematic review and meta-analysis comprising evidence based on different research methods and study designs (e.g., modeling studies), to address the existing uncertainty about the efficacy and effectiveness of wearing a mask targeting the community setting for limiting the spread of COVID-19.

A pragmatic ecologic study, involving 49 countries, used data from the European Center for Disease Prevention and Control (ECDC) and investigated the association between face mask use in the community and cumulative number of cases of COVID-19 infection per million inhabitants, discovering that face mask use was negatively associated with number of COVID-19 cases (coef. −326; 95% CI −601 to −51, P = 0.021) (68).

The results of this ecological study and of the individual-level studies included in the review are in line with our findings, supporting the use of face masks for reducing the transmission and acquisition of respiratory viral infections in the community.

Strength and Limitations

Our review included experimental laboratory research and mathematical modeling studies to complement observations studies and trials, for obtaining a more complete picture on mortality and viral load reduction, filtering capacity and population coverage which are important factors influencing the R0. We adopted full methodological rigor within a much shorter time-frame compared to traditional reviews, using enhanced processes. We also critically assessed the risk of bias of included studies (randomized controlled studies and observational studies) and infeasibility of mathematical modeling studies.

Our systematic review has some limitations. Only a minority of the included studies looked at COVID-19, mainly addressed by modeling studies. We did not investigate the balance of pros and cons of wearing a mask. On one hand, the use of face masks may provide a false sense of security leading to suboptimal physical distancing, poor respiratory etiquette and hand hygiene—and possibly not staying at home when ill. There is a risk that improper removal of the face mask, handling of a contaminated face mask or an increased tendency to touch the face while wearing a mask by healthy persons might actually increase the risk of transmission (10). On the other hand, the fears related to the paradoxical increase of the infectious risk for their improper use are entirely theoretical, based on preconception without real foundation. Education campaigns should be encouraged for assuring proper use (10).

We reported adjusted estimates from two out of three cluster RCTs, because one RCT (35) might have unreliable results due to low usage of face masks in participants: indeed, a low usage of masks was reported in the face mask group, with adherence of only 25% among participants. In contrast, a moderate proportion of participants in the control group (49%) used face masks daily and intermittently. This undermines the reliability of results. We performed sensitivity analysis in order to present routine situations in the community but the included three places (schools, universities and in the general community) have different characteristics (e.g., open/closed space, potential confounder/interaction variable).

We did not appraise the quality of laboratory experimental studies since we did not find appropriate tools for measuring it. Similarly, for mathematical models we used the unfeasibility appraisal, a proxy of quality assessment, which is more appropriate given the nature of the studies. As for the quantitative-deterministic studies, we acknowledge that such models, especially when SIR-based, do not provide estimates of events, but rather describe what could happen in the future with respect to a predefined set of initial conditions. Namely, they help stakeholders in understanding how the situation could evolve in the future if different actions are adopted today. It follows that pitfalls of such models can be due to mis-specified initial conditions.

With new publications on COVID-19 related prediction models rapidly entering the medical literature, this systematic review cannot be viewed as an up to date list of all currently available prediction models. Furthermore, there were some studies among the ones we have reviewed that were available only as preprints; such studies might actually bring new insights after the peer-reviewing process.

Challenges and Opportunities for Public Health

The speed of the worldwide spread of the SAR-COV-2 virus, leading to a severe pandemic for which there is no effective treatment or vaccine and limited knowledge on disease behavior, and the uncertainty regarding the role of asymptomatic individuals in the transmission of the virus, call for Public Health infection prevention and control measures, even in the absence of evidence or in the presence of low quality scientific evidence. A recent systematic review found that, in this pandemic, the proportion of asymptomatic cases ranged from 4 to 41% (69). In this light, universal masking in the community may mitigate the extent of transmission of COVID-19 and may be a necessary adjunctive public health measure (70).

The evidence-based medicine should be used with acumen. The evidence-based GRADE approach suggest that whenever the evidence in favor to the intervention is low but the risks related to the averted implementation could be high, drastic measures can be adopted even in the absence of solid evidence, if the conditions are met (71).

The SARS-COV-2 pandemic is a life-threatening condition to such an extent as to indicate the need of accepting a minimal risk, assuming there is such a risk (i.e., mask costs), of the community intervention (i.e., face mask use), considering the notable benefit of its implementation, even if the evidence-base is of low quality. Deferring these measures, on the other hand, can have a negative effect on health policy decisions. This is called “precautionary principle”: “when human activities may lead to morally unacceptable harm that is scientifically plausible but uncertain, actions shall be taken to avoid or diminish that harm” (72, 73). The evidence, albeit imperfect, in support of the use of masks in this context are justifiable and sufficient in light of this principle. Although evidence-based medicine rightly looks suspiciously at tests of low methodological quality, at the same time it does not completely dismiss them, when circumstances are appropriate, as in this case (8).

And, when it comes to parachuting from a plane that is crashing, you wear it even if no trial has ever shown its effectiveness compared to a control group that launched without (74).

It should be emphasized that the use of face masks in the community should be considered only as a complementary measure and not as a replacement for the core preventive measures that are recommended to reduce community transmission including physical distancing, staying home when ill, teleworking/home working if possible, respiratory etiquette, meticulous hand hygiene and avoiding touching the face, nose, eyes, and mouth (10). In conclusion, the use of face masks as single intervention is not sufficient to stop the spread of COVID19 and a full package of the above mentioned interventions is the safest and the most recommended approach.

Data Availability Statement

Data can be found in Supplementary Material and the dataset is stored at the following repository https://osf.io/uvjgq/.

Author Contributions

DC and AN carried out the literature search, conducted screenings, extracted data, and completed the risk of bias assessment. AF, LI, DDA, and CR provided a critical revision of the manuscript. SG and GC conceived and drafted the manuscript and performed the statistical analyses. ADM extracted data and assessed quality of modeling studies. PI conceived and drafted the manuscript, interpreted the data, wrote the discussion, and guarantor of the data. CM and GT interpreted the data and revised the manuscript for important intellectual content. All authors approved the final version of the manuscript.

Disclaimer

The views and opinions expressed in this article are those of the author Andrea del Monaco and do not involve the responsibility of the Bank of Italy nor the ESCB.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2020.594269/full#supplementary-material

Abbreviations

aOR, Adjusted Odds Ratio; CI, Confidence Interval; COVID-19, Coronavirus disease 2019; CDC, Centers for Disease Control and Prevention; CHARMS, Checklist for critical Appraisal and data extraction for systematic Reviews of prediction Modeling Studies; ECDC, European Center for Disease Prevention and Control; GRADE, Grades of Recommendation, Assessment, Development and Evaluation; MERS, Middle East respiratory syndrome; MOOSE, Guidelines for Meta-analysis and Systematic reviews of observational studies; NOS, Newcastle Ottawa scale for non-randomized studies; PRISMA, Preferred reporting items for systematic reviews and meta-analyses; PROBAST, Prediction model Risk Of Bias Assessment Tool; RCT, Randomized Controleld Trials; RR, Risk Ratio; QUADRIAC, QUAntitative-Deterministic models Risk of Infeasibility Assessment Checklist; SARS, severe acute respiratory syndrome; SARS-CoV-2, severe acute respiratory syndrome coronavirus-2; SR, Systematic Reviews; SOF, Summary of Findings; WHO, World Health Organization.

References

1. 2020a World Health Organization. Advice on the Use of Masks in the Context of COVID-19. 6 April (2020). Available online at: https://www.who.int/publications-detail/advice-on-the-use-of-masks-in-the-community-during-home-care-and-in-healthcare-settings-in-the-context-of-the-novel-coronavirus-(2019-ncov)-outbreak (accessed May 26, 2020).

Google Scholar

2. 2020d World Health Organization. Modes of Transmission of Virus Causing COVID-19: Implications for IPC Precaution Recommendations. Scientific brief 29 March (2020). WHO/2019-nCoV/Sci_Brief/Transmission_modes/2020.2. Available online at: https://www.who.int/news-room/commentaries/detail/modes-of-transmission-of-virus-causing-covid-19-implications-for-ipc-precaution-recommendations World Health Organization (accessed May 26, 2020).

Google Scholar

3. Chen J. Pathogenicity and transmissibility of 2019-nCoV-A quick overview and comparison with other emerging viruses. Microb Infect. (2020) 22:69–71. doi: 10.1016/j.micinf.2020.01.004

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Read J. Coronavirus 2019-nCoV: early estimation of epidemiological parameters and epidemic predictions. medRxiv. (2020). doi: 10.1101/2020.01.23.20018549

CrossRef Full Text | Google Scholar

5. 2020c World Health Organization. Coronavirus Disease 2019 (COVID-19): Situation Report-46. (2020). https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports (accessed May 26, 2020).

Google Scholar

6. Prevention. CfDCa. Laboratory-Confirmed Influenza Hospitalizations. Preliminary cumulative rates as of May 16 (2020). Available online at: https://gis.cdc.gov/GRASP/Fluview/FluHospRates.html (accessed May 26, 2020).

Google Scholar

7. Prevention. CfDCa. COVIDView. A Weekly Surveillance Summary of U.S. COVID-19 Activity. Key Updates for Week 20, ending May 16. (2020). Available online at: https://www.cdc.gov/coronavirus/2019-ncov/covid-data/covidview/index.html (accessed May 26, 2020)

Google Scholar

8. Greenhalgh T, Schmid MB, Czypionka T, Bassler D, Gruer L. Face masks for the public during the covid-19 crisis. Bmj. (2020) 369:m1435. doi: 10.1136/bmj.m1435

PubMed Abstract | CrossRef Full Text | Google Scholar

9. b. World Health Organization. Coronavirus Disease (2019). (COVID-19): Situation Report. (2020). Available online at: https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports. https://reliefweb.int/sites/reliefweb.int/files/resources/20201201_Weekly_Epi_Update_16.pdf (accessed May 26, 2020).

Google Scholar

10. ECDC. European Centre for Disease Prevention and Control. Using face masks in the community. Stockholm (2020). Available online at: https://wwwecdceuropaeu/sites/default/files/documents/COVID-19-use-face-masks-communitypdf (accessed July 4, 2020).

Google Scholar

11. Ngonghala CN, Iboi E, Eikenberry S, Scotch M, MacIntyre CR, Bonds MH, et al. Mathematical assessment of the impact of non-pharmaceutical interventions on curtailing the 2019 novel Coronavirus. Mathem Biosci. (2020) 325:108364. doi: 10.1016/j.mbs.2020.108364

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Howard. Face Masks Against COVID-19: An Evidence Review. (2020). doi: 10.20944/preprints202004.0203.v1

CrossRef Full Text | Google Scholar

13. Eikenberry SE, Mancuso M, Iboi E, Phan T, Eikenberry K, Kuang Y, et al. To mask or not to mask: Modeling the potential for face mask use by the general public to curtail the COVID-19 pandemic. Infect Dis Model. (2020) 5:293–308. doi: 10.1016/j.idm.2020.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

14. CDC. Recommendation Regarding the Use of Cloth Face Coverings, Especially in Areas of Significant Community-Based Transmission. (2020). CDC (2020). Available online at: https://www.cdc.gov/coronavirus/2019-ncov/prevent-getting-sick/cloth-face-cover.html (accessed May 26, 2020).

Google Scholar

15. WHO. World Health Organization. Non-Pharmaceutical Public Health Measures for Mitigating the Risk and Impact of Epidemic and Pandemic Influenza 2019. Licence: CC BY-NC-SA 3.0 IGO. (2019). Available online at: https://apps.who.int/iris/handle/10665/329439

Google Scholar

16. Bartoszko JJ, Farooqi MAM, Alhazzani W, Loeb M. Medical masks vs N95 respirators for preventing COVID-19 in healthcare workers: A systematic review and meta-analysis of randomized trials. Influenza Other Resp Viruses. (2020) 14:365–73. doi: 10.1111/irv.12745

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Saunders-Hastings P, Crispo JAG, Sikora L, Krewski D. Effectiveness of personal protective measures in reducing pandemic influenza transmission: a systematic review and meta-analysis. Epidemics. (2017) 20:1–20. doi: 10.1016/j.epidem.2017.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Wong VW, Cowling BJ, Aiello AE. Hand hygiene and risk of influenza virus infections in the community: a systematic review and meta-analysis. Epidemiol Infect. (2014) 142:922–32. doi: 10.1017/S095026881400003X

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Iannone P, Castellini G, Coclite D, Napoletano A, Fauci AJ, Iacorossi L, et al. The need of health policy perspective to protect Healthcare Workers during COVID-19 pandemic. A GRADE rapid review on the N95 respirators effectiveness. PLoS ONE. (2020) 15:e0234025. doi: 10.1371/journal.pone.0234025

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Petrosillo N, Viceconte G, Ergonul O, Ippolito G, Petersen E. COVID-19, SARS and MERS: are they closely related? Clin Microbiol Infect. (2020) 26:729–34.

PubMed Abstract | Google Scholar

21. Abdelrahman Z, Li M, Wang X. Comparative review of SARS-CoV-2, SARS-CoV, MERS-CoV, and influenza a respiratory viruses. Front Immunol. (2020) 11:552909.

PubMed Abstract | Google Scholar

22. Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. Open Med. (2009) 3:e123–30. doi: 10.1371/journal.pmed.1000097

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA. (2000) 283:2008–12. doi: 10.1001/jama.283.15.2008

PubMed Abstract | CrossRef Full Text | Google Scholar

24. O'Connor D, Green S, Higgins J. Defining the review question and developing criteria for including studies. In: JPT Higgins, S Green, editors. Cochrane Handbook for Systematic Reviews of Interventions (Wiley Cochrane Series) (Hardcover). Wiley-Blackwell. (2008).

Google Scholar

25. Moons KG, de Groot JA, Bouwmeester W, Vergouwe Y, Mallett S, Altman DG, et al. Critical appraisal and data extraction for systematic reviews of prediction modelling studies: the CHARMS checklist. PLoS Med. (2014) 11:e1001744. doi: 10.1371/journal.pmed.1001744

PubMed Abstract | CrossRef Full Text | Google Scholar

26. DerSimonian R, Kacker R. Random-effects model for meta-analysis of clinical trials: an update. Contemp Clin Trials. (2007) 28:105–14. doi: 10.1016/j.cct.2006.04.004

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. Bmj. (2011) 343:d5928. doi: 10.1136/bmj.d5928

PubMed Abstract | CrossRef Full Text | Google Scholar

28. NOS. The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomised Studies in Meta-analyses. Ottawa: Ottawa Hospital Research Institute. Available online at: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed May 26, 2020).

Google Scholar

29. Wolff RF, Moons KGM, Riley RD, Whiting PF, Westwood M, Collins GS, et al. PROBAST: a tool to assess the risk of bias and applicability of prediction model studies. Ann Inter Med. (2019) 170:51–8. doi: 10.7326/M18-1376

CrossRef Full Text | Google Scholar

30. Porgo TV, Norris SL, Salanti G, Johnson LF, Simpson JA, Low N, et al. The use of mathematical modeling studies for evidence synthesis and guideline development: A glossary. Res Synth Methods. (2019) 10:125–33. doi: 10.1002/jrsm.1333

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Huguet A, Hayden JA, Stinson J, McGrath PJ, Chambers CT, Tougas ME, et al. Judging the quality of evidence in reviews of prognostic factor research: adapting the GRADE framework. System Rev. (2013) 2:71. doi: 10.1186/2046-4053-2-71

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Aiello AE, Murray GF, Perez V, Coulborn RM, Davis BM, Uddin M, et al. Mask use, hand hygiene, and seasonal influenza-like illness among young adults: a randomized intervention trial. J Infect Dis. (2010) 201:491–8. doi: 10.1086/650396

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Aiello AE, Perez V, Coulborn RM, Davis BM, Uddin M, Monto AS. Facemasks, hand hygiene, and influenza among young adults: a randomized intervention trial. PLoS ONE. (2012) 7:e29744. doi: 10.1371/journal.pone.0029744

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Al-Jasser FS, Kabbash IA, AlMazroa MA, Memish ZA. Patterns of diseases and preventive measures among domestic hajjis from Central, Saudi arabia [complete republication]. Eastern Mediterranean Health J. (2013) 19 (Suppl. 2):S34–41. doi: 10.26719/2013.19.Supp2.S34

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Alfelali M. Facemask vs. No Facemask in Preventing Viral Respiratory Infections During Hajj: A Cluster Randomised Open Label Trial. (2019). Available online at: https://ssrn.com/abstract=3349234

Google Scholar

36. Javid B, Balaban NQ. Impact of population mask wearing on COVID-19 post lockdown. Infectious Microbes and Diseases, (2020). doi: 10.1097/IM9.0000000000000029

CrossRef Full Text | Google Scholar

37. Bae S, Kim MC, Kim JY, Cha HH, Lim JS, Jung J, et al. Effectiveness of surgical and cotton masks in Blocking SARS-CoV-2: a controlled comparison in 4 patients. Ann Internal Med. (2020) 173:W22–W23. doi: 10.7326/M20-1342

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Balaban V. Protective practices and respiratory illness among US travelers to the 2009. Hajj J Travel Med. (2012) 19:163–8. doi: 10.1111/j.1708-8305.2012.00602.x

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Brienen NC, Timen A, Wallinga J, van Steenbergen JE, Teunis PF. The effect of mask use on the spread of influenza during a pandemic. Risk Analysis. (2010) 30:1210–8. doi: 10.1111/j.1539-6924.2010.01428.x

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Chen SC, Liao CM. Modelling control measures to reduce the impact of pandemic influenza among schoolchildren. Epidemiol Infect. (2008) 136:1035–45. doi: 10.1017/S0950268807009284

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Choudhry AJ, Al-Mudaimegh KS, Turkistani AM, Al-Hamdan NA. Hajj-associated acute respiratory infection among hajjis from Riyadh. East Mediterr Health J. (2006) 12:300–9.

PubMed Abstract | Google Scholar

42. Cui J, Zhang Y, Feng ZL, Guo SB, Zhang Y. Influence of asymptomatic infections for the effectiveness of facemasks during pandemic influenza. MBE. (2019) 16:3936–46. doi: 10.3934/mbe.2019194

PubMed Abstract | CrossRef Full Text | Google Scholar

43. D'Orazio M, Bernardini G, Quagliarini E. How to restart? An agent-based simulation model towards the definition of strategies for COVID-19 “second phase” in public buildings. arXiv:2004.12927v1. (2020). Available online at: https://arxiv.org/abs/2004.12927v1

Google Scholar

44. Davies A, Thompson KA, Giri K, Kafatos G, Walker J, Bennett A. Testing the efficacy of homemade masks: would they protect in an influenza pandemic? Disaster Med Public Health Preparedness. (2013) 7:413–8. doi: 10.1017/dmp.2013.43

PubMed Abstract | CrossRef Full Text | Google Scholar

45. De Kai G, Goldstein G-P, Morgunov A, Nangalia V. Universal masking is urgent in the COVID-19 pandemic: SEIR and agent based models, empirical validation, policy recommendations. arXiv:2004.13553v1 [physics.soc-ph]. (2020).

Google Scholar

46. Deris Z. The prevalence of acute respiratory symptoms and role of protective measures among malaysian hajj pilgrims. J Travel Med. (2010) 17:82–8. doi: 10.1111/j.1708-8305.2009.00384.x

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Emamian M. Respiratory tract infections and its preventive measures among hajj Pilgrims, 2010. A Nested Case Control Study. Int J Prev Med. (2013) 4:1030*5.

PubMed Abstract | Google Scholar

48. Guha S, Mejia-Alfaro A, Hariharan P, Myers MR. Effectiveness of facemasks for pediatric populations against submicron-sized aerosols. Am J Infect Control. (2015) 43:871–7. doi: 10.1016/j.ajic.2015.03.032

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Kim C. Is abdominal obesity associated with the 2009 influenza A (H1N1) pandemic in Korean school-aged children? Influenza Other Respir Viruses. (2012) 6:313–7. doi: 10.1111/j.1750-2659.2011.00318.x

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Lai AC, Poon CK, Cheung AC. Effectiveness of facemasks to reduce exposure hazards for airborne infections among general populations. J R Soc Interface. (2012) 9:938–48. doi: 10.1098/rsif.2011.0537

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Lau JT, Tsui H, Lau M, Yang X. SARS transmission, risk factors, and prevention in Hong Kong. Emerg Infect Dis. (2004) 10:587–92. doi: 10.3201/eid1004.030628

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Li Y, Guo YP, Wong KC, Chung WY, Gohel MD, Leung HM. Transmission of communicable respiratory infections and facemasks. J Multidiscipl Healthcare. (2008) 1:17–27. doi: 10.2147/JMDH.S3019

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Makison Booth C, Clayton M, Crook B, Gawn JM. Effectiveness of surgical masks against influenza bioaerosols. J Hospital Infect. (2013) 84:22–6. doi: 10.1016/j.jhin.2013.02.007

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Milton DK, Fabian MP, Cowling BJ, Grantham ML, McDevitt JJ. Influenza virus aerosols in human exhaled breath: particle size, culturability, and effect of surgical masks. PLoS Pathogens. (2013) 9:e1003205. doi: 10.1371/journal.ppat.1003205

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Mniszewski S, Del Valle S, Priedhorsky R, Hyman J, Hickman K. Understanding the impact of face mask usage through epidemic simulation of large social networks. In: Chapter in Intelligent Systems Reference Library. (2014) 52:97–115. doi: 10.1007/978-3-642-39149-1_8

CrossRef Full Text | Google Scholar

56. Rengasamy S, Eimer B, Shaffer RE. Simple respiratory protection–evaluation of the filtration performance of cloth masks and common fabric materials against 20-1000 nm size particles. Ann Occupational Hygiene. (2010) 54:789–98. doi: 10.1093/annhyg/meq044

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Tian L, Xuefei Li X, Qi F, Q-Y T, Tang V, Liu J, et al. Calibrated Intervention and Containment of the COVID-19 Pandemic. arXiv. (2020)

Google Scholar

58. Tracht SM, Del Valle SY, Hyman JM. Mathematical modeling of the effectiveness of facemasks in reducing the spread of novel influenza A (H1N1). PLoS ONE. (2010) 5:e9018. doi: 10.1371/journal.pone.0009018

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Tracht SM, Del Valle SY, Edwards BK. Economic analysis of the use of facemasks during pandemic (H1N1) 2009. J Theoret Biol. (2012) 300:161–72. doi: 10.1016/j.jtbi.2012.01.032

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Uchida M. Effectiveness of vaccination and wearing masks on seasonal influenza in Matsumoto City, Japan, in the 2014/2015 season: an observational study among all elementary schoolchildren. Prev Med Rep. (2016) 5:86–91. doi: 10.1016/j.pmedr.2016.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

61. van der Sande M, Teunis P, Sabel R. Professional and home-made face masks reduce exposure to respiratory infections among the general population. PLoS One. (2008) 3:e2618. doi: 10.1371/journal.pone.0002618

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Wu J. Risk Factors for SARS among persons without known contact with SARS patients, Beijing, China. Emerg Infect Dis. (2004) 10:210–6. doi: 10.3201/eid1002.030730

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Yan J, Guha S, Hariharan P, Myers M. Modeling the effectiveness of respiratory protective devices in reducing influenza outbreak. Risk Analysis. (2019) 39:647–61. doi: 10.1111/risa.13181

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Zhang L, Peng Z, Ou J, Zeng G, Fontaine RE, Liu M, et al. Protection by face masks against influenza A(H1N1)pdm09 virus on trans-Pacific passenger aircraft, 2009. Emerg Infect Dis. (2013) 19:1403–10. doi: 10.3201/eid1909.121765

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Jefferson T, Foxlee R, Del Mar C, Dooley L, Ferroni E, Hewak B, et al. Physical interventions to interrupt or reduce the spread of respiratory viruses: systematic review. BMJ. (2008) 336:77–80. doi: 10.1136/bmj.39393.510347.BE

CrossRef Full Text | Google Scholar

66. Liang M, Gao L, Cheng C, Zhou Q, Uy JP, Heiner K, et al. Efficacy of face mask in preventing respiratory virus transmission: A systematic review and meta-analysis. Travel Med Infect Dis. (2020) 2020:101751. doi: 10.1016/j.tmaid.2020.101751

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Chu DK, Akl EA, Duda S, Solo K, Yaacoub S, Schunemann HJ, 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) 395:1973–87. doi: 10.1016/j.jvs.2020.07.040

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Kenyon C. Widespread use of face masks in public may slow the spread of SARS CoV-2:2 an ecological study. medRxiv preprint. (2020) doi: 10.1101/2020.03.31.20048652

CrossRef Full Text | Google Scholar

69. Byambasuren O, Cardona M, Bell K, Clark J, McLaws M-L, Glasziou P. Estimating the extent of true asymptomatic COVID-19 and its potential for community transmission: systematic review and meta-analysis. medRxiv Preprint. (2020) doi: 10.2139/ssrn.3586675

CrossRef Full Text | Google Scholar

70. Cheng VC, Wong SC, Chuang VW, So SY, Chen JH, Sridhar S, et al. The role of community-wide wearing of face mask for control of coronavirus disease (2019). (COVID-19) epidemic due to SARS-CoV-2. J Infect. (2020). 81:107–14. doi: 10.1016/j.jinf.2020.04.024

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Andrews JC, Schunemann HJ, Oxman AD, Pottie K, Meerpohl JJ, Coello PA, et al. GRADE guidelines: 15. Going from evidence to recommendation-determinants of a recommendation's direction and strength. J Clin Epidemiol. (2013) 66:726–35. doi: 10.1016/j.jclinepi.2013.02.003

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Commission E. The Precautionary Principle: Decision Making Under Uncertainty. (2017). Available online at: https://ec.europa.eu/environment/integration/research/newsalert/pdf/precautionary_principle_decision_making_under_uncertainty_FB18_en.pdf (accessed July 4, (2020).

Google Scholar

73. The precautionary principle. EPRS | European Parliamentary Research Service. (2005). doi: 10.2861/821468

CrossRef Full Text | Google Scholar

74. Smith GC, Pell JP. Parachute use to prevent death and major trauma related to gravitational challenge: systematic review of randomised controlled trials. BMJ. (2003) 327:1459–61. doi: 10.1136/bmj.327.7429.1459

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: pandemics, face mask, prevention and control [MeSH], SARS—CoV−2, COVID−19, disease outbreaks, community, systematic review

Citation: Coclite D, Napoletano A, Gianola S, del Monaco A, D'Angelo D, Fauci A, Iacorossi L, Latina R, Torre GL, Mastroianni CM, Renzi C, Castellini G and Iannone P (2021) Face Mask Use in the Community for Reducing the Spread of COVID-19: A Systematic Review. Front. Med. 7:594269. doi: 10.3389/fmed.2020.594269

Received: 12 August 2020; Accepted: 09 December 2020;
Published: 12 January 2021.

Edited by:

Yoav Keynan, University of Manitoba, Canada

Reviewed by:

Zulma Vanessa Rueda, Pontifical Bolivarian University, Colombia
Diamantis Plachouras, European Centre for Disease Prevention and Control (ECDC), Sweden
Lorenzo Bertizzolo, Université Paris Descartes, France

Copyright © 2021 Coclite, Napoletano, Gianola, del Monaco, D'Angelo, Fauci, Iacorossi, Latina, Torre, Mastroianni, Renzi, Castellini and Iannone. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Silvia Gianola, c2lsdmlhLmdpYW5vbGEmI3gwMDA0MDtncnVwcG9zYW5kb25hdG8uaXQ=

These authors share first authorship

These authors share last authorship

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