Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link

Disclaimer: Early release articles are not considered as final versions. Any changes will be reflected in the online version in the month the article is officially released.

Volume 27, Number 8—August 2021
Research

Social Distancing, Mask Use, and Transmission of Severe Acute Respiratory Syndrome Coronavirus 2, Brazil, April–June 2020

Marcelo Rodrigues GonçalvesComments to Author , Rodrigo Citton Padilha dos Reis, Rodrigo Pedroso Tólio, Lucia Campos Pellanda, Maria Inês Schmidt, Natan Katz, Sotero Serrate Mengue, Pedro C. Hallal, Bernardo L. Horta, Mariangela Freitas Silveira, Roberto Nunes Umpierre, Cynthia Goulart Bastos-Molina, Rodolfo Souza da Silva, and Bruce B. Duncan
Author affiliations: Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil (M.R. Gonçalves, R.C.P. Reis, R.P. Tólio, M.I. Schmidt, N. Katz, S.S. Mengue, R.N. Umpierre, C.G. Bastos-Molina, R.S. da Silva, B.B. Duncan); Hospital de Clínicas de Porto Alegre, Porto Alegre (M.R. Gonçalves, M.I. Schmidt, R.N. Umpierre, C.G. Bastos-Molina, R.S. da Silva, B.B. Duncan); Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre (L.C. Pellanda); Municipal Health Department, Porto Alegre (N. Katz); Universidade Federal de Pelotas, Pelotas, Brazil (P.C. Hallal, B.L. Horta, M.F. Silveira); Universidade do Vale dos Sinos (UNISINOS), São Leopoldo, Brazil (C.G. Bastos-Molina)

Suggested citation for this article

Abstract

We assessed the associations of social distancing and mask use with symptomatic, laboratory-confirmed severe acute respiratory syndrome coronavirus 2 infection in Porto Alegre, Brazil. We conducted a population-based case-control study during April–June 2020. Municipal authorities furnished case-patients, and controls were taken from representative household surveys. In adjusted logistic regression analyses of 271 case-patients and 1,396 controls, those reporting moderate to greatest adherence to social distancing had 59% (odds ratio [OR] 0.41, 95% CI 0.24–0.70) to 75% (OR 0.25, 95% CI 0.15–0.42) lower odds of infection. Lesser out-of-household exposure (vs. going out every day all day) reduced odds from 52% (OR 0.48, 95% CI 0.29–0.77) to 75% (OR 0.25, 95% CI 0.18–0.36). Mask use reduced odds of infection by 87% (OR 0.13, 95% CI 0.04–0.36). In conclusion, social distancing and mask use while outside the house provided major protection against symptomatic infection.

The coronavirus disease (COVID-19) pandemic has spread worldwide (1). The rapid transmission of the causative agent, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has produced a high death toll, threatening health systems and creating huge challenges for governments and societies.

Until advances in the development and distribution of vaccines or treatment reduce the risk for COVID-19 complications to levels permitting near-normal day-to-day functioning, societies continue to require simple public health approaches to control pandemic spread, including mask use and social distancing. Several cohort studies in hospital settings have shown benefits of both interventions (2). However, in community settings, where these approaches have the greatest potential to limit viral spread and halt the pandemic, documented support for their use comes mostly from ecologic studies and, indirectly, from findings related to previous pandemics of other coronaviruses. Only a few studies (3), including a retrospective case-control study of asymptomatic contacts (4), a randomized trial (5), and a study at sea (6), have evaluated their effectiveness against community transmission of SARS-CoV-2 on the basis of individual-level exposure and outcome measurements. Their relevance remains embroiled in controversy. To help close this gap, we evaluated the association of mask use and social distancing with incident, symptomatic, laboratory-confirmed SARS-CoV-2 infection in a population-based case-control study.

Methods

We conducted a population-based, case-control study in Porto Alegre, the capital of Rio Grande do Sul State, Brazil, which has an estimated population of 1,483,771 (7). The ethics committee of the Hospital de Clínicas de Porto Alegre approved our study (approval no. 31499420.5.0000.5327), and the Brazilian National Ethics Committee (approval no. 30415520.2.0000.5313) approved the accompanying seroprevalence surveys. All participants gave prior informed consent, in written form by the controls and verbally for case-patients.

On March 19, 2020, state officials mandated school and nonessential business closure and travel restrictions and ordered citizens to stay at home unless going to essential services (8). On May 8, 2020, Porto Alegre’s mayor issued a series of orders and recommendations for mask use. These mandates, with only slight alterations, remained in force in Porto Alegre throughout the period of this study. However, social distancing and mask use were not universally adopted; prominent leaders questioned their necessity and supported widely publicized gatherings, frequently without mask use.

We obtained case-patients from the Municipal Health Department, given that notification of COVID-19 cases is mandatory. The list consisted of all persons (excluding healthcare professionals) who tested positive for SARS-CoV-2 by reverse transcription PCR or antibody testing through June 19, 2020, in Porto Alegre. With rare exceptions, case-patients were receiving medical care, because testing during this period was limited and available only for symptomatic persons. Cases were identified in hospitals and primary care settings. We then contacted persons >18 years of age whose date of symptom onset was on or after April 28, 2020. Before deeming a case-patient nonrespondent, we attempted >10 calls on different days at different hours, as well as attempting contact through short message service, WhatsApp, other social media, and physical mail. We excluded persons working in healthcare settings because our focus was community transmission. We also excluded deceased persons and persons who resided outside the municipality. When the case-patient could not be interviewed, we obtained responses from a proxy (i.e., a close contact, either a family member or caretaker).

Controls were the seronegative persons in 3 representative community surveys of SARS-CoV-2 antibody prevalence in Porto Alegre conducted during May 9–11, May 23–25, and June 26–28, 2020 (9,10). For the surveys, 50 of Porto Alegre’s census tracts were selected with probability proportional to size. Within each, during each survey, 10 households were selected systematically; if no one was home or residents refused participation, we used the neighboring residence. A resident of each home was then selected at random for interview.

Controls underwent a brief interview, including questions on social distancing, mask use, and sociodemographics. Seropositivity was determined by a point-of-care rapid antibody test (L.C. Pellanda et al., unpub. data, https://www.medrxiv.org/content/10.1101/2020.05.06.20093476v1). For case-patients, we conducted telephone interviews by using the same questions applied in the surveys.

Case-patients and controls were queried by trained interviewers using standardized questionnaires: “Regarding the social distancing recommended by health authorities, that is, staying at home and avoiding contact with other people, how much do you think you have managed to do?” Reply choices were 1, very little; 2, little; 3, some; 4, a great deal; and 5, practically isolated from everyone.

In response to “What has been your routine of activities?” participants opted among the following choices: 1, go out every day, all day, to work or other regular activity; 2, go out every day for some activity; 3, go out from time to time to shop and stretch my legs; 4, go out only for essential things like buying food; and 5, stay at home all the time. We created and categorized a social distancing score by summing responses to each of these questions when taken as an ordinal scale.

Mask use was queried for all case-patients but queried for controls only during the last seroprevalence survey. In response to “Do you use a mask when you leave home?” case-patients opted between yes and no and controls among yes, sometimes, and no. For modeling, we merged the replies yes and sometimes. For case-patients and controls, we defined income as mean head-of-household monthly income on the respondent’s census tract.

We calculated sample size by using an α of 0.05 and 80% power: to detect an odds ratio of 2 would require 93 case-patients and 372 controls. We described continuous variables by mean (SD) or median (interquartile range) and categorical variables by frequency (percentage). When information on household size was missing, we used the mean household size of the respondent’s census tract. Participants with other missing values were excluded from analyses. We investigated associations of social distancing and mask use through prespecified logistic regression analyses. We defined the pandemic moment as the date of symptom onset for case-patients and as 10 days before the date of interview for controls. We performed all analyses by using the statistical software package R version 4.0.2 (https://cran.r-project.org) (11).

Results

Figure 1

Flowchart of COVID-19 case-patient and controls, Porto Alegre, Brazil, April–June 2020. COVID-19, coronavirus disease.

Figure 1. Flowchart of COVID-19 case-patient and controls, Porto Alegre, Brazil, April–June 2020. COVID-19, coronavirus disease.

Of all initial case-patients, after excluding deceased persons and those who were not part of the target population, 813 case-patients were eligible for contact (Figure 1). We established contact with 467 (57.4%) and found an additional 184 ineligible. Of the remaining 283 persons, 12 refused participation or provided incomplete social distancing information, leaving 271 case-patients. We interviewed 237 (87.5%) directly and 34 (12.5%) by proxy. If the proportion of actual eligible case-patients among the 813 initially eligible persons was the same as among those contacted (283/467), the 271 cases represent a response rate of 55.0% among those actually eligible. Comparison of the Municipal Health Department case data showed that case-patients in the final sample differed little from those not included in terms of sex (43.9% [95% CI 37.9%–50.0%] men among those included vs. 48.3% [95% CI 44.7%–58.6%] men among those excluded) and age (46.0 [95% CI 44.0–48.0] years for those included vs. 48.0 [95% CI 46.2–49.8] years for those excluded).

For controls, of 3,065 households approached, 1,177 (38.4%) were vacant or without residents at home, residents refused in 388 (12.7%) households, and 4 seropositive persons were excluded; a total of 1,496 (48.8%) potential controls were contacted (12). An additional 70 were <18 years old and data on race were missing for 30, leaving 1,396 (45.5%) for analyses. Comparison of controls in the final sample with the 30 persons for whom data were missing demonstrated they were also similar in sex (38.5% [95% CI 35.9%–41.0%] men for final controls vs. 36.7% [95% CI 21.9%–54.5%] men for those with data missing) and age (49.7 [95% CI 48.8–50.6] for final controls vs. 52.3 [95% CI 44.1–60.5] years for those with data missing).

Our controls were more frequently women and were somewhat older than the average of the adult population of Porto Alegre (Table 1) (13). Case-patients, compared to controls, were more frequently men, Black, and younger; had a lower level of education; and lived in larger households (Table 2). Case-patients were less likely to adhere to social distancing. In the variable summarizing social distancing, case-patients more frequently practiced least (16.2% vs. 7.2% for controls) or little (26.6% vs. 15.5% for controls) social distancing. Reported mask use was common. After we excluded those reporting to stay at home all the time, only 10 (2.4%) controls and 14 (7.1%) case-patients reported not using masks when out.

Figure 2

Number of case-patients (n = 271) by date of coronavirus disease symptom onset in study of face masks, social distancing, and transmission of severe acute respiratory syndrome coronavirus 2, Porto Alegre, Brazil, April–June 2020. Green bars indicate dates of interviews of controls (n = 1,396): May 9–11, May 23–25, and June 26–28.

Figure 2. Number of case-patients (n = 271) by date of coronavirus disease symptom onset in study of face masks, social distancing, and transmission of severe acute respiratory syndrome coronavirus 2, Porto...

We compared the temporal distribution of symptom onset of case-patients and the 3 interview periods for controls (Figure 2). On average, symptom onset in case-patients was slightly less than a week before the interview date of controls (Table 2).

In crude analyses (Table 3, model 1), moderate or high adherence to social distancing and being practically isolated from everyone all reduced risk for infection. Multiple adjustments (models 2 and 3) produced little change. In model 3, those with moderate adherence to social distancing were 72% (OR 0.28, 95% CI 0.16–0.50) and those with high adherence 75% (OR 0.25, 95% CI 0.15–0.42) less likely to become infected. Persons who reported they were practically isolated from everyone were 59% (OR 0.41, 95% CI 0.24–0.70) less likely to become infected. When we excluded proxy interviews (model 4), the association of being practically isolated from everyone became stronger (OR 0.34, 95% CI 0.20–1.60).

In similar models (Table 3), lesser activity of any degree reduced the odds of infection compared to leaving home daily for the whole day. Relatively little confounding was present, and in models adjusted for all covariates, going out for some activities every day reduced odds by 74% (OR 0.26, 95% CI 0.13–0.49), going out from time to time reduced odds by 61% (OR 0.39, 95% CI 0.25–0.61), and going out just for essential activities reduced odds by 75% (OR 0.25, 95% CI 0.18–0.36). After we excluded proxy interviews (model 4), staying home all the time also provided a major reduction in odds (OR 0.25, 95% CI 0.13–0.44).

When these 2 measures were joined in a categorical summary measure of social distancing (Table 3), practicing much distancing reduced the adjusted odds of becoming infected by 67% (OR 0.33, 95% CI 0.22–0.52) and most distancing reduced odds by 62% (OR 0.38, 95% CI 0.23–0.62), in comparison to least distancing. After excluding proxy interviews, the association became graded; odds were 73% lower (OR 0.27, 95% CI 0.16–0.46) among persons who practiced the most social distancing.

Because information on mask use was only obtained during the third seroprevalence survey, we compared use for the 464 controls in this survey with 229 case-patients of a similar pandemic moment (symptom onset <10 days before the second survey). Considering all those with mask data during this period, crude analyses demonstrated that mask use reduced odds of infection by 88% (OR 0.12, 95% CI 0.04–0.30), and after adjustments, including the summary distancing score (Table 4, model 3), by 90% (OR 0.10, 95% CI 0.03–0.25). No interaction was seen between mask use and social distancing (OR 0.96, 95% CI 0.60–1.58). The association was similar in the restricted sample, which removed those who reported staying home all the time (87%; OR 0.13, 95% CI 0.04–0.36) and, in addition, when proxy respondents were removed (88%; OR 0.12, 95% CI 0.04–0.35). In a sensitivity analysis in which “sometimes” mask use was joined with “no” rather than with “always,” mask use reduced odds of infection (model 3) by 64% (OR 0.36, 95% CI 0.17–0.74).

Finally, when we adjusted social distancing associations for mask use in an analysis limited to controls from the third survey and cases of similar pandemic moment, we found little change in associations with social distancing. There was 50% (OR 0.51, 95% CI 0.27–0.93) lesser risk for infection with little social distancing, 67% (OR 0.33, 95% CI 0.19–0.60) with much social distancing, and 59% (OR 0.41, 95% CI 0.21–0.80) with the most social distancing.

Discussion

In this population-based case-control study of COVID-19 conducted during a period of low-level to mid-level viral transmission in a major city in Brazil, mask use and adherence to social distancing resulted in major protection against symptomatic SARS-CoV-2 infection. Even after adjusting for various risk factors, adults who reported moderate or greater adherence to distancing recommendations reduced their odds of infection by one half to two thirds, and those who reported using masks when out reduced their risk by 87%. Because we excluded persons in healthcare settings, our findings directly address the use of these measures for protection against COVID-19 in the general community.

Evidence supporting the use of nonpharmacologic public health measures to slow viral spread of SARS-CoV-2 in communities has come mainly from ecologic studies documenting large inverse associations between greater use of these measures and viral spread (1417). Evidence based on individual-level analyses, which come almost exclusively from studies of severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome or from investigations in hospitals, have findings similar to ours: that risk approximately doubled with each additional meter of proximity to known infected persons, and that mask use reduced risk for transmission by 85% (OR 0.15, 95% CI 0.07–0.34) (2). Similar, although weaker, protection in a SARS-CoV-2 outbreak in a specific setting (the USS Roosevelt aircraft carrier) was found with greater use of face coverings (OR 0.30, 95% CI 0.17–0.52), avoidance of common areas (OR 0.56, 95% CI 0.37–0.86), and increased distance from others (OR 0.52, 95% CI 0.34–0.79) (6).

Very few individual-level studies have been reported on the effect of these measures on community transmission of SARS-CoV-2 (18). A case-control study of asymptomatic contacts in Thailand documented a risk reduction of 77% with mask use and 85% with distancing greater than 1 meter (4), and a study from Wuhan, China, showed mask use at home during the lockdown provided protection (19). An additional report ascertained that greater mask use reduced risk for predicted COVID-19 by 63% (S. Kwon et al., unpub. data, https://www.medrxiv.org/content/10.1101/2020.11.11.20229500v1). Finally, a cross-sectional study from Vermont, USA, with only 10 cases showed some protection in crude analyses (20).

A randomized trial in Denmark (5) that suggested lower, nonsignificant protection (OR 0.82, 95% CI 0.54–1.23) of mask use, although based on a potentially stronger design, had major methodologic problems (21,22). First, mask use was limited; only 46% reported full adherence. Second, 84% of outcomes were detected by antibody testing, leading an editorial accompanying the publication (21) to note that, given the extremely low incidence of cases, “all of the antibody-positive results in both intervention and control groups could have been false positives.” When the study analyzed the subset of healthcare-diagnosed cases (15 participants), masks provided a greater, though not statistically significant, protection (OR 0.52, 95% CI 0.18–1.53). Third, the trial’s short study periods (1 month), coupled with low antibody test sensitivity in early disease (30% <7 days and 72% during days 8–14) (23), could have resulted in the inclusion during the initial 2 weeks of case-patients who had contacted the disease before trial initiation. Similarly, during the final 2 weeks of the study period, some infections could have been missed by antibody testing, also not being detected by home-based reverse transcription PCR of uncertain sensitivity at close-out. Finally, because the intervention did not include face mask use by other household members, some cases could have resulted from home exposure, limiting the applications of the trial to current community settings, in which a greater fraction of other household members would also be using masks when out.

Our study provides estimates for easily interpretable measures—percentage effectiveness of social distancing and masking in protecting against infection—in the general community, the setting of greatest relevance for controlling the pandemic. The study occurred during a period of low to moderate transmission. Rio Grande do Sul State seroprevalence data suggest that ≈0.5% of the population became infected and 57 (3.8/100,000 population) COVID-19 deaths occurred in Porto Alegre during our ≈2-month study period (24).

The first potential limitation of our study was that response rates for case-patients (55.0%) and controls (45.5%) were low, and differential nonparticipation could introduce selection bias. Whereas not being available to participate could be associated with less social distancing, additional factors could explain the low response. Among case-patients, the frequent address changes identified when contact was achieved suggest that many case-patients on the initial list were ineligible because they were nonresidents who had furnished a false address to gain access to care. In addition, telemarketing and telephone scams lead many to ignore calls from unknown numbers. Of note, however, if these persons did not respond because they were away from their landline telephones, their inclusion would have resulted in even stronger associations. Among controls, refusal to participate was uncommon (12.7%); vacant residences were the main cause of nonresponse. Although interviews occurred on weekends, the limited attempts made to locate absent residents could have resulted in enrollment of controls who were more likely to practice social distancing. If so, this factor could have resulted in an overreport of the true effect. However, other reasons could explain the high vacancy rate, such as residents visiting vacation homes or relatives; residents, especially in apartments or other housing with restricted access, not responding to strangers; and residences being temporarily vacant. Our adjustment for age, sex, and other covariates could have at least partially controlled for these differential responses.

Second, some exposure misclassification was possible, because questions about mask use and social distancing were unvalidated and limited in detail, having been taken from the community serology survey providing the controls. As such, we were unable to address differences in protection when indoors, outdoors, or indoors in specific settings.

Third, full adjustment for pandemic moment in analyses of mask use was not possible, because controls with data on mask use were all interviewed in a period shortly after case-patients began experiencing symptoms. However, given that this period was short and followed mandated mask use, a temporal trend in mask use would probably have been small and thus have had little effect on our estimates.

Fourth, controls could include persons who had received a misdiagnosis of false-negative. However, given low seroprevalence and our test’s 86.4% sensitivity and 99.6% specificity (L.C. Pellanda, unpub. data), we estimate that misdiagnosis would likely have occurred in only 1 control.

Fifth, as the serology survey did not include occupation, we could not exclude healthcare workers among controls. Because healthcare workers would likely adhere to greater social distancing and mask use, their inclusion among controls could have falsely strengthened our findings. However, only ≈5% of the workforce in Brazil are healthcare workers (25), so we do not believe that their inclusion produced an appreciable error. In addition, errors because of lack of control for unmeasured confounding (e.g., from other occupational or residual socioeconomic differences or from recent travel) are always possible.

Sixth, a specific finding—lesser protection of those who reported being practically isolated from everyone and those who reported staying at home all the time (Table 3, model 3)—could weaken confidence in our social distancing results. However, as suggested by the additional analysis removing proxy responses (model 4), the lack of a graded dose-response in the model 3 associations could have been because of the greater risk level of case-patients who reported they were isolated but actually resided in assisted living.

Finally, application of our findings to settings with circulating virus variants or to persons who have received vaccination can only be speculated. In the case of circulating variants, risk for infection among those distancing and using masks will probably be greater, but risk among those not distancing or not using masks will also be greater. In the case of vaccination, however, risk for infection would be lower for all. We know of no a priori reason, however, to presume that the relative protection of distancing and mask use in these settings would be either lesser or greater than we report.

The primary strength of our report is that, as a population-based study, it avoids the risk for selection bias typical of less representative designs. It is sufficiently large to permit precise confidence intervals for our estimates of the benefit of protective measures. Furthermore, because our cases were detected at a time when testing was limited to symptomatic persons seeking care, the protection we found was against becoming a clinically relevant case. Finally, and perhaps most vital, our findings are based on individual-level analyses and thus permit estimation of percent reduction of risk, a direct and simple way to communicate the magnitude of individual protection afforded by these simple public health measures.

Given the hurdles faced in vaccine production, distribution, and acceptance, and the increasing emergence of virus variants, mass vaccination is unlikely to suffice to control the pandemic in the near future in many parts of the world. During this period and continuing into the future phase of maintaining viral control, simple public health measures, principally social distancing and mask use, will remain crucial options to minimize viral spread. The expression of their benefit in easy-to-grasp terms should help stimulate and maintain adherence to social distancing and mask use during this period.

In conclusion, we found that social distancing and mask use while away from home provided major protection against symptomatic SARS-CoV-2 infection. Our easily grasped and generalizable estimates of protection against transmission lend support to previous, frequently less direct, assessments. Our findings support the contention that greater use of simple public health measures in the community provides major protection against symptomatic infection.

Dr. Gonçalves is a family physician, epidemiologist, and associate professor of the Social Medicine Department and Postgraduate Program in Epidemiology at the Federal University of Rio Grande do Sul. Though his main research interests are health services evaluation, chronic disease, and telehealth, in recent months he has been actively engaged in clinical and research activities related to confronting the coronavirus disease pandemic.

Top

Acknowledgment

We thank Amanda de Carvalho Robaina, Juarez de Lima dos Santos Filho, and Viviane Horn de Melo, who supervised case interviews.

Top

References

  1. World Health Organization. WHO coronavirus disease (COVID-19) dashboard [cited 2020 Sep 9]. https://covid19.who.int
  2. Chu  DK, Akl  EA, Duda  S, Solo  K, Yaacoub  S, Schünemann  HJ, et al.; COVID-19 Systematic Urgent Review Group Effort (SURGE) study authors. 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;395:197387. DOIPubMed
  3. Chou  R, Dana  T, Jungbauer  R, Weeks  C. Update alert 3: masks for prevention of respiratory virus infections, including SARS-CoV-2, in health care and community settings. Ann Intern Med. 2020;173:169. DOIPubMed
  4. Doung-Ngern  P, Suphanchaimat  R, Panjangampatthana  A, Janekrongtham  C, Ruampoom  D, Daochaeng  N, et al. Case-control study of use of personal protective measures and risk for SARS-CoV 2 infection, Thailand. Emerg Infect Dis. 2020;26:260716. DOIPubMed
  5. Bundgaard  H, Bundgaard  JS, Raaschou-Pedersen  DET, von Buchwald  C, Todsen  T, Norsk  JB, et al. Effectiveness of adding a mask recommendation to other public health measures to prevent SARS-CoV-2 infection in Danish mask wearers: a randomized controlled trial. Ann Intern Med. 2021;174:33543. DOIPubMed
  6. Payne  DC, Smith-Jeffcoat  SE, Nowak  G, Chukwuma  U, Geibe  JR, Hawkins  RJ, et al.; CDC COVID-19 Surge Laboratory Group. SARS-CoV-2 infections and serologic responses from a sample of U.S. Navy service members—USS Theodore Roosevelt, April 2020. MMWR Morb Mortal Wkly Rep. 2020;69:71421. DOIPubMed
  7. Brazilian Institute of Geography and Statistics. Porto Alegre [cited 2020 Sep 9]. https://www.ibge.gov.br/cidades-e-estados/rs/porto-alegre.html
  8. PROCERGS. Decree No. 55.118, of March 16, 2020. Establishes complementary measures to prevent contagion by COVID-19 (new coronavirus) within the State. Official Register of the State of Rio Grande do Sul, Porto Alegre [in Portuguese]. 2020 Mar 17 [cited 2020 Nov 13]. https://www.diariooficial.rs.gov.br/materia?id=395443
  9. Hallal  PC, Horta  BL, Barros  AJD, Dellagostin  OA, Hartwig  FP, Pellanda  LC, et al. Trends in the prevalence of COVID-19 infection in Rio Grande do Sul, Brazil: repeated serological surveys. Cien Saude Colet. 2020;25(suppl 1):2395401. DOIPubMed
  10. Barros  AJD, Victora  CG, Menezes  AMB, Horta  BL, Hartwig  F, Victora  G, et al. Social distancing patterns in nine municipalities of Rio Grande do Sul, Brazil: the Epicovid19/RS study. Rev Saude Publica. 2020;54:75. DOIPubMed
  11. R: The R Project for Statistical Computing [cited 2020 Sep 19]. https://www.r-project.org/
  12. Silveira  MF, Barros  AJD, Horta  BL, Pellanda  LC, Victora  GD, Dellagostin  OA, et al. Population-based surveys of antibodies against SARS-CoV-2 in Southern Brazil. Nat Med. 2020;26:11969. DOIPubMed
  13. SIDRA. IBGE Automatic Recovery System. National Annual Continuous Household Sample Survey–PNADC/A [cited 2020 Sep 21]. https://sidra.ibge.gov.br/pesquisa/pnadca/tabelas
  14. Courtemanche  C, Garuccio  J, Le  A, Pinkston  J, Yelowitz  A. Strong social distancing measures in the United States reduced the COVID-19 growth rate. Health Aff (Millwood). 2020;39:123746. DOIPubMed
  15. Lyu  W, Wehby  GL. Community use of face masks and COVID-19: evidence from a natural experiment of state mandates in the US. Health Aff (Millwood). 2020;39:141925. DOIPubMed
  16. Islam  N, Sharp  SJ, Chowell  G, Shabnam  S, Kawachi  I, Lacey  B, et al. Physical distancing interventions and incidence of coronavirus disease 2019: natural experiment in 149 countries. BMJ. 2020;370:m2743. DOIPubMed
  17. Haug  N, Geyrhofer  L, Londei  A, Dervic  E, Desvars-Larrive  A, Loreto  V, et al. Ranking the effectiveness of worldwide COVID-19 government interventions. Nat Hum Behav. 2020;4:130312. DOIPubMed
  18. Chou  R, Dana  T, Jungbauer  R, Weeks  C, McDonagh  MS. Update alert: masks for prevention of respiratory virus infections, including SARS-CoV-2, in health care and community settings. Ann Intern Med. 2020;173:W86. DOIPubMed
  19. Centers for Disease Control and Prevention. Coronavirus disease 2019 (COVID-19) scientific brief: community use of cloth masks to control the spread of SARS-CoV-2. 2020 [cited 2020 Nov 13]. https://www.cdc.gov/coronavirus/2019-ncov/more/masking-science-sars-cov2.html
  20. van den Broek-Altenburg  EM, Atherly  AJ, Diehl  SA, Gleason  KM, Hart  VC, MacLean  CD, et al. Jobs, housing, and mask wearing: cross-sectional study of risk factors for COVID-19. JMIR Public Health Surveill. 2021;7:e24320. DOIPubMed
  21. Frieden  TR, Cash-Goldwasser  S. Of Masks and Methods. Ann Intern Med. 2021;174:4212. DOIPubMed
  22. Haber  NA, Wieten  SE, Smith  ER. Letter of concern regarding »Reduction in COVID-19 infection using surgical facial masks outside the healthcare system«. Dan Med J. 2020;67:A205063.PubMed
  23. Deeks  JJ, Dinnes  J, Takwoingi  Y, Davenport  C, Spijker  R, Taylor-Phillips  S, et al.; Cochrane COVID-19 Diagnostic Test Accuracy Group. Antibody tests for identification of current and past infection with SARS-CoV-2. Cochrane Database Syst Rev. 2020;6:CD013652.PubMed
  24. Dados Covid-19 em Porto Alegre [cited 2020 Sep 10]. https://mhbarbian.shinyapps.io/covid19_poa/
  25. Machado  MH, Oliveira  ES, Moyses  NMN. Trends in the health labor market in Brazil. In: Pierantoni C, dal Poz MR, France T, editors. Working in health: quantitative and qualitative approaches. Vol. 1. Rio de Janeiro (Brazil): Center for Studies and Research in Collective Health, State University of Rio de Janeiro; 2011. p. 103–116 [cited 2021 Apr 9]. http://www.ensp.fiocruz.br/observarh/arquivos/TendenciasTrabalho.pdf

Top

Figures
Tables

Top

Suggested citation for this article: Gonçalves MR, Reis RCP, Tólio RP, Pellanda LC, Schmidt MI, Katz N, et al. Social distancing, mask use, and transmission of severe acute respiratory syndrome coronavirus 2, Brazil, April–June 2020. Emerg Infect Dis. 2021 Aug [date cited]. https://doi.org/10.3201/eid2708.204757

DOI: 10.3201/eid2708.204757

Original Publication Date: June 03, 2021

Table of Contents – Volume 27, Number 8—August 2021

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Marcelo Rodrigues Gonçalves, Postgraduate Program in Epidemiology, School of Medicine, Federal University of Rio Grande do Sul, Rua Ramiro Barcelos, 2400, Porto Alegre, Rio Grande do Sul, Brazil

Send To

10000 character(s) remaining.

Top

Page created: May 19, 2021
Page updated: June 16, 2021
Page reviewed: June 16, 2021
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external