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Volume 27, Number 9—September 2021
Dispatch

A Community-Adapted Approach to SARS-CoV-2 Testing for Medically Underserved Populations, Rhode Island, USA

Author affiliations: The Rhode Island Public Health Institute, Providence, Rhode Island, USA (M. Murphy, C. Sutten Coats, Y. Malyuta, E. Adams, T. Arnold, P.A. Chan, A. Nunn); Brown University, Providence (M. Murphy, I. Dhrolia, J. Tao, P.A. Chan, A. Nunn); The Miriam Hospital, Providence (A. Zanowick-Marr, S. Napoleon, P.A. Chan)

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Abstract

We developed a testing program for severe acute respiratory syndrome coronavirus 2 in an urban Latinx neighborhood in Providence, Rhode Island, USA. Approximately 11% of Latinx participants (n = 180) tested positive. Culturally tailored, community-based programs that reduce barriers to testing help identify persons at highest risk for coronavirus disease.

As of May 2021, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had infected >154 million globally and caused >3.2 million deaths (1). The United States accounts for ≈21% of coronavirus disease (COVID-19) cases and related deaths worldwide (1). Vaccines are a highly effective transmission prevention tool. However, SARS-CoV-2 testing, contact tracing, and quarantining are among the few effective prevention measures available to the public that are proven to reduce transmission in the setting of variable vaccine availability and uptake (2). The COVID-19 disease burden has disproportionately affected Black and Latinx populations in the United States (3,4). These health disparities in racial and ethnic minority populations are driven by complex social and structural factors, such as a paucity of health services, absence of culturally tailored services, and economic barriers that affect adherence to quarantine guidelines (5,6). These disparities have been further compounded by fragmented SARS-CoV-2 testing policies in the United States, which have not prioritized testing for medically underserved racial and ethnic minority communities (2).

Rhode Island experienced high rates of SARS-CoV-2 infection early in the pandemic and has been recognized for expanding testing early across the state (5). Policies in Rhode Island evolved in tandem with the pandemic and availability of testing supplies. In April 2020, faced with limited testing supplies and healthcare personnel, officials in Rhode Island restricted SARS-CoV-2 testing to prescheduled appointments for symptomatic persons with recent travel histories (7,8). By June, testing recommendations in Rhode Island had evolved to include populations considered at high risk for COVID-19, and the state has since maintained one of the highest per capita testing rates in the United States (7,8). However, most testing locations required appointments and were limited to symptomatic patients, and services were not offered in most urban communities, where infection rates were highest.

As seen elsewhere in the United States, the Latinx community in Rhode Island has been disproportionately affected by COVID-19 (9). The Latinx community constitutes just 14% of the population in Rhode Island; the most represented countries and territories are Mexico (35%), Cuba (29%), Spain (11.7%), and Puerto Rico (8.9%). However, the Latinx community accounts for 38% of positive SARS-CoV-2 tests and 33% of COVID-19–related hospitalizations in the state (1,8).

The Study

In June 2020, to respond to the unmet need for culturally tailored SARS-CoV-2 testing services, we opened a multilingual, community-based site for testing by PCR in Providence, Rhode Island (7). This program was supported by the Rhode Island Department of Health. We partnered with a local community cultural center to develop a culturally tailored model for SARS-CoV-2 testing in urban neighborhoods with large numbers of Latinx residents and high rates of COVID-19 infection. The cultural center was a well-known space for community gatherings, artist performances, and religious services. The testing site was staffed by trained medical personnel including clinical providers and volunteers. We designed the testing model to accept all walk-ins; offer drive-through and walk-up testing; provide onsite access to bilingual testing services in English, Spanish, and Portuguese (with additional language services provided by tele-interpretation); offer patients multiple modalities for accessing test results (in person, by telephone, postal mail, or online portal for patients with email addresses); provide testing regardless of insurance status, provider referral, in-state residency, or clinical manifestation; and forego out-of-pocket costs. We also worked with Latinx community leaders to promote our testing program on Latinx radio, Facebook, and other social media; conducted outreach to sexual and gender minority communities on social media platforms; and partnered with established community resources (e.g., cultural centers, churches) to promote testing by word of mouth. All persons who underwent testing were required to provide their legal name and date of birth, proof of identity and address (e.g., state identification card, utility bill, bank statement, etc.), contact information (i.e., address, phone number), and insurance information if applicable. We did not collect information related to immigration or in-state residency status to avoid introducing perceived barriers to testing. A healthcare provider at our facility contacted every person who tested positive for SARS-CoV-2 as soon as results were available. Patients were then connected with available support services, such as food and housing resources. The Department of Health also contacted patients to support additional transmission prevention activities.

During June 8–August 8, 2020, a total of 498 persons in the community underwent testing at this site; 40% of the sample identified as Latinx. Approximately ≈5% of all persons (Table 1) and 11% of Latinx participants were SARS-CoV-2–positive, compared with a statewide positive rate of 2%–3% (10). Furthermore, although 40% of the sample self-identified as Latinx, Latinx persons constituted 80% of positive case-patients. Latinx persons had 7 times higher odds of testing positive (crude odds ratio [OR] 7.03, 95% CI 2.58–19.19) than did non-Latinx persons (Table 2).

Figure 1

Geographic distribution of 498 persons tested for severe acute respiratory syndrome coronavirus 2 by Rhode Island Public Health Institute staff, Rhode Island, USA, June 8–August 8, 2020. Color scale indicates number of persons tested by ZIP code. Five patients had unknown ZIP codes and 16 were from out of state.

Figure 1. Geographic distribution of 498 persons tested for severe acute respiratory syndrome coronavirus 2 by Rhode Island Public Health Institute staff, Rhode Island, USA, June 8–August 8, 2020. Color scale indicates...

Figure 2

Geographic distribution of 28 persons receiving a positive test result for severe acute respiratory syndrome coronavirus 2 from testing performed by Rhode Island Public Health Institute staff during June 8–August 8, 2020. Color scale indicates number of persons testing positive by ZIP code. One patient had an unknown ZIP code.

Figure 2. Geographic distribution of 28 persons receiving a positive test result for severe acute respiratory syndrome coronavirus 2 from testing performed by Rhode Island Public Health Institute staff during June 8–August...

Although we designed our program to respond to unmet need for urban SARS-CoV-2 testing, it attracted persons from throughout the city of Providence and the state of Rhode Island (Figure 1). However, the greatest number of positive SARS-CoV-2 tests were from persons who lived in the surrounding ZIP codes (Figure 2), a geographic area experiencing high rates of community transmission.

Only 39% of all patients in this sample were men, but they represented 59% of all COVID-19 cases. Being male was associated with 2.96 times higher odds of testing positive (crude OR 2.96, 95% CI 1.28–6.84). Sexual minorities accounted for ≈40% of the sample, and gender minorities accounted for 12% of the sample. However, sexual and gender minorities had far lower rates of COVID-19 infection; 90% of persons who tested positive for SARS-CoV-2 were cisgender and heterosexual.

Conclusions

Our experience suggests that SARS-CoV-2 testing models that reduce barriers to care can successfully reach medically underserved communities that have high rates of COVID-19 infection. Culturally tailored approaches might be critical for identifying Latinx populations unaware of their SARS-CoV-2 infection (10). Not requiring health insurance or physician orders for testing, not charging payment, and offering walk-up and drive-through testing enabled widespread participation in our testing program. Offering multiple means of bilingual communication, including text, phone, email, traditional mail, and an online portal, also enabled communication with otherwise hard-to-reach patients. Although our findings are notable, they would be strengthened by an increased sample size to better characterize differences observed in the study population. Our outreach strategies were effective, but additional efforts in future initiatives could further improve testing outreach.

Our program provides a useful framework for reducing barriers to SARS-CoV-2 testing services in underserved communities, including sexual and gender minorities and Latinx populations who otherwise might not be tested for SARS-CoV-2. Perhaps the greatest challenge to replicating and sustaining this model is developing a viable funding model. Despite our program’s success in enabling testing for persons at elevated risk for COVID-19, the human and financial resources needed to maintain this testing site design might limit its ability to be implemented in resource-limited environments. The need for culturally tailored testing programs will continue even as vaccination programs are enacted across the country. Currently, reimbursement-based and traditional medical service delivery models often operate at a financial loss; greater public funding support is needed to sustain culturally tailored, low-barrier testing models that address ethnic and racial disparities in SARS-CoV-2 infection.

Dr. Murphy is medical director of The Rhode Island Public Health Institute’s Open Door Health Clinic (an LGBTQ+-focused primary care clinic in inner-city Providence), and an assistant professor of medicine at Brown University. His research focuses on linkage to community-based HIV prevention, including access to preexposure prophylaxis, for medically underserved populations.

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Acknowledgment

This research was supported in part by National Institutes of Health/National Institute of Allergy and Infectious Diseases grant R25AI140490 and National Institutes of Health/National Institute of General Medical Sciences grant U54GM115677.

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References

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  7. National Governors Association. Rhode Island—coronavirus state actions. 2020 Mar 9 [cited 2020 Sep 11]. https://www.nga.org/coronavirus-state-actions/rhode-island/
  8. Johns Hopkins Coronavirus Resource Center. Impact of opening and closing decisions by state: a look at how social distancing measures have influenced trends in COVID-19 cases and deaths in Rhode Island [cited 2020 Dec 11]. https://coronavirus.jhu.edu/data/state-timeline/new-confirmed-cases/rhode-island
  9. Macias Gil  R, Marcelin  JR, Zuniga-Blanco  B, Marquez  C, Mathew  T, Piggott  DA. COVID-19 pandemic: disparate health impact on the Hispanic/Latinx population in the United States. J Infect Dis. 2020;222:15925. DOIPubMedGoogle Scholar
  10. Rhode Island Department of Health (RIDOH). COVID-19 Rhode Island data [cited 2020 Dec 11]. https://docs.google.com/spreadsheets/d/1c2QrNMz8pIbYEKzMJL7Uh2dtThOJa2j1sSMwiDo5Gz4/edit#gid=31350783

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Cite This Article

DOI: 10.3201/eid2709.204874

Original Publication Date: August 05, 2021

Table of Contents – Volume 27, Number 9—September 2021

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Amy Nunn, Rhode Island Public Health Institute, 7 Central St, Providence, RI 02907, USA

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Page created: June 23, 2021
Page updated: August 18, 2021
Page reviewed: August 18, 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.
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