Find Resources
Emerging Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and produce early results that are consistent with the objectives of the activities and thus indicate effectiveness.
RELEASE DATE:
Summary Report/Recommendations
This paper contains a review of the role of telehealth and digital care solutions, application types, and current COVID-19 policies. The study includes information for medical staff on the potential of digital technologies to provide support during and after the pandemic.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
RELEASE DATE:
Summary Report/Recommendations
This article provides a brief overview of a framework to incorporate data and community engagement into a targeted approach to promote equitable testing and treatment of COVID-19, and to address underlying social determinant of health risks that disproportionately burden racial minority communities.
Emerging Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and produce early results that are consistent with the objectives of the activities and thus indicate effectiveness.
RELEASE DATE:
Summary Report/Recommendations
This report uses preliminary data on COVID-19 mortality rates among Asian Minnesotans. It draws attention to the disproportionate COVID-19 mortality rates among Hmong, Karen, and Karenni residents to demonstrate the critical importance of data disaggregation.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
RELEASE DATE:
Summary Report/Recommendations
To begin bridging the gap in knowledge about COVID-19 risk among sexual minority adults, the Centers for Disease Control and Prevention examined disparities between sexual minority and heterosexual adults in the prevalence of underlying conditions with strong or mixed evidence of associations with severe COVID-19-related illness, by using data from the 2017–2019 Behavioral Risk Factor Surveillance System (BRFSS). Collecting data on sexual orientation in COVID-19 surveillance and other studies would improve knowledge about disparities in infection and adverse outcomes by sexual orientation, thereby informing more equitable responses to the pandemic.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
RELEASE DATE:
Summary Report/Recommendations
This report highlights how disaggregating Native Hawaiian, Pacific Islander, and Asian race data can aid in identifying racial disparities among specific subpopulations, and highlights the importance of partnering with communities to develop culturally responsive outreach teams, and tailored public health interventions, and vaccination campaigns to more effectively address health disparities.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
RELEASE DATE:
Summary Report/Recommendations
This article documents the efforts of the Native Hawaiian and Pacific Islander COVID-19 Response, Recovery, and Resilience Team, a partnership of academic, government, and community organizations. Their goal was to analyze the utilization, public reporting, and quality of race and ethnicity health data to inform policy changes and promote equity. Through this partnership, the group created solutions for issues such as aggregation of Native Hawaiians and Pacific Islanders in health data, how data is reported through the health department, and discussions with testing labs and health institutions to create more standardized race and ethnicity data.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
RELEASE DATE:
Summary Report/Recommendations
This article explores how the relationships between vaccine site density, vaccination rates, and social vulnerability are connected across metropolitan and non-metropolitan areas in the U.S. The study uses CDC Social Vulnerability Index data combined with vaccination site density data to examine how vaccination site placement can benefit highly vulnerable populations. The results determined that while areas with higher socioeconomic vulnerability contain a large density of vaccination sites, this does not affect the low vaccination rates found in these communities. Other methods besides vaccination site placement must be considered to overcome these barriers in vaccination rates.
Novel Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and are in the process of generating evidence of effectiveness or may not yet be tested.
RELEASE DATE:
Summary Report/Recommendations
This article shows efforts of six grant-funded regional partners to create a usable public health analytic system to address health inequities among COVID-19 positive cases on an individual patient level. The article highlights the many challenges of this Multistate Data Strategy, including lack of standardization across data sources, missing data fields, and different state-level reporting requirements. However, the ability to produce this analytic system in real time, including a standardized COVID-19 data dictionary, demonstrates the necessity for healthcare administrators to utilize deidentified patient-level data in order to provide better care for state residents, particularly in disadvantaged communities.