WASHINGTON, D.C. – U.S. Senator Tammy Baldwin has joined a group of Democrats in the Senate and House to reintroduce the bicameral Equitable Data Collection and Disclosure on COVID-19 Act. The bill would require the Department of Health and Human Services (HHS) to collect and report racial and other demographic data on COVID-19 testing, treatment, vaccination, and fatality rates and use all available surveillance systems to post daily updates on the CDC website showing data disaggregated by race, ethnicity, sex, age, socioeconomic status, disability status, county, and other demographic information.
“Health disparities have contributed to higher rates of COVID-19 cases and deaths in communities of color. In particular, the pandemic has disproportionately impacted the Black and Latinx communities. This legislation will require the CDC to collect and publicly release all demographic data on COVID-19 testing, treatment, hospitalizations and deaths, so we can learn more and provide the resources necessary to combat the spread of this virus and better support underserved communities in Wisconsin and across this country,” said Senator Baldwin.
From the beginning of this pandemic, Black, brown, and American Indian/Alaska Native (AI/AN) people in the United States have suffered the largest burden of illness, hospitalization and death from COVID19. The Centers for Disease Control and Prevention (CDC) reports that AI/AN people are nearly four times as likely as white people to be hospitalized for COVID-19, and that Black and Hispanic/Latino people are about twice as likely to die of COVID-19 as white people. Nonetheless, significant gaps in data reporting remain. Even a year into the pandemic, race and ethnicity data is available for only half (51%) of COVID-19 cases.
Specifically, the Equitable Data Collection and Disclosure on COVID-19 Act would require the reporting of the following data disaggregated by race, ethnicity, sex, age, socioeconomic status, disability status, county, and other demographic information:
It would also authorize $50 million in emergency supplemental funding to HHS to conduct or support data collection on the racial and ethnic implications of COVID-19, including supporting capacity building in state and local health departments to collect and transmit racial and ethnic data. Finally, it creates a Commission on Ensuring Data for Health Equity to provide guidance on how to better collect and analyze demographic data in responding to future public health emergencies.
The legislation is led by Senator Elizabeth Warren (D-MA) and Representatives Ayanna Pressley (D-MA), Barbara Lee (D-CA), Robin Kelly (D-IL), and Karen Bass (D-CA). In addition to Senator Baldwin, the legislation is co-sponsored by Senators Richard Blumenthal (D-CT), Cory Booker (D-NJ), Tim Kaine (D-VA) Amy Klobuchar (D-MN), Edward J. Markey (D-MA), Jeff Merkley (D-OR), Jacky Rosen (D-NV), Debbie Stabenow (D-MI), Chris Van Hollen (D-MD), and Ron Wyden (D-OR), and Representatives Adriano Espaillat (D-NY), Brenda L. Lawrence (D-MI), Gregory W. Meeks (D-NY), Val B. Demings (D-FL), Alexandria Ocasio-Cortez (D-NY), Dwight Evans (D-PA), Rashida Tlaib (D-MI), Bonnie Watson Coleman (D-NJ), Grace Meng (D-NY), Lisa Blunt Rochester (D-DE), Kweisi Mfume (D-MD), Henry C. "Hank" Johnson (D-GA), Yvette D. Clarke (D-NY), and Diana DeGette (D-CO).
The Equitable Data Collection and Disclosure on COVID-19 Act is endorsed by the National Birth Equity Collaborative, Seattle Indian Health Board, and National Council of Urban Indian Health.