Federal bill targets maternal health data gaps during disease outbreaks

What does this do?

HR 8807 directs $190 million to the CDC and NIH to collect data on pregnancy outcomes during public health emergencies, expand maternal health surveys, review pregnancy-related deaths, and research ways to reduce risks to pregnant people and newborns. The bill requires the government to publish this data publicly and update it at least monthly during an emergency, while protecting individual patient privacy. It also creates a task force to develop official recommendations for safe and respectful maternity care during emergencies, covering topics such as telehealth, mental health screening, access to midwives and doulas, and care for uninsured or undocumented pregnant people.

Who does it affect?

Pregnant women and new mothers nationwide are the primary people affected, with particular focus on Black, Hispanic, Native American, and low-income women who have historically experienced worse health outcomes. Health care providers, midwives, doulas, public health departments, and state and tribal governments would also be involved in carrying out the programs and following the new guidance.

Why does it matter?

Public health emergencies such as disease outbreaks create gaps in data about how pregnancy outcomes are affected, and no standardized federal guidance currently exists for maternity care during those events. The bill would establish data collection systems and care recommendations that could shape how providers, states, and tribes respond to future emergencies affecting pregnant and postpartum people.

What does it cost, and who pays?

• $190M total allocated
• Funds CDC and NIH programs
• Covers data, research, maternal care