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Data to Save Moms Act
12/15/2023, 4:07 PM
Summary of Bill S 1599
The bill aims to address the rising rates of maternal mortality in the country by requiring states to report data on pregnancy-related deaths to the Centers for Disease Control and Prevention (CDC). This data will be used to identify trends and risk factors associated with maternal mortality, with the ultimate goal of developing strategies to prevent these deaths.
Additionally, the Data to Save Moms Act seeks to improve the quality of data collected by standardizing reporting requirements across states and providing funding for states to implement these requirements. The bill also includes provisions to improve data collection on maternal morbidity, or severe complications related to pregnancy and childbirth. Overall, the Data to Save Moms Act is a bipartisan effort to address the growing crisis of maternal mortality in the United States by improving data collection and analysis. By better understanding the factors contributing to maternal deaths, policymakers and healthcare providers can work towards implementing effective interventions to save the lives of mothers across the country.
Congressional Summary of S 1599
Data to Save Moms Act
This bill expands data collection and research on maternal morbidity and mortality among racial and ethnic minority groups.
Specifically, the bill adds requirements to certain grants awarded by the Centers for Disease Control and Prevention (CDC) for maternal mortality review committees. To the extent practicable, grant-funded committees must
- use the most up-to-date indicators of severe maternal morbidity;
- review deaths caused by suicide, overdose, or other behavioral health conditions attributed to or aggravated by pregnancy or childbirth; and
- consult with representatives of communities disproportionately affected by adverse maternal outcomes about nonclinical factors that may contribute to those outcomes.
The CDC may also award grants to committees to increase their engagement with local communities, such as by bringing on community representatives as committee members.
Additionally, the Centers for Medicare & Medicaid Services and the Agency for Healthcare Research and Quality must consult with stakeholders to review maternal health data collection processes and quality measures and make recommendations to improve them.
The Department of Health and Human Services must also support studies on adverse maternal health outcomes among American Indian and Alaska Native populations and other racial and ethnic minority groups.
