First Place Winner
Policy Memo: Lowering Preventable Maternal Deaths in Rural Georgia
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Gabrielle Delima (1), Amanda Engstrom (2), Emily Michels (3), Jay Qiu (4)
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Keywords: maternal mortality; rural; Certified Nurse Midwives (CNM); tax credit; preventive care
Executive Summary: Georgia’s maternal mortality rate (MMR) is one of the highest in the U.S. and shows few signs of improvement, despite government intervention. Women living in rural areas are exposed to significantly higher risk than their urban counterparts and have reduced access to life-saving health care. 60% of Georgia’s maternal deaths are preventable, however the lack of available providers—especially in rural areas—makes it hard to address these avoidable issues. As such, we propose an amendment to the Georgia legal code that would allow Certified Nurse Midwives (CNM) to practice independently, removing unnecessary restrictions on the low-risk and routine care that they are trained to provide. This change could lower systemic and individual health care costs while allowing an existing workforce to augment preventive care efforts.
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References
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Gabrielle Delima is a 4th year graduate student in the Microbiology and Molecular Genetics program at Emory University. She uses reverse genetics to map genetic determinants underlying influenza A virus gene expression as it pertains to host adaptation. After earning her PhD, Gabrielle plans to pursue a career in science policy and outreach.
Amanda Engstrom just received her PhD in Biochemistry and Cell Biology from Emory University. Her research focused on the mechanism of neuronal cell death in Alzheimer’s disease and other related dementias. She will continue her research as a post- doctoral fellow. In addition to scientific research, Amanda is interested in science policy, STEM outreach, and being part of innovative mechanisms to communicate science to general audiences.
Emily Michels operates as a liaison between science, tech, and policy, working to educate policymakers and companies on the importance of ethical and scientifically sound internal and external policies. After working as a health policy analyst in Colorado, she received her Masters of Bioethics from Emory University in May 2020 with focuses on the ethics of HIV genetic sequencing-based interventions, community engagement, and artificial intelligence in health care.
Jay Qiu is a genetic counseling student in the Emory Genetic Counseling Training Program. His research is focused on the public’s opinion and understanding of the limitations of direct-to-consumer genetic testing. He has an active interest in science and health policy and is passionate about the implementation of genomic research into clinical practice.
Acknowledgements
The authors would like to acknowledge the Emory Science Advocacy Network (EScAN) at Emory University especially Alyssa Scott, Erin King, Julia de Amorim, and Emily Hill for their comments on this publication.
Disclaimer
The authors disclose that they have no conflict of interest in this form.
Amanda Engstrom just received her PhD in Biochemistry and Cell Biology from Emory University. Her research focused on the mechanism of neuronal cell death in Alzheimer’s disease and other related dementias. She will continue her research as a post- doctoral fellow. In addition to scientific research, Amanda is interested in science policy, STEM outreach, and being part of innovative mechanisms to communicate science to general audiences.
Emily Michels operates as a liaison between science, tech, and policy, working to educate policymakers and companies on the importance of ethical and scientifically sound internal and external policies. After working as a health policy analyst in Colorado, she received her Masters of Bioethics from Emory University in May 2020 with focuses on the ethics of HIV genetic sequencing-based interventions, community engagement, and artificial intelligence in health care.
Jay Qiu is a genetic counseling student in the Emory Genetic Counseling Training Program. His research is focused on the public’s opinion and understanding of the limitations of direct-to-consumer genetic testing. He has an active interest in science and health policy and is passionate about the implementation of genomic research into clinical practice.
Acknowledgements
The authors would like to acknowledge the Emory Science Advocacy Network (EScAN) at Emory University especially Alyssa Scott, Erin King, Julia de Amorim, and Emily Hill for their comments on this publication.
Disclaimer
The authors disclose that they have no conflict of interest in this form.
DISCLAIMER: The findings and conclusions published herein are solely attributed to the author and not necessarily endorsed or adopted by the Journal of Science Policy and Governance. Articles are distributed in compliance with copyright and trademark agreements.
ISSN 2372-2193
ISSN 2372-2193
