Public and population health evidence helps us understand how we deliver and integrate services that affect the health of communities, and how we promote healthy communities.
As our blog series has highlighted, the removal of public health data has impeded research and has serious implications for the scientific enterprise. In response, several crowdsourcing efforts have emerged in an imperfect effort to fill the gap.
Research nominated as the best abstract for each theme from the 2025 Call for Abstracts explores topics related to how prepared hospitals are for the next pandemic, gender differences in primary care physician earnings and outcomes, and methods for decomposing heterogeneous treatment effects.
The first installment of our blog series on open data highlights its critical role in driving public health and scientific research and explores the threats it faces despite longstanding bipartisan support to make federally-funded data freely available to the public.
One of the key datasets for maternal and child health, The Pregnancy Risk Assessment Monitoring System (PRAMS), has been taken offline and there is uncertainty if it will be made accessible again. The continuation of PRAMS, either at the federal or state level, is necessary to monitor and improve maternal and child health outcomes.
AHRQ's research and implementation support improves the health of all communities. Given the recent changes and reductions in force at HHS, it is imperative that the work to improve care at the local level continues.
AHRQ pioneers initiatives that break down barriers to care and improve health for rural Americans. Given the recent announcement on the reorganization of HHS, we’re highlighting AHRQ’s crucial role in rural health care.
AcademyHealth, in partnership with Econometrica and Family Voices, launch a new project to develop a prioritized research agenda to build the evidence needed to optimize school-based mental health services for children and youth with special health care needs (CYSHCN). This project is funded through the Eugene Washington PCORI Engagement Award Program, an initiative of the Patient-Centered Outcomes Research Institute® (PCORI®) (#EASCS-38921).
As lead clinicians for their states with responsibility for overseeing clinical care and stewardship of resources, Medicaid Medical Directors propose policy recommendations to ensure equitable access to cell and gene therapies.
Reflections on the past 10 years of state-university partnerships reaffirm that SUPLN members’ commitment to deepening connections, embracing improved data analytics, and promoting evidence-based policymaking will remain strong.
State-university partnerships create opportunities for early career researchers to engage in impactful, data-driven policy work that would be difficult to achieve through traditional academic paths alone.
