Only 4% of NIH prevention projects target health disparities, revealing a major gap between equity research and real-world implementation.
A growing body of evidence shows that pediatric cardiology remains stuck in the first 2 generations of health equity research—documenting and describing disparities—while few studies have advanced to the intervention stage to work on eliminating these disparities.1
In the words of Keila N. Lopez, MD, MPH, director of transition medicine in pediatric cardiology and associate professor of pediatrics at Baylor College of Medicine, “We talk about lifespan health disparities and that they exist, and then we talk about how they exist, and did you also know that they exist and continue to exist?” Although there is a lot of conversation around social determinants of health, very little third-generation research has been done.
At the American Heart Association (AHA) 2025 Scientific Sessions, Lopez argued that to truly improve access to pediatric cardiovascular care, equity research must be translated into policy action and patient-centered advocacy. Only about 4% of current NIH prevention projects include interventions that specifically target health disparities, Lopez noted, calling this a “huge missed opportunity” to translate knowledge into real-world change.
Keila N. Lopez, MD, MPH | Image credit: Texas Children's Hospital

Lopez argued that equity research must intentionally connect to health policy. Nearly half of all US children are covered through Medicaid or the Children’s Health Insurance Program (CHIP), and recent policy changes threaten to widen coverage gaps.2 States that did not expand Medicaid leave an estimated 1.6 million children without affordable health insurance, and cuts to Medicaid could cause 3 in 10 young adults to lose access to care.1 These changes have direct implications for children with congenital heart disease, whose long-term outcomes depend on continuous coverage and specialist access.
In response to ongoing funding cuts and grant terminations, Lopez encouraged researchers to frame health equity as beneficial to everyone when writing grants, not just the underserved patients they’re trying to target. “That means, when you're writing your grants, when you're doing your proposals, you need to talk about how health equity matters for everyone,” she emphasized. “We already know this. Focus on the everyone part of this to be able to get our grants funded.”
Pediatric cardiology can learn from adult cardiovascular research, Lopez added, which has made greater strides in translating findings into policy. “If we do not figure out how to translate our research to policymakers and figure out ways to speak with them, we will never be able to have a seat at the table,” Lopez warned. “We will never be able to have agency with our patients and with policymakers and have funding for our research.”
Research also shows that financial hardship remains a persistent burden for families navigating pediatric heart disease. In one national survey, about half of families reported economic strain due to medical bills, which frequently resulted in food insecurity and delayed or skipped care.3 Notably, these challenges affected both Medicaid recipients and privately insured families, suggesting that underinsurance in the US can be just as damaging as being uninsured.
At AHA 2025, Lopez called on clinicians to engage in advocacy at every level, including within their own institutions.1 Pediatric cardiologists, she noted, have some of the lowest patient referrals to the Make-A-Wish Foundation—while hematologists and oncologists are referring children at a 76% rate, cardiologists are only referring 33%. Increasing these opportunities for patients and their families can improve well-being and strengthen trust in the health care system beyond the clinic.
“If you're competitive, and I know that you all are because you're pediatric cardiologists, remember this is an opportunity to even just bring advocacy for joy for your patients,” Lopez said. “It’s a small task.”
On a broader level, fostering a culture of advocacy means integrating equity into both research and training. Health equity is now a formal part of pediatric cardiology curricula, but Lopez emphasized that embedding these principles requires everyday practice changes, ensuring interpreter access, accommodating families’ needs, and using research data to shape policy.
To move the field forward, Lopez said every study must consider 2 core questions: does this research improve equity for all patients, and does it have policy potential? Equity-driven research, she emphasized, must be designed to drive system-level change, not simply document persistent gaps.
“Is this research allowing me to then use this platform and the data that will be generated from the research to then speak with a policymaker? If it doesn't, you should consider adding aspects that perhaps will allow for that to happen,” Lopez concluded.
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