“…Although many care guidelines recognize the impact of social needs on pediatric health outcomes, they now need to suggest concrete, evidence-based recommendations about how to change care for children experiencing these barriers and can follow the examples set forth for adult populations with diabetes mellitus and hypertension. 8,9 Using updated guidelines, clinical decision support tools in electronic health records can then combine information from patients' social histories and medical histories to routinely recommend clinical care adjustments, such as lower cost and nonrefrigerated medications or follow-up care that accommodates transportation or digital access barriers, so that all encounters become opportunities to ensure pediatric care meets the needs of families experiencing socioeconomic barriers to health promotion and disease management. 10 Finally, to enable research and facilitate ongoing learning about what interventions lead to better child health, pediatric clinical teams must develop workflows to document both social risks and interventions taken to either reduce or mitigate the impacts of those risks on health.…”