Takeaways
- A structured, system-wide clinical pathway increased pediatric lipid screening rates from 36% to 69% in less than 18 months.
- Screening improvements were greater in the 9–11-year age group than in older adolescents.
- Multimodal quality improvement approaches—including EHR prompts and clinician engagement—may further close screening gaps.
Universal lipid screening for children and adolescents improved markedly following implementation of a system-based clinical pathway, according to new findings presented at the 2025 American Heart Association Scientific Sessions.1
Pediatric dyslipidemias are among the most treatable causes of cardiovascular disease (CVD). Early detection of lipid abnormalities allows for timely management to reduce future CVD risk. The National Heart, Lung, and Blood Institute (NHLBI) Expert Panel guidelines, issued in 2011, recommend universal lipid screening for children aged 9 to 11 years and again at 17 to 21 years. Selective screening is advised for younger children beginning at age 2 years if there is a family history of early cardiovascular disease, familial hypercholesterolemia, obesity, hypertension, diabetes, or other risk factors such as chronic kidney disease or inflammatory disorders.2
Despite these recommendations, screening rates remain suboptimal in the United States. According to contemporary estimates, fewer than half of children and adolescents receive lipid screening. To address this gap, researchers from Nemours Children’s Health in Wilmington, Delaware, developed a quality improvement initiative aimed at increasing adherence to screening recommendations within their health system.1
“The SMART aim was to increase lipid screening rates in children and adolescents seen within a primary care network from 36% to 80% within 12 months,” the authors stated.
A multidisciplinary team of preventive cardiologists, primary care leadership, and improvement specialists collaborated across 38 clinics in three states to design and implement a standardized clinical pathway. The pathway included universal lipid panel screening for all eligible patients, targeted screening for those with positive familial hypercholesterolemia questionnaires or risk factors, and clear management guidance for abnormal results. The team employed plan-do-study-act (PDSA) cycles to test and refine interventions and used statistical process control charts to monitor outcomes and identify meaningful variation over time.