Abstract 4361336: Exploring Disparities in Pediatric Wolff-Parkinson-White Patients by Race and Ethnicity: Results of a Multicenter Ambispective Registry
Abstract 4361336: Exploring Disparities in Pediatric Wolff-Parkinson-White Patients by Race and Ethnicity: Results of a Multicenter Ambispective Registry
Where did the research take place?
The study site has not been established. Author addresses may differ from where the research occurred.
US · Author affiliation · country only
Cleveland Clinic Children's, Pepper Pike, Ohio, United StatesLocation evidence
Salt Lake City, US · Author affiliation
Primary Children's Hospital, Salt Lake City, Utah, United StatesLocation evidence
New York City, US · Author affiliation
NYU Langone Medical Center, New York, New York, United StatesLocation evidence
Providence, US · Author affiliation
Providence Sacred Heart Children's Hospital, Spokane, Washington, United StatesLocation evidence
Spokane, US · Author affiliation
Providence Sacred Heart Children's Hospital, Spokane, Washington, United StatesLocation evidence
Pittsburgh, US · Author affiliation
Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United StatesLocation evidence
Chicago, US · Author affiliation
Ann&Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United StatesLocation evidence
Ann Arbor, US · Author affiliation
University of Michigan, Ann Arbor, Michigan, United StatesLocation evidence
Omaha, US · Author affiliation
Children's Specialty Physician, Omaha, Nebraska, United StatesLocation evidence
Philadelphia, US · Author affiliation
Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United StatesLocation evidence
Nashville, US · Author affiliation
Vanderbilt University Medical Center, Nashville, Tennessee, United StatesLocation evidence
La Grange, US · Author affiliation
Advocate Children's Hospital, La Grange Park, Illinois, United StatesLocation evidence
Vancouver, CA · Author affiliation
British Columbia, Vancouver, British Columbia, CanadaLocation evidence
IN · Author affiliation · country only
Sri Jayadeva Institute of Cardiovascular Sciences and Research, Kamataka, IndiaLocation evidence
Toronto, CA · Author affiliation
THE HOSPITAL FOR SICK CHILDREN, Toronto, Ontario, CanadaLocation evidence
San Francisco, US · Author affiliation
UCSF Benioff Children's Hosp, San Francisco, California, United StatesLocation evidence
Boise, US · Author affiliation
St Luke's Boise, Boise, Idaho, United StatesLocation evidence
Edmonton, CA · Author affiliation
STOLLERY CHILDRENS HOSPITAL, Edmonton, Alberta, CanadaLocation evidence
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Original abstract
Background: Social determinants of health —including socioeconomic status, race and ethnicity, and access to care—affect health outcomes and contribute to disparities in disease burden and treatment. We sought to describe racial and ethnic differences in pediatric WPW patients (pts), focusing on healthcare utilization, management, and life-threatening events (LTEs) using a multicenter registry. Methods: Data were extracted from the international ambispective WPW registry, which enrolled pts age < 21 years (2017- 2024). Demographics, clinical presentation, ED visits, hospital/ICU admissions, antiarrhythmic use, and EP study (EPS) (transesophageal and/or invasive) were compared by race (White vs. non-White) and ethnicity (Hispanic vs. non-Hispanic). LTEs were defined as sudden death (SD), aborted SD, or pre-excited AF with rapid conduction or hemodynamic instability. Logistic regression model adjusting for age at enrollment was performed to evaluate associations between race and total and invasive EPS rates. Results: 1118 pts from 23 centers were included. Racial distribution was White (87%), Black (6%), Asian (3%), others (1%), and > 1 race (3%). Most pts with reported ethnicity were non-Hispanic (NH) (93%). Compared to White pts, non-White pts were more likely to have congenital heart disease and persistent pre-excitation but less likely to require ICU admission or undergo EPS, including invasive EPS (Table 1). There were no significant racial differences in age at presentation at EPS, symptoms at presentation, hospitalization, antiarrhythmic drug use, or LTEs at presentation or f/u. In logistic regression models adjusting for age at enrollment, race was not significantly associated with invasive EPS (p=0.067). However, White pts were significantly more likely to undergo any EPS than non-White pts (OR 1.82, 95% CI 1.05–3.14). With respect to ethnicity, Hispanic pts underwent EPS at a younger age than NH pts (12.13 vs. 13.28 yrs, p=0.033). There were no other significant management or outcome differences between ethnic groups. Conclusion: Racial disparities in healthcare utilization and management strategies exist among pediatric WPW pts, with non-White pts less likely to undergo any EPS despite higher rates of persistent pre-excitation. Rates of LTE, however, were similar between racial and ethnic groups. Future studies should focus on exploring causes of racial disparities that would inform targeted interventions to promote equitable care.