| Literature DB >> 32500288 |
Laura M Gaydos1, Kristin Sommerhalter2, Cheryl Raskind-Hood3, Olushola Fapo2, George Lui4, Daphne Hsu5, Alissa Van Zutphen2,6, Jill Glidewell7, Sherry Farr7, Fred H Rodriguez8, Trenton Hoffman3, Wendy Book8.
Abstract
With increasing survival trends for children and adolescents with congenital heart defects (CHD), there is a growing need to focus on transition from pediatric to adult specialty cardiac care. To better understand parental perspectives on the transition process, a survey was distributed to 451 parents of adolescents with CHD who had recent contact with the healthcare system in Georgia (GA) and New York (NY). Among respondents, 90.7% reported excellent, very good or good health-related quality of life (HRQoL) for their adolescent. While the majority of parents (77.8%) had been told by a provider about their adolescent's need to transition to adult specialty cardiac care, most reported concerns about transitioning to adult care. Parents were most commonly concerned with replacing the strong relationship with pediatric providers (60.7%), locating an appropriate adult provider (48.7%), and accessing adult health insurance coverage (43.6%). These findings may offer insights into transition planning for adolescents with CHD.Entities:
Keywords: CHD; Cardiology; Congenital; Heart defects; Transition
Mesh:
Year: 2020 PMID: 32500288 PMCID: PMC9109153 DOI: 10.1007/s00246-020-02378-z
Source DB: PubMed Journal: Pediatr Cardiol ISSN: 0172-0643 Impact factor: 1.838