Background: Our objective was to characterize the education and employment history of young adults with congenital heart defects (CHD) living in the United States.
Methods: The 2016-2019 Congenital Heart Survey To Recognize Outcomes, Needs, and well-beinG collected data from young adults (ages 19-38) with CHD identified from active birth defect in Arkansas, Arizona, and Atlanta, Georgia. Educational attainment, employment history, and special education between kindergarten and 12th grade were self-/proxy-reported. Respondent percentages were standardized to the eligible population by CHD severity, birth year, site, sex, and maternal race/ethnicity and compared by CHD severity using p values from Z-scores. Log-binomial prevalence ratios (aPRs) assessed associations between respondent characteristics and outcomes, adjusting for CHD severity, age group, sex, race/ethnicity, and site. Employment models also adjusted for education. Point estimates were compared to the 2018 American Community Survey (ACS) 5-year general population estimates.
Results: Among 1438 respondents, 28.3% attained ≥ bachelor's degree and 22.1% were unemployed for ≥ 12 months. Estimates were comparable by CHD severity (aPRs ~1.0) and similar to general population estimates (in ACS, 21% attained ≥ bachelor's degree and 26% were unemployed). About 25.3% of adults with CHD received special education, more commonly adults with severe (32.9%) than nonsevere CHD (23.5%, p = 0.01).
Conclusions: Among young adults with CHD, educational attainment and employment did not substantially differ by CHD severity or from general population rates. One in four used special education between kindergarten and 12th grade. Clinical guidelines recommend ongoing educational and vocational support to individuals with CHD as needed so this population continues to thrive.
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http://dx.doi.org/10.1002/bdr2.2452 | DOI Listing |
Front Public Health
March 2025
Orthopedics, Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Objective: To investigate the prevalence of scoliosis and congenital heart disease (CHD) in the same area and to explore the relationship between them according to a joint school screening.
Methods: All students aged 6-15 years in 20 schools in Jinghong City, Yunnan Province, China was screened for scoliosis and CHD. Scoliosis screening completed through the Adam's forward bending test with scoliometer measurement, and CHD screening completed through auscultation combined with portable echocardiography (ECHO).
J Adv Nurs
March 2025
College of Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Aim: To examine the relationship between frailty status, family functioning, and quality of life in adolescents with congenital heart disease (CHD).
Background: Frailty is a rarely assessed health outcome in adolescents. Despite advances in paediatric CHD treatment, potential complications may cause frailty, affecting family dynamics and quality of life.
Front Pediatr
February 2025
Pediatric Cardiology Center, Sichuan Provincial Women's and Children's Hospital/The Affiliated Women's and Children's Hospital of Chengdu Medical College, Chengdu, Sichuan, China.
Objective: This study evaluates the clinical value of α-Hydroxybutyrate Dehydrogenase (α-HBDH), Cardiac Troponin I (cTnI), and B-Type Natriuretic Peptide (BNP) in the perioperative diagnosis of heart failure in children with congenital heart disease (CHD).
Methods: A retrospective analysis was performed on data from 107 children with CHD who underwent surgery between March 2022 and March 2023. Patients were categorized based on the European Society of Cardiology (ESC) cardiac function grading into three groups (Grades I-III) and further into heart failure (HF) and non-HF groups.
Cureus
February 2025
Internal Medicine, Hospital Militar Escuela "Dr. Alejandro Dávila Bolaños", Managua, NIC.
Congenital heart diseases are structural abnormalities of the heart with functional repercussions on the patient's hemodynamics. At the time of diagnosis, most patients are in childhood, and the clinical course exhibits a wide spectrum of severity, ranging from mild conditions that do not affect the quality of life to severe presentations that may lead to death. Under this concept, we present the case of a 45-year-old patient who was diagnosed in childhood with a ventricular septal defect for which he did not receive any treatment or intervention.
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March 2025
Growth Network CrescNet, Leipzig University, 04103, Leipzig, Germany.
Treatment options and therefore general health in children with congenital heart defects (CHD) improved tremendously over the last decades. Growth is an important marker to evaluate healthy development, especially in patients with chronic diseases. This study aimed to evaluate growth in children with CHD compared to their healthy peers.
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