Education and employment as young adults living with spina bifida transition to adulthood in the USA: A study of the National Spina Bifida Patient Registry.


Journal

Developmental medicine and child neurology
ISSN: 1469-8749
Titre abrégé: Dev Med Child Neurol
Pays: England
ID NLM: 0006761

Informations de publication

Date de publication:
06 2023
Historique:
revised: 06 10 2022
received: 31 01 2022
accepted: 12 10 2022
pmc-release: 01 06 2024
medline: 10 5 2023
pubmed: 18 11 2022
entrez: 17 11 2022
Statut: ppublish

Résumé

To describe the education and employment transition experience of young adults with spina bifida (YASB) and investigate factors associated with employment. We queried education and employment data from the US National Spina Bifida Patient Registry from 2009 to 2019. We applied generalized estimating equations models to analyze sociodemographic and disease-related factors associated with employment. A total of 1909 participants (850 males, 1059 females) aged 18 to 26 years contributed 4379 annual visits. Nearly 84% had myelomeningocele and, at last visit, the median age was 21 years (mean 21 years 5 months, SD 2 years 10 months). A total of 41.8% had at least some post-high school education, and 23.9% were employed. In a multivariable regression model, employment was significantly associated with education level, lower extremity functional level, bowel continence, insurance, and history of non-shunt surgery. This large, national sample of YASB demonstrated low rates of post-secondary education attainment and employment and several potentially modifiable factors associated with employment. Specific sociodemographic, medical, and functional factors associated with employment are important for clinicians to consider when facilitating transition for YASB into adulthood. Additional research is needed to understand the impact of cognitive functioning and social determinants of health on transition success in YASB. There were low education attainment and employment rates in a large sample of young adults with spina bifida. Specific sociodemographic, medical, and functional factors are associated with employment. Some employment-associated factors, such as continence and self-management skills, are modifiable.

Identifiants

pubmed: 36385606
doi: 10.1111/dmcn.15456
pmc: PMC10415865
mid: NIHMS1917385
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

821-830

Subventions

Organisme : ACL HHS
ID : U01DD001279
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001268
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001279
Pays : United States
Organisme : ACL HHS
ID : U01DD001093
Pays : United States
Organisme : ACL HHS
ID : U01DD001062
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001057
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001275
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001237
Pays : United States
Organisme : ACL HHS
ID : U01DD001057
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD000738
Pays : United States
Organisme : ACL HHS
ID : U01DD001065
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001280
Pays : United States
Organisme : ACL HHS
ID : U01DD001235
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001235
Pays : United States
Organisme : ACL HHS
ID : U01DD001268
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD000742
Pays : United States
Organisme : ACL HHS
ID : U01DD001275
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001082
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001093
Pays : United States
Organisme : ACL HHS
ID : U01DD001240
Pays : United States
Organisme : ACL HHS
ID : U01DD001262
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001278
Pays : United States
Organisme : ACL HHS
ID : U01DD001270
Pays : United States
Organisme : ACL HHS
ID : U01DD001274
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD000740
Pays : United States
Organisme : ACL HHS
ID : U01DD001266
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD000774
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001265
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001062
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001240
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001274
Pays : United States
Organisme : ACL HHS
ID : U01DD001280
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001262
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001270
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001065
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD000743
Pays : United States
Organisme : ACL HHS
ID : U01DD001237
Pays : United States
Organisme : ACL HHS
ID : U01DD001272
Pays : United States
Organisme : ACL HHS
ID : U01DD001265
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001266
Pays : United States
Organisme : NCBDD CDC HHS
ID : U01 DD001272
Pays : United States
Organisme : ACL HHS
ID : U01DD001278
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Published 2022. This article is a U.S. Government work and is in the public domain in the USA.

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Auteurs

Tiebin Liu (T)

Birth Defects Monitoring and Research Branch, Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Lijing Ouyang (L)

Birth Defects Monitoring and Research Branch, Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

William O Walker (WO)

Division of Developmental Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
University of Washington School of Medicine, Seattle, Washington, USA.

John S Wiener (JS)

Division of Urology, Duke University Medical Center, Durham, North Carolina, USA.

Jason Woodward (J)

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Jonathan Castillo (J)

Division of Developmental Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.

Hadley M Wood (HM)

Cleveland Clinic, Glickman Urological and Kidney Institute, Cleveland, Ohio, USA.

Stacy T Tanaka (ST)

Department of Urology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Richard Adams (R)

University of Texas Southwestern Medical Center; Scottish Rite for Children, Dallas, Texas, USA.

Kathryn A Smith (KA)

Children's Hospital Los Angeles, Los Angeles, California, USA.
Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Joseph O'Neil (J)

Riley Hospital for Children, Indianapolis, Indiana, USA.

Tonya R Williams (TR)

Birth Defects Monitoring and Research Branch, Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Elisabeth A Ward (EA)

Birth Defects Monitoring and Research Branch, Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Universal Consulting Services, Inc, Consultant to Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Robin M Bowman (RM)

Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.

Catharine Riley (C)

Birth Defects Monitoring and Research Branch, Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

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Classifications MeSH