Literature DB >> 29571933

Disparities in Access to Healthcare Transition Services for Adolescents with Down Syndrome.

James Nugent1, Gregory Gorman2, Christine R Erdie-Lalena3.   

Abstract

OBJECTIVE: To compare healthcare transition planning in adolescents with Down syndrome with adolescents with other special healthcare needs. STUDY
DESIGN: Data were drawn from the 2009-2010 National Survey of Children with Special Health Care Needs, a nationally representative sample with 17 114 adolescents aged 12-17 years. Parents were asked whether providers and the study child had discussed shifting to an adult provider, changing healthcare needs, maintaining health insurance coverage, and taking responsibility for self-care. The transition core outcome was a composite measure based on the results of these 4 questions. Multivariable logistic regression determined the association between Down syndrome and the transition core outcome as well as each of the 4 individual component measures.
RESULTS: Although 40% of adolescents with other special healthcare needs met the transition core outcome, 11.0% of adolescents with Down syndrome met this outcome. Adolescents with Down syndrome were less likely to be encouraged to take responsibility for their health (32.2% vs 78.4%). After adjustment for demographic, socioeconomic, and health-related factors, adolescents with Down syndrome had 4 times the odds of not meeting the transition core outcome. For the component measures, Down syndrome adolescents had 4 times the odds of not being encouraged to take responsibility for self-care. Medical home access increased the odds of transition preparation.
CONCLUSIONS: Adolescents with Down syndrome experience disparities in access to transition services. Provider goals for adolescents with Down syndrome should encourage as much independence as possible in their personal care and social lives.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Trisomy 21; adolescence; children with special healthcare needs; medical home; transition to adulthood

Mesh:

Year:  2018        PMID: 29571933     DOI: 10.1016/j.jpeds.2018.01.072

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  7 in total

1.  Description of Daily Living Skills and Independence: A Cohort from a Multidisciplinary Down Syndrome Clinic.

Authors:  Kavita Krell; Kelsey Haugen; Amy Torres; Stephanie L Santoro
Journal:  Brain Sci       Date:  2021-07-30

2.  Global, Regional, and National Burden and Trends of Down Syndrome From 1990 to 2019.

Authors:  Liyuan Chen; Lifei Wang; Yi Wang; Haishan Hu; Yuan Zhan; Zhilin Zeng; Lidan Liu
Journal:  Front Genet       Date:  2022-07-15       Impact factor: 4.772

3.  Destination unknown: Parents and healthcare professionals' perspectives on transition from paediatric to adult care in Down syndrome.

Authors:  Vincent J T Peters; Levinus A Bok; Lieke de Beer; Joyce J M van Rooij; Bert R Meijboom; Jan Erik H Bunt
Journal:  J Appl Res Intellect Disabil       Date:  2022-06-05

Review 4.  Disparities and outcomes of patients living with Down Syndrome undergoing healthcare transitions from pediatric to adult care: A scoping review.

Authors:  Karan Varshney; Rosemary Iriowen; Kayla Morrell; Preshon Pillay; Alexander Fossi; Mary M Stephens
Journal:  Am J Med Genet A       Date:  2022-06-10       Impact factor: 2.578

5.  Demographic and Clinical Characteristics Associated With Adherence to Guideline-Based Polysomnography in Children With Down Syndrome.

Authors:  Philip D Knollman; Christine H Heubi; Susan Wiley; David F Smith; Sally R Shott; Stacey L Ishman; Jareen Meinzen-Derr
Journal:  Otolaryngol Head Neck Surg       Date:  2020-09-15       Impact factor: 5.591

Review 6.  Care Coordination Needs of Families of Children with Down Syndrome: A Scoping Review to Inform Development of mHealth Applications for Families.

Authors:  Beth Skelton; Kathleen Knafl; Marcia Van Riper; Louise Fleming; Veronica Swallow
Journal:  Children (Basel)       Date:  2021-06-29

7.  Opportunities, barriers, and recommendations in down syndrome research.

Authors:  James A Hendrix; Angelika Amon; Leonard Abbeduto; Stamatis Agiovlasitis; Tarek Alsaied; Heather A Anderson; Lisa J Bain; Nicole Baumer; Anita Bhattacharyya; Dusan Bogunovic; Kelly N Botteron; George Capone; Priya Chandan; Isabelle Chase; Brian Chicoine; Cécile Cieuta-Walti; Lara R DeRuisseau; Sophie Durand; Anna Esbensen; Juan Fortea; Sandra Giménez; Ann-Charlotte Granholm; Laura J Hahn; Elizabeth Head; Hampus Hillerstrom; Lisa M Jacola; Matthew P Janicki; Joan M Jasien; Angela R Kamer; Raymond D Kent; Bernard Khor; Jeanne B Lawrence; Catherine Lemonnier; Amy Feldman Lewanda; William Mobley; Paul E Moore; Linda Pollak Nelson; Nicolas M Oreskovic; Ricardo S Osorio; David Patterson; Sonja A Rasmussen; Roger H Reeves; Nancy Roizen; Stephanie Santoro; Stephanie L Sherman; Nasreen Talib; Ignacio E Tapia; Kyle M Walsh; Steven F Warren; A Nicole White; Guang William Wong; John S Yi
Journal:  Transl Sci Rare Dis       Date:  2021-04-15
  7 in total

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