Literature DB >> 20796162

Employment impact and financial burden for families of children with fragile X syndrome: findings from the National Fragile X Survey.

L Ouyang1, S Grosse, M Raspa, D Bailey.   

Abstract

BACKGROUND: The employment impact and financial burden experienced by families of children with fragile X syndrome (FXS) has not been quantified in the USA.
METHOD: Using a national fragile X family survey, we analysed data on 1019 families with at least one child who had a full FXS mutation. Out-of-pocket expenditures related to fragile X were reported. We used logistic regression to examine the role of insurance, number of affected children, and number of total co-occurring conditions in predicting the financial burden and employment impact of FXS, while adjusting for race, education, marital status and other sociodemographic predictors.
RESULTS: Almost half of families affected by FXS reported that they had experienced an increased financial burden and nearly 60% stated that they had had to change work hours or stop work because of FXS. Families with health insurance that met family needs were significantly less likely to report an excess financial burden. The type of insurance (private or public) was not associated with the reported financial burden. Affected children's mutation status, especially male children with the full mutation, was associated with employment impact. The total number of co-occurring conditions was associated with both financial burden and employment impact.
CONCLUSIONS: Families affected by FXS experienced a significant employment impact and financial burden. Policies designed to help families with FXS need to take into consideration the dimension of co-occurring conditions.
© 2010 The Authors. Journal of Intellectual Disability Research © 2010 Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2010        PMID: 20796162     DOI: 10.1111/j.1365-2788.2010.01320.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  15 in total

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2.  Use of state administrative data sources to study adolescents and young adults with rare conditions.

Authors:  J A Royer; J W Hardin; S McDermott; L Ouyang; J R Mann; O D Ozturk; J Bolen
Journal:  J Gen Intern Med       Date:  2014-08       Impact factor: 5.128

3.  A comparison of family financial and employment impacts of fragile X syndrome, autism spectrum disorders, and intellectual disability.

Authors:  Lijing Ouyang; Scott D Grosse; Catharine Riley; Julie Bolen; Ellen Bishop; Melissa Raspa; Donald B Bailey
Journal:  Res Dev Disabil       Date:  2014-04-20

Review 4.  Public Health Literature Review of Fragile X Syndrome.

Authors:  Melissa Raspa; Anne C Wheeler; Catharine Riley
Journal:  Pediatrics       Date:  2017-06       Impact factor: 7.124

5.  The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views.

Authors:  Colin Reilly; Lelia Murtagh; Joyce Senior
Journal:  J Genet Couns       Date:  2015-01-19       Impact factor: 2.537

6.  The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia.

Authors:  Emma K Baker; Sheena Arora; David J Amor; Perrin Date; Meagan Cross; James O'Brien; Chloe Simons; Carolyn Rogers; Stephen Goodall; Jennie Slee; Chris Cahir; David E Godler
Journal:  J Autism Dev Disord       Date:  2021-07-22

7.  The economic burden of fragile x syndrome: healthcare resource utilization in the United States.

Authors:  Patricia Sacco; Gorana Capkun-Niggli; Xin Zhang; Rosemary Jose
Journal:  Am Health Drug Benefits       Date:  2013-03

8.  Caregiver Burden in Fragile X Families.

Authors:  Ana-Maria Iosif; Andres F Sciolla; Khyati Brahmbhatt; Andreea L Seritan
Journal:  Curr Psychiatry Rev       Date:  2013-02-01

9.  Biobehavioral composite of social aspects of anxiety in young adults with fragile X syndrome contrasted to autism spectrum disorder.

Authors:  Jane E Roberts; Jordan E Ezell; Amanda J Fairchild; Jessica Klusek; Angela J Thurman; Andrea McDuffie; Leonard Abbeduto
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2018-10-11       Impact factor: 3.568

10.  Caregiver opinions about fragile X population screening.

Authors:  Donald B Bailey; Ellen Bishop; Melissa Raspa; Debra Skinner
Journal:  Genet Med       Date:  2011-09-13       Impact factor: 8.822

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