Literature DB >> 28092296

Qualitative Analysis of Parental Observations on Quality of Life in Australian Children with Down Syndrome.

Nada Murphy1, Amy Epstein, Helen Leonard, Elise Davis, Dinah Reddihough, Andrew Whitehouse, Peter Jacoby, Jenny Bourke, Katrina Williams, Jenny Downs.   

Abstract

OBJECTIVE: There are many challenges to health, functioning, and participation for children with Down syndrome; yet, the quality-of-life (QOL) domains important for this group have never been clearly articulated. This study investigated parental observations to identify QOL domains in children with Down syndrome and determined whether domains differed between children and adolescents.
METHODS: The sample comprised 17 families whose child with Down syndrome was aged 6 to 18 years. Primary caregivers took part in semistructured telephone interviews to explore aspects of their child's life that were satisfying or challenging. Qualitative thematic analysis was implemented using a grounded theory framework to identify domains. The coded data set was divided into 2 groups (childhood and adolescence) at 3 age cut points to observe whether differences existed between the coded domains and domain elements: (1) 6 to 11 years with 12 to 18 years; (2) 6 to 13 years with 14 to 18 years; and (3) 6 to 15 years with 16 to 18 years.
RESULTS: Eleven domains were identified: physical health, behavior and emotion, personal value, communication, movement and physical activity, routines and predictability, independence and autonomy, social connectedness and relationships, variety of activities, nature and outdoors, and access to services. No differences in domains and domain elements were identified across childhood and adolescence.
CONCLUSION: Our data form a preliminary framework from which to design investigations of the child's perspectives on life quality and suggest a range of necessary supports and services.

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Mesh:

Year:  2017        PMID: 28092296      PMCID: PMC5285501          DOI: 10.1097/DBP.0000000000000385

Source DB:  PubMed          Journal:  J Dev Behav Pediatr        ISSN: 0196-206X            Impact factor:   2.225


  20 in total

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2.  Development of a condition-specific measure of quality of life for children with cerebral palsy: empirical thematic data reported by parents and children.

Authors:  E Waters; E Maher; L Salmon; D Reddihough; R Boyd
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3.  Patterns of participation and enjoyment in adolescents with Down syndrome.

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Journal:  Res Dev Disabil       Date:  2012-01-11

Review 4.  Quality of life: its definition and measurement.

Authors:  D Felce; J Perry
Journal:  Res Dev Disabil       Date:  1995 Jan-Feb

5.  Conceptualizing a quality of life framework for girls with Rett syndrome using qualitative methods.

Authors:  Amy Epstein; Helen Leonard; Elise Davis; Katrina Williams; Dinah Reddihough; Nada Murphy; Andrew Whitehouse; Jenny Downs
Journal:  Am J Med Genet A       Date:  2015-12-21       Impact factor: 2.802

6.  Variation over time in medical conditions and health service utilization of children with Down syndrome.

Authors:  Kelly Thomas; Jenny Bourke; Sonya Girdler; Ami Bebbington; Peter Jacoby; Helen Leonard
Journal:  J Pediatr       Date:  2011-02       Impact factor: 4.406

7.  Morbidity and medication in a large population of individuals with Down syndrome compared to the general population.

Authors:  Myriam Alexander; Hans Petri; Yingjie Ding; Christoph Wandel; Omar Khwaja; Nadia Foskett
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8.  Problem behavior of individuals with Down syndrome in a nationwide cohort assessed in late adolescence.

Authors:  Helma B M van Gameren-Oosterom; Minne Fekkes; Jacobus P van Wouwe; Symone B Detmar; Anne Marie Oudesluys-Murphy; Paul H Verkerk
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9.  Quality of life of adolescents with cerebral palsy: perspectives of adolescents and parents.

Authors:  Elise Davis; Amy Shelly; Elizabeth Waters; Andrew Mackinnon; Dinah Reddihough; Roslyn Boyd; H Kerr Graham
Journal:  Dev Med Child Neurol       Date:  2009-01-26       Impact factor: 5.449

10.  Development, problem behavior, and quality of life in a population based sample of eight-year-old children with Down syndrome.

Authors:  Helma B M van Gameren-Oosterom; Minne Fekkes; Simone E Buitendijk; Ashna D Mohangoo; Jeanet Bruil; Jacobus P Van Wouwe
Journal:  PLoS One       Date:  2011-07-21       Impact factor: 3.240

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  5 in total

1.  Psychometric properties of the Quality of Life Inventory-Disability (QI-Disability) measure.

Authors:  Jenny Downs; Peter Jacoby; Helen Leonard; Amy Epstein; Nada Murphy; Elise Davis; Dinah Reddihough; Andrew Whitehouse; Katrina Williams
Journal:  Qual Life Res       Date:  2018-11-20       Impact factor: 4.147

2.  Devising a Missing Data Rule for a Quality of Life Questionnaire-A Simulation Study.

Authors:  Peter Jacoby; Andrew Whitehouse; Helen Leonard; Jacinta Saldaris; Scott Demarest; Tim Benke; Jenny Downs
Journal:  J Dev Behav Pediatr       Date:  2022-01-24       Impact factor: 2.988

Review 3.  Family Variables and Quality of Life in Children with Down Syndrome: A Scoping Review.

Authors:  Anna Lee; Kathleen Knafl; Marcia Van Riper
Journal:  Int J Environ Res Public Health       Date:  2021-01-07       Impact factor: 3.390

4.  Parental perspectives on the quality of life of children with Down syndrome.

Authors:  Elisa Fucà; Paolo Galassi; Floriana Costanzo; Stefano Vicari
Journal:  Front Psychiatry       Date:  2022-08-12       Impact factor: 5.435

Review 5.  Care Coordination Needs of Families of Children with Down Syndrome: A Scoping Review to Inform Development of mHealth Applications for Families.

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Journal:  Children (Basel)       Date:  2021-06-29
  5 in total

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