Literature DB >> 20478692

Self and proxy rating of quality of life in adults with intellectual disabilities: results from the DISQOL study.

Silke Schmidt1, Mick Power, Ann Green, Ramona Lucas-Carrasco, Erhan Eser, Eva Dragomirecka, Marcello Fleck.   

Abstract

The aim of this study was to analyze the agreement between self and proxy reports of quality of life (QoL) in people with intellectual disabilities and to examine the factors which contribute to these differences. The study was conducted across six international centres in a sample of 614 adults with intellectual disabilities as well as two different samples of proxies (N=874) including both professional carers and relatives. QoL was assessed with the disability version of the WHOQOL-BREF. In both proxy samples results show a significant moderate association between the persons' QoL-assessment and the assessment of their proxies in all of the five QoL domains. There were significant mean differences in most items which varied in their direction. In general, people with disabilities rated their QoL higher than their proxies except for two items from the physical domain. The factors which most significantly contributed to these differences were proxy knowledge of the person as well as the WHODAS-disability score. Cross-cultural differences in the magnitude of concordance were observed. As a conclusion, the study shows a good agreement between the person-proxy QoL-assessments, and that the factors associated with disagreement are limited in this study. Future studies should elaborate the stability of concordance over time. Copyright (c) 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20478692     DOI: 10.1016/j.ridd.2010.04.013

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


  7 in total

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Authors:  Roslyn A Prichard; Fei-Li Zhao; Julee Mcdonagh; Stephen Goodall; Patricia M Davidson; Phillip J Newton; Ben Farr-Wharton; Christopher S Hayward
Journal:  Qual Life Res       Date:  2021-01-02       Impact factor: 4.147

2.  Meeting the 24-h movement guidelines and health-related outcomes among youth with autism spectrum disorder: a seven-country observational study.

Authors:  Chunxiao Li; Justin A Haegele; Fenghua Sun; Maria Luiza Tanure Alves; Stefanie Hwee Chee Ang; Jihyun Lee; Kwok Ng; Isabella Dos Santos Alves; Sean Healy; Wendy Yajun Huang; Pauli Rintala; Jernice Sing Yee Tan; Yandan Wu; Hannah Yang; Eija Kärnä; Hyokju Maeng; André Lisandro Schliemann; Ding Ding
Journal:  Child Adolesc Psychiatry Ment Health       Date:  2022-06-23       Impact factor: 7.494

3.  The factors associated with care-related quality of life of adults with intellectual disabilities in England: implications for policy and practice.

Authors:  Stacey Rand; Juliette Malley
Journal:  Health Soc Care Community       Date:  2016-04-24

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Authors:  Stacey Rand; James Caiels; Grace Collins; Julien Forder
Journal:  Health Qual Life Outcomes       Date:  2017-05-19       Impact factor: 3.186

5.  Capturing the complexity of healthcare for people with Down syndrome in quality indicators - a Delphi study involving healthcare professionals and patient organisations.

Authors:  Francine A van den Driessen Mareeuw; Antonia M W Coppus; Diana M J Delnoij; Esther de Vries
Journal:  BMC Health Serv Res       Date:  2020-07-27       Impact factor: 2.655

6.  Perceptions of people with mild intellectual disability and their family members about family-based social capital in the Netherlands.

Authors:  Sanne A H Giesbers; Alexander H C Hendriks; Richard P Hastings; Andrew Jahoda; Tess Tournier; Petri J C M Embregts
Journal:  Health Soc Care Community       Date:  2021-05-12

7.  Is it feasible to assess self-reported quality of life in individuals who are deaf and have intellectual disabilities?

Authors:  Johannes Fellinger; Magdalena Dall; Joachim Gerich; Maria Fellinger; Katharina Schossleitner; William Joseph Barbaresi; Daniel Holzinger
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2020-09-14       Impact factor: 4.328

  7 in total

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