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Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two
PURPOSE: To examine children’s health-related quality of life and parents’ satisfaction with life and explore the association between the two in families where a child has a rare disorder. METHODS: We used a cross-sectional study design. A questionnaire was sent to parents of 439 school children (6–...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844436/ https://www.ncbi.nlm.nih.gov/pubmed/24010895 http://dx.doi.org/10.1186/1477-7525-11-152 |
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author | Johansen, Heidi Dammann, Brede Andresen, Inger-Lise Fagerland, Morten Wang |
author_facet | Johansen, Heidi Dammann, Brede Andresen, Inger-Lise Fagerland, Morten Wang |
author_sort | Johansen, Heidi |
collection | PubMed |
description | PURPOSE: To examine children’s health-related quality of life and parents’ satisfaction with life and explore the association between the two in families where a child has a rare disorder. METHODS: We used a cross-sectional study design. A questionnaire was sent to parents of 439 school children (6–18 years) with congenital rare disorders. Children’s health-related quality of life (HRQOL) was examined by Pediatric Quality of Life Inventory(TM) 4.0 (PedsQL) Norwegian version. Satisfaction with life was examined by Satisfaction with Life Scale (SWLS). RESULTS: The response rate was 48% (n = 209). The average age of the children was 12 years and 50% were girls. The parents scored their children with reduced physical, emotional, social and school functioning. The reductions were greatest in the physical area. Parents scored average to high on SWLS but significantly lower than the general Norwegian population. There was a positive association between parental SWLS and the children’s social functioning and school functioning. CONCLUSION: Children with congenital, rare disorders often require assistance from many parts of the public service system. Caring for their physical needs should not conflict with their educational and social needs. It is important that the children’s school-life is organized so that the diagnosis does not interfere with the children’s education and social life more than necessary. |
format | Online Article Text |
id | pubmed-3844436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38444362013-12-02 Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two Johansen, Heidi Dammann, Brede Andresen, Inger-Lise Fagerland, Morten Wang Health Qual Life Outcomes Research PURPOSE: To examine children’s health-related quality of life and parents’ satisfaction with life and explore the association between the two in families where a child has a rare disorder. METHODS: We used a cross-sectional study design. A questionnaire was sent to parents of 439 school children (6–18 years) with congenital rare disorders. Children’s health-related quality of life (HRQOL) was examined by Pediatric Quality of Life Inventory(TM) 4.0 (PedsQL) Norwegian version. Satisfaction with life was examined by Satisfaction with Life Scale (SWLS). RESULTS: The response rate was 48% (n = 209). The average age of the children was 12 years and 50% were girls. The parents scored their children with reduced physical, emotional, social and school functioning. The reductions were greatest in the physical area. Parents scored average to high on SWLS but significantly lower than the general Norwegian population. There was a positive association between parental SWLS and the children’s social functioning and school functioning. CONCLUSION: Children with congenital, rare disorders often require assistance from many parts of the public service system. Caring for their physical needs should not conflict with their educational and social needs. It is important that the children’s school-life is organized so that the diagnosis does not interfere with the children’s education and social life more than necessary. BioMed Central 2013-09-08 /pmc/articles/PMC3844436/ /pubmed/24010895 http://dx.doi.org/10.1186/1477-7525-11-152 Text en Copyright © 2013 Johansen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Johansen, Heidi Dammann, Brede Andresen, Inger-Lise Fagerland, Morten Wang Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title | Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title_full | Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title_fullStr | Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title_full_unstemmed | Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title_short | Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
title_sort | health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844436/ https://www.ncbi.nlm.nih.gov/pubmed/24010895 http://dx.doi.org/10.1186/1477-7525-11-152 |
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