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Health-related quality of life of Canadian children and youth prenatally exposed to alcohol
BACKGROUND: In Canada, the incidence of Fetal Alcohol Spectrum Disorder (FASD) has been estimated to be 1 in 100 live births. Caused by prenatal exposure to alcohol, FASD is the leading cause of neuro-developmental disabilities among Canadian children, and youth. Objective: To measure the health-rel...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1617087/ https://www.ncbi.nlm.nih.gov/pubmed/17040571 http://dx.doi.org/10.1186/1477-7525-4-81 |
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author | Stade, Brenda C Stevens, Bonnie Ungar, Wendy J Beyene, Joseph Koren, Gideon |
author_facet | Stade, Brenda C Stevens, Bonnie Ungar, Wendy J Beyene, Joseph Koren, Gideon |
author_sort | Stade, Brenda C |
collection | PubMed |
description | BACKGROUND: In Canada, the incidence of Fetal Alcohol Spectrum Disorder (FASD) has been estimated to be 1 in 100 live births. Caused by prenatal exposure to alcohol, FASD is the leading cause of neuro-developmental disabilities among Canadian children, and youth. Objective: To measure the health-related quality of life (HRQL) of Canadian children and youth diagnosed with FASD. METHODS: A prospective cross-sectional study design was used. One-hundred and twenty-six (126) children and youth diagnosed with FASD, aged 8 to 21 years, living in urban and rural communities throughout Canada participated in the study. Participants completed the Health Utilities Index Mark 3 (HUI3). HUI3 measures eight health attributes: vision, hearing, speech, ambulation, dexterity, emotion, cognition, and pain. Utilities were used to measure a single cardinal value between 0 and 1.0 (0 = all-worst health state; 1 = perfect health) to reflect the global HRQL for that child. Mean HRQL scores and range of scores of children and youth with FASD were calculated. A one-sample t-test was used to compare mean HRQL scores of children and youth with FASD to those from the Canadian population. RESULTS: Mean HRQL score of children and youth with FASD was 0.47 (95% CI: 0.42 to 0.52) as compared to a mean score of 0.93 (95% CI: 0.92 to 0.94) in those from the general Canadian population (p < 0.001). Children demonstrated moderate to severe dysfunction on the single-attributes of cognition and emotion. CONCLUSION: Children and youth with FASD have significantly lower HRQL than children and youth from the general Canadian population. This finding has significant implications for practice, policy development, and research. |
format | Text |
id | pubmed-1617087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16170872006-10-19 Health-related quality of life of Canadian children and youth prenatally exposed to alcohol Stade, Brenda C Stevens, Bonnie Ungar, Wendy J Beyene, Joseph Koren, Gideon Health Qual Life Outcomes Research BACKGROUND: In Canada, the incidence of Fetal Alcohol Spectrum Disorder (FASD) has been estimated to be 1 in 100 live births. Caused by prenatal exposure to alcohol, FASD is the leading cause of neuro-developmental disabilities among Canadian children, and youth. Objective: To measure the health-related quality of life (HRQL) of Canadian children and youth diagnosed with FASD. METHODS: A prospective cross-sectional study design was used. One-hundred and twenty-six (126) children and youth diagnosed with FASD, aged 8 to 21 years, living in urban and rural communities throughout Canada participated in the study. Participants completed the Health Utilities Index Mark 3 (HUI3). HUI3 measures eight health attributes: vision, hearing, speech, ambulation, dexterity, emotion, cognition, and pain. Utilities were used to measure a single cardinal value between 0 and 1.0 (0 = all-worst health state; 1 = perfect health) to reflect the global HRQL for that child. Mean HRQL scores and range of scores of children and youth with FASD were calculated. A one-sample t-test was used to compare mean HRQL scores of children and youth with FASD to those from the Canadian population. RESULTS: Mean HRQL score of children and youth with FASD was 0.47 (95% CI: 0.42 to 0.52) as compared to a mean score of 0.93 (95% CI: 0.92 to 0.94) in those from the general Canadian population (p < 0.001). Children demonstrated moderate to severe dysfunction on the single-attributes of cognition and emotion. CONCLUSION: Children and youth with FASD have significantly lower HRQL than children and youth from the general Canadian population. This finding has significant implications for practice, policy development, and research. BioMed Central 2006-10-13 /pmc/articles/PMC1617087/ /pubmed/17040571 http://dx.doi.org/10.1186/1477-7525-4-81 Text en Copyright © 2006 Stade 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 Stade, Brenda C Stevens, Bonnie Ungar, Wendy J Beyene, Joseph Koren, Gideon Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title | Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title_full | Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title_fullStr | Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title_full_unstemmed | Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title_short | Health-related quality of life of Canadian children and youth prenatally exposed to alcohol |
title_sort | health-related quality of life of canadian children and youth prenatally exposed to alcohol |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1617087/ https://www.ncbi.nlm.nih.gov/pubmed/17040571 http://dx.doi.org/10.1186/1477-7525-4-81 |
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