69 research outputs found
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-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
Understanding discrepancies in parent-child reporting of emotional and behavioural problems: Effects of relational and socio-demographic factors
<p>Abstract</p> <p>Background</p> <p>Discrepancies between parents and children in their assessment of children's mental health affect the evaluation of need for services and must be taken seriously. This article presents the differences between parents' and children's reports of the children's symptoms and social impairment, based on the results of the Strengths and Difficulties Questionnaire (SDQ). The interrelationship between relational aspects and socio-demographic factors with patterns of disagreement are explored.</p> <p>Methods</p> <p>Differences in the prevalence and means of SDQ symptom and impact scores were obtained from 8,154 primary school children, aged between 10 and 13 years, and their parents. Agreement between matched pairs was measured using Pearson's and Spearman's rho correlations. Socio-demographic variables, communication patterns and parental engagement were analysed as possible correlates of informant discrepancies using bivariate and multivariate logistic regression models.</p> <p>Results</p> <p>In general, although children reported more symptoms, they reported less impact of perceived difficulties than parents. The parents were more consistent in their evaluation of symptoms and impact than were the children. Exploration of highly discrepant subgroups showed that, when children reported the most symptoms and impact, qualitative aspects of the parent-child relationship and family structure seemed to be more powerful predictors of disagreement than were gender of the child and socio-demographic variables. When parents reported the most symptoms and impact, low parental educational level, low income and male gender of the child played an additional role.</p> <p>Conclusions</p> <p>Our findings underline the importance of paying attention to child reports of emotional-behavioural difficulties, particularly when parents do not identify these problems. Considerations on what meaning parent-child discrepancy might have in the context of the parent-child relationship or the family's psychosocial status should be integrated in the overall understanding of the child's situation and subsequent recommendations.</p
ADHD in girls and boys – gender differences in co-existing symptoms and executive function measures
Concordância de informações de adolescentes e suas mães em inquérito de saúde
OBJETIVO: Estimar o grau de concordância entre informações obtidas de trabalhadores adolescentes e suas mães em inquérito de saúde. MÉTODOS: Os dados provêm de inquérito populacional, de base domiciliar, conduzido com amostra aleatória de superfície de residentes da área urbana de Salvador, capital do Estado da Bahia. A amostra compõe-se de 82 pares de adolescentes trabalhadores de 10 a 14 anos de idade e suas mães. Após entrevista com os adolescentes, numa outra visita, suas mães foram convidadas a responder um questionário similar por um entrevistador cego. Sintomas respiratórios, depressivos, alterações do padrão do sono e problemas na vizinhança e na escola foram as variáveis analisadas. O grau de concordância foi estimado com proporções de acordo e Índice Kappa. RESULTADOS: Estimativas de acordo foram, em geral, baixas, com as mães fornecendo mais freqüentemente respostas positivas que os adolescentes, determinando vieses negativos, ou seja, estimativas menores, caso os resultados se baseassem no informante. A confiabilidade foi mais elevada entre os meninos em comparação com as meninas, para todas variáveis exceto para alterações do padrão de sono. Para sintomas depressivos, o nível de escolaridade da mãe se associou negativamente com o grau de concordância. CONCLUSÕES: Informações obtidas de adolescentes diferem das obtidas de suas mães. Baixas concordâncias não equivalem a um problema de validade, que deverá ser avaliada em estudos futuros para essa população
The Diagnostic Interview for Children and Personality Inventory for Children in Studies of Children at Risk for Anxiety Disorders or Depression
DOES IT PAY TO DISCHARGE THE CHRONIC PATIENT? A 2 YEAR FOLLOW-UP OF 338 CHRONIC PATIENTS
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