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1.
J Child Neurol ; 22(2): 143-50, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-17621474

RESUMEN

The medical, educational, and psychosocial outcomes of 3224 subjects (age range, 7-33 years; mean age, 20.06 years; SD, 5.74) diagnosed and treated in the Institute for Child Development in Tel Aviv between the years 1975 and 1994 were assessed by a telephone interview. Results indicate that only 9% of the subjects are seriously disabled, and 8% are mentally retarded. Over the years, subjects were referred to the Child Development Center at an increasingly younger age, probably reflecting greater professional and parental awareness of the importance of early intervention. The nature of interventions changed, so that physiotherapy, occupational therapy, and psychological guidance were more often provided. While more children were referred to special education at kindergarten, the percentage of those graduating from regular schools has increased. Most completed 12 years of schooling and successfully acquired full or partial matriculation certificates. As adults, most function independently; fulfill civic obligations, such as their army service; are fully employed; and express satisfaction with their life. These results suggest that children with developmental disabilities who receive early intervention are likely to be functionally independent and to be satisfied with their lives, although they continue to need medical services and require some government support. Further studies are essential to examine the correlation of specific risk factors and early interventions with outcome.


Asunto(s)
Adaptación Psicológica , Discapacidades del Desarrollo/epidemiología , Discapacidades del Desarrollo/psicología , Vigilancia de la Población , Adolescente , Adulto , Distribución de Chi-Cuadrado , Niño , Demografía , Escolaridad , Femenino , Estado de Salud , Humanos , Estudios Longitudinales , Masculino , Reproducibilidad de los Resultados , Estudios Retrospectivos , Encuestas y Cuestionarios , Teléfono
2.
J Child Neurol ; 25(1): 36-42, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19502577

RESUMEN

Cerebral palsy, typically diagnosed in childhood, clearly continues into adulthood. This study describes the long-term medical, functional, educational, and psychosocial outcomes of people with cerebral palsy. Of the 203 people with cerebral palsy diagnosed and treated at the Child Development Center in Tel Aviv between 1975 and 1994, 163 (80%; age range 8-30 years, mean age 18.9 years, and median age 19 years) participated in a cross-sectional telephone survey. Half the respondents have chronic health problems: 78% report they experience gross motor disability, of whom 22% are wheelchair users; 30% to 50% need help in various activities of daily living; 35% have mental retardation; 79% completed 12 years or more of schooling; 78% live with their parents; 25% have served in the army; 23% have a driver's license; and 23% work in competitive employment. The large majority is involved in varied leisure activities and report a high level of life satisfaction.


Asunto(s)
Parálisis Cerebral/epidemiología , Actividades Cotidianas , Adolescente , Adulto , Conducción de Automóvil , Parálisis Cerebral/complicaciones , Parálisis Cerebral/psicología , Niño , Estudios de Cohortes , Discinesias/epidemiología , Discinesias/etiología , Escolaridad , Empleo , Femenino , Estudios de Seguimiento , Estado de Salud , Vivienda , Humanos , Discapacidad Intelectual/epidemiología , Discapacidad Intelectual/etiología , Masculino , Padres , Veteranos , Silla de Ruedas , Adulto Joven
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