期刊论文详细信息
Brain Sciences
The Impact of Health and Social Services on the Quality of Life in Families of Adults with Autism Spectrum Disorder (ASD): A Focus Group Study
Aldina Venerosi1  Marta Borgi1  Francesca Cirulli1  Barbara Trimarco2  Maurizio Ferraro2  Cinzia Correale2  Fiorenzo Laghi3 
[1] Center for Behavioral Sciences and Mental Health, Istituto Superiore di Sanità, 00161 Rome, Italy;Cooperativa Sociale Agricola Integrata «Giuseppe Garibaldi», 00179 Rome, Italy;Department of Developmental and Social Psychology, Sapienza University of Rome, 00185 Rome, Italy;
关键词: autism spectrum disorders;    parents;    health;    social;    services;    quality of life model;   
DOI  :  10.3390/brainsci12020177
来源: DOAJ
【 摘 要 】

Background: Autism spectrum disorder (ASD) is a complex developmental condition that affects the whole family. The gap between childrens’ needs and their satisfaction, especially regarding what concerns the presence of social and healthcare services, is still a source of burden, particularly after the transition to adulthood. Our study aimed to gather a comprehensive view on how parents of adults with ASD perceive (and interact with) health and social services, and how the provision of care impacts family quality of life with the aim to advise ASD intervention programs. The goal is to identify specific areas of change useful to influence autism intervention strategies so that they more effectively meet the needs of young people with autism and their families. Methods: We conducted two focus groups with parents of young adults with ASD. A semi-structured focus group methodology was adopted. The QoL conceptual framework guided data collection and analysis as part of a directed theory-driven content analysis approach. Results: The lack of structured care pathways and the low level of integration of different services were the main limits reported by parents during the focus group, while a shared positive perception of the experience conducted together as caring families emerged. Conclusions: The experience here reported claims for a greater role of the institutions in order to facilitate the building of networks that are really inclusive for persons with autism in society and to support the implementation of innovative solutions for the welfare system. Furthermore, parents stressed the need for the provision of support to the family.

【 授权许可】

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