What do parents expect from a genetic diagnosis of their child with intellectual disability?

被引:9
作者
Dikow, Nicola [1 ]
Moog, Ute [1 ]
Karch, Stephanie [2 ]
Sander, Anja [3 ]
Kilian, Samuel [3 ]
Blank, Rainer [4 ]
Reuner, Gitta [2 ]
机构
[1] Heidelberg Univ, Inst Human Genet, Heidelberg, Germany
[2] Univ Childrens Hosp, Clin 1, Sect Neuropediat & Inborn Errors Metab, Heidelberg, Germany
[3] Heidelberg Univ, Inst Med Biometry & Informat, Heidelberg, Germany
[4] Ctr Child Neurol & Social Pediat Maulbronn, Maulbronn, Germany
关键词
genetic diagnosis; intellectual disability; parental expectations; quality of life; DEVELOPMENTAL-DISABILITIES; INDIVIDUALS; UNCERTAINTY; MOTHERS; IMPACT; ADOLESCENTS; DISORDERS; VALIDITY; YIELD; DELAY;
D O I
10.1111/jar.12602
中图分类号
G44 [教育心理学];
学科分类号
0402 ; 040202 ;
摘要
Background Caring for a child with intellectual disability (ID) has been associated with increased social and psychological burdens. Diagnostic and prognostic uncertainty may enhance emotional stress in families. Method The present authors assessed the motivations, expectations, mental health, physical health and the quality of life of 194 parents whose children with intellectual disability were undergoing a genetic diagnostic workup. Results Most parents considered a diagnosis highly relevant for their own emotional relief, their child's therapies and education, or family planning. Parental mental health was significantly lower compared with the normative sample, but physical health was not different. The severity of the child's intellectual disability correlated negatively with their parents' mental and physical health, quality of life, and positively with parental anxiety. Conclusion Healthcare providers should be aware of the disadvantages facing families with intellectually disabled children. Receiving practical, social and psychological support as well as genetic testing might be particularly relevant for families with severely disabled children.
引用
收藏
页码:1129 / 1137
页数:9
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