Behavior problems and health-related quality of life in Dravet syndrome

被引:53
作者
Sinoo, Claudia [1 ]
de Lange, Iris Marie-Louise [1 ]
Westers, Paul [2 ]
Gunning, Willem Boudewijn [3 ]
Jongmans, Marian Jacqueline [4 ,5 ]
Brilstra, Eva Henriette [1 ]
机构
[1] Univ Utrecht, Dept Med Genet, Univ Med Ctr Utrecht, Utrecht, Netherlands
[2] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] Stichting Epilepsie Instellingen Nederland, Zwolle, Netherlands
[4] Univ Utrecht, Dept Child Family & Educ Studies, Utrecht, Netherlands
[5] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Neonatol, Utrecht, Netherlands
关键词
Dravet syndrome; Epilepsy; SCN1A; Behavior problems; Health-related quality of life; Cognitive impairment; SEVERE MYOCLONIC EPILEPSY; INTELLECTUAL DISABILITY; PEDIATRIC EPILEPSY; SCN1A MUTATIONS; DOWN-SYNDROME; CHILDREN; COMORBIDITIES; SATISFACTION; MANAGEMENT; DIAGNOSIS;
D O I
10.1016/j.yebeh.2018.11.029
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Objective: Behavior problems in Dravet syndrome (DS) are common and can impact the lives of patients tremendously. The current study aimed to give more insight into (1) the prevalence of a wide range of specific behavior difficulties and aspects of health-related quality of life (HRQoL) in patients with DS compared with the general population (gp) and patients with epilepsy without DS. (2) the relations between these behavior problems and different aspects of HRQoL, and (3) the associations between seizure frequency, cognitive impairment (CI), behavior problems, and HRQoL, based on a conceptual model. Methods: One hundred and sixteen patients (aged between 2 and 67 years), affected by SCN1A-related seizures, were included in the study. Eighty-five were patients with DS, 31 were patients with epilepsy without DS. Behavior problems were measured using the Child/Adult Behavior Checklist (C/ABCL), HRQoL was measured using the Pediatric Quality of Life Inventory (PedsQL) Measurement Model. Other characteristics were obtained by clinical assessments, medical records, and semi-structured telephone interviews with parents. Comparisons between patients with DS, patients without DS, and the gp were calculated by the exact goodness of fit chi(2) analyses, relations between subscales were analyzed using Pearson's correlations, and the conceptual model was tested in a path analysis. Results: (1) Patients with DS show significantly more behavior problems compared with the gp and patients with epilepsy without DS. A total of 56.5% of patients with DS scored in the borderline and clinical ranges for total behavior problems. Problems with attention were most prevalent; 62.3% of patients with DS scored in the borderline and clinical ranges. Health-related quality of life was significantly lower for patients with DS compared with the gp and patients without DS. Physical and social functioning scores were especially low and decreased even more in the older age categories. (2) Problems with attention, aggression, and withdrawn behavior were most related to social functioning. Somatic problems and anxiety/depression were most related to emotional functioning. (3) Cognitive impairment and behavior problems were both independent predictors of poorer HRQoL in patients with DS, with behavior problems being the strongest predictor. Seizure frequency was only indirectly related to HRQoL, mediated by cognitive impairment. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:217 / 227
页数:11
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