Comorbidities and predictors of health-related quality of life in Dravet syndrome: A 10-year, prospective follow-up study

被引:14
|
作者
Makiello, Phoebe [1 ]
Feng, Tony [1 ]
Dunwoody, Benjamin [1 ]
Steckler, Felix [1 ]
Symonds, Joseph [1 ,2 ]
Zuberi, Sameer M. [1 ,2 ]
Dorris, Liam [1 ,2 ]
Brunklaus, Andreas [1 ,2 ,3 ]
机构
[1] Royal Hosp Children, Paediat Neurosci Res Grp, Glasgow, Scotland
[2] Univ Glasgow, Sch Hlth & Wellbeing, Glasgow, Scotland
[3] Royal Hosp Children, Off Block,Zone 2,1345 Govan Rd, Glasgow G51 4TF, Scotland
关键词
comorbidity; Dravet syndrome; HRQOL; SCN1A; severe myoclonic epilepsy of infancy; SMEI; SEVERE MYOCLONIC EPILEPSY; FENFLURAMINE; MORTALITY; COHORT;
D O I
10.1111/epi.17531
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective Dravet syndrome (DS) is a severe developmental and epileptic encephalopathy, leading to reduced health-related quality of life (HRQOL). Prospective outcome data on HRQOL are sparse, and this study investigated long-term predictors of HRQOL in DS.Methods One hundred thirteen families of SCN1A-positive patients with DS, who were recruited as part of our 2010 study were contacted at 10-year follow-up, of which 68 (60%) responded. The mortality was 5.8%. Detailed clinical and demographic information was available for each patient. HRQOL was evaluated with two epilepsy-specific instruments, the Impact of Pediatric Epilepsy Scale (IPES) and the Epilepsy & Learning Disabilities Quality of Life Questionnaire (ELDQOL); a generic HRQOL instrument, the Pediatric Quality of Life Inventory (PedsQL); and a behavioral screening tool, the Strength and Difficulties Questionnaire (SDQ).Results Twenty-eight patients were 10-15 years of age (0-5 years at baseline) and 40 were >= 16 years of age (>= 6 years at baseline). Patients 0- to 5-years-old at baseline showed a significant decline in mean scores on the PedsQL total score (p = .004), physical score (p < .001), cognitive score (p = .011), social score (p = .003), and eating score (p = .030) at follow-up. On multivariate regression, lower baseline and follow-up HRQOL for the whole cohort were associated with worse epilepsy severity and a high SDQ total score (R-2 = 33% and 18%, respectively). In the younger patient group, younger age at first seizure and increased severity of epilepsy were associated with a lower baseline HRQOL (R-2 = 35%). In the older age group, worse epilepsy severity (F = 6.40, p = .016, R-2 = 14%) and the use of sodium-channel blockers were independently associated with a lower HRQOL at 10-year follow-up (F = 4.13, p = .05, R-2 = 8%).Significance This 10-year, prospective follow-up study highlights the significant HRQOL-associated cognitive, social, and physical decline particularly affecting younger patients with DS. Sodium channel blocker use appears to negatively impact long-term HRQOL, highlighting the importance of early diagnosis and disease-specific management in DS.
引用
收藏
页码:1012 / 1020
页数:9
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