Minderhoud Crista A, Postma Amber, Jansen Floor E, Zinkstok Janneke R, Verhoeven Judith S, Berghuis Bianca, Otte Wim M, Jongmans Marian J, Braun Kees P J, Brilstra Eva H
Department of Child Neurology, UMCU Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
Department of Psychiatry, UMCU Brain Center, University Medical Center Utrecht, 3583CX Utrecht, The Netherlands.
Brain Commun. 2024 Aug 26;6(5):fcae285. doi: 10.1093/braincomms/fcae285. eCollection 2024.
This cohort study aims to describe the evolution of disease features and health-related quality of life per life stage in Dravet syndrome and other -related non-Dravet seizure disorders which will enable treating physicians to provide tailored care. Health-related quality of life and disease features were assessed cross-sectionally in participants with a related seizure disorder, categorized per age group for Dravet syndrome, and longitudinally over seven years follow-up (2015-2022). Data were collected from questionnaires, medical records, and semi-structured telephonic interviews. Health-related quality of life was measured with the Paediatric Quality of Life Inventory, proxy-reported for participants with Dravet syndrome and for participants with non-Dravet aged younger than 18 years old and self-reported for participants with non-Dravet over 18 years old. Associations between health-related quality of life and disease features were explored with multivariable regression analyses, cross-sectionally in a cohort of 115 patients with Dravet and 48 patients with generalized epilepsy with febrile seizures plus and febrile seizures (non-Dravet) and longitudinally in a cohort of 52 Dravet patients and 13 non-Dravet patients. In the cross-sectional assessment in 2022, health-related quality of life was significantly lower in Dravet syndrome, compared to non-Dravet and normative controls. Health-related quality of life in the School and Psychosocial domain was significantly higher in older Dravet age groups. A higher health-related quality of life was associated with fewer behavioural problems [ = -1.1; 95% confidence interval (CI), (-1.4 to -0.8)], independent walking ( = 8.5; 95%CI (4.2-12.8)), compared to the use of a wheelchair), and fewer symptoms of autonomic dysfunction ( = -2.1, 95%CI (-3.2 to -1.0)). Longitudinally, health-related quality of life was significantly higher seven years later in the course of disease in Dravet participants (Δ8.9 standard deviation (SD) 18.0, < 0.05), mediated by a lower prevalence of behavioural problems ( = -1.2, 95%CI (-2.0 to -0.4)), lower seizure frequency ( = -0.1, 95%CI (-0.2 to -0.0)) and older age ( = 0.03, 95%CI (0.01-0.04)). In summary, health-related quality of life was significantly higher at older age in Dravet syndrome. This finding may reflect the benefits of an advanced care strategy in recent years and a ceiling of severity of disease symptoms, possibly resulting in an increased wellbeing of parents and patients. The strong association with behavioural problems reinforces the need to incorporate a multidisciplinary approach, tailored to the age-specific needs of this patient group, into standard care.
这项队列研究旨在描述德拉韦综合征及其他相关非德拉韦癫痫性疾病在每个生命阶段的疾病特征演变和健康相关生活质量,这将使治疗医生能够提供个性化护理。对患有相关癫痫性疾病的参与者进行了横断面健康相关生活质量和疾病特征评估,根据德拉韦综合征的年龄组进行分类,并进行了为期七年的纵向随访(2015 - 2022年)。数据通过问卷、病历和半结构化电话访谈收集。使用儿童生活质量量表测量健康相关生活质量,对于德拉韦综合征参与者以及18岁以下的非德拉韦参与者由代理人报告,对于18岁以上的非德拉韦参与者则由其自我报告。通过多变量回归分析探讨了健康相关生活质量与疾病特征之间的关联,横断面分析纳入了115例德拉韦患者以及48例伴有热性惊厥附加症和热性惊厥(非德拉韦)的全身性癫痫患者,纵向分析纳入了52例德拉韦患者和13例非德拉韦患者。在2022年的横断面评估中,与非德拉韦患者和正常对照组相比,德拉韦综合征患者的健康相关生活质量显著更低。在德拉韦年龄较大的年龄组中,学校和心理社会领域的健康相关生活质量显著更高。健康相关生活质量较高与行为问题较少(β = -1.1;95%置信区间(CI),(-1.4至 -0.8))、能够独立行走(β = 8.5;95%CI(4.2 - 12.8),与使用轮椅相比)以及自主神经功能障碍症状较少(β = -2.1,95%CI(-3.2至 -1.0))相关。纵向来看,德拉韦参与者在疾病过程中七年后的健康相关生活质量显著更高(Δ8.9标准差(SD)18.0,P < 0.05),这是由行为问题患病率较低(β = -1.2,95%CI(-2.0至 -0.4))、癫痫发作频率较低(β = -0.1,95%CI(-0.2至 -0.0))以及年龄较大(β = 0.03,95%CI(0.01 - ))介导的。总之,德拉韦综合征患者年龄较大时健康相关生活质量显著更高。这一发现可能反映了近年来先进护理策略的益处以及疾病症状严重程度的上限,可能导致家长和患者的幸福感增加。与行为问题的强烈关联强化了将针对该患者群体特定年龄需求的多学科方法纳入标准护理的必要性。