Abstract 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 SCN1A­-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 SCN1A-related seizure disorder, categorized per age group for Dravet syndrome, and longitudinally over seven years follow-up (2015-2022). Data was collected from questionnaires, medical records, and semi-structured telephonic interviews. Health-related quality of life was measured with the Pediatric 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 Dravet patients 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 less behavioral problems (β=-1.1, 95% confidence interval(CI) (-1.4 to -0.8)), independent walking (β=8.5, 95%CI(4.2 to 12.8)), compared to use of a wheelchair) and fewer symptoms of autonomic dysfunction (β=-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, p&amp;lt;0.05), mediated by a lower prevalence of behavioral problems (β=-1.2, 95%CI(-2.0 to -0.4)), lower seizure frequency (β=-0.1, 95%CI(-0.2 to -0.0)) and older age (β=0.03, 95%CI(0.01 to 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 behavioral problems reinforces the need to incorporate a multidisciplinary approach, tailored to the age-specific needs of this patient group, into standard care.

Quality of life in SCN1A-related seizure disorders across the lifespan