Content area
Objective
To assess the burden of Dravet syndrome (DS) and Lennox–Gastaut syndrome (LGS), including managing seizure and nonseizure symptoms, on patients and caregivers.
Methods
Data were drawn from the Adelphi Real World DS and LGS Disease Specific Programme™, a cross‐sectional survey in Asia (China, Japan), Europe (France, Germany, Italy, Spain, United Kingdom), and the United States of America between July 2022 and August 2023. Neurologists/pediatric neurologists reported demographics, clinical characteristics, and nonseizure symptoms for up to 10 consecutively consulting patients. Caregivers provided data on patient nonseizure symptoms, quality of life (QoL), satisfaction with treatment, and caregiver burden. Analyses were descriptive.
Results
Physicians (
Significance
In this study, considerable burden in DS and LGS management and care was driven by nonseizure symptoms, suggesting a need for treatments that manage the broad spectrum of disease symptoms.
Plain Language Summary
We asked doctors and caregivers to tell us about the symptoms that patients with Dravet syndrome and Lennox–Gastaut syndrome have. We asked how the symptoms affect the lives of the patients as well as the caregivers. We found that seizures have a big impact on the health and well‐being of patients and caregivers. We also found that other symptoms not caused by seizures have a big impact on patients and their caregivers.
Details
; Villanueva, Vicente 2
; Dlugos, Dennis 3
; Benitez, Arturo 1
; Taylor, Yasmin 4
; Olsen, Stevie 4
; Connolly, Hannah 4
; Lai, Sophie 4
; Andrews, J. Scott 1
1 Takeda Development Center Americas, Inc., Cambridge, Massachusetts, USA
2 Hospital Universitario y Politécnico La Fe, Valencia, Spain, Member of ERN EpiCARE,
3 The Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA
4 Adelphi Real World, Bollington, UK