Impact of Prolonged Seizures on Patients’ and Caregivers’ Quality of Life (P1-9.014)
Describe experiences of people with epilepsy (PwE) living with prolonged seizures (PS) and their caregivers, identify unmet needs, determine greatest areas of burden, and assess impact on quality of life (QoL).
Authors
- David M. Kaye (ORCID: https://orcid.org/0000-0003-4058-0372)
- Michele Manzo
- J. Eric Piña-Garza
- Cédric Laloyaux
- Tanya Bhatia
- Joseph Sirven
- Shelly Meitzler
- Rebecca Burns
- Andrea Wilkinson
- Susan Linn
- Shalee Cunneen
Institutions
- Epilepsy Foundation (US)
- Children’s Hospital at TriStar Centennial (US)
- TSC Alliance (US)
- Mayo Clinic in Arizona (US)
- Epilepsy Foundation (AU)
- National Patient Safety Foundation (US)
Publication Details
- Journal
- Neurology
- Published
- 2025-04-07
- DOI
- https://doi.org/10.1212/wnl.0000000000210527
- Primary Topic
- Epilepsy research and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00