Health-related quality of life and unmet needs of people with epilepsy and their family caregivers: A systematic scoping review

Introduction: People with epilepsy can experience limitations in their everyday lives due to their condition, impacting on health-related quality of life (HRQOL). We synthesized evidence on HRQOL and unmet needs in adult people with epilepsy and their family caregivers to provide a comprehensive overview of the impact of epilepsy and to identify opportunities for healthcare service improvements.

Methods: Systematic literature searches were conducted in CINAHL, Embase, Ovid MEDLINE, APA PsychInfo, Scopus, and grey literature databases (12 August 2024). Articles with primary quantitative, qualitative, or mixed methods data covering HRQOL outcomes or unmet needs of adults with epilepsy, their family caregivers, or healthcare professionals as proxies were included. A reflexive thematic framework analysis approach was taken to interpret findings.

Results: Searches yielded 5451 unique publications of which 139 were included. Most publications covered only quantitative data (n = 97, 69.8 %) and utilized a cross-sectional design (n = 121, 87.1 %). All domains of HRQOL (physical, cognitive, emotional/mental, social, and spiritual functioning) were impacted by epilepsy, and intercorrelated. High seizure burden and low socioeconomic status were consistently linked to poor HRQOL outcomes. Adverse HRQOL outcomes were related to high levels of illness intrusiveness, uncertainty, and low levels of perceived control. Caregiver burden was notable. People with epilepsy reported a range of information, healthcare communication, psycho-social and lifestyle, and education/vocational needs.

Discussion: Epilepsy impacts patient and caregiver HRQOL outcomes, highlighting profound illness intrusiveness. Addressing unmet needs may enhance clinical care and empower people with epilepsy and their caregivers to better cope with their condition, improving HRQOL.

Registration: INPLASY202510047.

Contributors

Florien Boele, Carissa Jensen, Gemma Madigan Johnson, Annemarie Lammers-Spijker, Aysun Altinbas, Lydia van den Berg, Kamala Broekman-Labinac, Rolf Fronczek, Maaike Schuur, Gemma Vonk, Maeike Zijlmans, Gerhard Visser, Jaap Reijneveld

Publication

Journal: Epilepsy & Behavior
Volume: 171
Issue:
Pages: -
Year: 2025
DOI: https://doi.org/10.1016/j.yebeh.2025.110601

Further Study Information

Current Stage: Completed
Date:
Funding source(s): This work was partly supported by the Anna Teding van Berkhout Stichting.


Health Area

Disease Category: Neurology

Disease Name: Epilepsy

Target Population

Age Range: 18 - 120

Sex: Either

Nature of Intervention:

Stakeholders Involved

Study Type

- Systematic review of outcomes measured in trials

Method(s)

- Systematic review