Parental experiences and perspectives on the value of seizure detection while caring for a child with epilepsy: A qualitative study

Publication date

2021-11

Authors

van Westrhenen, Anouk
de Lange, Wendela
Hagebeuk, Eveline E O
Lazeron, Richard H C
Thijs, Roland D
Kars, Marijke CORCID 0000-0001-5680-4559ISNI 0000000389716592

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Document Type

Article

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Abstract

INTRODUCTION: Caring for a child with epilepsy has a significant impact on parental quality of life. Seizure unpredictability and complications, including sudden unexpected death in epilepsy (SUDEP), may cause high parental stress and increased anxiety. Nocturnal supervision with seizure detection devices may lower SUDEP risk and decrease parental burden of seizure monitoring, but little is known about their added value in family homes. METHODS: We conducted semi-structured in-depth interviews with parents of children with refractory epilepsy participating in the PROMISE trial (NCT03909984) to explore the value of seizure detection in the daily care of their child. Children were aged 4-16 years, treated at a tertiary epilepsy center, had at least one nocturnal major motor seizure per week, and used a wearable seizure detection device (NightWatch) for two months at home. Data were analyzed using inductive thematic analysis. RESULTS: Twenty three parents of nineteen children with refractory epilepsy were interviewed. All parents expressed their fear of missing a large seizure and the possible consequences of not intervening in time. Some parents felt the threat of child loss during every seizure, while others thought about it from time to time. The fear could fluctuate over time, mainly associated with fluctuations of seizure frequency. Most parents described how they developed a protective behavior, driven by this fear. The way parents handled the care of their child and experienced the burden of care influenced their perceptions on the added value of NightWatch. The experienced value of NightWatch depended on the amount of assurance it could offer to reduce their fear and the associated protective behavior as well as their resilience to handle the potential extra burden of care, due to false alarms or technical problems. CONCLUSION: Healthcare professionals and device companies should be aware of parental protective behavior and the high parental burden of care and develop tailored strategies to optimize seizure detection device care.

Keywords

Burden of care, Implementation, Parental caregiving, Seizure detection devices, Sudden unexpected death in epilepsy (SUDEP), Clinical Neurology, Neurology, Behavioral Neuroscience, Journal Article

Citation

van Westrhenen, A, de Lange, W F M, Hagebeuk, E E O, Lazeron, R H C, Thijs, R D & Kars, M C 2021, 'Parental experiences and perspectives on the value of seizure detection while caring for a child with epilepsy : A qualitative study', Epilepsy & Behavior, vol. 124, 108323. https://doi.org/10.1016/j.yebeh.2021.108323