Exploratory study identifies unique quality of life priorities in epilepsy and non-epileptic spell populations, suggesting a need for tailored measurement approaches.
A distinct core outcome set (COS) for measuring quality of life (QOL) among people with epilepsy syndrome (ES) and non-epileptic spells (NES) has not yet been established, and further studies are needed to understand this patient population’s priorities in QOL measurement.
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Cui et al. (2026) studied this question.
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