Abstract
BackgroundLockdown due to the SARS‐CoV‐2 pandemic became a challenge to maintain care for patients with epilepsy; we aimed to find out how the pandemic affected them.MethodsWe sent an online 22‐item questionnaire to patients from our outpatient clinic, a reference centre in Spain for drug‐resistant epilepsy, inquiring about the effects of lockdown, from March to May 2020.ResultsWe sent the survey to 627 patients; 312 (58% women) sent a complete response and were included. Of all respondents, 57% took >2 antiseizure medications. One‐third of respondents (29%) declared an associated cognitive or motor disability. A minority had confirmed infection with SARS‐CoV‐2 (1.92%). Seizure frequency remained like usual in 56% of patients, while 31.2% reported an increase. Less than 10% needed emergent assistance. Almost half reported anxiety or depression, and 25% increased behavioural disorders. Mood (F: 5.40; p: 0.002) and sleep disorders (F = 2.67; p: 0.05) were associated with increase in seizure frequency. Patients were able to contact their physicians when needed and were open to a future telematic approach to follow‐up visits.ConclusionsSeizure frequency and severity remained unchanged in most patients during the lockdown. Mood and sleep disorders were common and associated with seizure worsening. Patients were open to telematic care in the future.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have