2021
DOI: 10.1016/j.yebeh.2021.107800
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Impact of COVID-19 on the lives and psychosocial well-being of persons with epilepsy during the third trimester of the pandemic: Results from an international, online survey

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Cited by 19 publications
(38 citation statements)
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References 30 publications
(51 reference statements)
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“…Difficulties in accessing health care for epilepsy treatment was a common finding in our survey, as well as with ASM supplies, in agreement with data published in other nations regardless of the national income [17,21,24,26,27]. Telemedicine was scarcely provided in our sample compared to other countries [11,[21][22][23][24][25].…”
Section: Discussionsupporting
confidence: 88%
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“…Difficulties in accessing health care for epilepsy treatment was a common finding in our survey, as well as with ASM supplies, in agreement with data published in other nations regardless of the national income [17,21,24,26,27]. Telemedicine was scarcely provided in our sample compared to other countries [11,[21][22][23][24][25].…”
Section: Discussionsupporting
confidence: 88%
“…During the pandemic, people have faced a higher level of stress. Daily updates on the number of cases and mortality, lack of information about the virus, false news, uncertainty about the future, and the need for social isolation resulted in increased psychological problems and sleep disorders, more intense in PWE [16,17]. Surveys carried out in several countries point out significant impact of the pandemic in this population [11,17].…”
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confidence: 99%
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“…Increased seizure frequency, difficulties in obtaining antiseizure medications, cancelled appointments and investigations, alterations in sleep patterns, mood changes, mental health difficulties, and caregiver stress and anxiety have all been reported. 1 , 2 , 3 For PWE who are newly diagnosed and their caregivers, the pandemic has been especially challenging, with limited and/or reduced access to in-person support services and agencies, isolation from family members and friends, and the stress of coping with the uncertainty of a new diagnosis.…”
mentioning
confidence: 99%
“…Furthermore, sleep disturbances, lack of adherence to antiseizure medications, increased seizure frequency, and lack of access to health care, all of which have been cited during the COVID pandemic, may have the potential to impact mortality in PWE. 1 , 2 , 3 , 10 Failure to discuss SUDEP among PWE and their caregivers may also lead to feelings of anger, frustration, and distrust of health care professionals.…”
mentioning
confidence: 99%