Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study
•The COVID-19 and Epilepsy (COV-E) global surveys were launched in May 2020.•UK respondents (n = 463) report changes in seizure frequency, mental health, and sleep.•Discussion of risk, including of SUDEP, was infrequent even before the pandemic.•COVID-19 is having far-reaching consequences on people...
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creator | Thorpe, Jennifer Ashby, Samantha Hallab, Asma Ding, Ding Andraus, Maria Dugan, Patricia Perucca, Piero Costello, Daniel French, Jacqueline A. O'Brien, Terence J. Depondt, Chantal Andrade, Danielle M. Sengupta, Robin Delanty, Norman Jette, Nathalie Newton, Charles R. Brodie, Martin J. Devinsky, Orrin Helen Cross, J. Sander, Josemir W. Hanna, Jane Sen, Arjune |
description | •The COVID-19 and Epilepsy (COV-E) global surveys were launched in May 2020.•UK respondents (n = 463) report changes in seizure frequency, mental health, and sleep.•Discussion of risk, including of SUDEP, was infrequent even before the pandemic.•COVID-19 is having far-reaching consequences on people with epilepsy.•Our study exemplifies the importance of delivering optimal care to mitigate risk.
The COVID-19 pandemic has caused global anguish unparalleled in recent times. As cases rise, increased pressure on health services, combined with severe disruption to people’s everyday lives, can adversely affect individuals living with chronic illnesses, including people with epilepsy. Stressors related to disruption to healthcare, finances, mental well-being, relationships, schooling, physical activity, and increased isolation could increase seizures and impair epilepsy self-management.
We aim to understand the impact that COVID-19 has had on the health and well-being of people with epilepsy focusing on exposure to increased risk of seizures, associated comorbidity, and mortality. We designed two online surveys with one addressing people with epilepsy directly and the second for caregivers to report on behalf of a person with epilepsy.
The survey is ongoing and has yielded 463 UK-based responses by the end of September 2020. Forty percent of respondents reported health changes during the pandemic (n = 185). Respondents cited a change in seizures (19%, n = 88), mental health difficulties (34%, n = 161), and sleep disruption (26%, n = 121) as the main reasons. Thirteen percent found it difficult to take medication on time. A third had difficulty accessing medical services (n = 154), with 8% having had an appointment canceled (n = 39). Only a small proportion reported having had discussions about epilepsy-related risks, such as safety precautions (16%, n = 74); mental health (29%, n = 134); sleep (30%, n = 140); and Sudden Unexpected Death in Epilepsy (SUDEP; 15%, n = 69) in the previous 12 months.
These findings suggest that people with epilepsy are currently experiencing health changes, coupled with inadequate access to services. Also, there seems to be a history of poor risk communication in the months preceding the pandemic. As the UK witnesses a second COVID-19 wave, those involved in healthcare delivery must ensure optimal care is provided for people with chronic conditions, such as epilepsy, to ensure that avoidable morbidity and mortality is prevented during |
doi_str_mv | 10.1016/j.yebeh.2020.107658 |
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The COVID-19 pandemic has caused global anguish unparalleled in recent times. As cases rise, increased pressure on health services, combined with severe disruption to people’s everyday lives, can adversely affect individuals living with chronic illnesses, including people with epilepsy. Stressors related to disruption to healthcare, finances, mental well-being, relationships, schooling, physical activity, and increased isolation could increase seizures and impair epilepsy self-management.
We aim to understand the impact that COVID-19 has had on the health and well-being of people with epilepsy focusing on exposure to increased risk of seizures, associated comorbidity, and mortality. We designed two online surveys with one addressing people with epilepsy directly and the second for caregivers to report on behalf of a person with epilepsy.
The survey is ongoing and has yielded 463 UK-based responses by the end of September 2020. Forty percent of respondents reported health changes during the pandemic (n = 185). Respondents cited a change in seizures (19%, n = 88), mental health difficulties (34%, n = 161), and sleep disruption (26%, n = 121) as the main reasons. Thirteen percent found it difficult to take medication on time. A third had difficulty accessing medical services (n = 154), with 8% having had an appointment canceled (n = 39). Only a small proportion reported having had discussions about epilepsy-related risks, such as safety precautions (16%, n = 74); mental health (29%, n = 134); sleep (30%, n = 140); and Sudden Unexpected Death in Epilepsy (SUDEP; 15%, n = 69) in the previous 12 months.
These findings suggest that people with epilepsy are currently experiencing health changes, coupled with inadequate access to services. Also, there seems to be a history of poor risk communication in the months preceding the pandemic. As the UK witnesses a second COVID-19 wave, those involved in healthcare delivery must ensure optimal care is provided for people with chronic conditions, such as epilepsy, to ensure that avoidable morbidity and mortality is prevented during the pandemic, and beyond.</description><identifier>ISSN: 1525-5050</identifier><identifier>EISSN: 1525-5069</identifier><identifier>DOI: 10.1016/j.yebeh.2020.107658</identifier><identifier>PMID: 33341393</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Caregivers - standards ; Chronic illness ; Coronavirus ; COVID-19 - epidemiology ; COVID-19 - prevention & control ; Delivery of Health Care - methods ; Delivery of Health Care - standards ; Epilepsy - epidemiology ; Epilepsy - therapy ; Female ; Humans ; Longitudinal Studies ; Male ; Mental health ; Middle Aged ; Pandemics - prevention & control ; Pilot Projects ; Risk Factors ; Seizures ; Self-Management - methods ; Sudden Unexpected Death in Epilepsy - epidemiology ; Sudden Unexpected Death in Epilepsy - prevention & control ; SUDEP ; Surveys and Questionnaires ; United Kingdom - epidemiology ; Young Adult</subject><ispartof>Epilepsy & behavior, 2021-02, Vol.115, p.107658-107658, Article 107658</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020 Elsevier Inc. All rights reserved. 2020 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-aca2209d2fe39ed343e35fdf15015c731ed034c2e19294562394c255bd8732fd3</citedby><cites>FETCH-LOGICAL-c459t-aca2209d2fe39ed343e35fdf15015c731ed034c2e19294562394c255bd8732fd3</cites><orcidid>0000-0002-8452-5319 ; 0000-0002-0812-6041 ; 0000-0003-1781-2892 ; 0000-0002-1220-2588 ; 0000-0001-6041-9661 ; 0000-0002-3901-7980 ; 0000-0002-8948-4763 ; 0000-0001-6997-3669</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.yebeh.2020.107658$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33341393$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thorpe, Jennifer</creatorcontrib><creatorcontrib>Ashby, Samantha</creatorcontrib><creatorcontrib>Hallab, Asma</creatorcontrib><creatorcontrib>Ding, Ding</creatorcontrib><creatorcontrib>Andraus, Maria</creatorcontrib><creatorcontrib>Dugan, Patricia</creatorcontrib><creatorcontrib>Perucca, Piero</creatorcontrib><creatorcontrib>Costello, Daniel</creatorcontrib><creatorcontrib>French, Jacqueline A.</creatorcontrib><creatorcontrib>O'Brien, Terence J.</creatorcontrib><creatorcontrib>Depondt, Chantal</creatorcontrib><creatorcontrib>Andrade, Danielle M.</creatorcontrib><creatorcontrib>Sengupta, Robin</creatorcontrib><creatorcontrib>Delanty, Norman</creatorcontrib><creatorcontrib>Jette, Nathalie</creatorcontrib><creatorcontrib>Newton, Charles R.</creatorcontrib><creatorcontrib>Brodie, Martin J.</creatorcontrib><creatorcontrib>Devinsky, Orrin</creatorcontrib><creatorcontrib>Helen Cross, J.</creatorcontrib><creatorcontrib>Sander, Josemir W.</creatorcontrib><creatorcontrib>Hanna, Jane</creatorcontrib><creatorcontrib>Sen, Arjune</creatorcontrib><creatorcontrib>on behalf of the COVID-19 and Epilepsy (COV-E) Study Group</creatorcontrib><creatorcontrib>COVID-19 and Epilepsy (COV-E) Study Group</creatorcontrib><title>Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study</title><title>Epilepsy & behavior</title><addtitle>Epilepsy Behav</addtitle><description>•The COVID-19 and Epilepsy (COV-E) global surveys were launched in May 2020.•UK respondents (n = 463) report changes in seizure frequency, mental health, and sleep.•Discussion of risk, including of SUDEP, was infrequent even before the pandemic.•COVID-19 is having far-reaching consequences on people with epilepsy.•Our study exemplifies the importance of delivering optimal care to mitigate risk.
The COVID-19 pandemic has caused global anguish unparalleled in recent times. As cases rise, increased pressure on health services, combined with severe disruption to people’s everyday lives, can adversely affect individuals living with chronic illnesses, including people with epilepsy. Stressors related to disruption to healthcare, finances, mental well-being, relationships, schooling, physical activity, and increased isolation could increase seizures and impair epilepsy self-management.
We aim to understand the impact that COVID-19 has had on the health and well-being of people with epilepsy focusing on exposure to increased risk of seizures, associated comorbidity, and mortality. We designed two online surveys with one addressing people with epilepsy directly and the second for caregivers to report on behalf of a person with epilepsy.
The survey is ongoing and has yielded 463 UK-based responses by the end of September 2020. Forty percent of respondents reported health changes during the pandemic (n = 185). Respondents cited a change in seizures (19%, n = 88), mental health difficulties (34%, n = 161), and sleep disruption (26%, n = 121) as the main reasons. Thirteen percent found it difficult to take medication on time. A third had difficulty accessing medical services (n = 154), with 8% having had an appointment canceled (n = 39). Only a small proportion reported having had discussions about epilepsy-related risks, such as safety precautions (16%, n = 74); mental health (29%, n = 134); sleep (30%, n = 140); and Sudden Unexpected Death in Epilepsy (SUDEP; 15%, n = 69) in the previous 12 months.
These findings suggest that people with epilepsy are currently experiencing health changes, coupled with inadequate access to services. Also, there seems to be a history of poor risk communication in the months preceding the pandemic. As the UK witnesses a second COVID-19 wave, those involved in healthcare delivery must ensure optimal care is provided for people with chronic conditions, such as epilepsy, to ensure that avoidable morbidity and mortality is prevented during the pandemic, and beyond.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Caregivers - standards</subject><subject>Chronic illness</subject><subject>Coronavirus</subject><subject>COVID-19 - epidemiology</subject><subject>COVID-19 - prevention & control</subject><subject>Delivery of Health Care - methods</subject><subject>Delivery of Health Care - standards</subject><subject>Epilepsy - epidemiology</subject><subject>Epilepsy - therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Mental health</subject><subject>Middle Aged</subject><subject>Pandemics - prevention & control</subject><subject>Pilot Projects</subject><subject>Risk Factors</subject><subject>Seizures</subject><subject>Self-Management - methods</subject><subject>Sudden Unexpected Death in Epilepsy - epidemiology</subject><subject>Sudden Unexpected Death in Epilepsy - prevention & control</subject><subject>SUDEP</subject><subject>Surveys and Questionnaires</subject><subject>United Kingdom - epidemiology</subject><subject>Young Adult</subject><issn>1525-5050</issn><issn>1525-5069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9P3DAQxS3UCijlEyBVPvaSxX_iJEYCCW23BQmJHtpeLa89Yb1N4mA7W-23r7cLq_bSk-3x770ZzUPogpIZJbS6XM-2sITVjBG2q9SVaI7QKRVMFIJU8s3hLsgJehfjmhBKBafH6IRzXlIu-Snyi43uJp3c8ISDiz9x8ngEP3aAf7m0wjC6Dsa4xXYKOyatAM8ff9x_KqjEox4s9M5c4a8BOte7QYctbt1gMxpxG3z_KigWOKbJbt-jt63uIpy_nGfo--fFt_ld8fD45X5--1CYUshUaKMZI9KyFrgEy0sOXLS2pYJQYWpOwRJeGgZUMlmKinGZX0IsbVNz1lp-hm72vuO07MEaGFLQnRqD6_OMymun_v0Z3Eo9-Y2qK9lUDckGH18Mgn-eICbVu2ig6_QAfoqKlXVeZsWaKqN8j5rgYwzQHtpQonZRqbX6E5XaRaX2UWXVh78nPGhes8nA9R6AvKeNg6CicTAYsC6AScp6998GvwFOA6aX</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Thorpe, Jennifer</creator><creator>Ashby, Samantha</creator><creator>Hallab, Asma</creator><creator>Ding, Ding</creator><creator>Andraus, Maria</creator><creator>Dugan, Patricia</creator><creator>Perucca, Piero</creator><creator>Costello, Daniel</creator><creator>French, Jacqueline A.</creator><creator>O'Brien, Terence J.</creator><creator>Depondt, Chantal</creator><creator>Andrade, Danielle M.</creator><creator>Sengupta, Robin</creator><creator>Delanty, Norman</creator><creator>Jette, Nathalie</creator><creator>Newton, Charles R.</creator><creator>Brodie, Martin J.</creator><creator>Devinsky, Orrin</creator><creator>Helen Cross, J.</creator><creator>Sander, Josemir W.</creator><creator>Hanna, Jane</creator><creator>Sen, Arjune</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8452-5319</orcidid><orcidid>https://orcid.org/0000-0002-0812-6041</orcidid><orcidid>https://orcid.org/0000-0003-1781-2892</orcidid><orcidid>https://orcid.org/0000-0002-1220-2588</orcidid><orcidid>https://orcid.org/0000-0001-6041-9661</orcidid><orcidid>https://orcid.org/0000-0002-3901-7980</orcidid><orcidid>https://orcid.org/0000-0002-8948-4763</orcidid><orcidid>https://orcid.org/0000-0001-6997-3669</orcidid></search><sort><creationdate>20210201</creationdate><title>Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study</title><author>Thorpe, Jennifer ; Ashby, Samantha ; Hallab, Asma ; Ding, Ding ; Andraus, Maria ; Dugan, Patricia ; Perucca, Piero ; Costello, Daniel ; French, Jacqueline A. ; O'Brien, Terence J. ; Depondt, Chantal ; Andrade, Danielle M. ; Sengupta, Robin ; Delanty, Norman ; Jette, Nathalie ; Newton, Charles R. ; Brodie, Martin J. ; Devinsky, Orrin ; Helen Cross, J. ; Sander, Josemir W. ; Hanna, Jane ; Sen, Arjune</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-aca2209d2fe39ed343e35fdf15015c731ed034c2e19294562394c255bd8732fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Caregivers - standards</topic><topic>Chronic illness</topic><topic>Coronavirus</topic><topic>COVID-19 - epidemiology</topic><topic>COVID-19 - prevention & control</topic><topic>Delivery of Health Care - methods</topic><topic>Delivery of Health Care - standards</topic><topic>Epilepsy - epidemiology</topic><topic>Epilepsy - therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Mental health</topic><topic>Middle Aged</topic><topic>Pandemics - prevention & control</topic><topic>Pilot Projects</topic><topic>Risk Factors</topic><topic>Seizures</topic><topic>Self-Management - methods</topic><topic>Sudden Unexpected Death in Epilepsy - epidemiology</topic><topic>Sudden Unexpected Death in Epilepsy - prevention & control</topic><topic>SUDEP</topic><topic>Surveys and Questionnaires</topic><topic>United Kingdom - epidemiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thorpe, Jennifer</creatorcontrib><creatorcontrib>Ashby, Samantha</creatorcontrib><creatorcontrib>Hallab, Asma</creatorcontrib><creatorcontrib>Ding, Ding</creatorcontrib><creatorcontrib>Andraus, Maria</creatorcontrib><creatorcontrib>Dugan, Patricia</creatorcontrib><creatorcontrib>Perucca, Piero</creatorcontrib><creatorcontrib>Costello, Daniel</creatorcontrib><creatorcontrib>French, Jacqueline A.</creatorcontrib><creatorcontrib>O'Brien, Terence J.</creatorcontrib><creatorcontrib>Depondt, Chantal</creatorcontrib><creatorcontrib>Andrade, Danielle M.</creatorcontrib><creatorcontrib>Sengupta, Robin</creatorcontrib><creatorcontrib>Delanty, Norman</creatorcontrib><creatorcontrib>Jette, Nathalie</creatorcontrib><creatorcontrib>Newton, Charles R.</creatorcontrib><creatorcontrib>Brodie, Martin J.</creatorcontrib><creatorcontrib>Devinsky, Orrin</creatorcontrib><creatorcontrib>Helen Cross, J.</creatorcontrib><creatorcontrib>Sander, Josemir W.</creatorcontrib><creatorcontrib>Hanna, Jane</creatorcontrib><creatorcontrib>Sen, Arjune</creatorcontrib><creatorcontrib>on behalf of the COVID-19 and Epilepsy (COV-E) Study Group</creatorcontrib><creatorcontrib>COVID-19 and Epilepsy (COV-E) Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Epilepsy & behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thorpe, Jennifer</au><au>Ashby, Samantha</au><au>Hallab, Asma</au><au>Ding, Ding</au><au>Andraus, Maria</au><au>Dugan, Patricia</au><au>Perucca, Piero</au><au>Costello, Daniel</au><au>French, Jacqueline A.</au><au>O'Brien, Terence J.</au><au>Depondt, Chantal</au><au>Andrade, Danielle M.</au><au>Sengupta, Robin</au><au>Delanty, Norman</au><au>Jette, Nathalie</au><au>Newton, Charles R.</au><au>Brodie, Martin J.</au><au>Devinsky, Orrin</au><au>Helen Cross, J.</au><au>Sander, Josemir W.</au><au>Hanna, Jane</au><au>Sen, Arjune</au><aucorp>on behalf of the COVID-19 and Epilepsy (COV-E) Study Group</aucorp><aucorp>COVID-19 and Epilepsy (COV-E) Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study</atitle><jtitle>Epilepsy & behavior</jtitle><addtitle>Epilepsy Behav</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>115</volume><spage>107658</spage><epage>107658</epage><pages>107658-107658</pages><artnum>107658</artnum><issn>1525-5050</issn><eissn>1525-5069</eissn><abstract>•The COVID-19 and Epilepsy (COV-E) global surveys were launched in May 2020.•UK respondents (n = 463) report changes in seizure frequency, mental health, and sleep.•Discussion of risk, including of SUDEP, was infrequent even before the pandemic.•COVID-19 is having far-reaching consequences on people with epilepsy.•Our study exemplifies the importance of delivering optimal care to mitigate risk.
The COVID-19 pandemic has caused global anguish unparalleled in recent times. As cases rise, increased pressure on health services, combined with severe disruption to people’s everyday lives, can adversely affect individuals living with chronic illnesses, including people with epilepsy. Stressors related to disruption to healthcare, finances, mental well-being, relationships, schooling, physical activity, and increased isolation could increase seizures and impair epilepsy self-management.
We aim to understand the impact that COVID-19 has had on the health and well-being of people with epilepsy focusing on exposure to increased risk of seizures, associated comorbidity, and mortality. We designed two online surveys with one addressing people with epilepsy directly and the second for caregivers to report on behalf of a person with epilepsy.
The survey is ongoing and has yielded 463 UK-based responses by the end of September 2020. Forty percent of respondents reported health changes during the pandemic (n = 185). Respondents cited a change in seizures (19%, n = 88), mental health difficulties (34%, n = 161), and sleep disruption (26%, n = 121) as the main reasons. Thirteen percent found it difficult to take medication on time. A third had difficulty accessing medical services (n = 154), with 8% having had an appointment canceled (n = 39). Only a small proportion reported having had discussions about epilepsy-related risks, such as safety precautions (16%, n = 74); mental health (29%, n = 134); sleep (30%, n = 140); and Sudden Unexpected Death in Epilepsy (SUDEP; 15%, n = 69) in the previous 12 months.
These findings suggest that people with epilepsy are currently experiencing health changes, coupled with inadequate access to services. Also, there seems to be a history of poor risk communication in the months preceding the pandemic. As the UK witnesses a second COVID-19 wave, those involved in healthcare delivery must ensure optimal care is provided for people with chronic conditions, such as epilepsy, to ensure that avoidable morbidity and mortality is prevented during the pandemic, and beyond.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33341393</pmid><doi>10.1016/j.yebeh.2020.107658</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8452-5319</orcidid><orcidid>https://orcid.org/0000-0002-0812-6041</orcidid><orcidid>https://orcid.org/0000-0003-1781-2892</orcidid><orcidid>https://orcid.org/0000-0002-1220-2588</orcidid><orcidid>https://orcid.org/0000-0001-6041-9661</orcidid><orcidid>https://orcid.org/0000-0002-3901-7980</orcidid><orcidid>https://orcid.org/0000-0002-8948-4763</orcidid><orcidid>https://orcid.org/0000-0001-6997-3669</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Adolescent Adult Caregivers - standards Chronic illness Coronavirus COVID-19 - epidemiology COVID-19 - prevention & control Delivery of Health Care - methods Delivery of Health Care - standards Epilepsy - epidemiology Epilepsy - therapy Female Humans Longitudinal Studies Male Mental health Middle Aged Pandemics - prevention & control Pilot Projects Risk Factors Seizures Self-Management - methods Sudden Unexpected Death in Epilepsy - epidemiology Sudden Unexpected Death in Epilepsy - prevention & control SUDEP Surveys and Questionnaires United Kingdom - epidemiology Young Adult |
title | Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study |
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