Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study.
Adolescent
Adult
COVID-19
/ epidemiology
Caregivers
/ standards
Delivery of Health Care
/ methods
Epilepsy
/ epidemiology
Female
Humans
Longitudinal Studies
Male
Middle Aged
Pandemics
/ prevention & control
Pilot Projects
Risk Factors
Self-Management
/ methods
Sudden Unexpected Death in Epilepsy
/ epidemiology
Surveys and Questionnaires
United Kingdom
/ epidemiology
Young Adult
Chronic illness
Coronavirus
Mental health
SUDEP
Seizures
Journal
Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
28
10
2020
revised:
22
11
2020
accepted:
22
11
2020
pubmed:
21
12
2020
medline:
23
2
2021
entrez:
20
12
2020
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 33341393
pii: S1525-5050(20)30838-6
doi: 10.1016/j.yebeh.2020.107658
pmc: PMC7698680
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
107658Subventions
Organisme : NINDS NIH HHS
ID : U24 NS107201
Pays : United States
Organisme : NINDS NIH HHS
ID : U54 NS100064
Pays : United States
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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