The Impact of COVID-19 on Fatigue in Multiple Sclerosis

Q1 Nursing
Zade Abou-Rass, Jennie Feldpausch, Prudence Plummer, Nora E. Fritz
{"title":"The Impact of COVID-19 on Fatigue in Multiple Sclerosis","authors":"Zade Abou-Rass, Jennie Feldpausch, Prudence Plummer, Nora E. Fritz","doi":"10.7224/1537-2073.2023-031","DOIUrl":null,"url":null,"abstract":"\n \n \n Although the COVID-19 quarantine required everyone to make lifestyle changes, it may have had especially profound implications for individuals who experience multiple sclerosis (MS)-related fatigue. Individuals with MS who suffer from fatigue are already predisposed to inactivity and social isolation and are at risk of worsening symptoms. The objective of this study was to examine the impact of the COVID-19 national quarantine and related restrictions on the mental, emotional, and physical fatigue in persons with MS in the United States.\n \n \n \n We conducted a survey open to all adults (> 18 years) with MS within the United States. The survey gathered demographic information and asked how the COVID-19 pandemic impacted their physical, mental, and emotional fatigue.\n \n \n \n The survey was completed by 600 individuals, 478 with relapsing MS and 122 with progressive MS. There was a significant 2-way interaction for time by fatigue type; both physical and emotional fatigue significantly increased during the pandemic (P < .01) and remained significantly higher after the pandemic than prior to the pandemic (P < .01). Mental fatigue increased significantly during the pandemic (P < .01) and although it remained higher, on average, after the pandemic, it was not significantly different than prepandemic.\n \n \n \n Individuals with MS experienced increases in physical, mental, and emotional fatigue over the course of the COVID-19 quarantine. Even after the lifting of quarantine restrictions, these levels have not returned to baseline. To adequately address fatigue, it is critical that health care professionals inquire about all types of fatigue in persons with MS.\n","PeriodicalId":14150,"journal":{"name":"International journal of MS care","volume":"43 47","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of MS care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7224/1537-2073.2023-031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Nursing","Score":null,"Total":0}
引用次数: 0

Abstract

Although the COVID-19 quarantine required everyone to make lifestyle changes, it may have had especially profound implications for individuals who experience multiple sclerosis (MS)-related fatigue. Individuals with MS who suffer from fatigue are already predisposed to inactivity and social isolation and are at risk of worsening symptoms. The objective of this study was to examine the impact of the COVID-19 national quarantine and related restrictions on the mental, emotional, and physical fatigue in persons with MS in the United States. We conducted a survey open to all adults (> 18 years) with MS within the United States. The survey gathered demographic information and asked how the COVID-19 pandemic impacted their physical, mental, and emotional fatigue. The survey was completed by 600 individuals, 478 with relapsing MS and 122 with progressive MS. There was a significant 2-way interaction for time by fatigue type; both physical and emotional fatigue significantly increased during the pandemic (P < .01) and remained significantly higher after the pandemic than prior to the pandemic (P < .01). Mental fatigue increased significantly during the pandemic (P < .01) and although it remained higher, on average, after the pandemic, it was not significantly different than prepandemic. Individuals with MS experienced increases in physical, mental, and emotional fatigue over the course of the COVID-19 quarantine. Even after the lifting of quarantine restrictions, these levels have not returned to baseline. To adequately address fatigue, it is critical that health care professionals inquire about all types of fatigue in persons with MS.
COVID-19 对多发性硬化症患者疲劳的影响
尽管 COVID-19 隔离要求每个人改变生活方式,但它可能对那些因多发性硬化症(MS)而感到疲劳的人产生了特别深远的影响。疲劳的多发性硬化症患者本来就容易缺乏活动和社交孤立,并面临症状恶化的风险。本研究旨在探讨 COVID-19 国家隔离及相关限制对美国多发性硬化症患者精神、情绪和身体疲劳的影响。 我们对美国所有患有多发性硬化症的成年人(18 岁以上)进行了一次公开调查。调查收集了人口统计学信息,并询问 COVID-19 大流行对他们的身体、精神和情绪疲劳有何影响。 共有 600 人完成了调查,其中 478 人患有复发性多发性硬化症,122 人患有进行性多发性硬化症。疲劳类型与时间之间存在明显的双向交互作用;在大流行期间,身体和情绪疲劳均明显增加(P < .01),大流行后仍明显高于大流行前(P < .01)。精神疲劳在大流行期间明显增加(P < .01),虽然在大流行后平均仍然较高,但与大流行前相比没有明显差异。 在 COVID-19 隔离期间,多发性硬化症患者的身体、精神和情绪疲劳均有所增加。即使在取消检疫限制后,这些水平也没有恢复到基线。为了充分解决疲劳问题,医护人员必须询问多发性硬化症患者的各种疲劳情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
International journal of MS care
International journal of MS care Nursing-Advanced and Specialized Nursing
CiteScore
3.00
自引率
0.00%
发文量
40
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信