Why so Blue? (Or Should I Say Red?) Recognizing the Emotional Impact of Psoriasis on Patients and Family Members: A Qualitative Study.

Q3 Medicine
Ashley M Snyder, Vanina L Taliercio, Bianca E Rich, Adelheid U Brandenberger, Lisa B Webber, Abram P Beshay, Joshua E Biber, Rachel Hess, Jamie Lw Rhoads, Aaron M Secrest
{"title":"Why so Blue? (Or Should I Say Red?) Recognizing the Emotional Impact of Psoriasis on Patients and Family Members: A Qualitative Study.","authors":"Ashley M Snyder, Vanina L Taliercio, Bianca E Rich, Adelheid U Brandenberger, Lisa B Webber, Abram P Beshay, Joshua E Biber, Rachel Hess, Jamie Lw Rhoads, Aaron M Secrest","doi":"10.1177/24755303211069335","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Psoriasis is a chronic skin condition with significant effects on quality of life, including impacts on emotional health. However, these experiences are not always addressed in clinic visits, despite their potential for significant effects on daily life. This study is part of a larger project on the effects of psoriasis on quality of life. The current information was analyzed separately because the amount of information on emotional impacts mentioned by participants was so significant that it warranted a separate analysis to thoroughly assess these experiences. <b>Objective:</b> To describe emotional consequences of psoriasis for patients and their family members. <b>Methods:</b> This project was conducted at an academic medical center in Utah. Experiences were discussed in interviews and focus groups with 25 patients and 11 family members. Thematic analysis was used to determine themes and subthemes. <b>Results:</b> This study sheds light on the damaging effects of psoriasis on emotional well-being, illustrating the challenges patients face from internal conflict, consequences for family members trying to cope with psoriasis in a loved one, and judgment from others who do not understand psoriasis and its challenges. <b>Conclusion:</b> Living with psoriasis leads to emotional consequences that may be left unaddressed in clinic visits, yet these experiences contribute significantly to quality of life. The stories told through this study can help clinicians understand how to identify and address emotional concerns to improve care for psoriasis patients and, as a result, improve quality of life for both patients and their families.</p>","PeriodicalId":36656,"journal":{"name":"Journal of Psoriasis and Psoriatic Arthritis","volume":"7 1","pages":"60-66"},"PeriodicalIF":0.0000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11361524/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Psoriasis and Psoriatic Arthritis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/24755303211069335","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/2/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Psoriasis is a chronic skin condition with significant effects on quality of life, including impacts on emotional health. However, these experiences are not always addressed in clinic visits, despite their potential for significant effects on daily life. This study is part of a larger project on the effects of psoriasis on quality of life. The current information was analyzed separately because the amount of information on emotional impacts mentioned by participants was so significant that it warranted a separate analysis to thoroughly assess these experiences. Objective: To describe emotional consequences of psoriasis for patients and their family members. Methods: This project was conducted at an academic medical center in Utah. Experiences were discussed in interviews and focus groups with 25 patients and 11 family members. Thematic analysis was used to determine themes and subthemes. Results: This study sheds light on the damaging effects of psoriasis on emotional well-being, illustrating the challenges patients face from internal conflict, consequences for family members trying to cope with psoriasis in a loved one, and judgment from others who do not understand psoriasis and its challenges. Conclusion: Living with psoriasis leads to emotional consequences that may be left unaddressed in clinic visits, yet these experiences contribute significantly to quality of life. The stories told through this study can help clinicians understand how to identify and address emotional concerns to improve care for psoriasis patients and, as a result, improve quality of life for both patients and their families.

为什么这么蓝?(或者我应该说红色?)认识到银屑病对患者和家庭成员的情绪影响:一项定性研究
背景:牛皮癣是一种对生活质量有显著影响的慢性皮肤病,包括对情绪健康的影响。然而,这些经历并不总是在诊所就诊中得到解决,尽管它们对日常生活有潜在的重大影响。这项研究是一个关于牛皮癣对生活质量影响的大型项目的一部分。目前的信息是单独分析的,因为参与者提到的情绪影响的信息量非常大,需要单独分析来彻底评估这些经历。目的:描述牛皮癣患者及其家属的情绪后果。方法:本项目在犹他州的一个学术医疗中心进行。对25名患者和11名家属进行访谈和焦点小组讨论。主题分析用于确定主题和副主题。结果:本研究揭示了牛皮癣对情绪健康的破坏性影响,说明了患者面临的内部冲突的挑战,家庭成员试图应对亲人患牛皮癣的后果,以及其他人不了解牛皮癣及其挑战的判断。结论:患有牛皮癣会导致情绪后果,这些后果可能在诊所就诊时未得到解决,但这些经历对生活质量有重要影响。通过本研究讲述的故事可以帮助临床医生了解如何识别和解决情绪问题,以改善对牛皮癣患者的护理,从而提高患者及其家人的生活质量。
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
CiteScore
1.30
自引率
0.00%
发文量
19
×
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