在 COVID-19 大流行期间与罕见遗传病共存:对患有 Li-Fraumeni 综合征的青少年的定性研究

Rare Pub Date : 2024-01-01 DOI:10.1016/j.rare.2024.100034
Allison Werner-Lin , Payal P. Khincha , Ashley S. Thompson , Camella Rising , Alix Sleight , Catherine Wilsnack , Patrick Boyd , Alexandra Feldman , Rowan Forbes Shepherd , Sharon A. Savage
{"title":"在 COVID-19 大流行期间与罕见遗传病共存:对患有 Li-Fraumeni 综合征的青少年的定性研究","authors":"Allison Werner-Lin ,&nbsp;Payal P. Khincha ,&nbsp;Ashley S. Thompson ,&nbsp;Camella Rising ,&nbsp;Alix Sleight ,&nbsp;Catherine Wilsnack ,&nbsp;Patrick Boyd ,&nbsp;Alexandra Feldman ,&nbsp;Rowan Forbes Shepherd ,&nbsp;Sharon A. Savage","doi":"10.1016/j.rare.2024.100034","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>The COVID-19 pandemic caused large-scale shifts in healthcare access and delivery that impacted the availability of routine care, such as cancer screening. Vulnerable populations, including those with rare cancer-prone genetic disease, faced considerable difficulties in managing their cancer risk. Studies characterizing the specific impacts of the pandemic on physical, mental, and emotional well-being for individuals with rare cancer-prone syndromes are emerging. This study used a patient-centered perspective to characterize how young adults with Li-Fraumeni syndrome (LFS), an inherited cancer predisposition syndrome with nearly 100 % lifetime risk of cancer, managed their physical and mental health during the first year of the COVID-19 pandemic.</p></div><div><h3>Methods</h3><p>This exploratory, qualitative cohort study was conducted between March and July of 2021 as part of the National Cancer Institute's Li-Fraumeni Study. Thirty adolescents and young adults (22 female, 8 male, median age 31 years, range 18–41) with a confirmed pathogenic <em>TP53</em> variant completed a semi-structured qualitative interview. An interdisciplinary team conducted Thematic Content Analysis on verbatim transcribed data.</p></div><div><h3>Results</h3><p>Most participants (22/30, 77 %) completed cancer screening during the first year of the pandemic, with a median perceived delay of 5 months (range 2–12 months) and with financial COVID-19-related burden (55 %). While participants reported satisfaction with telehealth-based services, they also reported challenges establishing new clinical relationships and a clear preference for in-person clinical care. Most participants reported negative or mixed impacts of COVID-19 on mental health (21/30, 70 %). Social network changes were reported by 22 (73 %), and almost all participants experienced negative or mixed emotions such as loss, grief, and isolation, to adaptations necessitated by COVID-19 in their social structure.</p></div><div><h3>Conclusions</h3><p>The COVID-19 pandemic had detrimental effects on the physical, emotional, and social health in young adults with Li-Fraumeni, including disruptions in care. These data highlight the need for integrative strategies to be in place prior to future pandemics to prioritize and support vulnerable populations, such as those with rare disease, and to manage unforeseen large-scale shifts in healthcare access and social structure.</p></div>","PeriodicalId":101058,"journal":{"name":"Rare","volume":"2 ","pages":"Article 100034"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2950008724000176/pdfft?md5=7f01362a794bd82c9af5daf628554d8d&pid=1-s2.0-S2950008724000176-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Living with rare genetic disease during the COVID-19 pandemic: A qualitative study of adolescents and young adults with Li-Fraumeni syndrome\",\"authors\":\"Allison Werner-Lin ,&nbsp;Payal P. Khincha ,&nbsp;Ashley S. Thompson ,&nbsp;Camella Rising ,&nbsp;Alix Sleight ,&nbsp;Catherine Wilsnack ,&nbsp;Patrick Boyd ,&nbsp;Alexandra Feldman ,&nbsp;Rowan Forbes Shepherd ,&nbsp;Sharon A. Savage\",\"doi\":\"10.1016/j.rare.2024.100034\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>The COVID-19 pandemic caused large-scale shifts in healthcare access and delivery that impacted the availability of routine care, such as cancer screening. Vulnerable populations, including those with rare cancer-prone genetic disease, faced considerable difficulties in managing their cancer risk. Studies characterizing the specific impacts of the pandemic on physical, mental, and emotional well-being for individuals with rare cancer-prone syndromes are emerging. This study used a patient-centered perspective to characterize how young adults with Li-Fraumeni syndrome (LFS), an inherited cancer predisposition syndrome with nearly 100 % lifetime risk of cancer, managed their physical and mental health during the first year of the COVID-19 pandemic.</p></div><div><h3>Methods</h3><p>This exploratory, qualitative cohort study was conducted between March and July of 2021 as part of the National Cancer Institute's Li-Fraumeni Study. Thirty adolescents and young adults (22 female, 8 male, median age 31 years, range 18–41) with a confirmed pathogenic <em>TP53</em> variant completed a semi-structured qualitative interview. An interdisciplinary team conducted Thematic Content Analysis on verbatim transcribed data.</p></div><div><h3>Results</h3><p>Most participants (22/30, 77 %) completed cancer screening during the first year of the pandemic, with a median perceived delay of 5 months (range 2–12 months) and with financial COVID-19-related burden (55 %). While participants reported satisfaction with telehealth-based services, they also reported challenges establishing new clinical relationships and a clear preference for in-person clinical care. Most participants reported negative or mixed impacts of COVID-19 on mental health (21/30, 70 %). Social network changes were reported by 22 (73 %), and almost all participants experienced negative or mixed emotions such as loss, grief, and isolation, to adaptations necessitated by COVID-19 in their social structure.</p></div><div><h3>Conclusions</h3><p>The COVID-19 pandemic had detrimental effects on the physical, emotional, and social health in young adults with Li-Fraumeni, including disruptions in care. These data highlight the need for integrative strategies to be in place prior to future pandemics to prioritize and support vulnerable populations, such as those with rare disease, and to manage unforeseen large-scale shifts in healthcare access and social structure.</p></div>\",\"PeriodicalId\":101058,\"journal\":{\"name\":\"Rare\",\"volume\":\"2 \",\"pages\":\"Article 100034\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2950008724000176/pdfft?md5=7f01362a794bd82c9af5daf628554d8d&pid=1-s2.0-S2950008724000176-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rare\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2950008724000176\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950008724000176","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景COVID-19 大流行导致医疗服务的获取和提供发生了大规模的变化,影响了癌症筛查等常规医疗服务的提供。弱势群体,包括那些患有罕见癌症易感基因病的人,在控制癌症风险方面面临着相当大的困难。关于大流行病对罕见癌症易感综合征患者的身体、精神和情绪的具体影响的研究正在出现。本研究采用以患者为中心的视角,描述了患有李-弗劳米尼综合征(LFS)的年轻成年人在 COVID-19 大流行的第一年是如何管理自己的身心健康的,李-弗劳米尼综合征是一种遗传性癌症易感综合征,终生患癌风险几乎为 100%。30名确诊为致病性TP53变异体的青少年(22名女性,8名男性,中位年龄31岁,18-41岁不等)完成了半结构化定性访谈。一个跨学科小组对逐字记录的数据进行了主题内容分析。结果大多数参与者(22/30,77%)在大流行的第一年完成了癌症筛查,中位延迟时间为 5 个月(2-12 个月),经济负担与 COVID-19 相关(55%)。虽然参与者对基于远程医疗的服务表示满意,但他们也表示在建立新的临床关系方面面临挑战,并明确倾向于亲自接受临床治疗。大多数参与者报告了 COVID-19 对心理健康的负面影响或混合影响(21/30,70%)。22名参与者(73%)报告了社会网络的变化,几乎所有参与者都经历了负面或混合情绪,如失落、悲伤和孤独,他们的社会结构必须适应 COVID-19 的影响。这些数据凸显了在未来大流行之前制定综合战略的必要性,以优先考虑和支持弱势群体(如罕见病患者),并管理医疗服务和社会结构中不可预见的大规模变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Living with rare genetic disease during the COVID-19 pandemic: A qualitative study of adolescents and young adults with Li-Fraumeni syndrome

Background

The COVID-19 pandemic caused large-scale shifts in healthcare access and delivery that impacted the availability of routine care, such as cancer screening. Vulnerable populations, including those with rare cancer-prone genetic disease, faced considerable difficulties in managing their cancer risk. Studies characterizing the specific impacts of the pandemic on physical, mental, and emotional well-being for individuals with rare cancer-prone syndromes are emerging. This study used a patient-centered perspective to characterize how young adults with Li-Fraumeni syndrome (LFS), an inherited cancer predisposition syndrome with nearly 100 % lifetime risk of cancer, managed their physical and mental health during the first year of the COVID-19 pandemic.

Methods

This exploratory, qualitative cohort study was conducted between March and July of 2021 as part of the National Cancer Institute's Li-Fraumeni Study. Thirty adolescents and young adults (22 female, 8 male, median age 31 years, range 18–41) with a confirmed pathogenic TP53 variant completed a semi-structured qualitative interview. An interdisciplinary team conducted Thematic Content Analysis on verbatim transcribed data.

Results

Most participants (22/30, 77 %) completed cancer screening during the first year of the pandemic, with a median perceived delay of 5 months (range 2–12 months) and with financial COVID-19-related burden (55 %). While participants reported satisfaction with telehealth-based services, they also reported challenges establishing new clinical relationships and a clear preference for in-person clinical care. Most participants reported negative or mixed impacts of COVID-19 on mental health (21/30, 70 %). Social network changes were reported by 22 (73 %), and almost all participants experienced negative or mixed emotions such as loss, grief, and isolation, to adaptations necessitated by COVID-19 in their social structure.

Conclusions

The COVID-19 pandemic had detrimental effects on the physical, emotional, and social health in young adults with Li-Fraumeni, including disruptions in care. These data highlight the need for integrative strategies to be in place prior to future pandemics to prioritize and support vulnerable populations, such as those with rare disease, and to manage unforeseen large-scale shifts in healthcare access and social structure.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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