Living with rare genetic disease during the COVID-19 pandemic: A qualitative study of adolescents and young adults with Li-Fraumeni syndrome

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
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Abstract

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.

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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
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。
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