The Impact of the Unknown: Patient Experiences with Uncertainty in Sarcoidosis.

IF 9.5 1区 医学 Q1 CRITICAL CARE MEDICINE
Chest Pub Date : 2025-07-01 DOI:10.1016/j.chest.2025.06.025
Kristen R Mathias, Michelle N Eakin, Katrina E Hauschildt, Edward S Chen, Nisha A Gilotra, Nancy W Lin, Catherine A Bonham, Michelle Sharp
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引用次数: 0

Abstract

Background: Individuals with sarcoidosis face many sources of illness uncertainty, including diagnostic delays, unpredictable therapeutic efficacy and toxicity, and disease-associated morbidity and mortality. Patient perspectives on illness uncertainty in sarcoidosis have not been critically evaluated and offer an opportunity for providers to contextualize and prioritize gaps in care and patient support.

Research question: How do patients with sarcoidosis describe their lived experiences with the disease and challenges they face in receiving care?

Study design and methods: We conducted semi-structured qualitative interviews with patients with biopsy-proven pulmonary sarcoidosis receiving treatment for the disease who were seen at a tertiary sarcoidosis center of excellence. Interviews examined patient experiences of living with sarcoidosis including their journey with diagnosis, treatment, and monitoring of disease activity. Transcripts were coded and categorized into themes and subthemes. Saturation was defined as at least 3 interviews without new information.

Results: Twenty-five participants completed semi-structured interviews. The median age was 60 years, with 64% of the participants being female and 68% identifying as Black. The impact of illness uncertainty was a shared component of their care journeys. Key themes that emerged were 1) the burden of limited disease awareness 2) uncertainty about sarcoidosis management, and 3) the unpredictability of disease progression. Uncertainty emerged as a major challenge that contributed to delays in care, poor disease control, and/or psychological distress.

Interpretation: Our findings are the first to highlight the impact of patients' illness uncertainty on sarcoidosis disease outcomes and psychological distress. Individuals living with sarcoidosis may benefit by addressing the psychosocial impact of uncertainty. Individuals living with sarcoidosis may benefit significantly from targeted interventions to mitigate the impact of illness uncertainty.

未知的影响:结节病患者的不确定性经验。
背景:结节病患者面临许多疾病不确定性的来源,包括诊断延迟,不可预测的治疗效果和毒性,以及疾病相关的发病率和死亡率。结节病患者对疾病不确定性的看法尚未得到严格评估,并为提供者提供了一个机会,以确定护理和患者支持方面的差距。研究问题:结节病患者如何描述他们与疾病的生活经历以及他们在接受治疗时面临的挑战?研究设计和方法:我们对在三级结节病卓越中心就诊的经活检证实正在接受治疗的肺结节病患者进行了半结构化定性访谈。访谈检查了结节病患者的生活经历,包括他们的诊断、治疗和疾病活动监测过程。抄本被编码并分类为主题和副主题。饱和被定义为至少3次没有新信息的采访。结果:25名参与者完成了半结构化访谈。中位年龄为60岁,64%的参与者是女性,68%的参与者是黑人。疾病不确定性的影响是他们护理旅程的一个共同组成部分。出现的关键主题是:1)疾病意识有限的负担;2)结节病管理的不确定性;3)疾病进展的不可预测性。不确定性成为造成护理延误、疾病控制不良和/或心理困扰的主要挑战。解释:我们的发现首次强调了患者疾病不确定性对结节病疾病结局和心理困扰的影响。结节病患者可以通过解决不确定性的社会心理影响而获益。患有结节病的个体可以从有针对性的干预措施中显著受益,以减轻疾病不确定性的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chest
Chest 医学-呼吸系统
CiteScore
13.70
自引率
3.10%
发文量
3369
审稿时长
15 days
期刊介绍: At CHEST, our mission is to revolutionize patient care through the collaboration of multidisciplinary clinicians in the fields of pulmonary, critical care, and sleep medicine. We achieve this by publishing cutting-edge clinical research that addresses current challenges and brings forth future advancements. To enhance understanding in a rapidly evolving field, CHEST also features review articles, commentaries, and facilitates discussions on emerging controversies. We place great emphasis on scientific rigor, employing a rigorous peer review process, and ensuring all accepted content is published online within two weeks.
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