Using photovoice to investigate patient experiences of lupus nephritis in Canada.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY Lupus Science & Medicine Pub Date : 2024-11-07 DOI:10.1136/lupus-2024-001265
Francesca S Cardwell, Susan J Elliott, Megan R W Barber, Kim Cheema, Sydney George, Adrian Boucher, Ann Elaine Clarke
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Abstract

Objective: Lupus nephritis (LN) is a major cause of morbidity and mortality, affecting up to 60% of patients with systemic lupus erythematosus (SLE). The perspectives of patients with SLE have been explored; however, little is known of the lived experiences of patients with LN.

Methods: Patients aged ≥18 years with biopsy-proven pure or mixed International Society of Nephrology/Renal Pathology Society Class III, IV or V LN were purposefully recruited from a Canadian lupus cohort to participate in a photovoice (visual-narrative participatory research method) exercise. Participants took photos of what LN means to them, impacts on daily life and factors impacting LN management. Photos were shared and discussed in focus groups.

Results: 13 individuals with LN participated (92.3% were female; mean (SD) age was 41.7 (14.0) years). The mean (SD) number of photos shared per participant was 4.2 (0.9). Photos (n=54) depicted activities/settings that contribute to well-being (n=15), the participants themselves (n=13), healthcare experiences (n=10), home (n=4), community (n=2), friends (n=2), work (n=2) and other challenges (n=6). All participants described physical and psychosocial impacts of living with LN. Although 12 mentioned activities/settings that contribute to well-being (eg, time in natural environments), participants were consistently reminded of limitations imposed by LN due to physical symptoms, challenges presented by the physical environment and the altered life trajectories experienced. Participants discussed the dual burden of LN and the associated medication journey; side effects and medication-related financial challenges were highlighted by ten and five participants, respectively.

Conclusions: Participants reported a substantial psychosocial burden associated with altered life trajectories, the dual burden of LN and the associated medication journey, and the conflicting role of the physical environment. The need for flexibility (ie, from employers, themselves) is an essential component of navigating altered life trajectories.

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在加拿大,利用摄影自选来调查狼疮性肾炎患者的经历。
目的:狼疮性肾炎(LN)是发病和死亡的主要原因之一,高达60%的系统性红斑狼疮(SLE)患者都会患上该病。人们对系统性红斑狼疮患者的视角进行了探讨,但对 LN 患者的生活经历却知之甚少:从加拿大狼疮队列中有目的地招募了年龄≥18 岁、活检证实患有纯合子或混合性国际肾脏病学会/肾脏病理学学会 III、IV 或 V 级 LN 的患者,让他们参加摄影选言(视觉叙事参与式研究方法)活动。参与者拍摄照片,记录 LN 对他们的意义、对日常生活的影响以及影响 LN 管理的因素。照片在焦点小组中进行分享和讨论:13 名 LN 患者参加了此次活动(92.3% 为女性;平均(标清)年龄为 41.7(14.0)岁)。每位参与者分享照片的平均(标清)数量为 4.2 (0.9)张。照片(n=54)描述了有助于身心健康的活动/环境(n=15)、参与者本人(n=13)、医疗保健经历(n=10)、家庭(n=4)、社区(n=2)、朋友(n=2)、工作(n=2)和其他挑战(n=6)。所有参与者都描述了与 LN 共同生活对身体和心理的影响。尽管有 12 位参与者提到了有助于身心健康的活动/环境(例如,在自然环境中度过的时间),但他们始终认为 LN 带来的限制是由于身体症状、物理环境带来的挑战以及生活轨迹的改变。参与者讨论了 LN 和相关药物治疗带来的双重负担;分别有 10 名和 5 名参与者强调了副作用和与药物治疗相关的经济挑战:与会者报告了与生活轨迹改变、LN 和相关药物治疗的双重负担以及物理环境的冲突作用相关的巨大社会心理负担。对灵活性的需求(即来自雇主和自身的需求)是驾驭改变后的生活轨迹的重要组成部分。
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
Lupus Science & Medicine
Lupus Science & Medicine RHEUMATOLOGY-
CiteScore
5.30
自引率
7.70%
发文量
88
审稿时长
15 weeks
期刊介绍: Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.
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