Aboul-Hassan Deena, Summerville Johari, Yalavarthi Bhaavna, Farahani Nikki, Yu Christine, Xiao Lillian Z, Rajgarhia Sia, Clauw Daniel J, Kahlenberg J Michelle, DeJonckheere Melissa, Bergmans Rachel S
Medical School, Department of Anesthesiology, University of Michigan, Ann Arbor, United States.
Medical School, Department of Internal Medicine, University of Michigan, Ann Arbor, United States.
Disabil Health J. 2025 Apr;18(2):101713. doi: 10.1016/j.dhjo.2024.101713. Epub 2024 Oct 23.
Black people have disproportionately high morbidity and mortality due to systemic lupus erythematosus (SLE). Features of social and occupational environments can protect against poor health outcomes.
We aimed to characterize how SLE intersects with interpersonal relationships and employment among Black adults to inform tailored care approaches and public policies that could alleviate racial inequities in SLE.
We used a qualitative, interpretive description approach that involved semi-structured interviews with Black adults who had SLE. The interview guide included questions about SLE diagnosis, impacts on day-to-day life, and symptom management. We analyzed the de-identified transcripts using inductive, thematic analysis with input from representatives of the study population. Our theme development focused on how SLE (i.e., symptoms, severity, management) intersected with interpersonal relationships and employment.
This study included 30 interviews (97 % female, age range = 18-65 years). Among participants, 30 % were not working due to unemployment or disability and 23 % reported a lack of emotional support. Our analysis resulted in three main themes: 1) The bi-directional relationship between employment and SLE; 2) The positive and negative effects of connecting with other people who have SLE; and 3) The moderating role of relationships with family and friends, and the impact on self-identity.
This study describes features of social and occupational environments that influence SLE management and wellbeing. Our results highlight directions for further study that could identify and address how systemic racism affects race-based inequities in SLE.
由于系统性红斑狼疮(SLE),黑人的发病率和死亡率高得不成比例。社会和职业环境的特征可以预防不良健康结果。
我们旨在描述SLE与黑人成年人的人际关系和就业之间的交叉情况,为能够减轻SLE中种族不平等现象的量身定制的护理方法和公共政策提供信息。
我们采用了定性的、解释性描述方法,对患有SLE的黑人成年人进行了半结构化访谈。访谈指南包括有关SLE诊断、对日常生活的影响以及症状管理的问题。我们使用归纳性主题分析方法,在研究人群代表的参与下,对去识别化的访谈记录进行了分析。我们的主题开发重点是SLE(即症状、严重程度、管理)如何与人际关系和就业交叉。
本研究包括30次访谈(97%为女性,年龄范围为18 - 65岁)。在参与者中,30%因失业或残疾而未工作,23%报告缺乏情感支持。我们的分析产生了三个主要主题:1)就业与SLE之间的双向关系;2)与其他患有SLE的人建立联系的积极和消极影响;3)与家人和朋友关系的调节作用以及对自我认同的影响。
本研究描述了影响SLE管理和幸福感的社会和职业环境特征。我们的结果突出了进一步研究的方向,这些研究可以确定并解决系统性种族主义如何影响SLE中基于种族的不平等问题。