Shohet Merav, Nguyen Nicole H, Stern Lauren D, Waikar Sushrut S, Schmidt Insa M
Boston University College & Graduate School of Arts and Sciences, Department of Anthropology, Boston, MA.
Boston University Sargent College of Health and Rehabilitation Sciences, Boston, MA.
Kidney Med. 2023 Aug 25;5(11):100717. doi: 10.1016/j.xkme.2023.100717. eCollection 2023 Nov.
RATIONALE & OBJECTIVE: Racial and ethnic minority groups in the United States are disproportionately affected by chronic kidney disease and progressive kidney failure and face significantly more socioeconomic and psychosocial challenges. However, how such patients' social environment and stigmatization shape their illness experiences and abilities to cope before and during the coronavirus disease 2019 (COVID-19) pandemic has not been well documented, even as social scientific research predicts these groups' exponential vulnerability.
Qualitative study using semistructured interviews to elicit individual patient narratives about their personal illness experiences before and during the COVID-19 pandemic, any challenges they faced, and their sources of support.
SETTING & PARTICIPANTS: Using purposive sampling, we recruited 20 adult patients receiving maintenance hemodialysis from centers affiliated with a safety-net hospital in Boston, Massachusetts.
Interviews were audiotaped, transcribed, and analyzed using thematic content analysis to identify patients' challenges and supports before and during the pandemic.
Of the 20 patients in the study, 9 were women, and 18 self-identified as Black or African American. Three main themes emerged, whereby most patients described: (1) stigma and stigmatization as a central element of their life experience; (2) the pandemic as a difficult experience but not a complete rupture from their prepandemic life; and (3) social networks, particularly family, friends, and religious communities, as sources of support crucial to coping with their debilitating illness.
Whether the findings apply to other settings is unknown, as participants were recruited from centers in a single safety-net urban hospital setting.
Psychosocial and environmental factors, including institutional racism and stigmatization, play significant roles in amplifying the burdens shouldered by racial and ethnic minority individuals with kidney disease who now also face the COVID-19 pandemic that has since turned endemic. The results of this study can inform the development of policy interventions aimed at alleviating tensions and structural conditions that impinge on kidney disease patients' wellbeing and health outcomes.
PLAIN-LANGUAGE SUMMARY: Members of racial and ethnic minority groups in the United States experience the highest rates of progressive kidney failure and face significantly more socioeconomic and psychosocial challenges. We interviewed 20 patients who receive maintenance hemodialysis treatment from centers affiliated with a safety-net hospital. Patients described stigmatization as a central element of their life experience and the pandemic as a difficult challenge (but not a complete rupture) that added to their struggles with illness-related, race-related, and class-related stigmas. Social networks, particularly family, friends, and religious communities, are key sources of support crucial to coping with illness. Findings from this study can inform health care providers and community workers and guide the development of policy interventions to provide better support for these patients.
美国的少数族裔群体受慢性肾脏病和进行性肾衰竭的影响尤为严重,面临着更多的社会经济和心理社会挑战。然而,在2019冠状病毒病(COVID-19)大流行之前及期间,这类患者的社会环境和污名化如何塑造他们的患病经历及应对能力,即便社会科学研究预测这些群体极易受到影响,相关记录仍不完善。
采用半结构式访谈的定性研究,以获取患者个人关于COVID-19大流行之前及期间的患病经历、所面临的任何挑战以及支持来源的叙述。
采用目的抽样法,我们从马萨诸塞州波士顿一家安全网医院附属中心招募了20名接受维持性血液透析的成年患者。
访谈进行录音、转录,并采用主题内容分析法进行分析,以确定大流行之前及期间患者的挑战和支持因素。
研究中的20名患者中,9名是女性,18名自我认定为黑人或非裔美国人。出现了三个主要主题,大多数患者描述:(1)污名和被污名化是他们生活经历的核心要素;(2)大流行是一段艰难经历,但并非与大流行前的生活完全脱节;(3)社会网络,尤其是家人朋友和宗教团体,是应对其衰弱疾病至关重要的支持来源。
由于参与者是从单一安全网城市医院环境中的中心招募的,这些发现是否适用于其他环境尚不清楚。
心理社会和环境因素,包括制度性种族主义和污名化,在加重少数族裔肾病患者的负担方面发挥着重要作用,这些患者现在还面临着已成为地方病的COVID-19大流行。本研究结果可为旨在缓解影响肾病患者福祉和健康结果的紧张局势和结构性状况的政策干预措施的制定提供参考。
美国少数族裔群体经历进行性肾衰竭的比例最高,面临更多的社会经济和心理社会挑战。我们采访了20名从安全网医院附属中心接受维持性血液透析治疗的患者。患者将被污名化描述为其生活经历的核心要素,将大流行描述为一项艰难挑战(但并非完全脱节),这加剧了他们与疾病相关、种族相关和阶级相关污名的斗争。社会网络,尤其是家人、朋友和宗教团体,是应对疾病至关重要的支持关键来源。本研究结果可为医疗保健提供者和社区工作者提供参考,并指导政策干预措施的制定,以便为这些患者提供更好的支持。