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The effect of social support on depression in African American women diagnosed with systemic lupus erythematosus.

机译:社会支持对诊断为系统性红斑狼疮的非洲裔美国女性抑郁症的影响。

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摘要

Systemic lupus erythematosus (SLE) affects more African American women than any other group, and with greater level of morbidity and mortality. There are a myriad of challenges facing the African American woman diagnosed with SLE and there have been very few studies that addressed these challenges. Socio-economic factors such as education, occupation, income, and lifestyles play a significant role the misdiagnosis, delayed diagnosis, and poor disease management, placing the African American female at greater risk for earlier and more serious organ system involvement than other groups living with SLE. The magnitude of depression in SLE is not fully known because of the many factors impeding clear understanding. Yet, there have been few studies that examined SLE and depression in relation to social support. This study was undertaken to examine perceptions of the relationship between social support and depression among African American women living with SLE and to explore the relationship among depression, social support and the frequency and intensity of SLE flares. A purposeful sample of ten African American women between 30 and 50 years old, diagnosed with SLE for at least two years, and experiencing mild to severe depression as determined by the Beck Depression Inventory-II, were recruited from members of two community-based lupus support groups in a large metropolitan area. The lived experience of depression from the perspective of the African American women is unique and can be fully understood only through the lens of the individuals living with SLE. Depression is poorly understood and is often mistaken as a part of the SLE rather than a comorbid condition. As such it can remain untreated, placing the individual at a greater risk for more frequent SLE flares and further deepened the depression. Grounded theory was used to collect and analyze data from semi-structured interviews with the participants. Data analysis revealed many of the challenges experienced by African American women living with SLE. Additionally, participants reported using a variety of coping strategies to confront the challenges of living with SLE. The study's findings indicate that social support plays an important role in the development of coping strategies in the management of SLE and depression in African American women. Limitations of the study include the small sample size and homogeneity of the participants. However, although the study's findings cannot be generalized beyond the present sample, there was wide agreement among the participants on the challenges of living with SLE and helpful coping strategies. The study's findings provide an opportunity to explore the experiences of African American women living with SLE and elucidate potential interventions for this group and health care professionals who work with them.
机译:系统性红斑狼疮(SLE)对非裔美国女性的影响比其他任何群体都要多,发病率和死亡率也更高。被诊断患有SLE的非洲裔美国妇女面临着众多挑战,而针对这些挑战的研究很少。社会经济因素(如教育,职业,收入和生活方式)在误诊,延迟诊断和不良疾病管理中起着重要作用,这使非裔美国女性比其他同居人群更容易发生更早和更严重的器官系统受累。 SLE。由于许多因素妨碍人们清楚地了解,SLE的抑郁程度尚不完全清楚。但是,很少有研究针对社会支持与SLE和抑郁症进行研究。这项研究的目的是检查对患有SLE的非洲裔美国妇女社会支持与抑郁之间关系的看法,并探讨抑郁,社会支持与SLE发作频率和强度之间的关系。从两个社区狼疮患者中招募了有目的的10名30至50岁,被诊断为SLE至少两年并且经历了轻度至重度抑郁症的非洲裔美国妇女(根据贝克抑郁量表II的调查结果)。大城市地区的支持小组。从非洲裔美国妇女的角度来看,抑郁症的真实经历是独特的,只有通过SLE患者的个人才能充分理解。人们对抑郁症了解甚少,常常被误认为是SLE的一部分,而不是合并症。因此,它可能得不到治疗,从而使个体更有可能发生更频繁的SLE耀斑,并进一步加重了抑郁症。扎根理论被用来收集和分析来自参与者半结构化访谈的数据。数据分析显示,患有SLE的非洲裔美国妇女面临着许多挑战。此外,参与者报告说使用了多种应对策略来应对SLE的生活挑战。该研究结果表明,社会支持在应对非洲裔美国妇女SLE和抑郁症的应对策略中起着重要作用。该研究的局限性包括样本量小和参与者的同质性。但是,尽管该研究的结果无法在当前样本范围之外进行概括,但参与者之间就SLE生活和有效应对策略所面临的挑战达成了广泛共识。这项研究的发现为探索非洲裔美国人患有SLE的妇女提供了一个机会,并阐明了该人群和与之合作的医疗保健专业人员的潜在干预措施。

著录项

  • 作者

    Howe, Monica G.;

  • 作者单位

    Adler School of Professional Psychology.;

  • 授予单位 Adler School of Professional Psychology.;
  • 学科 Psychology Clinical.
  • 学位 Psy.D.
  • 年度 2009
  • 页码 74 p.
  • 总页数 74
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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