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尼日利亚白癜风患者的生活体验:一项参与性解释现象学分析

The experience of living with vitiligo in Nigeria: A participatory Interpretative Phenomenological Analysis.

作者信息

Taylor Nick, Maduesesi Ogo, Vasiliou Vasilis S, Thompson Andrew R

机构信息

The University of Sheffield, UK.

Unmind, UK.

出版信息

J Health Psychol. 2025 Apr;30(5):1120-1135. doi: 10.1177/13591053241261684. Epub 2024 Jul 30.

Abstract

Vitiligo is a visible depigmenting skin condition, particularly noticeable on Black skin. There is widespread misunderstanding of the condition. Using a participatory form of Interpretative Phenomenological Analysis (IPA), we conducted eight semi-structured interviews with Nigerians living with vitiligo. Participants described their initial attempts to understand the condition, which typically drew on both traditional illness beliefs, religious influences, and the biomedical disease model. All participants reported experiencing marked stigmatization and discrimination. Participants experienced distress associated with thoughts about the personal meaning of the disease including its impact on their appearance and from concerns about anticipated and direct discrimination. Despite the wide-ranging impact, the participants' narratives also contained references to the development of strategies that maintained wellbeing. This study provides valuable insights into the role of faith and traditional beliefs in both the experience and management of vitiligo in Nigeria. These insights can be used to develop individual and community interventions.

摘要

白癜风是一种皮肤色素脱失性疾病,在黑色皮肤上尤为明显。人们对这种疾病存在广泛的误解。我们采用参与式解释现象学分析(IPA)方法,对八名患白癜风的尼日利亚人进行了半结构化访谈。参与者描述了他们最初尝试理解病情的过程,这通常借鉴了传统疾病观念、宗教影响以及生物医学疾病模型。所有参与者都报告遭受了明显的污名化和歧视。参与者因思考疾病的个人意义(包括其对外表的影响)以及对预期和直接歧视的担忧而感到痛苦。尽管影响广泛,但参与者的叙述中也提到了维持幸福感的策略的发展。本研究为信仰和传统信念在尼日利亚白癜风的体验和管理中的作用提供了有价值的见解。这些见解可用于制定个人和社区干预措施。

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