精神疾病污名化对专业知识发展和实践的影响:从结构性暴力角度看跨专业健康教育框架

Sebastian Gyamfi PhD, MPhil, Cheryl Forchuk PhD, RN, Isaac Luginaah PhD, FAAS
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引用次数: 0

摘要

精神疾病患者(PWMI)继续遭受公众的耻辱,并带来负面后果。最近的病耻感论述指出,权力差异是在社会环境中形成与精神疾病相关的病耻感的关键。众所周知,对PWMI的社会不公正存在于轶事和文献论述中。污名是公众态度和行为的产物,这些态度和行为表现为标签、刻板印象、偏见、认知分离、地位丧失和歧视,这些反应可能包括对现有权力关系差异所支撑的社会行为的经历、预期、感知或个人认可的压力和与尊重相关的评价。这种社会不公正(不公平待遇)对残疾人的潜在后果可能导致耻辱及其后遗症,包括低社会经济地位、压力、低自尊、失业、无家可归、排斥和侵犯人权。本文提出了一个跨专业健康教育框架,并讨论了这种不公平的社会待遇对医疗保健专业人员专业知识发展和实践的影响,以期改善协作和患者护理结果。一种更加协作的护理模式,即服务使用者和临床医生相互认为对方知识渊博,有共同的力量来实现健康的结果,使患者在自己不足的领域获得更大的能力。
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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Implications of the stigma of mental illness for professional knowledge development and practice: An Interprofessional Health Education framework from structural violence perspectives

Persons with mental illness (PWMI) continue to encounter stigma from the public with negative outcomes. Recent stigma discourse points to power differentials as key in shaping stigma related to mental illness within social settings. The perceived social injustice towards PWMI is known to exist both anecdotally and in documented discourses. Stigma constitutes the product of public attitudes and behaviors that characterize labeling, stereotyping, prejudice, cognitive separation, status loss, and discrimination that lead to responses that may include stress and esteem-related appraisal of experienced, anticipated, perceived, or personal endorsement of societal actions that are anchored by existing power relational differentials. The potential consequence of such societal injustices (unfair treatments) towards PWMI may result in stigma and its sequels, including low socioeconomic status, stress, low self-esteem, unemployment, homelessness, exclusion, and human rights abuse. This paper proposes an Interprofessional Health Education framework and discusses the implications of such unfair social treatments for Professional knowledge development and practice among healthcare professionals, with the view to improving collaboration and patient care outcomes. A more collaborative model of care, where service users and clinicians regard each other as knowledgeable with shared power to achieve healthy outcomes, empowers patients even more in areas where they fall short.

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