土著重病患者的文化宣传。

Jeanna A Ford, Constance Dahlin
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摘要

美国原住民(I.A. )重病患者及其家人的需求得不到满足。这一群体通常被视为少数中的少数。在 I.A. 人口中,存在着许多健康挑战,导致了严峻的医疗状况。历史创伤和对医疗保健系统的不信任影响了这一边缘人群获得高质量的姑息关怀服务。考虑到一系列社会、精神和文化问题,跨专业团队需要增加对 I.A. 人口的具体了解,以确保提供全面的、文化敏感的护理。本文通过一个案例研究,回顾了身患重病的 I.A. 人士的需求和基本技能。目的是让姑息关怀临床医生掌握相关知识,为患有重病的 I.A. 人及其社区提供文化敏感性和一致的关怀。
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Cultural Advocacy for Indigenous Individuals With Serious Illness.

Indigenous American (I.A.) individuals with serious illness and their families have unmet needs. Often, this group is viewed as a minority within a minority. Numerous health challenges exist within the I.A. populations resulting in dire health care situations. Historical trauma and mistrust of the healthcare system impacts access to quality palliative care by this marginalized population. Given the range of social, spiritual, and cultural issues, the interprofessional team needs increased knowledge specific to the I.A. population to ensure holistic, culturally sensitive care. Utilizing a case study, this article reviews of the needs of I.A. individuals with serious illness and essential skills. The aim is empower palliative care clinicians the knowledge to provide culturally sensitive and congruent care to I.A. individuals with serious illness and their community.

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