与文化和语言多元化社区合作,推广超出预期的姑息关怀。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Ann Dadich, Gregory Crawford, Peter Laintoll, Issac Zangre, Kamal Dahal, Dalia Albrezi, Cathie Jeffs, Aileen Collier
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引用次数: 0

摘要

导言:鉴于长期以来阻碍综合姑息关怀的障碍,尤其是对文化和语言多元化社区而言,本文展示了一种与叙利亚、不丹和非洲社区接触的方法,以便与这些社区的成员一起并从他们那里了解出色的姑息关怀:本研究采用了 POSH-VRE 方法,该方法将医疗保健中的积极组织学术研究(POSH)与视频反思人种学(VRE)相结合。叙利亚、不丹和非洲社区的成员(n = 14)参加了一个焦点小组或一次访谈,以思考对姑息关怀的理解;对美好死亡的概念化;姑息关怀在其社区的典型实施方式和原因;相关影响;以及文化和语言多样性社区与公共姑息关怀服务之间的关系。在讨论过程中,我们还参考了之前关于精彩姑息关怀研究的视频录像,并邀请参与者回顾这些视频录像。采用反思性主题分析法对焦点小组和访谈的视频录像和文字记录进行了分析:结果:参与者对姑息关怀的理解和实施方式存在很大差异。对一些人来说,死亡是一个禁忌话题,而对另一些人来说,死亡是必须面对的现实,尤其是在战乱地区。同样,虽然医生受到高度评价,但参与者对他们应如何实施姑息关怀和预知死亡持有不同的观点,特别是因为家庭成员被认为是姑息关怀的关键部分。为了改善对罹患生命垂危疾病的不同文化和语言社区人群的关怀,与会者强调了三个机会。这些机遇包括避免一概而论、优先考虑文化群体的需求和偏好以及利用社区网络:本研究展示了如何利用 POSH-VRE 增强对姑息关怀的相互理解。具体而言,不丹人、非洲人和叙利亚人社区的成员展示了不同文化和语言社区在需求、偏好和习俗方面的多样性。因此,放弃对文化群体希望如何被转诊和护理的假设,采用公共卫生的姑息关怀方法,既以人口为基础又以人为中心的关怀方法,很可能会促进综合姑息关怀:不丹、非洲和叙利亚社区的成员作为参与者和共同研究者为本研究做出了贡献,为数据的分析和解释以及文章的撰写做出了贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation

Introduction

Given longstanding barriers that obstruct integrated palliative care, particularly for culturally and linguistically diverse communities, this article demonstrates a way to engage with Syrian, Bhutanese and African communities to learn about brilliant palliative care with and from members of these communities.

Methods

This study involved the methodology of POSH-VRE, which combines positive organisational scholarship in healthcare (POSH) with video-reflexive ethnography (VRE). Members of the Syrian, Bhutanese, and African communities (n = 14) participated in a focus group or an interview to consider understandings of palliative care; conceptualisations of a good death; how and why palliative care was typically enacted in their communities; the associated effects; as well as the relationship between culturally and linguistically diverse communities and public palliative care services. Discussions were aided by video recordings captured during the previous study on brilliant palliative care, which participants were invited to review. Video recordings and transcripts of the focus groups and interview were analysed using reflexive thematic analysis.

Results

The participants demonstrated considerable variability in the ways that palliative care was understood and enacted. For some, death was a taboo topic, while for others, it was a reality that was required to face, particularly in war-torn regions. Similarly, while doctors were held in high regard, participants held different views about how they should enact palliative care and the anticipation of death, particularly because family members were deemed to be a pivotal part of palliative care. To improve the care of people of culturally and linguistically diverse communities who experience a life-limiting illness, participants highlighted three opportunities. These included the avoidance of generalisations, prioritising the needs and preferences of cultural groups, and leveraging the community network.

Conclusion

This study demonstrated how reciprocal understandings of palliative care were potentiated using POSH-VRE. Specifically, the members of the Bhutanese, African and Syrian communities demonstrated diversity in the needs, preferences, and customs of culturally and linguistically diverse communities. As such, integrated palliative care is likely to be bolstered by relinquishing assumptions about how cultural groups wish to be referred to and cared for and adopting a public health approach to palliative care that embraces both a population-based and person-centred approach to care.

Patient or Public Contribution

Members of the Bhutanese, African and Syrian communities contributed to this study as participants and co-researchers, contributing to the analysis and interpretation of the data and in the preparation of the article.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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