描述一群遭遇社会经济不平等并接受姑息关怀的城市患者的特征和症状概况:一项描述性探索分析。

IF 2.7 Q2 HEALTH CARE SCIENCES & SERVICES
Palliative Care and Social Practice Pub Date : 2024-08-01 eCollection Date: 2024-01-01 DOI:10.1177/26323524241264880
Harrison Moore, Cara Bablitz, Anna Santos Salas, Heather Morris, Aynharan Sinnarajah, Sharon M Watanabe
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引用次数: 0

摘要

背景:遭受社会经济不平等待遇的人健康状况较差,在接受姑息关怀和临终关怀方面面临障碍。有必要为这部分服务不足的人群量身定制姑息关怀项目:目的:了解一群经历社会经济不平等并接受姑息关怀的城市患者的特征和症状概况:设计:对患者数据集进行描述性探索分析。该患者数据集是通过一项试点研究产生的,研究对象是社会经济不平等且患有局限生命疾病的患者,他们接受了基于社区的姑息关怀干预:该干预项目在姑息关怀外展和倡导团队(Palliative Care Outreach and Advocacy Team)中进行,为期一年,该团队是加拿大艾伯塔省埃德蒙顿市的一家社区城市姑息关怀诊所,为经历社会经济不平等的患者提供服务。参与者必须年满 18 周岁,能够用英语交流,因患局限生命的疾病而需要姑息关怀,并同意参与研究:共有 25 名参与者参加了研究。参与者主要为男性和原住民,经历过贫困和住房不稳定,并患有转移性癌症。与同城的社区姑息关怀人群相比,我们的参与者对疼痛、呼吸急促和焦虑的评价更为严重。大多数患者死于住院临终关怀医院(73%):我们的分析深入揭示了需要姑息关怀的人群中研究不足、服务欠缺的情况。鉴于参与者的症状严重程度较高,我们的分析强调了以人为本的姑息关怀的重要性。我们建议,对于患有生命垂危疾病的患者,应考虑社会经济不平等问题。还需要进一步的研究来探讨为那些面临社会经济不平等的人提供姑息关怀的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Describing the characteristics and symptom profile of a group of urban patients experiencing socioeconomic inequity and receiving palliative care: a descriptive exploratory analysis.

Background: Individuals experiencing socioeconomic inequity have worse health outcomes and face barriers to palliative and end-of-life care. There is a need to develop palliative care programs tailored to this underserved population.

Objectives: To understand the characteristics and symptom profiles of a group of urban patients experiencing socioeconomic inequity and receiving palliative care.

Design: Descriptive exploratory analysis of a patient dataset. The patient dataset was generated through a pilot research study with patients experiencing socioeconomic inequity and life-limiting illness who received a community-based palliative care intervention.

Methods: The intervention took place over 1 year in the Palliative Care Outreach and Advocacy Team, a community-based urban palliative care clinic in Edmonton, Alberta, Canada, serving persons experiencing socioeconomic inequity. Participants had to be at least 18 years of age, be able to communicate in English, require palliative care for a life-limiting illness, and be able to consent to inclusion in the study.

Results: Twenty-five participants were enrolled. Participants predominantly identified as male and Indigenous, experienced poverty and housing instability, and had metastatic cancer. Our participants rated their pain, shortness of breath, and anxiety as more severe than the broader community-based palliative care population in the same city. Most patients died in inpatient hospices (73%).

Conclusion: Our analysis provides an in-depth picture of an understudied, underserved population requiring palliative care. Given the higher symptom severity experienced by participants, our analysis highlights the importance of person-centered palliative care. We suggest that socioeconomic inequity should be considered in patients with life-limiting illnesses. Further research is needed to explore palliative care delivery to those facing socioeconomic inequity.

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来源期刊
Palliative Care and Social Practice
Palliative Care and Social Practice Nursing-Advanced and Specialized Nursing
CiteScore
2.90
自引率
0.00%
发文量
37
审稿时长
9 weeks
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