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Journal of Social Work in End-of-Life & Palliative Care最新文献

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Social Workers as Leaders for Facilitating Trauma-Informed Palliative Care in the Outpatient Palliative Care Clinic. 社会工作者作为促进门诊姑息治疗诊所创伤知情姑息治疗的领导者。
IF 1.6 Q3 Social Sciences Pub Date : 2023-10-01 Epub Date: 2023-12-01 DOI: 10.1080/15524256.2023.2262157
Jennifer DiBiase

Palliative care social workers are trained to identify how trauma manifests over the course of serious and chronic illness. This expertise can guide patients and team members to ensure a trauma-informed experience of care. This paper identifies the growth of outpatient palliative care clinics as an opportunity for palliative care social workers to emphasize this clinical skill set and assume a leadership role in the implementation of trauma-informed practices early in the trajectory of serious illness.

姑息护理社会工作者接受培训,以确定创伤在严重和慢性疾病过程中的表现。这种专业知识可以指导患者和团队成员确保创伤知情的护理体验。本文将门诊姑息治疗诊所的发展确定为姑息治疗社会工作者强调这一临床技能集的机会,并在严重疾病早期实施创伤知情实践中发挥领导作用。
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引用次数: 0
The Experience of Living with a Chronic Illness: A Qualitative Study among End-Stage Renal Disease Patients. 慢性病患者的生活经验:终末期肾病患者的定性研究。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-07-11 DOI: 10.1080/15524256.2023.2229034
Ginu George Powathil, Anish Kr

The prevalence of End-Stage Renal Disease (ESRD) has been rising over time and substantially affects morbidity and mortality. ESRD requires lifelong treatment, and as a result, patients experience multiple physical and psychosocial stressors. ESRD patients struggle to retain their jobs, social lives, financial flexibility, and diet restrictions of liquids and solid foods. The present study aims to understand the experiences of ESRD patients undergoing hemodialysis. The study was conducted at Eldho Mor Baselious Dialysis Center in Perumbavoor, Kerala, in the hemodialysis outpatient unit. The Biopsychosocial model was used as the theoretical framework of the study. As the goal of the study was to investigate the inner experiences of ESRD patients, a qualitative research approach was employed. Twelve respondents were selected for the study using purposive sampling, and the data were organized and analyzed using Colaizzi's descriptive phenomenological method. Four theme categories emerged from data analysis: decline in physical function, psychosocial distress, economic hardships, and impact on the support system. The study shows that ESRD patients experience significant psychosocial and health-related issues. The role of the clinical social worker is vital as there is a need for social work interventions to resolve the psychosocial issues of patients with ESRD.

终末期肾病(ESRD)的患病率随着时间的推移而上升,并对发病率和死亡率产生重大影响。ESRD需要终身治疗,因此,患者会经历多种身体和心理压力。ESRD患者很难保住自己的工作、社交生活、经济灵活性以及液体和固体食物的饮食限制。本研究旨在了解ESRD患者进行血液透析的经验。这项研究是在喀拉拉邦佩伦巴沃的Eldho Mor Baselious透析中心血液透析门诊部进行的。生物心理社会模型被用作研究的理论框架。由于本研究的目的是调查ESRD患者的内心经历,因此采用了定性研究方法。采用有目的的抽样方法选择了12名受访者进行研究,并使用Colaizzi的描述性现象学方法对数据进行了组织和分析。数据分析得出四个主题类别:身体功能下降、心理痛苦、经济困难和对支持系统的影响。研究表明,ESRD患者经历了重大的心理社会和健康问题。临床社会工作者的作用至关重要,因为需要社会工作干预来解决ESRD患者的心理社会问题。
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引用次数: 0
Pathways of Individuals Experiencing Serious Illness While Homeless: An Exploratory 4-Point Typology from the RASCAL-UP Study. 无家可归者经历严重疾病的途径:RASCAL-UP研究的4点类型学探索。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-18 DOI: 10.1080/15524256.2023.2223772
Ian M Johnson, Michael A Light

The shifting age demographics of those experiencing homelessness in the United States expose shortcomings and barriers within homelessness response services and safety-net healthcare to address serious illness. The purpose of this study is to describe the common trajectories of patients concurrently experiencing homelessness and serious illness. As a part of the Research, Action, and Supportive Care at Later-life for Unhoused People (RASCAL-UP) study, the study uses patient charts (n = 75) from the only specialty palliative care program in the U.S. specifically for people experiencing homelessness. Through a thematic mixed-method analysis, a four-point typology of care pathways taken by people experiencing homelessness while seriously ill is introduced: (1) aging and dying-in-place within the housing care system; (2) frequent transitions during serious illness; (3) healthcare institutions as housing; and (4) housing as palliation. Implications of this exploratory typology include targeted, site-specific interventions for supporting goal-concordant patient care and assisting researchers and policy makers in appreciating heterogeneity in experience and need among older and chronically ill people experiencing homelessness and housing precarity.

美国无家可归者年龄结构的变化暴露了无家可归者应对服务和解决严重疾病的安全网医疗保健方面的缺陷和障碍。本研究的目的是描述同时经历无家可归和严重疾病的患者的常见轨迹。作为“无人居住者的研究、行动和晚年支持性护理”(RASCAL-UP)研究的一部分,该研究使用了患者图表(n = 75),这是美国唯一一个专门针对无家可归者的专业姑息治疗项目。通过主题混合方法分析,介绍了重病期间无家可归者所采取的护理途径的四点类型:(1)住房护理系统中的老龄化和死亡;(2) 在严重疾病期间频繁转换;(3) 医疗机构作为住房;以及(4)作为缓和的住房。这种探索性类型的含义包括有针对性的、针对特定地点的干预措施,以支持目标一致的患者护理,并协助研究人员和政策制定者了解无家可归和住房不稳定的老年人和慢性病患者的经验和需求的异质性。
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引用次数: 1
Stretching a Penny: Completing a Rapid Needs Assessment for a Nonprofit Community-Based Hospice Wellness Center in Ontario, Canada. 花一分钱:为加拿大安大略省一家非营利社区临终关怀健康中心完成快速需求评估。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-29 DOI: 10.1080/15524256.2023.2229037
Michael R Bennett, Carly Charron, Patricia Valcke

The literature pertaining to community-based hospice wellness centres, especially concerning program evaluation, is sparse. This article describes the development and implementation of a mixed-method, rapid needs assessment for a nonprofit community-based hospice wellness centre in Ontario, Canada. As part of the needs assessment, a survey and focus groups were performed to elicit responses from service users. Individuals registered for services and wellness centre attendees were asked about their needs, opinions, and preferences to help guide future program and service options. Findings and recommendations are presented for programming and service options, and implications for future program evaluation projects are discussed. The methodology of this time and cost-efficient evaluation provides insights that can be utilized by other hospice wellness centres facing similar challenges of time, money, and program evaluation expertise constraints. The findings and recommendations may inform program and service offerings at other Canadian hospice wellness centres.

关于社区临终关怀健康中心的文献,特别是关于项目评估的文献很少。本文描述了加拿大安大略省一家非营利性社区临终关怀健康中心的混合方法快速需求评估的开发和实施。作为需求评估的一部分,进行了一项调查和焦点小组,以征求服务用户的回应。注册服务的个人和健康中心参与者被问及他们的需求、意见和偏好,以帮助指导未来的计划和服务选择。对方案和服务选项提出了调查结果和建议,并讨论了对未来方案评估项目的影响。这种时间和成本效益评估的方法提供了一些见解,可供其他面临类似时间、金钱和项目评估专业知识限制挑战的临终关怀健康中心使用。这些发现和建议可能会为加拿大其他临终关怀健康中心的计划和服务提供信息。
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引用次数: 0
Bearing Witness: The Power of Presence. 见证:存在的力量。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-02 DOI: 10.1080/15524256.2023.2219407
Aline Demerjian
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引用次数: 0
Editor Introduction. 编辑简介。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 DOI: 10.1080/15524256.2023.2248808
Ellen L Csikai
Welcome to another issue! In a look ahead to the final issue of this volume, the issue will contain reflections and practice concepts and innovations manuscripts that were submitted in response to a “call” pertaining to trauma-informed practice within endof-life and palliative care. This issue begins with the thoughtful reflections of three authors: Demerjian, Abrams and Olsen. I am always impressed with these reflections that definitely give pause to spur on our own reflection or to learn a new or different way to view. This issue’s “Practice Concepts and Innovations,” brings awareness to a vital part of communication and quality of life and near the end of life: the ability to hear. Hughes describes a hearing aid loan program that provided hearing aids to individuals to their benefit as well as their caregivers. The author discusses the intervention, partnerships formed and challenges identified in implementing this type of program. Social workers may wish to consider designing a similar problem with partners as a resource for hearing loss within hospice and palliative care settings. The first of the research articles, highlights the prevalence of end-stage renal and the experiences of individuals in hemodialysis. Because ESRD is a chronic illness with deterioration in kidney function over time, even with following treatment plans, it often comes with many physical and psychosocial stressors. Powathil & AR describe a qualitative study conducted in a dialysis center in India. The participants described their decline in physical functioning and psychosocial concerns, including social support system changes and economic hardships. The authors place these results within their cultural context. What remains similar is the need for social work interventions to help individuals and families cope with the stressors of this end stage disease. When someone has a serious illness, it seems most would assume that treatment of the illness should bring about at least some relief from symptoms that may be causing distress. It is often not widely acknowledged by health care professionals that there are other factors that could interfere with treatment, such as homelessness. Johnson and colleagues present a study examining the common experiences that people who have unstable housing and a concurrent serious illness may face while living with the illness and seeking treatment. The authors then craft these common experiences found into a typology of pathways that may be seen. These include aging and dying within the housing care system, frequent transitions, “use” of health facilities as housing and stable housing seen as palliative (providing comfort). Practitioners and policy advocates can utilize this typology to bring further attention to this growing problem. Next, Bennett and colleagues share a methodology utilized for a rapid needs assessment that was used for a nonprofit community-based hospice wellness center. Multiple methods of data collection was used
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引用次数: 0
Challenges and Innovations in Hospice Care during the COVID-19 Pandemic: A Scoping Review. 新冠肺炎大流行期间临终关怀的挑战和创新:范围界定综述。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-30 DOI: 10.1080/15524256.2023.2229036
Patricia Dobríková, Regina Scheitel, Audrey Roulston

In addition to addressing nursing and medical needs, the social needs of patients within hospice care require assessment (i.e., relationships, isolation, loneliness, societal inclusion or exclusion, negotiating adequate formal and informal support, or living with a life-limiting condition). The objectives of this scoping review are to examine the challenges of adult patients in receipt of hospice care during the COVID-19 pandemic and to identify innovative changes to care during the pandemic. The methodology of the scoping review follows the Joanna Briggs Institute framework developed in 2015. The context included hospice services (inpatient, outpatient and community). In August 2022, PubMed and SAGE journals were searched from 2020 onwards for studies published in English, which focused on COVID-19, hospice, social, support and challenges. Titles and abstracts were independently screened by two reviewers against agreed criteria. Fourteen studies were included. Data were independently extracted by authors. Emerging themes were loss due to COVID-19 restrictions, challenges for staff, barriers to communication and transition to Telemedicine, and positive effects of the pandemic. Pivoting to Tele-medicine and restricting visitors reduced the risk of spreading coronavirus but resulted in patients being socially isolated from loved ones, and a reliance on technology to have sensitive conversations.

除了解决护理和医疗需求外,临终关怀患者的社会需求还需要评估(即关系、隔离、孤独、社会包容或排斥、协商适当的正式和非正式支持,或生活在限制生命的条件下)。本范围审查的目的是审查成年患者在新冠肺炎大流行期间接受临终关怀的挑战,并确定大流行期间护理的创新变化。范围界定审查的方法遵循乔安娜·布里格斯研究所2015年制定的框架。背景包括临终关怀服务(住院、门诊和社区)。2022年8月,从2020年起,PubMed和SAGE杂志搜索了以英语发表的研究,这些研究侧重于新冠肺炎、临终关怀、社会、支持和挑战。标题和摘要由两名评审员根据商定的标准进行独立筛选。包括14项研究。数据由作者独立提取。新出现的主题是新冠肺炎限制造成的损失、工作人员面临的挑战、沟通障碍和向远程医疗的过渡以及疫情的积极影响。转向远程医疗和限制访客降低了冠状病毒传播的风险,但导致患者与亲人社交隔离,并依赖技术进行敏感对话。
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引用次数: 0
Hearing Aid Loan Program for Hearing Loss at the End of Life. 针对临终听力损失的助听器贷款计划。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-27 DOI: 10.1080/15524256.2023.2229038
M Courtney Hughes, Diane ScheckLong, King Chung

This article describes a hearing aid loan program to provide free amplification devices for patients at the end of life to help them communicate more effectively at this critical time. It includes steps for establishing such a program, addressing challenges, and the role of the informal caregiver throughout the intervention. Healthcare professionals and social workers are encouraged to develop similar programs and use the information here as helpful suggestions to consider for their programs.

这篇文章描述了一项助听器贷款计划,为生命末期的患者提供免费的放大设备,帮助他们在这个关键时刻更有效地沟通。它包括建立这样一个计划的步骤,应对挑战,以及在整个干预过程中非正式护理人员的作用。鼓励医疗保健专业人员和社会工作者制定类似的计划,并将此处的信息作为他们计划的有用建议。
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引用次数: 0
Agency as a Key to Identity. 代理是身份的关键。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-06-02 DOI: 10.1080/15524256.2023.2219411
Elizabeth Abrahams
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引用次数: 0
Sitting with Helplessness. 无助地坐着。
IF 1.6 Q3 Social Sciences Pub Date : 2023-07-01 Epub Date: 2023-07-04 DOI: 10.1080/15524256.2023.2231160
Catherine Olsen
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引用次数: 0
期刊
Journal of Social Work in End-of-Life & Palliative Care
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