“应该有一个随叫随到的护士”:医疗补助辅助生活中低收入老年人的复杂护理需求。

IF 2.1 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Journal of palliative medicine Pub Date : 2025-08-01 Epub Date: 2025-04-10 DOI:10.1089/jpm.2024.0445
Komal Patel Murali, Rebecca K F Lassell, Abraham A Brody, Dena Schulman-Green, Daniel David
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引用次数: 0

摘要

背景:在美国,近100万老年人居住在辅助生活设施中,这些设施旨在为他们提供安全、自主的生活支持。然而,低收入居民,特别是在医疗补助机构的低收入居民,由于资源有限,医疗和社会复杂护理需求得不到满足,大病沟通有限。目的:本研究的目的是探讨低收入老年人在医疗补助辅助生活中所经历的复杂护理需求和严重疾病沟通挑战。方法:对来自纽约市一家医疗补助机构的17名60岁及以上严重疾病居民的父母定性研究数据进行定性二级框架分析。住院医师完成埃德蒙顿症状评估量表并参加半结构化访谈。本研究在国家姑息治疗共识项目的指导下,重点关注姑息治疗领域的居民经验,复杂的护理需求和沟通。结果:居民主要是黑人和西班牙裔,近三分之一的人有无家可归或使用避难所的历史,他们经历了很高的症状负担。出现了四个关键主题:(1)生活质量下降;(2)症状负担高,获得护理的机会有限,居民报告疼痛、疲劳和情绪困扰;(3)在就医过程中存在沟通缺口,导致挫折感和被忽视感;(4)分散的医疗协调,加剧了医疗系统的孤立感和不信任。结论:研究结果表明,在复杂的护理需求和大病沟通方面,医疗补助支持的辅助生活居民面临着巨大的挑战。迫切需要以社区为基础的干预措施,以增加护理机会,改善症状管理,促进有效的沟通,最终支持居民的生活质量和健康结果。加强对工作人员的培训和政策改革是解决这些系统性保健障碍的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"There Should Be a Nurse on Call": Complex Care Needs of Low-Income Older Adults in Medicaid-Supported Assisted Living.

Background: In the United States, nearly 1 million older adults reside in assisted living facilities, which aim to provide support for safe, autonomous living. However, low-income residents, especially those in Medicaid-supported facilities, experience unmet medical and social complex care needs and limited serious illness communication due to limited resources. Objective: The objective of this study was to explore the complex care needs and serious illness communication challenges experienced by low-income older adults in Medicaid-supported assisted living. Methods: A qualitative secondary framework analysis was conducted on data from a parent qualitative study involving 17 residents aged 60 and older with serious illnesses at a Medicaid-supported facility in New York City. Residents completed the Edmonton Symptom Assessment Scale and participated in semistructured interviews. This study was guided by the National Consensus Project for Quality Palliative Care, focusing on the residents' experiences, complex care needs, and communication within palliative care domains. Results: Residents were predominantly Black and Hispanic, with nearly one-third having a history of homelessness or shelter use, and they experienced a high symptom burden. Four key themes emerged: (1) compromised quality of life; (2) high symptom burden and limited access to care, with residents reporting pain, fatigue, and emotional distress; (3) communication gaps while navigating health care, resulting in frustration and feelings of being unheard; and (4) fragmented care coordination, which exacerbated feelings of isolation and mistrust in the health care system. Conclusion: The findings reveal that Medicaid-supported assisted living residents encounter substantial challenges related to complex care needs and serious illness communication. There is an urgent need for community-based interventions to enhance care access, improve symptom management, and facilitate effective communication, ultimately supporting the residents' quality of life and health outcomes. Enhanced training for staff and policy changes are key to addressing these systemic barriers to care.

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来源期刊
Journal of palliative medicine
Journal of palliative medicine 医学-卫生保健
CiteScore
3.90
自引率
10.70%
发文量
345
审稿时长
2 months
期刊介绍: Journal of Palliative Medicine is the premier peer-reviewed journal covering medical, psychosocial, policy, and legal issues in end-of-life care and relief of suffering for patients with intractable pain. The Journal presents essential information for professionals in hospice/palliative medicine, focusing on improving quality of life for patients and their families, and the latest developments in drug and non-drug treatments. The companion biweekly eNewsletter, Briefings in Palliative Medicine, delivers the latest breaking news and information to keep clinicians and health care providers continuously updated.
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