“They Are Lost Souls”: Medicare Home Care Nurses’ Perceptions of Medicare’s Inadequate Coverage of Homebound Persons With Alzheimer’s Disease

IF 0.8 Q4 NURSING
William Cabin
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Abstract

Alzheimer’s disease is a major and increasing cause of illness and death in the United States, imposing significant social, economic, and psychological burdens on patients and their caregivers. This article explores the perceptions of Medicare home health nurses as to the impact of Medicare home health requirements on their decisions to admit, treat, cope with, and meet patient care needs of Alzheimer’s disease patients. It presents an exploratory study, which resulted from a gap in the literature review that found only 3 studies and 1 article since 1965. The study is based on interviews of a convenience sample of 37 home care nurses from 5 home health agencies in the New York City metropolitan area. Analysis followed the grounded theory 3-stage coding of interview data: open, axial, and selective coding. This research methodology was used because it was developed for interpreting qualitative data in the absence of a pre-existing theory. Five themes emerged from interviews: (1) Most Medicare home health patients have some level of Alzheimer’s disease (AD). Medicare home care regulations: (2) restrict nurses’ admissions of persons with AD and lack a mandatory evidence-based assessment for AD; (3) restrict the care that nurses can order for persons with AD; (4) do not cover evidence-based non-pharmacological interventions for AD patients ; and (5) nurses use 3 coping strategies to deal with the restrictions: most as conformists, others as innovators, some as rebels. Policymakers are urged to consider legislation expanding coverage of home-based, evidence-based non-pharmacological interventions for persons with Alzheimer’s disease; expanding Medicare home care social work services to allow delivery of appropriate services; requiring an evidence-based Alzheimer’s disease assessment at intake and as part of the OASIS; additional reimbursement for home health agencies treating Medicare homebound persons with Alzheimer’s disease.
“他们是迷失的灵魂”:医疗保险家庭护理护士对老年痴呆症患者的医疗保险覆盖不足的看法
在美国,阿尔茨海默病是一个主要且日益增加的疾病和死亡原因,给患者及其护理人员带来了巨大的社会、经济和心理负担。这篇文章探讨了医疗保险家庭健康护士对医疗保险家庭健康要求对他们决定接纳、治疗、应对和满足阿尔茨海默病患者护理需求的影响。这是一项探索性研究,这是由于文献综述的空白,自1965年以来只有3项研究和1篇文章。该研究基于对纽约市大都会地区5家家庭健康机构的37名家庭护理护士的访谈。分析采用扎根理论对访谈数据进行三阶段编码:开放编码、轴向编码和选择性编码。之所以使用这种研究方法,是因为它是在没有预先存在的理论的情况下为解释定性数据而开发的。访谈中出现了五个主题:(1)大多数医疗保险家庭健康患者都有不同程度的阿尔茨海默病(AD)。医疗保险家庭护理规定:(2)限制护士接收AD患者,缺乏对AD的强制性循证评估;(3)限制护士对AD患者的护理安排;(4)不涵盖针对AD患者的循证非药物干预措施;(5)护士使用3种应对策略来应对这些限制:大多数是循规蹈矩,有些是创新者,有些是反叛者。敦促政策制定者考虑立法,扩大对阿尔茨海默病患者以家庭为基础、循证的非药物干预措施的覆盖范围;扩大医疗保险家庭护理社会工作服务,以便提供适当的服务;要求在摄入时进行基于证据的阿尔茨海默病评估,并作为OASIS的一部分;为家庭保健机构治疗老年痴呆症患者提供额外报销。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
18.20%
发文量
29
期刊介绍: Home Health Care Management & Practice is a comprehensive resource for clinicians, case managers, and administrators providing home and community based health care. Articles address diverse issues, ranging from individual patient care and case management to the human resource management and organizational operations management and administration of organizations and agencies. Regular columns focus on research, legal issues, psychosocial perspectives, accreditation and licensing, compliance, management, and cultural diversity. Specific topics include treatment, care and therapeutic techniques, cultural competence, family caregivers, equipment management, human resources, home health center.
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