与非裔美国人痴呆症护理提供者未满足需求相关的因素。

P J Desin, A M Caban-Holt, E L Abner, L J Van Eldik, F A Schmitt
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引用次数: 26

摘要

种族和少数民族目前占美国人口的20%;到2050年,这一数字预计将上升到42%。因此,阿尔茨海默病(AD)是65岁及以上人群的第五大死亡原因,在这些人群中可能会增加。这些人群的大多数痴呆症护理来自家人和朋友,特别是社会经济地位较低的家庭。为了确定未满足的需求,对30名非裔美国痴呆症护理人员进行了访谈。与会者表示对正式服务的需求有限,例如支援小组、法律咨询、个案管理和家政服务。相反,普遍表达的需求是白天的临时护理,尤其是对家庭和社会支持的渴望。许多照顾者表示需要其他家庭成员在这一过程中分担责任;因此,照顾者支持的方法,解决多个家庭成员的照顾提供可能是有益的这一组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Associated with Unmet Needs among African-American Dementia Care Providers.

Racial and ethnic minorities currently comprise 20% of the U.S. population; in 2050, this figure is expected to rise to 42%. As a result, Alzheimer's disease (AD), the 5th leading cause of death for people aged 65 and older, is likely to increase in these groups. Most dementia caregiving for these populations comes from family and friends, especially among families with lower socioeconomic status. A convenience sample of 30 African-American dementia caregivers was interviewed to determine unmet needs. Participants expressed a limited desire for formal services, such as support groups, legal advice, case management, and homemaker services. Instead, commonly expressed needs were daytime respite care and especially a desire for family and social support. Many caregivers expressed a need for other family members to share responsibility in the process; therefore, methods for caregiver support that address multiple family members in care provision may be beneficial for this group.

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