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本文引用的文献

1
Health impact on caregivers of providing informal care to a cognitively impaired older adult: rural versus urban settings.为认知障碍老年人提供非正式护理对农村和城市地区护理人员的健康影响。
Can J Rural Med. 2004 Winter;9(1):15-23.
2
Rural practitioners' experiences in dementia diagnosis and treatment.乡村医生在痴呆症诊断与治疗方面的经验。
Aging Ment Health. 2004 Sep;8(5):422-9. doi: 10.1080/13607860410001725018.
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Including older people with dementia in research: challenges and strategies.将患有痴呆症的老年人纳入研究:挑战与策略。
Aging Ment Health. 2003 Sep;7(5):351-62. doi: 10.1080/1360786031000150685.
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Alzheimer disease in the US population: prevalence estimates using the 2000 census.美国人口中的阿尔茨海默病:利用2000年人口普查数据进行的患病率估计
Arch Neurol. 2003 Aug;60(8):1119-22. doi: 10.1001/archneur.60.8.1119.
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Transitions in spousal caregiving.配偶照顾的转变。
Gerontologist. 2003 Apr;43(2):230-41. doi: 10.1093/geront/43.2.230.
6
The role of cultural factors on clients' attitudes toward caregiving, perceptions of service delivery, and service utilization.文化因素对客户在照护态度、服务提供认知及服务利用方面的作用。
Home Health Care Serv Q. 2002;21(3-4):65-88. doi: 10.1300/J027v21n03_04.
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Rural families caring for a relative with dementia: barriers to use of formal services.农村地区照顾痴呆症亲属的家庭:使用正规服务的障碍
Soc Sci Med. 2002 Oct;55(7):1129-42. doi: 10.1016/s0277-9536(01)00255-6.
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Essential information and support needs of family caregivers.
Patient Educ Couns. 2002 Jun;47(2):95-100. doi: 10.1016/s0738-3991(01)00194-x.
9
Decision-making for persons with cognitive impairment and their family caregivers.认知障碍者及其家庭照顾者的决策制定。
Am J Alzheimers Dis Other Demen. 2002 Jul-Aug;17(4):237-44. doi: 10.1177/153331750201700406.
10
Spouse caregivers' perceptions of influence of dementia on marriage.配偶照顾者对痴呆症对婚姻影响的看法。
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生活在农村社区的阿尔茨海默病患者及其家庭护理人员的信息和服务需求。

Information and service needs of persons with Alzheimer's disease and their family caregivers living in rural communities.

作者信息

Edelman Perry, Kuhn Daniel, Fulton Bradley R, Kyrouac Gregory A

机构信息

Mather LifeWays Institute on Aging, Evanston, IL 60201, USA.

出版信息

Am J Alzheimers Dis Other Demen. 2006 Aug-Sep;21(4):226-33. doi: 10.1177/1533317506290664.

DOI:10.1177/1533317506290664
PMID:16948286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10833300/
Abstract

This study aimed to identify the information and service needs of persons with Alzheimer's disease (AD) and their family caregivers living in rural communities and to assess differences and similarities in each partner's perspective. In an outpatient clinic setting, a self-report survey was completed by 100 caregivers, while a similar survey was used to interview 100 persons with mild to moderate AD. The survey assessed respondents' interest in information or services related to 22 topics about AD and various aspects of coping with the disease. Although more caregivers than persons with AD reported interest in each topic, 8 of the top 10 topics endorsed by each group of respondents were the same. However, analysis of responses by dyads revealed substantial disagreement in terms of each partner's interest in information and services. Patient and family education, as well as referrals for services, must take into account each partner's unique perspective and needs.

摘要

本研究旨在确定生活在农村社区的阿尔茨海默病(AD)患者及其家庭护理人员的信息和服务需求,并评估每个伴侣观点中的差异和相似之处。在门诊环境中,100名护理人员完成了一份自我报告调查,同时使用类似的调查对100名轻度至中度AD患者进行了访谈。该调查评估了受访者对与AD相关的22个主题以及应对该疾病的各个方面的信息或服务的兴趣。尽管报告对每个主题感兴趣的护理人员比AD患者多,但每组受访者认可的前10个主题中有8个是相同的。然而,对二元组反应的分析显示,每个伴侣对信息和服务的兴趣存在很大分歧。患者和家庭教育以及服务转介必须考虑到每个伴侣的独特观点和需求。