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本文引用的文献

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Racial differences in knowledge and beliefs about Alzheimer disease.关于阿尔茨海默病的知识和认知方面的种族差异。
Alzheimer Dis Assoc Disord. 2009 Apr-Jun;23(2):110-6. doi: 10.1097/WAD.0b013e318192e94d.
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Diagnosis and assessment of Alzheimer's disease in diverse populations.不同人群中阿尔茨海默病的诊断与评估
Alzheimers Dement. 2008 Jul;4(4):305-9. doi: 10.1016/j.jalz.2008.03.001. Epub 2008 Apr 21.
3
Reaction to a dementia diagnosis in individuals with Alzheimer's disease and mild cognitive impairment.阿尔茨海默病和轻度认知障碍患者对痴呆症诊断的反应。
J Am Geriatr Soc. 2008 Mar;56(3):405-12. doi: 10.1111/j.1532-5415.2007.01600.x. Epub 2008 Jan 5.
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Prevalence of dementia in the United States: the aging, demographics, and memory study.美国痴呆症患病率:老龄化、人口统计学与记忆研究
Neuroepidemiology. 2007;29(1-2):125-32. doi: 10.1159/000109998. Epub 2007 Oct 29.
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Public opinion about Alzheimer disease among blacks, hispanics, and whites: results from a national survey.黑人群体、西班牙裔群体和白人群体对阿尔茨海默病的公众看法:一项全国性调查的结果
Alzheimer Dis Assoc Disord. 2007 Jul-Sep;21(3):232-40. doi: 10.1097/WAD.0b013e3181461740.
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Who refuses the diagnostic assessment for dementia in primary care?在初级医疗保健中,谁会拒绝进行痴呆症的诊断评估?
Int J Geriatr Psychiatry. 2006 Jun;21(6):556-63. doi: 10.1002/gps.1524.
7
Mild cognitive impairment is early-stage Alzheimer disease: time to revise diagnostic criteria.轻度认知障碍即早期阿尔茨海默病:是时候修订诊断标准了。
Arch Neurol. 2006 Jan;63(1):15-6. doi: 10.1001/archneur.63.1.15.
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Cultural factors in dementia: perspectives from the anthropology of aging.
Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19(4):272-4. doi: 10.1097/01.wad.0000190806.13126.55.
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Cultural diversity in Alzheimer disease: the interface between biology, belief, and behavior.阿尔茨海默病中的文化多样性:生物学、信仰与行为之间的交汇点。
Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19(4):250-5. doi: 10.1097/01.wad.0000190802.03717.20.
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African American, Chinese, and Latino family caregivers' impressions of the onset and diagnosis of dementia: cross-cultural similarities and differences.非裔美国人、华裔和拉丁裔家庭护理人员对痴呆症发病和诊断的印象:跨文化的异同
Gerontologist. 2005 Dec;45(6):783-92. doi: 10.1093/geront/45.6.783.

成年黑人和白人家庭成员对痴呆症诊断的态度。

Black and white adult family members' attitudes toward a dementia diagnosis.

作者信息

Connell Cathleen M, Roberts J Scott, McLaughlin Sara J, Carpenter Brian D

机构信息

Department of Health Behavior, University of Michigan School of Public Health, 109 South Observatory Street, Ann Arbor, MI 48109, USA.

出版信息

J Am Geriatr Soc. 2009 Sep;57(9):1562-8. doi: 10.1111/j.1532-5415.2009.02395.x. Epub 2009 Aug 13.

DOI:10.1111/j.1532-5415.2009.02395.x
PMID:19682136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6312886/
Abstract

OBJECTIVES

To examine potential benefits of and barriers to diagnosis from the perspective of black and white adults directly affected by Alzheimer's disease (AD).

DESIGN

Telephone survey.

SETTING

Convenience sample recruited from two U.S. metropolitan areas.

PARTICIPANTS

One hundred seventy-eight family members of people with AD, including current and former AD caregivers and immediate blood relatives of someone with AD.

MEASUREMENTS

Respondents were asked to rate the importance of eight benefits of and 16 barriers to obtaining a diagnosis.

RESULTS

Family members strongly endorse several benefits of obtaining a diagnosis, including getting information, finding out what is wrong with their relative, and prompting future planning. A majority of survey respondents did not endorse any barriers examined. Lack of a cure for AD and the belief that little can be done for someone with AD were the most frequently endorsed barriers. Black respondents endorsed five of the eight benefits more frequently than white respondents.

CONCLUSION

Black and white adults with a family member who has received an diagnosis of AD perceive a range of benefits and few barriers to the diagnostic process examined in this study. Their positive experiences might be instructive to families considering pursuing a diagnosis and to physicians who may be reluctant to offer screening or referral because of the belief that families have little to gain.

摘要

目的

从直接受阿尔茨海默病(AD)影响的黑人和白人成年人的角度,探讨诊断的潜在益处和障碍。

设计

电话调查。

地点

从美国两个大都市地区招募的便利样本。

参与者

178名AD患者的家庭成员,包括现任和前任AD护理者以及AD患者的直系血亲。

测量

要求受访者对获得诊断的八项益处和十六项障碍的重要性进行评分。

结果

家庭成员强烈认可获得诊断的多项益处,包括获取信息、弄清楚亲属的问题以及推动未来规划。大多数调查受访者不认可所考察的任何障碍。AD无法治愈以及认为对AD患者无能为力是最常被认可的障碍。黑人受访者比白人受访者更频繁地认可八项益处中的五项。

结论

有家庭成员被诊断患有AD的黑人和白人成年人认为在本研究中所考察的诊断过程有一系列益处且几乎没有障碍。他们的积极经历可能对考虑寻求诊断的家庭以及可能因认为家庭获益不大而不愿提供筛查或转诊的医生具有指导意义。