Caregivers in China: Knowledge of Mild Cognitive Impairment

被引:26
|
作者
Dai, Baozhen [1 ,2 ]
Mao, Zongfu [3 ]
Mei, John [4 ]
Levkoff, Sue [5 ]
Wang, Huali [6 ]
Pacheco, Misty [7 ]
Wu, Bei [8 ,9 ]
机构
[1] Jiangsu Univ, Sch Management, Zhenjiang, Peoples R China
[2] Jiangsu Univ, Res Inst New Rural Dev, Zhenjiang, Peoples R China
[3] Wuhan Univ, Sch Publ Hlth, Wuhan 430072, Peoples R China
[4] Harvard Univ, Dept Anthropol, Cambridge, MA 02138 USA
[5] Univ S Carolina, Coll Social Work, DeSaussure Coll, Columbia, SC 29208 USA
[6] Peking Univ, Inst Mental Hlth, Dementia Care & Res Ctr, Beijing 100871, Peoples R China
[7] Univ Hawaii Manoa, Honolulu, HI 96822 USA
[8] Duke Univ, Sch Nursing, Durham, NC 27706 USA
[9] Duke Univ, Global Hlth Inst, Durham, NC USA
来源
PLOS ONE | 2013年 / 8卷 / 01期
基金
美国国家卫生研究院;
关键词
ALZHEIMER-DISEASE; HIGH-RISK; CARE; DEMENTIA; ONSET; PREVALENCE; DIAGNOSIS; BURDEN;
D O I
10.1371/journal.pone.0053928
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study aimed to examine the experience and knowledge of mild cognitive impairment (MCI) among Chinese family caregivers of individuals with MCI. The sample was recruited from memory clinics in Zhongnan Hospital in Wuhan, China. In-depth semi-structured interviews were used. Thirteen family members of individuals diagnosed with MCI participated in the study. Data analysis revealed three themes: 1) initial recognition of cognitive decline; 2) experience of the diagnosis of MCI; 3) perception of cognitive decline as a normal part of aging. While family members recognized the serious consequences of memory loss (e. g. getting lost), they would typically not take their family members to see a doctor until something specific triggered their access to the medical care system. The Chinese traditional perception of dementia as part of normal aging may serve to lessen the stigma of individuals with MCI, while the term "laonian chidai" which literally translates to "stupid, demented elderly" may exacerbate the stigma associated with individuals with MCI. It is suggested that family members' worries may be relieved by improving their access to accurate knowledge of the disease, community-based and institutional care services, and culturally appropriately words are needed for MCI.
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页数:8
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