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阿尔茨海默病患者的非裔美国人和白人家庭照顾者的临终关怀及对死亡的反应

End of life care and reactions to death in African-American and white family caregivers of relatives with Alzheimer's disease.

作者信息

Owen J E, Goode K T, Haley W E

机构信息

University of Alabama at Birmingham, USA.

出版信息

Omega (Westport). 2001;43(4):349-61. doi: 10.2190/YH2B-8VVE-LA5A-02R2.

Abstract

Family caregivers for relatives with Alzheimer's Disease (AD) often experience significant stress-related problems in mental and physical health. Patients with AD often survive for protracted periods of time, placing an extensive burden of care on the caregiver prior to the patient's death. The present study addresses ethnic differences in the experience of AD caregivers around the time of their loved one's death, including life-sustaining treatment decisions and reactions to death. The results showed that, in our sample, more patients died in their homes than has been reported for deaths in the United States. African-American and White caregivers differed substantially in their reports of end of life care and subjective reactions to the death. Compared with White caregivers, African-American caregivers were less likely to make a decision to withhold treatment at the time of death, less likely to have their relative die in a nursing home, and reported less acceptance of the relative's death and greater perceived loss. Results suggest that death after AD caregiving deserves further study, and that ethnic differences in end of life care and bereavement may be of particular importance.

摘要

阿尔茨海默病(AD)患者的家庭护理人员常常在身心健康方面经历与压力相关的重大问题。AD患者通常会存活很长时间,在患者去世之前给护理人员带来沉重的护理负担。本研究探讨了AD患者护理人员在亲人去世前后的经历中的种族差异,包括维持生命治疗的决策和对死亡的反应。结果显示,在我们的样本中,在家中去世的患者比美国报道的死亡患者更多。非裔美国人和白人护理人员在临终关怀报告以及对死亡的主观反应方面存在显著差异。与白人护理人员相比,非裔美国护理人员在患者死亡时决定停止治疗的可能性较小,其亲属在养老院死亡的可能性较小,并且报告对亲属死亡的接受程度较低,感知到的损失更大。结果表明,AD护理后的死亡值得进一步研究,临终关怀和丧亲之痛中的种族差异可能尤为重要。

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