Family caregivers of people with dementia.

原文摘录 · 研究摘要约 2 分钟

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Family caregivers of people with dementia, often called the invisible second patients, are critical to the quality of life of the care recipients. The effects of being a family caregiver, though sometimes positive, are generally negative, with high rates of burden and psychological morbidity as well as social isolation, physical ill-health, and financial hardship. Caregivers vulnerable to adverse effects can be identified, as can factors which ameliorate or exacerbate burden and strain. Psychosocial interventions have been demonstrated to reduce caregiver burden and depression and delay nursing home admission. Comprehensive management of the patient with dementia includes building a partnership between health professionals and family caregivers, referral to Alzheimer's Associations, and psychosocial interventions where indicated.

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Brodaty H, Donkin M.. (2009). PMID: 19585957. 许可：cc by-nc-nd。摘要为原文，未做 AI 改写。

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https://europepmc.org/article/MED/19585957

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原文摘录 · 研究摘要

本文部分内容由 AI 辅助生成并人工整理；仅供学习参考，不构成心理诊断或治疗建议。引文如标注「待核验」，请勿直接引用。

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来源Brodaty H, Donkin M.. (2009). PMID: 19585957. 许可：cc by-nc-nd。摘要为原文，未做 AI 改写。

审校状态原文条目在来源中注明出处与许可；摘要类条目未逐条核验；研究摘要为英文原文，未做 AI 改写

Family caregivers of people with dementia.

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