阿尔茨海默病对美国护理人员的影响

IF 2 Q3 PSYCHOLOGY, CLINICAL
Health Psychology Research Pub Date : 2022-08-20 eCollection Date: 2022-01-01 DOI:10.52965/001c.37454
Megan Vu, Rohan Mangal, Thor Stead, Carlos Lopez-Ortiz, Latha Ganti
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引用次数: 7

摘要

背景/目的:阿尔茨海默病(AD)于1906年由Alois Alzheimer首次发现,已成为全球日益关注的健康问题,对个人和现代社会具有许多影响。随着痴呆症患者症状的不断恶化,他们的独立性也逐渐受到限制。因此,家庭成员和熟人往往成为病人的照顾者,并更多地参与维持病人的生活方式。本研究的作者试图研究是什么促使护理人员照顾阿尔茨海默病患者,以及阿尔茨海默病对他们的生活方式、身体、心理和社会健康的影响。方法:作者精心设计了一项包含14个问题的调查,并收集了200名护理人员关于阿尔茨海默病对他们的身体、情感和社会健康的影响的数据,以及他们的关键人口统计学和背景信息(例如,他们是否为阿尔茨海默病患者的护理人员)。结果:阿尔茨海默病护理者以家庭成员居多(78%)。阿尔茨海默病经常使护理人员与患者的关系变得紧张(47.5%),58%的参与护理人员报告了极端的压力水平,而65%的人意识到照顾患者是非常困难的。由于压力水平的增加,47%的参与护理人员睡眠减少;43%的人感到与家人更加孤立;35.5%的人没有寻求别人的帮助。爱和强烈的责任感似乎是护理人员照顾病人的主要动机。为病人担心(50%)、经济担忧(12.5%)、缺乏医疗经验(10.5%)和自身健康(10.5%)似乎是护理人员的主要压力源。护理人员依赖于许多支持系统和应对机制,最常见的是身体活动(54.5%)和酒精和大麻使用量增加(35.5%)。结论:尽管护理人员有支持系统,并找到了应对方法来减轻他们照顾AD患者的负担,但AD对护理人员的明显负面影响影响了他们的身体、心理和社会健康。由于目前还没有治愈阿尔茨海默病的方法,对护理人员的同情和更多的支持是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Alzheimer's Disease on Caregivers in the United States.

Background/objective: First discovered by Alois Alzheimer in 1906, Alzheimer's disease (AD) has become a growing global health concern with numerous implications for individuals and modern society. As patients' symptoms of dementia continue to worsen, they gradually grow more limited in their independence. As a result, family members and close acquaintances often become caregivers for the patient and become more involved in maintaining the patient's lifestyle. The authors of this research sought to study what motivates caregivers to look after AD patients and the impact of AD on their lifestyles and physical, mental, and social health.

Methods: The authors crafted a survey of fourteen questions and collected data from 200 caregivers regarding AD's impact on their physical, emotional, and social health along with their key demographic and background information (e.g. whether or not they are a caregiver for a patient with AD).

Results: The results indicate that most AD caregivers are family members (78%). AD often strains the caregiver's relationship with the patient (47.5%), and 58% of participating caregivers report extreme stress levels while 65% realize it is incredibly difficult to take care of a patient. Because of the increased levels of stress, 47% of participating caregivers sleep less; 43% feel more isolated from their family; and, 35.5% did not try to get help from others. Love and a strong sense of duty seem to be the primary motivation for caregivers to take care of a patient. Worry for the patient (50%), financial worries (12.5%), lack of medical experience (10.5%), and their own health (10.5%) seem to be the primary stressors for caregivers. Caregivers rely on numerous support systems and coping mechanisms, with physical activity (54.5%) and increased alcohol and marijuana usage (35.5%) the most frequent.

Conclusions: Although caregivers have support systems and found coping methods that would alleviate their burden of caring for a patient with AD, the clear negative impact AD has on caregivers affects their physical, mental, and social health. As there is currently no cure for AD, compassion and greater support for caregivers are necessary.

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来源期刊
Health Psychology Research
Health Psychology Research PSYCHOLOGY, CLINICAL-
CiteScore
2.90
自引率
0.00%
发文量
63
审稿时长
15 weeks
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