A systematic review of depressive and anxiety symptoms in caregivers of dementia patients.

Q3 Medicine
Despοina Deli, George Tsouvelas, Dimitrios Roukas, Manolis Mentis
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Abstract

The current number of dementia cases in Europe stands at 7.7 million, a figure projected to double by 2050. Caregivers of individuals with dementia experience a heightened burden compared to those caring for other chronically ill individuals, increasing the risk of depression and stress disorders. This systematic literature review, following PRISMA guidelines, explores the prevalence of anxiety and depressive symptoms in dementia caregivers. Searches in academic databases, restricted to studies from the last 15 years, identified 85 articles with 16 meeting the inclusion criteria. Results indicate significant caregiver burden, diminished self-reported quality of life, and a propensity for clinical depression. Depression and anxiety symptoms were more pronounced among female caregivers. Caregiver depression correlated with increased emergency department utilization by dementia patients, with a surge in depressive symptoms reported during the COVID-19 pandemic. Caregiving for dementia patients was associated with burnout, adversely impacting caregiver quality of life. Depression and anxiety symptoms in caregivers correlated with substance use. Sociodemographic variables, including low socioeconomic status, high urbanization levels, and older age, were associated with caregiver depression. Caregivers of individuals with Alzheimer's disease reported higher anxiety, burden, and depression scores compared to those assisting individuals with other dementias, particularly when neuropsychiatric symptoms were evident. The identification of the factors that are linked to the mental burden of caregivers allows mental health professionals to enhance symptom detection and provide tailored support, ultimately alleviating caregiver burden and improving dementia care quality. Systematic professional assistance and training opportunities through health policies can effectively alleviate caregiver burden.

痴呆症患者照护者抑郁和焦虑症状的系统回顾。
欧洲目前有 770 万痴呆症患者,预计到 2050 年这一数字将翻一番。与照顾其他慢性病患者相比,痴呆症患者的照顾者承受着更大的负担,从而增加了患抑郁症和应激障碍的风险。本系统性文献综述遵循 PRISMA 指南,探讨了痴呆症照护者中焦虑和抑郁症状的流行情况。在学术数据库中搜索仅限于过去 15 年内的研究,共发现 85 篇文章,其中 16 篇符合纳入标准。结果表明,照顾者负担沉重,自我报告的生活质量下降,并有临床抑郁倾向。女性护理者的抑郁和焦虑症状更为明显。照护者抑郁与痴呆症患者急诊使用率的增加有关,据报道,在 COVID-19 大流行期间,抑郁症状激增。照护痴呆症患者与职业倦怠有关,对照护者的生活质量产生不利影响。护理人员的抑郁和焦虑症状与药物使用有关。社会经济地位低、城市化水平高和年龄大等社会人口变量与护理人员抑郁有关。与协助其他痴呆症患者的护理人员相比,阿尔茨海默氏症患者的护理人员在焦虑、负担和抑郁方面的得分更高,尤其是在神经精神症状明显的情况下。找出与照护者精神负担相关的因素,可以让心理健康专业人员加强症状检测,并提供有针对性的支持,最终减轻照护者的负担,提高痴呆症照护质量。通过卫生政策提供系统的专业援助和培训机会,可以有效减轻照顾者的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychiatrike = Psychiatriki
Psychiatrike = Psychiatriki Medicine-Medicine (all)
CiteScore
2.60
自引率
0.00%
发文量
37
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