Burden of Care, Depression, and Anxiety Among Family Caregivers of People With Dementia.

IF 3 Q1 PRIMARY HEALTH CARE
Doaa S Abdelhalim, Marwa M Ahmed, Hoda A Hussein, Ola O Khalaf, Mai D Sarhan
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Abstract

Background: There are many challenges that entail caring for an individual with dementia, affecting not only the individual with the condition but also their caregivers. This can lead to increased burden, frustration, and depression among those taking care of them. A research gap exists concerning the care of people with dementia in Egypt, particularly regarding the mental health of caregivers. Limited studies have been conducted in Egypt, particularly focusing on the mental health of caregivers. This lack highlights the need to understand the prevalence and impact of caregiver burden in this population.

Objectives: The research aimed to evaluate the burden of dementia, levels of depression, and anxiety among family caregivers of individuals with dementia.

Methods: A cross-sectional study was conducted at a geriatric unit clinic of a psychiatric hospital in Cairo University, Egypt. Caregiver burden, anxiety, and depression were assessed using questionnaires. These questionnaires included the Zarit Burden Interview (ZBI), Generalized Anxiety Disorder scale (GAD-7), and Patient Health Questionnaire-9 (PHQ-9), together with demographic data on the patients and caregivers.

Results: The majority of the 141 participants (73% (n = 103)) were female, mostly daughters, with an average age of 40 years. Approximately 50% (n = 71) of the subjects exhibited mild to moderate burden, whereas 30% (n = 43) showed moderate to severe burden. About 31% (n = 44) of the subjects exhibited symptoms of moderate depression, whereas 9% (n = 13) had symptoms of severe depression. Furthermore, almost 43% (n = 60) of caregivers exhibited a moderate level of anxiety. Furthermore, a significant association was seen between caregiver burden and the presence of anxiety and depression.

Conclusion: This study showed a substantial burden in providing care, elevated levels of despair, and anxiety among caregivers of PWD. The findings highlight how important it is to develop targeted therapies and support systems in order to lessen the load on caregivers, advance their mental health, and improve overall care for both caregivers and their patients in Egypt. Policy-makers should prioritize investing in dementia-related support systems and services to empower caregivers and improve the quality of life for both caregivers and their patients.

痴呆症患者家庭照护者的照护负担、抑郁和焦虑。
背景:照顾痴呆症患者会面临许多挑战,不仅会影响患者本人,还会影响其照顾者。这可能会增加照顾者的负担、挫折感和抑郁情绪。在埃及,有关痴呆症患者护理,尤其是护理者心理健康方面的研究存在空白。在埃及开展的研究有限,尤其是针对护理人员心理健康的研究。这种缺乏凸显了了解护理者负担在这一人群中的普遍性和影响的必要性:研究旨在评估痴呆症患者家庭照顾者的痴呆症负担、抑郁水平和焦虑程度:在埃及开罗大学一家精神病医院的老年病科诊所进行了一项横断面研究。研究使用问卷对照顾者的负担、焦虑和抑郁程度进行了评估。这些问卷包括扎里特负担访谈(ZBI)、广泛性焦虑症量表(GAD-7)和患者健康问卷-9(PHQ-9),以及患者和照顾者的人口统计学数据:在 141 名参与者中,大多数(73%(n = 103))是女性,其中大部分是女儿,平均年龄为 40 岁。约 50% 的受试者(71 人)表现出轻度至中度负担,30% 的受试者(43 人)表现出中度至重度负担。约 31%(n = 44)的受试者表现出中度抑郁症状,而 9%(n = 13)的受试者表现出重度抑郁症状。此外,近 43% 的照顾者(n = 60)表现出中度焦虑。此外,护理人员的负担与焦虑症和抑郁症之间也存在着明显的联系:这项研究表明,残疾人护理者在提供护理方面负担沉重,绝望和焦虑程度升高。研究结果凸显了开发有针对性的疗法和支持系统的重要性,以减轻护理人员的负担,促进他们的心理健康,并改善埃及护理人员及其患者的整体护理。决策者应优先投资于与痴呆症相关的支持系统和服务,以增强护理人员的能力,改善护理人员及其患者的生活质量。
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
CiteScore
4.80
自引率
2.80%
发文量
183
审稿时长
15 weeks
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