Care needs of caregivers of the elderly with early-stage dementia

Hiromi Kimura, Kayoko Koga, Midori Nishio
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Abstract

Objective This study aimed to identify the care needs of family caregivers of elderly patients with early-stage dementia and examine support measures. Materials and Methods We conducted a self-administered questionnaire survey with 115 primary caregivers of outpatients who visited A City Community General Support Center or B University Hospital Department of Neurology for memory loss consultation. The questionnaire content included demographic characteristics, the care needs scale for caregivers of the elderly with early-stage dementia (Care Needs Scale), and the Japanese short version of the Zarit Burden Interview. The Medical Ethics Committee of Fukuoka University approved this study (approval number: M047). Of the 115 participants, 104 were included in the analysis after excluding 11 respondents with missing data. We divided the participants into a young group (under 65 years of age) and an old group (65 years of age or older) and compared the variables and each scale score using the Mann–Whitney U test. We also compared the correlations between the total score and subscale scores of the Care Needs Scale and each variable, in addition, we performed multiple regression analyses using the total score of the Care Needs Scale as the dependent variable. Results The young caregivers wanted to know how to take care, prevent deterioration, and deal with symptoms of early-stage dementia. They were trying to balance caregiving with work and housekeeping and reduce the stress and burden of long-term care. Older caregivers were confused about caregiving and wanted someone to talk about their situations. Conclusion Both groups shared that the family’s lack of understanding about caregiving and personal and role strains were associated with the care needs of caregivers of the elderly with early-stage dementia.
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早期痴呆症老人护理者的护理需求
目的 本研究旨在确定老年早期痴呆症患者家庭照顾者的护理需求,并研究支持措施。材料与方法 我们对到 A 市社区综合支援中心或 B 大学附属医院神经内科就诊的记忆力减退门诊患者的 115 位主要照护者进行了自填式问卷调查。问卷内容包括人口统计学特征、早期痴呆症老人护理者护理需求量表(Care Needs Scale)和日语简版 Zarit 负担访谈(Zarit Burden Interview)。福冈大学医学伦理委员会批准了这项研究(批准号:M047)。在 115 名参与者中,剔除 11 名数据缺失的受访者后,有 104 人被纳入分析。我们将参与者分为年轻组(65 岁以下)和年长组(65 岁或以上),并使用 Mann-Whitney U 检验比较了变量和每个量表的得分。我们还比较了护理需求量表的总分和分量表得分与各变量之间的相关性,此外,我们还以护理需求量表的总分为因变量进行了多元回归分析。结果 年轻的照护者希望了解如何进行照护、防止病情恶化以及应对早期痴呆症的症状。他们试图在护理与工作和家务之间取得平衡,减轻长期护理的压力和负担。年长的照护者对照护工作感到困惑,希望有人能谈谈他们的情况。结论 两个小组都认为,家人对照护工作缺乏了解以及个人和角色的压力与早期痴呆症老人照护者的照护需求有关。
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