养老院照顾者对痴呆症患者的负担:心理支持的重要性

S. Pinna
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引用次数: 3

摘要

背景:家庭照顾者是老年痴呆症患者医疗保健服务的重要组成部分。他们中的大多数人在将亲人送入长期护理机构后继续照顾他们。这种照顾的特点不同于那些与家庭照顾有关的照顾,很少在文献中研究。目的:探讨参加支持/心理教育小组和未参加支持/心理教育小组的老年痴呆患者照顾者负担演变的差异。方法:29例在我院接受标准康复治疗(≈90天)的痴呆患者的护理人员(7M-22F,年龄:59±7.8)在住院开始和结束时进行护理人员负担量表。这些护理人员参加了由训练有素的心理学家主持的支持/心理教育小组(每月两次,每次两小时)。我们得到的结果与没有参加接触的对照组进行了比较。采用单因素方差分析(ANOVA)和Student’s配对t检验(Student’s t配对组)。结果:两组在人口学变量上没有差异;两组相应的患者在临床/人口学和神经心理学变量方面也没有差异。只有参加小组的护理人员在项目结束时显著减轻了负担(p<0.001)。结论:我们的研究支持简单的病人不在家不足以预防和减轻照顾者负担的假设。支持/心理教育团体是家庭的基本资源,在疾病的每一个阶段和每一种情况下都应成为家庭保健的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Caregivers burden in nursing homes for patients with dementia: the importance of psychological support
Background: family caregivers are an essential part of healthcare services for elderly with dementia. Most of them continue caregiving for their relatives after admitting them to long-term care facilities. The characteristics of this caregiving differ from those related to caregiving in home-care settings and have been rarely studied in literature. Objective: to investigate the differences of burden evolution between caregivers of patients with dementia in a Nursing Home joining a support/psycho educational group and caregivers who did not. Methods: 29 caregivers (7M-22F, age: 59±7.8) of demented patients who were undergoing a standard rehabilitation program in our Institute (≈ 90 days) were administered the Caregiver Burden Inventory at the beginning and at the end of hospitalization. These caregivers took part in a support/ psycho educational group (two hours, twice a month) conducted by a trained psychologist. The results we obtained were compared to a control group, that did not participate to the encounters. Univariate analysis of variance (ANOVA) and Student’s paired t test (Student’s t paired groups) were conducted. Results: the two groups did not differ for demographical variables; the two correspondant groups of patients did not differ for clinical/demographical and neuropsychological variables, too. Only caregivers who participated to the group reduced their burden significantly at the end of the program (p<0.001). Conclusions: our study supports the hypothesis that the simple absence of a patient from home is not enough to prevent and reduce caregiver burden. Support/psycho educational groups are a fundamental resource for families and should be part of their healthcare in every stage of the disease and in every context.
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