了解负担:探索在安老院舍中痴呆症护理的关键因素。

Yi-Heng Chen, Li-Chan Lin, Pei-Hao Chen, I-Hsuan Lu
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引用次数: 0

摘要

背景:影响养老院提供痴呆护理的照顾者负担的因素是多方面的。文献中很少有研究同时调查了与痴呆症住院护理接受者及其正式护理者相关的变量。目的:本研究旨在评估痴呆症住院护理受助人的正式照顾者的照顾负担,并确定与这些照顾受助人和他们的照顾者相关的这种负担的重要预测因素。方法:本前瞻性横断面研究招募了206名注册护士和护理助理,以及来自6家养老院的256名痴呆症患者。采用结构化问卷调查的方法,收集护理人员的社会人口学特征、态度、痴呆护理知识、照顾者负担等数据,以及痴呆住院护理对象的社会人口学特征、日常功能能力、认知功能、神经精神症状等数据。结果:本研究中正式照护者报告有轻至中度照护负担。逐步线性回归分析发现,先前的痴呆症护理培训、对护理提供的信心、正式护理人员的态度、药物数量和居民的躁动/攻击水平是护理负担的重要预测因子,解释了32%的方差。出乎意料的是,照顾者的基本痴呆护理知识和居民的身体依赖等神经精神症状并没有被认为是照顾者负担的显著预测因素。结论/对实践的启示:本研究的结果强调了护理者的态度、信心和应对技能在决定护理负担方面的关键重要性,并指出并非所有的行为和心理症状都对护理负担产生同等影响。这些见解强调需要增强对正式护理人员的信心和积极态度,并通过药物和非药物方法有效管理居民的攻击行为,以改善与痴呆症护理相关的高护理人员负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding the Burden: Exploring Key Factors in Dementia Caregiving in Residential Care Homes.

Background: The factors of influence on caregiver burden with regard to dementia care provided in residential care homes are multifaceted. Few studies in the literature have simultaneously investigated the variables related to residential care recipients with dementia and their formal caregivers.

Purpose: This study was designed to assess caregiving burden in formal caregivers of residential care recipients with dementia and to identify significant predictors of this burden associated with these care recipients and their caregivers.

Methods: This prospective cross-sectional study enrolled 206 registered nurses and nursing assistants working as formal caregivers, as well as 256 residents with dementia across 6 residential care homes. Structured questionnaires were used to collect data on the sociodemographic characteristics, attitudes, dementia care knowledge, and caregiver burden of nursing staff, as well as data on the sociodemographic characteristics, daily functional ability, cognitive functioning, and neuropsychiatric symptoms of residential care recipients with dementia.

Results: The formal caregivers in this study reported experiencing mild to moderate care burden. Stepwise linear regression analysis identified prior dementia care training, confidence in care provision, and attitude in the formal caregivers and number of medications and agitation/aggression levels in the residents as significant predictors of caregiving burden, explaining 32% of the variance. Unexpectedly, the basic dementia care knowledge of the caregivers and the physical dependence and other neuropsychiatric symptoms of the residents were not identified as significant predictors of caregiver burden.

Conclusions/implications for practice: The findings of this study underscore the critical importance of caregiver attitude, confidence, and coping skills in determining caregiving burden, noting that not all behavioral and psychological symptoms impact this burden equally. These insights emphasize the need to enhance confidence and positive attitudes in formal caregivers and to effectively manage residents' aggressive behaviors through both pharmacological and nonpharmacological approaches to ameliorate the high caregiver burden associated with dementia care.

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