a Department of Health Sciences, Faculty of Medicine , Lund University , Lund , Sweden.
b University of Witten/Herdecke , Witten , Germany.
Aging Ment Health. 2017 Nov;21(11):1138-1146. doi: 10.1080/13607863.2016.1211621. Epub 2016 Jul 27.
OBJECTIVES: To investigate informal caregivers' psychological well-being and predicted increase in psychological well-being, when caring for persons with dementia (PwDs) living at home, related to caregiver, PwD and formal care (FC) factors. METHOD: A cohort study at baseline and 3 months' follow-up in eight European countries. Caregivers included (n = 1223) were caring for PwDs aged ≥ 65 years at home. Data on caregivers, PwDs and FC were collected using standardized instruments. Regression analysis of factors associated with caregiver psychological well-being at baseline and 3 months later was performed. RESULTS: Factors associated with caregiver psychological well-being at baseline were positive experience of caregiving, low caregiver burden, high quality of life (QoL) for caregivers, male gender of PwD, high QoL of PwD, few neuropsychiatric symptoms and depressive symptoms for the PwD. At follow-up, caregivers with increased psychological well-being experienced of quality of care (QoC) higher and were more often using dementia specific service. Predicting factors for caregivers' increased psychological well-being were less caregiver burden, positive experience of caregiving, less supervision of the PwD and higher caregiver QoL, if PwD were male, had higher QoL and less neuropsychiatric symptoms. Furthermore, higher QoC predicted increased caregivers' psychological well-being. CONCLUSION: Informal caregiving for PwDs living at home is a complex task. Our study shows that caregivers' psychological well-being was associated with, among other things, less caregiver burden and higher QoL. Professionals should be aware of PwD neuropsychiatric symptoms that might affect caregivers' psychological well-being, and provide proper care and treatment for caregivers and PwDs.
目的:调查居家照顾痴呆症患者(PwD)的非专业照护者的心理健康状况及其预期变化,相关因素包括照护者、PwD 和正式照顾(FC)因素。
方法:这是一项在八个欧洲国家进行的队列研究,在基线和 3 个月随访时进行。纳入的照护者(n=1223)正在照顾年龄≥65 岁的居家 PwD。使用标准化工具收集照护者、PwD 和 FC 的数据。对与基线和 3 个月后照护者心理福祉相关的因素进行回归分析。
结果:与基线时照护者心理福祉相关的因素包括积极的照护体验、低照护负担、照护者较高的生活质量(QoL)、PwD 为男性、PwD 较高的 QoL、较少的神经精神症状和抑郁症状。在随访时,心理福祉提高的照护者体验到更高的照顾质量(QoC),并且更常使用专门针对痴呆症的服务。预测照护者心理福祉提高的因素是照护负担减轻、积极的照护体验、对 PwD 的监督减少以及照护者 QoL 提高,如果 PwD 为男性、QoL 较高且神经精神症状较少。此外,较高的 QoC 预测了照护者心理福祉的提高。
结论:居家照顾 PwD 是一项复杂的任务。我们的研究表明,照护者的心理福祉与照护负担减轻和 QoL 提高等因素有关。专业人员应注意可能影响照护者心理福祉的 PwD 神经精神症状,并为照护者和 PwD 提供适当的照顾和治疗。
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