Sánchez-Martínez Vanessa, Cauli Omar, Corchón Silvia
Nursing Department, University of Valencia, 46010 Valencia, Spain.
Frailty Research Organized Group (FROG), University of Valencia, 46010 Valencia, Spain.
Diseases. 2024 Nov 14;12(11):292. doi: 10.3390/diseases12110292.
Family caregivers of people with neuropsychiatric conditions are at risk of caregiver burden and declining health. The aims of this study were to identify the impact of caring on long-term family caregivers and their unmet needs and to explore their self-care strategies for achieving a successful caregiving experience. A mixed-method study was conducted using semi-structured interviews and a questionnaire in which standardized, self-reported measures of burden, health behaviors, sleep, and mental well-being were administered. Participants were family caregivers of people with neuropsychiatric disorders. Convenience sampling of 28 caregivers: 13 of people with mental health disorders (schizophrenia and bipolar disorder) and 15 with Alzheimer's disease. Based on the analysis of the semi-structured interviews, data saturation was reached. Analysis of self-reported measures indicated that 32.1% of long-term caregivers had high caregiver burden, 64.3% had reduced quality of life, 39.3% had low sleep quality, 21.4% had low adherence to the Mediterranean diet, 50.0% had a physical activity below the recommendation, 42.9% had high anxiety symptoms, 35.7% had high depressive symptoms, and 71.4% had reduced self-care agency. Content analysis and statistical analysis were conducted. Two themes were identified: (1) the impact of long-term caregiving and unmet needs and (2) successful self-care strategies. Caregivers of people with Alzheimer's disease spent less time doing physical activity, had higher caregiver burden, and poorer health-related quality of life. The negative impact of caregiving could be prevented/managed by assessing the individual's circumstances for the development of cross-sectional self-care strategies involving physical, emotional, and social spheres.
患有神经精神疾病患者的家庭照顾者面临着照顾者负担和健康状况下降的风险。本研究的目的是确定照顾对长期家庭照顾者的影响及其未满足的需求,并探索他们实现成功照顾体验的自我照顾策略。采用半结构化访谈和问卷调查的混合方法进行研究,其中使用了标准化的自我报告测量工具来评估负担、健康行为、睡眠和心理健康状况。参与者是患有神经精神疾病患者的家庭照顾者。通过便利抽样选取了28名照顾者:其中13名照顾患有精神健康障碍(精神分裂症和双相情感障碍)的患者,15名照顾患有阿尔茨海默病的患者。基于对半结构化访谈的分析,达到了数据饱和。对自我报告测量结果的分析表明,32.1%的长期照顾者有较高的照顾者负担,64.3%的照顾者生活质量下降,39.3%的照顾者睡眠质量低,21.4%的照顾者对地中海饮食的依从性低,50.0%的照顾者身体活动水平低于推荐值,42.9%的照顾者有高度焦虑症状,35.7%有高度抑郁症状,71.4%的照顾者自我照顾能力下降。进行了内容分析和统计分析。确定了两个主题:(1)长期照顾的影响和未满足的需求;(2)成功的自我照顾策略。照顾患有阿尔茨海默病患者的照顾者进行体育活动的时间较少,照顾者负担较重,与健康相关的生活质量较差。通过评估个体情况来制定涉及身体、情感和社会领域的横断面自我照顾策略,可以预防/管理照顾带来的负面影响。