Assessment of psychological distress and quality of life of family caregivers caring for patients with chronic diseases at home.

IF 3.1 Q2 HEALTH CARE SCIENCES & SERVICES
Anastasia Stathopoulou, Georgios F Fragkiadakis
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Abstract

Introduction: Caring for the chronically ill at home is a particularly demanding process that can place a great burden on the caregiver. International and Greek studies underline and confirm this problem. In addition, family caregivers are not supported by the health systems of the different countries, especially in Greece, where the system relies mainly on the family to care for these patients, which is even more challenging during the Covid-19 pandemic.

Aim: The aim of this study is to evaluate the psychological burden of family caregivers of the chronically ill and the outcomes of care for these individuals. It also aims to assess the intensity of burden and changes in quality of life of family caregivers by demographic characteristics.

Methods: The sample of the study was a random sample and consisted of 102 family caregivers of chronically ill patients registered in home care of "Metaxa" hospital. The scales (BAKAS/BCOS) and (HADS) were used for data collection. SPSS 25 statistical package was used for statistical analysis of the results.

Results: The results of the study, calculated with the BCOS scale, show a low burden (-0.93) of family caregivers, patients with chronic diseases and moderate depression and anxiety. The results of the analysis associate the intensity of family caregiver burden with increased levels of anxiety and depression. The factors that affect burden are gender, with women having higher burden, living with the patient, and low education level. According to the HADS anxiety scale, family caregivers had an average score of 11, indicating a moderate level of anxiety, and for depression, the average score was 10.4, also indicating a moderate level of depression. The results indicate that the state needs to support family caregivers and take immediate action to create structures and implement actions to help families continue in their difficult roles in a pain-free manner.

家庭照顾者在家照顾慢性病患者的心理困扰和生活质量评估。
在家里照顾慢性病患者是一个特别费力的过程,可能会给照顾者带来很大的负担。国际和希腊研究强调并证实了这一问题。此外,不同国家的卫生系统并不支持家庭护理人员,特别是在希腊,该国的卫生系统主要依靠家庭来照顾这些患者,这在2019冠状病毒病大流行期间更具挑战性。目的:本研究的目的是评估慢性疾病家庭照顾者的心理负担和照顾这些个体的结果。它还旨在根据人口特征评估家庭照顾者的负担强度和生活质量的变化。方法:采用随机抽样的方法,选取102名在梅塔克萨医院家庭护理的慢性病患者的家庭护理人员作为研究样本。采用BAKAS/BCOS量表和HADS量表进行数据收集。采用SPSS 25统计软件包对结果进行统计分析。结果:采用BCOS量表计算的研究结果显示,家庭照顾者、慢性疾病患者、中度抑郁和焦虑的负担较低(-0.93)。分析结果表明,家庭照顾者负担的强度与焦虑和抑郁水平的增加有关。影响负担的因素有性别,女性负担较高,与患者同住,受教育程度低。根据HADS焦虑量表,家庭照顾者的平均得分为11分,表明焦虑程度中等;在抑郁方面,平均得分为10.4分,也表明抑郁程度中等。结果表明,国家需要支持家庭照顾者,并立即采取行动,建立结构和实施行动,帮助家庭以无痛的方式继续承担困难的角色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AIMS Public Health
AIMS Public Health HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.80
自引率
0.00%
发文量
31
审稿时长
4 weeks
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