慢性疾病患者与健康相关的生活质量和照顾者负担:一项横断面研究

IF 0.5 Q4 PRIMARY HEALTH CARE Family Medicine and Primary Care Review Pub Date : 2021-01-01 DOI:10.5114/FMPCR.2021.103184
Seyedmohammad Mirhosseini, M. Bazghaleh, M. Basirinezhad, A. Abbasi, H. Ebrahimi
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引用次数: 3

摘要

背景。癌症和2型糖尿病(T2D)作为两组流行的慢性疾病,与不同的社会、经济和情感后果相关,并且可以改变其照顾者的生活质量(QoL)。目标。本研究的目的是确定生活质量与癌症和T2D患者照顾者负担之间的关系。材料和方法。本研究对308名癌症合并T2D患者的护理人员进行了比较横断面研究。数据收集工具包括人口统计学特征表、SF-36生活质量表和护理负担量表(Novak和Guest)。数据采集采用方便抽样法。然后使用描述性统计和推理统计(线性向后逐步回归方法)进行数据分析。结果。肿瘤患者和T2D患者护理人员的平均年龄分别为41.30±13.12岁和41.86±12.78岁。两组照护者的照护负担和生活质量均分差异无统计学意义。照顾者生活质量与照顾者疾病呈显著正相关,照顾者受教育程度与照顾负担呈显著负相关。结论。慢性病患者照护者承受照顾负担,对其生活质量产生负向影响;因此,建议通过提供适当的精神、心理和社会支持来减轻护理负担,提高他们的生活质量。由于照护负担对照护者生活质量的负面影响,发展中国家应加强对慢性患者的照护服务。
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Health-related quality of life and caregiver’s burden in patients with chronic diseases: a cross-sectional study
Background. Cancer and type 2 diabetes (T2D), as two groups of prevalent chronic diseases, are associated with different social, economic and emotional consequences, and they can change the quality of life (QoL) of their caregivers. Objectives. The aim of the present study was to determine the relationship between QoL and the burden on caregivers of patients with cancer and T2D. Material and methods. This comparative cross-sectional study was conducted on 308 caregivers of patients with cancer and T2D. Data collection tools included a demographic characteristics form, SF-36 quality of life form and care burden inventory (Novak and Guest). Data was collected using the convenience sampling method. Data analysis was then carried out using descriptive and inferential statistics (linear backward stepwise regression method). Results. The mean age of the caregivers of patients with cancer and T2D was 41.30 ± 13.12 and 41.86 ± 12.78 years, respectively. There was no significant difference between the mean score of care burden and QoL in the two groups of caregivers. There was a significant direct relationship between caregivers’ QoL and caregivers' disease and a significant inverse relationship between caregivers’ education and caring burden. Conclusions. Caregivers of patients with chronic diseases suffer from care burden, which negatively affects their QoL; thus, it is recommended to reduce the care burden, increasing their QoL by providing appropriate mental, psychological, and social support. Due to the negative impact of caring burden on caregivers’ QoL, care services for chronic patients in developing countries should be strengthened.
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来源期刊
CiteScore
1.20
自引率
14.30%
发文量
18
审稿时长
12 weeks
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