Coping with stress by caregivers of patients under the care of the Home Palliative Care Team

被引:0
|
作者
Babiarczyk, Beata [1 ]
Slezinska, Beata [2 ]
Jaksz-Recmanik, Ewelina [1 ]
机构
[1] Uniwersytet Bielsko Bialski, Bielska Biala, Poland
[2] Beskidzkie Centrum Onkol Szpital Miejski, Bielska Biala, Poland
来源
关键词
stress factors; coping with stress strategies; terminal care; caregivers' burden;
D O I
10.5114/pm.2023.132903
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Introduction: Analysis of coping with stress strategies in the families of patients under the care of the Home Palliative Care Team (ZDOP). Material and methods: The survey was conducted between May and September 2022 in the city of Bielsko-Biala. A total of 84 family members of palliative patients were included. The diagnostic survey method was applied. MINI-COPE and our own designed questionnaire were used as the research tools. Results: All respondents were caregivers for cancer patients (n = 84; 100%). Most of the respon-dents were familiar with the assumptions of palliative care (n = 67; 79.8%) and were satisfied with the care of ZDOP (n = 76; 90.5%). For most respondents, especially those who were the main care-givers, the experienced situation was a physical, organizational, and mental burden. The factor that particularly increased the sense of burden was the poor mental condition of the respondents. Most of the respondents had somatic complaints that could indicate chronic stress (n = 66;78.6%), and its main sources were watching the suffering and pain of a loved one (n = 51; 60.7%), experiencing internal blockages (n = 35; 41.7%) or watching at the altered body of a loved one (n = 30; 35.7%). The respondents mentioned many fears related to caring for their loved ones (most often the fear that a loved one will die or suffer). Among the stress coping strategies, the respondents most often chose those related to active coping. However, a certain group of respondents, especially those who were older, less educated, and with a worse financial situation, showed a high level of helplessness and avoidance behaviours. Conclusions: Caregivers of palliative patients, in response to the burden in various domains, take actions referred to as ,,active coping", i.e. taking specific actions to overcome this situation.
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收藏
页码:119 / 129
页数:11
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