Amiri Parastoo, Niazkhani Zahra, Pirnejad Habibollah, Bahaadinbeigy Kambiz
Department of Health Information Technology, School of Allied Medical Sciences, Lorestan University of Medical Sciences, Khorramabad, Iran.
Nephrology and Kidney Transplant Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran.
BMJ Open. 2025 Jan 23;15(1):e088313. doi: 10.1136/bmjopen-2024-088313.
The aim of the present study was to explore the experiences and viewpoints of professional family caregivers in the management of behavioural and psychological symptoms of dementia (BPSDs) to identify the ecopsychosocial strategies applied by them.
Qualitative study.
Kerman, Iran.
Stories were collected from 40 professional family caregivers of dementia patients.
The guidelines of the National Consensus Project (NCP) of the USA served as the conceptual framework for the deductive thematic analysis of our qualitative data. A schematic of the entire process was performed in five steps.
30 stories relevant to the aim of this study were included in the analysis from April to June 2021. A majority of the stories were written by female caregivers. We identified 19 ecopsychosocial interventions, which covered the NCP dimensions except 'Care of the patient nearing the end of life'. More than half of these interventions were classified into psychological/psychiatric and physical aspects of care (57.8%). In addition to the care/support provided by special care units or home care, some caregivers believe that support from the government, various care organisations, social media and even other family members/friends is necessary to better manage BPSDs.
Despite limitations, such as having a small sample size and analysing only one story from each caregiver, our results indicate that dementia caregivers need more educational and cultural support in their ecopsychosocial strategies. Government involvement would yield more positive outcomes in managing BPSDs.
本研究旨在探讨专业家庭照护者在管理痴呆行为和心理症状(BPSD)方面的经历和观点,以确定他们所采用的生态心理社会策略。
定性研究。
伊朗克尔曼。
从40名痴呆患者的专业家庭照护者那里收集故事。
美国国家共识项目(NCP)的指南作为我们定性数据演绎主题分析的概念框架。整个过程的示意图分五步进行。
2021年4月至6月,分析纳入了30个与本研究目的相关的故事。大多数故事由女性照护者撰写。我们确定了19种生态心理社会干预措施,涵盖了NCP的各个维度,但不包括“临终患者护理”。这些干预措施中一半以上被归类为护理的心理/精神和身体方面(57.8%)。除了特殊护理单位或家庭护理提供的护理/支持外,一些照护者认为政府、各种护理组织、社交媒体甚至其他家庭成员/朋友的支持对于更好地管理BPSD是必要的。
尽管存在局限性,如样本量小且每位照护者仅分析一个故事,但我们的结果表明,痴呆照护者在其生态心理社会策略方面需要更多的教育和文化支持。政府的参与在管理BPSD方面将产生更积极的结果。