School of Psychology and Centre for Human Brain Health, University of Birmingham, Birmingham, UK.
Neuropsychol Rehabil. 2022 Aug;32(7):1643-1666. doi: 10.1080/09602011.2021.1922463. Epub 2021 Jun 4.
Providing long-term care for a family member diagnosed with a Prolonged Disorder of Consciousness (PDoC) can have a significant impact on the lives of family caregivers. This scoping review aimed to explore the current literature investigating the impact of caring for a person in a PDoC on family caregivers' Quality of Life (QOL), as categorized using the WHOQOL-BREF model. We observed that articles employing quantitative methodologies mostly reported QOL outcomes relating to negative feelings, thinking, learning, memory and concentration, and personal relationships. Articles employing qualitative methodologies mostly reported QOL outcomes relating to negative feelings, personal relationships, positive feelings, and health and social care accessibility and quality. A descriptive content analysis of the QOL outcomes highlighted the limitations of the current literature base in representing the complexities of the experiences of family members providing care for a person in a PDoC. To provide valuable and personalized support to caregivers, without pathologizing or medicalizing their distress, it is vital to characterize more accurately the contextual subtleties of each person's situation.
为被诊断患有持续性意识障碍(PDoC)的家庭成员提供长期护理会对家庭照顾者的生活产生重大影响。本范围综述旨在探讨当前研究照顾 PDoC 患者对家庭照顾者生活质量(QOL)影响的文献,使用 WHOQOL-BREF 模型进行分类。我们发现,采用定量方法的文章主要报告了与负面情绪、思维、学习、记忆和注意力以及人际关系有关的 QOL 结果。采用定性方法的文章主要报告了与负面情绪、人际关系、积极情绪以及健康和社会护理的可及性和质量有关的 QOL 结果。对 QOL 结果的描述性内容分析突出了当前文献基础在代表为 PDoC 患者提供护理的家庭成员的经历的复杂性方面的局限性。为了为照顾者提供有价值和个性化的支持,而不会使他们的痛苦变得病态或医学化,准确描述每个人情况的背景细微差别至关重要。