a Center of Excellence for Rehabilitation Medicine , Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University and De Hoogstraat Rehabilitation , Utrecht , The Netherlands.
b Department of Neurology , Brain Center Rudolf Magnus, University Medical Center Utrecht , Utrecht , The Netherlands.
Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):235-241. doi: 10.1080/21678421.2018.1534976. Epub 2019 Jan 18.
: To assess psychological distress levels over time in caregivers of patients in the early stage of amyotrophic lateral sclerosis (ALS) and to investigate the association between caregivers' coping styles and psychological distress over time. : Fifty-four caregivers were followed in a RCT of patients in the early stage of ALS. Questionnaires were administered at baseline, 4, 7, and 10 months. Psychological distress was assessed using the Hospital Anxiety and Depression Scale (HADS) and task-, emotion-, and avoidance-oriented coping styles were identified with the short version of the Coping Inventory for Stressful Situations (CISS-21). Analyses were performed using linear mixed models. : Caregivers' psychological distress increased by 0.24 points on the HADS per month ( = 0.01). An emotion-oriented coping style was positively associated with psychological distress in caregivers ( = 0.90, < 0.01), but did not influence the development of psychological distress over time. The avoidance-oriented coping style and the task-oriented coping style were not significantly related to psychological distress. : Feelings of distress increase in ALS caregivers during the course of the disease of the patient. Emotion-oriented coping is related to psychological distress; however, emotional coping and distress might represent overlapping constructs. Focusing on one coping style in the care for ALS caregivers may be too simplistic for the complex situations they face, as it ignores the fact that people may require different coping strategies in different situations
评估肌萎缩侧索硬化(ALS)早期患者的护理者随时间推移的心理困扰水平,并研究护理者应对方式与随时间推移的心理困扰之间的关系。
54 名护理者参与了一项 ALS 早期患者的 RCT 研究。在基线、4、7 和 10 个月时进行问卷调查。使用医院焦虑和抑郁量表(HADS)评估心理困扰,使用应激情境应对量表(CISS-21)的简短版本确定任务导向、情绪导向和回避导向的应对方式。使用线性混合模型进行分析。
护理者的 HADS 心理困扰每月增加 0.24 分( = 0.01)。情绪导向的应对方式与护理者的心理困扰呈正相关( = 0.90, < 0.01),但不会影响心理困扰随时间的发展。回避导向的应对方式和任务导向的应对方式与心理困扰没有显著关系。
在患者疾病的过程中,ALS 护理者的痛苦感会增加。情绪导向的应对与心理困扰有关;然而,情绪应对和困扰可能代表重叠的结构。在照顾 ALS 护理者时,仅关注一种应对方式可能过于简单,因为它忽略了一个事实,即人们在不同情况下可能需要不同的应对策略。