Fox Siobhán, Azman Atheerah, Timmons Suzanne
Centre for Gerontology and Rehabilitation, School of Medicine, University College Cork, Cork, Ireland.
Ann Palliat Med. 2020 Feb;9(Suppl 1):S34-S43. doi: 10.21037/apm.2020.02.04.
A diagnosis of Parkinson's disease (PD) has a significant psychological impact on both the person diagnosed and their loved ones, and can have a negative effect on family relationships. Caring for someone with a long-term progressing illness may cause anticipatory grief, i.e., experienced before a bereavement. This has been widely studied in illnesses such as dementia and cancer, but less so in relation to PD. The study aims were: (I) to demonstrate the occurrence of anticipatory grief experienced by carers of people with PD; (II) to explore how this grief relates to caregiver burden and caregiver depression and demographic variables.
Family carers of people with moderate to advanced PD (Hoehn & Yahr stages 3-5) were invited to complete a survey, including demographic questions and three questionnaires: Zarit Burden Interview (ZBI); 16-item Geriatric Depression Scale (GDS); and Anticipatory Grief Scale (AGS).
Anticipatory grief was common among carers of people with PD [mean AGS score =70.41; standard deviation (SD) =16.93; sample range, 38-102]. Though distinct concepts, carers with higher burden and depression scores also experienced more anticipatory grief symptoms. Carers experiencing higher anticipatory grief tended to be caring for someone of a younger age, displaying more non-motor symptoms, at a more advanced disease stage, and who considered either themselves and/or their loved one as depressed.
Carers of people with advanced PD experienced anticipatory grief, as well as depression and a high caregiver burden. To improve carer outcomes, our focus should include the period both before and after the death of a loved one, and carers should receive regular psychological assessment and support.
帕金森病(PD)的诊断对被诊断者及其亲人都会产生重大的心理影响,并可能对家庭关系产生负面影响。照顾患有长期进展性疾病的人可能会引发预期性悲伤,即在丧亲之痛之前就经历的悲伤。这在痴呆症和癌症等疾病中已得到广泛研究,但在帕金森病方面的研究较少。本研究的目的是:(I)证明帕金森病患者的照顾者经历预期性悲伤的情况;(II)探讨这种悲伤与照顾者负担、照顾者抑郁以及人口统计学变量之间的关系。
邀请中重度帕金森病患者(Hoehn & Yahr分期3 - 5期)的家庭照顾者完成一项调查,包括人口统计学问题以及三份问卷: Zarit负担访谈量表(ZBI);16项老年抑郁量表(GDS);以及预期性悲伤量表(AGS)。
预期性悲伤在帕金森病患者的照顾者中很常见[平均AGS得分 = 70.41;标准差(SD) = 16.93;样本范围为38 - 102]。尽管负担和抑郁得分是不同的概念,但负担和抑郁得分较高的照顾者也经历了更多的预期性悲伤症状。经历较高预期性悲伤的照顾者往往照顾的是年龄较小、表现出更多非运动症状、疾病处于更晚期且认为自己和/或其亲人抑郁的患者。
晚期帕金森病患者的照顾者经历了预期性悲伤、抑郁以及较高的照顾者负担。为了改善照顾者的状况,我们的关注应包括亲人去世前后的时期,照顾者应接受定期的心理评估和支持。