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帕金森病的姑息治疗需求:关注家庭照料者的预期性悲伤

Palliative care needs in Parkinson's disease: focus on anticipatory grief in family carers.

作者信息

Fox Siobhán, Azman Atheerah, Timmons Suzanne

机构信息

Centre for Gerontology and Rehabilitation, School of Medicine, University College Cork, Cork, Ireland.

出版信息

Ann Palliat Med. 2020 Feb;9(Suppl 1):S34-S43. doi: 10.21037/apm.2020.02.04.

Abstract

BACKGROUND

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.

METHODS

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).

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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)。

结果

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。

结论

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。

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