Symptom- and function-based trajectories of patients with dementia in hospital and community palliative care settings in the last two weeks of life: a retrospective cohort study.

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES BMC Palliative Care Pub Date : 2024-10-21 DOI:10.1186/s12904-024-01565-6
Minghui Tan, Xiwen Simon Qin, Claire E Johnson, Lin Xiao, Angus Cook, Jinfeng Ding, Juan Wang
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Abstract

Background: The prevalence of dementia is increasing worldwide and many people with the condition require some level of palliative care. However, the trajectories of function and symptom burden in palliative care services at the end of life remain unclear. This study aimed to describe and compare the longitudinal trajectories of function and symptom burden among patients with dementia between hospital versus palliative community care services in the last two weeks of life.

Methods: A retrospective cohort study used data from the Australian Palliative Care Outcomes Collaboration. Patients with dementia who died between 1 January 2013 and 31 December 2020 from the Australian Palliative Care Outcomes Collaboration. Four validated clinical instruments were used to collect outcomes on each individual's function and symptom distress and severity. Multilevel models were used to estimate the differences in clinical trajectories between hospital and community-based palliative care in the last two weeks of life.

Results: Patients with dementia tended to have low levels of distress for most symptoms but increasing levels of functional impairment. There were no or only marginally significant differences in the symptom trajectories between the community and hospital groups (OR ranged from 0.57 to 1.97). Although clinical trajectories of function were relatively similar between two groups, statistically higher functional indicators were observed for people when admitted to community palliative care services (OR = 0.42 and 2.27, respectively).

Conclusions: Our findings suggest that community-based palliative care services can be as effective as hospital-based care for many patients with dementia nearing the end of life. With appropriate support for families, community-based care could serve as a viable alternative to hospital-based care for some patients in the final stages of dementia.

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医院和社区姑息关怀机构中痴呆症患者生命最后两周的症状和功能轨迹:一项回顾性队列研究。
背景:痴呆症的发病率在全球范围内不断上升,许多痴呆症患者都需要一定程度的姑息关怀。然而,生命末期姑息治疗服务的功能和症状负担轨迹仍不清楚。本研究旨在描述和比较痴呆症患者在生命最后两周在医院和社区姑息关怀服务中的功能和症状负担的纵向轨迹:这是一项回顾性队列研究,使用的数据来自澳大利亚姑息治疗结果合作组织(Australian Palliative Care Outcomes Collaboration)。研究对象为2013年1月1日至2020年12月31日期间死亡的痴呆症患者,这些患者均来自澳大利亚姑息治疗结果合作组织(Australian Palliative Care Outcomes Collaboration)。四种经过验证的临床工具用于收集每个人的功能、症状困扰和严重程度的结果。采用多层次模型估算了医院姑息治疗与社区姑息治疗在患者生命最后两周的临床轨迹差异:结果:痴呆症患者大多数症状的痛苦程度较低,但功能障碍程度却在增加。社区组和医院组之间的症状轨迹没有或仅有微小差异(OR值介于0.57至1.97之间)。虽然两组患者的临床功能轨迹相对相似,但从统计学角度看,接受社区姑息关怀服务的患者的功能指标更高(OR = 0.42 和 2.27):我们的研究结果表明,对于许多临近生命终点的痴呆症患者而言,社区姑息关怀服务与医院姑息关怀服务同样有效。在为家属提供适当支持的情况下,对于一些处于痴呆症晚期的患者来说,社区姑息关怀服务可以作为医院姑息关怀服务的可行替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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