Lien Centre for Palliative Care, Duke-NUS Medical School, Singapore; Program in Health Services and Systems Research, Duke-NUS Medical School, Singapore.
Lien Centre for Palliative Care, Duke-NUS Medical School, Singapore.
J Am Med Dir Assoc. 2023 Sep;24(9):1427-1432. doi: 10.1016/j.jamda.2023.07.001. Epub 2023 Aug 8.
Family caregivers' perception that dementia is a terminal disease influence end-of-life (EoL) care of persons with severe dementia (PwSDs). Yet, this perception and the extent to which it changes over time is underexplored. We assessed PwSD caregivers' perception of dementia as a terminal disease and changes in this perception over time.
Prospective cohort.
Two hundred fifteen primary informal caregivers of community-dwelling PWSDs in Singapore were surveyed every 4 months over a period of 16 months.
We assessed the proportion of caregivers who perceived that dementia is a terminal disease and the extent to which it changed between the previous time points. Using mixed effects multinomial regression models, we assessed factors associated with caregivers' perception and changes in perception between consecutive time points.
At baseline, only 26% of the caregivers reported correctly that dementia is a terminal disease. This changed over time, not necessarily toward a correct perception. Caregivers of PwSDs with an acute medical condition in the last 4 months (risk ratio [RR] 2.19, 95% CI 1.21, 3.97) and those with higher functional dependence (RR 1.11, 95% CI 1.01,1.22) were more likely and those of older PwSDs were less likely (RR 0.87, 95% CI 0.81, 0.93) to perceive dementia as a terminal disease. Caregivers of PwSDs who had experienced an acute medical problem in the last 4 months (RR 1.58, 95% CI 1.00, 2.49) were also more likely to shift their perception toward being correct. Caregivers of PwSDs who had more agitation behaviors were more likely to shift their perception toward being incorrect (RR 1.04, 95% CI 1.00,1.07) CONCLUSIONS AND IMPLICATIONS: Few caregivers perceived dementia as terminal, and this perception changed over time and differed according to age and the health status of PwSD. Results have implications regarding the frequency of prognostic discussions.
家庭照顾者认为痴呆是一种终末期疾病,这会影响严重痴呆症患者(PwSD)的临终关怀。然而,这种认知以及其随时间变化的程度尚未得到充分探索。我们评估了 PwSD 照顾者对痴呆症作为终末期疾病的认知,以及这种认知随时间的变化。
前瞻性队列研究。
2015 年在新加坡对 215 名社区居住的 PwSD 的主要非正式照顾者进行了每 4 个月一次的调查,共进行了 16 个月。
我们评估了认为痴呆症是一种终末期疾病的照顾者的比例,以及他们在之前的时间点之间认知变化的程度。使用混合效应多项逻辑回归模型,我们评估了与照顾者的认知以及连续时间点之间认知变化相关的因素。
基线时,只有 26%的照顾者正确报告痴呆症是一种终末期疾病。这一情况随时间发生了变化,但并不一定朝着正确的认知发展。在过去 4 个月内有急性医疗状况的 PwSD 的照顾者(风险比 [RR]2.19,95%置信区间 [CI]1.21,3.97)和功能依赖程度较高的照顾者(RR1.11,95%CI1.01,1.22)更有可能,而年龄较大的 PwSD 的照顾者(RR0.87,95%CI0.81,0.93)则不太可能将痴呆症视为终末期疾病。在过去 4 个月内经历过急性医疗问题的 PwSD 的照顾者(RR1.58,95%CI1.00,2.49)也更有可能将其认知转变为正确。PwSD 出现激越行为的照顾者更有可能将其认知转变为不正确(RR1.04,95%CI1.00,1.07)。
很少有照顾者将痴呆症视为终末期疾病,这种认知随时间而变化,并且因 PwSD 的年龄和健康状况而异。结果对预后讨论的频率具有启示意义。