绘制最后的旅程:生命末期的脆弱轨迹和死亡原因。

Jianhong Xu, Jonathan Ka-Long Mak, Qian-Li Xue, Chenkai Wu
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引用次数: 0

摘要

背景:在现有的研究中,与衰老相关的虚弱变化已经得到了充分的证明。然而,关于衰弱在生命末期如何发展的证据有限。我们的目的是探索生命最后一年的脆弱轨迹,并探索这些轨迹的分布如何根据导致死亡的条件而不同。方法:基于英国生物银行(UK Biobank)的国家死亡登记关联数据,分析样本包括37,465名死者。使用医院衰弱风险评分(HFRS)获得死亡前1年的每月衰弱评分;(衡量脆弱程度的累积赤字)。使用潜在类别轨迹模型来估计脆弱性的轨迹。我们进一步分析了这些脆弱轨迹在导致死亡的不同条件下的分布。多项逻辑回归模型用于检验预测因子与脆弱轨迹之间的关联。结果:37465例死亡中,2895例(7.7%)死于神经退行性疾病。在这些死者中确定了三种不同的衰弱轨迹:快速进展的衰弱(6.9%),中度衰弱(21.1%)和晚期和稳定的衰弱(72.0%)。这些模式明显不同于其他死因的死者,后者表现为持续轻度虚弱(24.7%),中度和进行性虚弱(46.5%),以及晚期和进行性虚弱(28.8%)。与癌症患者相比,患有神经退行性疾病的个体具有更高的基线虚弱和晚期和稳定虚弱的主要轨迹。年龄较大、受教育程度较低和慢性疾病负担加重与晚期和进行性衰弱轨迹相关。结论:生命结束时的虚弱轨迹因死亡原因而异,神经退行性疾病的死者表现出更严重的虚弱。这些发现强调了早期识别虚弱和量身定制的临终关怀策略的必要性,特别是对于患有神经退行性疾病的个体,他们经常经历长期和严重的虚弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping the Final Journey: End-Of-Life Frailty Trajectories and Cause of Death.

Background: Frailty changes associated with aging have been well-documented in existing research. However, there is limited evidence on how frailty progresses during the end-of-life stage. We aimed to explore trajectories of frailty in the last year of life and explore how the distribution of these trajectories differs according to the conditions leading to death.

Methods: Based on national death registries linkage data in the UK Biobank, 37,465 decedents were included in the analytic sample. Monthly frailty scores were obtained for 1 year prior to death using the Hospital Frailty Risk Score (HFRS; a cumulative deficit measure of frailty). Latent class trajectory models were used to estimate trajectories of frailty. We further analyzed the distribution of these frailty trajectories across different conditions leading to death. Multinomial logistic regression models were applied to examine the associations between predictors and frailty trajectories.

Results: Among 37,465 decedents, 2895 (7.7%) died from neurodegenerative diseases. Three distinct frailty trajectories were identified among these decedents: rapidly progressive frailty (6.9%), moderate progression of frailty (21.1%), and advanced and stable frailty (72.0%). These patterns differed significantly from those observed in decedents with other causes of death, who exhibited persistently low frailty (24.7%), intermediate and progressive frailty (46.5%), and advanced and progressive frailty (28.8%). Compared to cancer decedents, individuals with neurodegenerative diseases had higher baseline frailty and a dominant trajectory of advanced and stable frailty. Older age, lower education, and greater chronic disease burden were associated with the advanced and progressive frailty trajectory.

Conclusions: Frailty trajectories at the end of life varied by cause of death, with neurodegenerative disease decedents exhibiting more severe frailty. These findings underscored the need for early identification of frailty and tailored end-of-life care strategies, particularly for individuals with neurodegenerative diseases who often experienced prolonged and severe frailty.

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