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法国阿尔茨海默病的资源使用与成本:GERAS观察性研究的18个月结果

Resource Use and Cost of Alzheimer's Disease in France: 18-Month Results from the GERAS Observational Study.

作者信息

Rapp Thomas, Andrieu Sandrine, Chartier Florence, Deberdt Walter, Reed Catherine, Belger Mark, Vellas Bruno

机构信息

LIRAES (EA4470), Université Paris Descartes-Sorbonne Paris Cité, Paris, France.

INSERM UMR1027, Toulouse University Hospital, Toulouse, France.

出版信息

Value Health. 2018 Mar;21(3):295-303. doi: 10.1016/j.jval.2017.09.019. Epub 2017 Nov 11.

Abstract

BACKGROUND

There is little longitudinal data on resource use and costs associated with Alzheimer's disease (AD) in France.

OBJECTIVES

To evaluate resource use and societal costs associated with AD in a French cohort of patients and their caregivers and the effect of patient cognitive decline on costs over an 18-month period.

METHODS

Community-dwelling patients with mild, moderate, or moderately severe/severe AD dementia (n = 419) were followed-up for 18 months. Total societal costs were estimated by applying 2010 unit costs to resource use, including outpatient visits, hospital days, institutionalization, and caregiver hours. Cognitive function was assessed by Mini-Mental State Examination scores.

RESULTS

Mean cumulative total costs over the 18-month period were €24,140 for patients with mild AD dementia, €34,287 for those with moderate AD dementia, and €44,171 for those with moderately severe/severe AD dementia (P < 0.001; ANOVA comparison between severity groups). The biggest contributor to total societal costs was caregiver informal care (>50% of total costs at all stages of AD dementia). Cognitive decline (≥3-point decrease in Mini-Mental State Examination score or institutionalization) was associated with a 12.5% increase in total costs (P = 0.02). Significant differences were observed across severity groups for caregiver time (P < 0.001); mean monthly caregiver time increased at each time point over the 18 months in each severity group.

CONCLUSIONS

Increasing severity of AD dementia in France is associated with increased use of resources as well as increased total societal and patient costs; informal care was the greatest cost contributor. Clinically meaningful cognitive decline is associated with significantly increased costs.

摘要

背景

在法国,关于阿尔茨海默病(AD)相关资源使用和成本的纵向数据很少。

目的

评估法国一组患者及其照料者中与AD相关的资源使用和社会成本,以及患者认知功能下降在18个月期间对成本的影响。

方法

对社区居住的轻度、中度或中度重度/重度AD痴呆患者(n = 419)进行了18个月的随访。通过将2010年单位成本应用于资源使用来估计总社会成本,资源使用包括门诊就诊、住院天数、机构化照料和照料者工时。通过简易精神状态检查表评分评估认知功能。

结果

轻度AD痴呆患者在18个月期间的平均累计总成本为24,140欧元,中度AD痴呆患者为34,287欧元,中度重度/重度AD痴呆患者为44,171欧元(P < 0.001;ANOVA比较严重程度组之间)。总社会成本的最大贡献者是照料者的非正式照料(在AD痴呆的所有阶段占总成本的>50%)。认知功能下降(简易精神状态检查表评分下降≥3分或机构化照料)与总成本增加12.5%相关(P = 0.02)。在照料者时间方面,不同严重程度组之间观察到显著差异(P < 0.001);在18个月期间,每个严重程度组的每个时间点,照料者平均每月时间都有所增加。

结论

法国AD痴呆严重程度的增加与资源使用增加以及总社会成本和患者成本增加相关;非正式照料是最大的成本贡献因素。具有临床意义的认知功能下降与成本显著增加相关。

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