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阿尔茨海默病患者非正式照护的经济评估及其决定因素

Economic valuation and determinants of informal care to people with Alzheimer's disease.

作者信息

Peña-Longobardo Luz María, Oliva-Moreno Juan

机构信息

Faculty of Law and Social Sciences, University of Castilla-La Mancha, Toledo, Spain.

出版信息

Eur J Health Econ. 2015 Jun;16(5):507-15. doi: 10.1007/s10198-014-0604-6. Epub 2014 May 7.

DOI:10.1007/s10198-014-0604-6
PMID:24802240
Abstract

OBJECTIVE

To estimate the monetary value of informal care to people with Alzheimer's disease (AD) in Spain and to identify the main determinants of the time of informal care.

DATA AND METHODS

We used the Survey on Disabilities, Autonomy and Dependency carried out in Spain in 2008 to obtain information on disabled individuals with Alzheimer and their informal caregivers. Assessment of informal care time was performed using three different approaches: the proxy good method, the opportunity cost method and the contingent valuation method. A statistical multivariate analysis--an ordered probit model--was performed to study the determinants of informal care provided.

RESULTS

The average number of required informal hours per year was 4,151. The cost per caregiver ranged from 31,839 to 52,760 euros under the proxy good method; it was estimated at 20,053 euros under the opportunity cost method; and it ranged between 18,680 and 29,057 euros under the contingent valuation method. The degree of dependency and the formal care services were the main variables that explained the variability of the informal time provided. When a person presents a very high level of dependency, the probability of receiving more than 100 h of informal care per week is 25.8% higher than a non-dependent person with AD. Formal in-home care complements informal caregiving, while formal care outside the home replaces it.

CONCLUSIONS

Informal care represents a high social cost in people with AD, regardless of the estimation method considered. A higher level of dependence is associated with more hours of informal care provided.

摘要

目的

评估西班牙阿尔茨海默病(AD)患者接受非正式照护的货币价值,并确定非正式照护时间的主要决定因素。

数据与方法

我们使用了2008年在西班牙进行的残疾、自主性和依赖性调查,以获取有关患有阿尔茨海默病的残疾个体及其非正式照护者的信息。使用三种不同方法评估非正式照护时间:替代商品法、机会成本法和条件估值法。进行了统计多变量分析——有序概率模型——以研究提供非正式照护的决定因素。

结果

每年所需的非正式照护平均时长为4151小时。在替代商品法下,每位照护者的成本在31839欧元至52760欧元之间;在机会成本法下估计为20053欧元;在条件估值法下则在18680欧元至29057欧元之间。依赖程度和正式照护服务是解释所提供非正式照护时间变异性的主要变量。当一个人具有非常高的依赖程度时,每周接受超过100小时非正式照护的概率比非依赖型AD患者高25.8%。正式的居家照护补充了非正式照护,而院外正式照护则取代了非正式照护。

结论

无论采用何种估计方法,非正式照护对AD患者而言都代表着高昂的社会成本。更高的依赖程度与提供更多时长的非正式照护相关。

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