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Article type: Research Article
Authors: Peña-Longobardo, Luz María; * | Oliva-Moreno, Juan
Affiliations: Faculty of Law and Social Sciences, Department of Economic Analysis, University of Castilla-La Mancha, Toledo, Spain
Correspondence: [*] Correspondence to: Luz María Peña-Longobardo, Universidad de Castilla la Mancha, Facultad de Ciencias Jurídicas y Sociales de Toledo, Análisis Económico y Finanzas, Cobertizo de San Pedro Mártir s/n, 45071 Toledo, Spain. Tel.: +34 925 26 88 00; Ext. 5043; E-mail: [email protected].
Abstract: Background:Alzheimer's disease constitutes one of the leading causes of burden of disease, and it is the third leading disease in terms of economic and social costs. Objective:To analyze the burden and problems borne by informal caregivers of patients who suffer from Alzheimer's disease in Spain. Data and Methods:We used the Survey on Disabilities, Autonomy and Dependency to obtain information on the characteristics of disabled people with Alzheimer's disease and the individuals who provide them with personal care. Additionally, statistical multivariate analyses using probit models were performed to analyze the burden placed on caregivers in terms of health, professional, and leisure/social aspects. Results:46% of informal caregivers suffered from health-related problems as a result of providing care, 90% had leisure-related problems, and 75% of caregivers under 65 years old admitted to suffering from problems related to their professional lives. The probability of a problem arising for an informal caregiver was positively associated with the degree of dependency of the person cared for. In the case of caring for a greatly dependent person, the probability of suffering from health-related problems was 22% higher, the probability of professional problems was 18% higher, and there was a 10% greater probability of suffering from leisure-related problems compared to non-dependents. Conclusions:The results show a part of the large hidden cost for society in terms of problems related to the burden lessened by the caregivers. This information should be a useful tool for designing policies focused toward supporting caregivers and improving their welfare.
Keywords: Alzheimer's disease, burden, caregivers, informal care, social costs
DOI: 10.3233/JAD-141374
Journal: Journal of Alzheimer's Disease, vol. 43, no. 4, pp. 1293-1302, 2015
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