Julio López-Bastida
University of Castilla–La Mancha
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Publication
Featured researches published by Julio López-Bastida.
European Journal of Health Economics | 2010
Julio López-Bastida; Juan Oliva; Fernando Antoñanzas; Anna García-Altés; Ramón Gisbert; Javier Mar; Jaume Puig-Junoy
The economic evaluation of health technologies has become a major tool in health policy in Europe for prioritizing the allocation of health resources and the approval of new technologies. The objective of this proposal was to develop guidelines for the economic evaluation of health technologies in Spain. A group of researchers specialized in economic evaluation of health technologies developed the document reported here, following the initiative of other countries in this framework, to provide recommendations for the standardization of methodology applicable to economic evaluation of health technologies in Spain. Recommendations appear under 17 headings or sections. In each case, the recommended requirements to be satisfied by economic evaluation of health technologies are provided. Each recommendation is followed by a commentary providing justification and compares and contrasts the proposals with other available alternatives. The economic evaluation of health technologies should have a role in assessing health technologies, providing useful information for decision making regarding their adoption, and they should be transparent and based on scientific evidence.
Neurology | 2006
Julio López-Bastida; Pedro Serrano-Aguilar; Lilisbeth Perestelo-Pérez; Juan Oliva-Moreno
Objectives: To examine the economic burden (direct and indirect costs) of Alzheimer disease (AD) and to analyze the impact on health-related quality of life (HRQOL) for patients with AD and caregivers in 2001 in the Canary Islands, Spain. Methods: Two hundred thirty-seven patients (61% of those contacted) were recruited from the Alzheimer’s Disease Association in the Canary Islands. Demographic, health resources utilization, informal care, indirect costs, and quality of life data were collected from primary caregivers of patients as proxy respondents. HRQOL was measured for patients and caregivers with the generic questionnaire EQ-5D. Results: The average annual cost per patient with AD was 28,198 (US
Amyotrophic Lateral Sclerosis | 2009
Julio López-Bastida; Lilisbeth Perestelo-Pérez; Fernando Montón-Álvarez; Pedro Serrano-Aguilar; Jose L. Alfonso-Sanchez
36,144). The most important categories of costs were for informal care and drugs. Costs increased with cognitive impairment with an average annual cost of 14,956 (US
BMC Health Services Research | 2012
Julio López-Bastida; Juan Oliva Moreno; Melany Worbes Cerezo; Lilisbeth Perestelo Peréz; Pedro Serrano-Aguilar; Fernando Montón-Álvarez
19,171) for mild, 25,562 (US
European Journal of Health Economics | 2005
Juan Oliva; Félix Lobo; Julio López-Bastida; Néboa Zozaya; Rosa Romay
32,765) for moderate, and 41,669 (US
European Journal of Health Economics | 2009
Juan Oliva-Moreno; Julio López-Bastida; Angel Luis Montejo-González; Rubén Osuna-Guerrero; Beatriz Duque-González
53,411) for severe patients. The total cost of patients with AD in Canary Islands was 259 (US
BMC Health Services Research | 2009
Julio López-Bastida; Juan Oliva-Moreno; Lilisbeth Perestelo-Pérez; Pedro Serrano-Aguilar
332) million. The HRQOL with the EQ-5D social tariff was 0.29 for patients and 0.67 for caregivers. The EQ-5D VAS (thermometer) score was 42 for patients and 62 for caregivers. Conclusions: Direct health care costs of AD represented 2.4% of the total public health care expenditure in the Canary Islands. Across all severity levels, we estimated a total annual cost of 10 (US
Globalization and Health | 2013
Julio López-Bastida; Mauro Boronat; Juan Oliva Moreno; Willemien Schurer
13) billion for AD patients older than 65 years in Spain. The degree of severity of the patients with AD substantially influenced the quality of life of the patients but not that of the caregivers.
Health Policy | 2012
Renata Linertová; Pedro Serrano-Aguilar; Manuel Posada-de-la-Paz; Manuel Hens-Pérez; Panos Kanavos; Domenica Taruscio; Arrigo Schieppati; Rumen Stefanov; Márta Péntek; Claudia Delgado; Johann-Matthias Graf von der Schulenburg; Ulf Persson; Karine Chevreul; Giovanni Fattore; Melany Worbes-Cerezo; Mark Sefton; Julio López-Bastida
Amyotrophic lateral sclerosis (ALS) is a process that leads to the functional disability of the individual in a relatively short period of time, with a very important limitation of autonomy and affecting the quality of life. We wished to determine the economic burden (direct and indirect costs), as well as health-related quality of life (HRQoL) in patients with ALS in Spain. A cross-sectional study was carried out on 63 patients with ALS during 2004. A retrospective assessment of the use of resources was obtained through questionnaires completed by the patients and/or the patients’ caregivers. The approach used was a cost-of-illness study based on a societal perspective. We assessed the HRQoL with the EQ-5D. Mean annual cost per patient with ALS was €36,194. The most important categories of costs were informal care, early retirement, medications, and orthopaedic devices. The mean EQ-5D index score was 0.18 and the mean EQ-5D VAS score was 29. Considerations of the costs related to caregiving to cope with the patients’ disabilities, as well as the high indirect costs resulting from early retirement in patients with ALS, should become a priority for health authorities in Spain. The patients’ HRQoL was very low and substantially influenced by the degree of severity of ALS.
Revista Espanola De Cardiologia | 2009
Juan Oliva; Julio López-Bastida; Santiago G. Moreno; Pedro Mata; Rodrigo Alonso
BackgroundCost-of-illness analysis is the main method of providing an overall vision of the economic impact of a disease. Such studies have been used to set priorities for healthcare policies and inform resource allocation. The aim of this study was to determine the economic burden and health-related quality of life (HRQOL) in the first, second and third years after surviving a stroke in the Canary Islands, Spain.MethodsCross-sectional, retrospective study of 448 patients with stroke based on ICD 9 discharge codes, who received outpatient care at five hospitals. The study was approved by the Research Ethics Committee of Nuestra Señora de la Candelaria University Hospital. Data on demographic characteristics, health resource utilization, informal care, labor productivity losses and HRQOL were collected from the hospital admissions databases and questionnaires completed by stroke patients or their caregivers. Labor productivity losses were calculated from physical units and converted into monetary units with a human capital-based method. HRQOL was measured with the EuroQol EQ-5D questionnaire. Healthcare costs, productivity losses and informal care costs were analyzed with log-normal, probit and ordered probit multivariate models.ResultsThe average cost for each stroke survivor was €17 618 in the first, €14 453 in the second and €12 924 in the third year after the stroke; the reference year for unit prices was 2004. The largest expenditures in the first year were informal care and hospitalizations; in the second and third years the main costs were for informal care, productivity losses and medication. Mean EQ-5D index scores for stroke survivors were 0.50 for the first, 0.47 for the second and 0.46 for the third year, and mean EQ-5D visual analog scale scores were 56, 52 and 55, respectively.ConclusionsThe main strengths of this study lie in our bottom-up-approach to costing, and in the evaluation of stroke survivors from a broad perspective (societal costs) in the first, second and third years after surviving the stroke. This type of analysis is rare in the Spanish context. We conclude that stroke incurs considerable societal costs among survivors to three years and there is substantial deterioration in HRQOL.