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dc.contributor.authorGómez, Laura E.
dc.contributor.authorMorán, M. Lucía
dc.contributor.authorSolís, Patricia
dc.contributor.authorPérez-Curiel, Patricia
dc.contributor.authorMonsalve, Asunción
dc.contributor.authorNavas Macho, Patricia 
dc.date.accessioned2025-01-22T12:13:42Z
dc.date.available2025-01-22T12:13:42Z
dc.date.issued2023
dc.identifier.citationGómez, L. E., Morán, L., Solís, P., Pérez-Curiel, P., Monsalve, A. & Navas, P. (2024). Health care for people with intellectual disability in Spain. Journal of Policy and Practice in Intellectual Disabilities, 21(1). https://doi.org/10.1111/JPPI.12455es_ES
dc.identifier.issn1741-1122
dc.identifier.urihttp://hdl.handle.net/10366/162284
dc.description.abstract[EN] We describe the healthcare system for people with intellectual disability (ID) in Spain. First, we provide general population statistics before focusing on the most recent prevalence data related to people with disability in general, and with ID in particular. We also discuss how health care is organized. Most of the Spanish population is covered by the public healthcare system, which is structured into primary care (first-level health services; easily accessible and capable of tackling the most common ailments) and specialized care (second-level health services; comprising the most complex and costly diagnostic and therapeutic resources). We then explain Spain's primary legislation that promotes the rights of people with disabilities, highlighting the importance of the United Nations Convention on the Rights of Persons with Disabilities (CRPD), which is enshrined in the Spanish General Law on the Rights of People with Disabilities and their Social Inclusion (Royal Legislative Decree 1/2013). Second, we describe the organization of Spanish disability support and health services, whose regulation is highly complex given that the autonomous regions set their own rules about coverage, services, and financing. Third, we present some recent studies that allow a better understanding of health care for people with ID in Spain, including a summary of the ongoing #Rights4MeToo project. We report specific data on the right to habilitation/rehabilitation. People with ID and professionals providing them with supports agreed that the most problematic aspects of health care for people with ID were the lack of: coordination across services, user-friendly information to maintain or improve their health, psychological treatments, preventive medical check-ups, and knowledge about disability among health professionals. There is a need to give people with ID priority access to services, reduce waiting times, increase the length of medical appointments, and create protocols and prevention campaigns targeting them.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectConvention on the Rights of Persons with Disabilitieses_ES
dc.subjecthealthes_ES
dc.subjecthealth carees_ES
dc.subjectintellectual disabilityes_ES
dc.subjectmental healthes_ES
dc.titleHealth care for people with intellectual disability in Spaines_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1111/jppi.12470es_ES
dc.identifier.doi10.1111/JPPI.12455
dc.relation.projectIDPID2019-105737RB-I00/ AEI/10.13039/501100011033es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1741-1130
dc.journal.titleJournal of Policy and Practice in Intellectual Disabilitieses_ES
dc.volume.number21es_ES
dc.issue.number1es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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