dc.contributor.author | Güeita Rodriguez, Javier | |
dc.contributor.author | Famoso Pérez, Pilar | |
dc.contributor.author | Salom Moreno, Jaime | |
dc.contributor.author | Carrasco Garrido, Pilar | |
dc.contributor.author | Pérez Corrales, Jorge | |
dc.contributor.author | Palacios Ceña, Domingo | |
dc.date.accessioned | 2020-10-22T09:49:36Z | |
dc.date.available | 2020-10-22T09:49:36Z | |
dc.date.issued | 2020 | |
dc.identifier.issn | 1660-4601 | spa |
dc.identifier.uri | http://hdl.handle.net/10641/2028 | |
dc.description.abstract | Rare diseases face serious sustainability challenges regarding the distribution of resources geared at health and social needs. Our aim was to describe the barriers experienced by parents of children with Rett Syndrome for accessing care resources. A qualitative case study was conducted among 31 parents of children with Rett syndrome. Data were collected through in-depth interviews, focus groups, researchers’ field notes and parents’ personal documents. A thematic analysis was performed and the Standards for Reporting Qualitative Research (SRQR) guidelines were followed. Three main themes emerged from the data: (a) essential health resources; (b) bureaucracy and social care; and (c) time management constraints. Parents have difficulties accessing appropriate health services for their children. Administrative obstacles exist for accessing public health services, forcing parents to bear the financial cost of specialized care. Time is an essential factor, which conditions the organization of activities for the entire family. Qualitative research offers insight into how parents of children with Rett syndrome experience access to resources and may help improve understanding of how Rett syndrome impacts the lives of both the children and their parents | spa |
dc.language.iso | eng | spa |
dc.publisher | International journal of environmental research and public health | spa |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 España | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es/ | * |
dc.subject | Health services accessibility | spa |
dc.subject | Rare disease | spa |
dc.subject | Rett syndrome | spa |
dc.subject | Qualitative research | spa |
dc.title | Challenges A ecting Access to Health and Social Care Resources and Time Management among Parents of Children with Rett Syndrome: A Qualitative Case Study. | spa |
dc.type | article | spa |
dc.description.version | post-print | spa |
dc.rights.accessRights | openAccess | spa |
dc.description.extent | 353 KB | spa |
dc.identifier.doi | 10.3390/ijerph17124466 | spa |
dc.relation.publisherversion | https://www.mdpi.com/1660-4601/17/12/4466 | spa |