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dc.contributor.authorMartí García, Celia 
dc.contributor.authorFernández Alcántara, Manuel
dc.contributor.authorSuárez López, Patricia
dc.contributor.authorRomero Ruiz, Carolina
dc.contributor.authorMuñoz Martín, Rocío
dc.contributor.authorGarcía Caro, María Paz 
dc.date.accessioned2021-01-27T13:25:41Z
dc.date.available2021-01-27T13:25:41Z
dc.date.issued2020-12-14
dc.identifier.citationMartí-García C, Fernández-Alcántara M, Suárez López P, Romero Ruiz C, Muñoz Martín Rí, Garcia-Caro MP. 2020. Experiences of family caregivers of patients with terminal disease and the quality of end-of-life care received: a mixed methods study. PeerJ 8:e10516 [http://doi.org/10.7717/peerj.10516]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/66080
dc.descriptionThis study is part of a research project financed in a public and competitive call by the Health Ministry of the Junta de Andalucía (Variability of clinical practice and conditioning factors in the implementation of end-of-life care processes, Ref no PI-0670 -2010). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.descriptionSupplemental information for this article can be found online at http://dx.doi.org/10.7717/ peerj.10516#supplemental-informationes_ES
dc.description.abstractThe aim of this study was to analyze the perceptions and experiences of relatives of patients dying from a terminal disease with regard to the care they received during the dying process, considering the oncological or non-oncological nature of the terminal disease, and the place where care was provided (at home, emergency department, hospital room, or palliative care unit). For this purpose, we conducted a mixed-methods observational study in which two studies were triangulated, one qualitative using semi-structured interviews (n = 30) and the other quantitative, using questionnaires (n = 129). The results showed that the perception of relatives on the quality of care was highly positive in the quantitative evaluation but more critical and negative in the qualitative interview. Experience of the support received and palliative measures was more positive for patients attended in hospital in the case of oncological patients but more positive for those attended at home in the case of non-oncological patients.es_ES
dc.description.sponsorshipHealth Ministry of the Junta de Andalucia PI-0670 -2010es_ES
dc.language.isoenges_ES
dc.publisherPeerJes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectPalliative carees_ES
dc.subjectQualitativees_ES
dc.subjectMixed methodses_ES
dc.subjectBereavement es_ES
dc.subjectRelativeses_ES
dc.subjectEnd-of-life carees_ES
dc.subjectCaregivers es_ES
dc.titleExperiences of family caregivers of patients with terminal disease and the quality of end-of-life care received: a mixed methods studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.7717/peerj.10516
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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Atribución 3.0 España
Except where otherwise noted, this item's license is described as Atribución 3.0 España