Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/213435
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Toro, Daniel del | - |
dc.contributor.author | Limonero, Joaquin T. | - |
dc.contributor.author | Guillén, Montserrat | - |
dc.contributor.author | Bolancé Losilla, Catalina | - |
dc.contributor.author | Navarro Vilarrubí, Sergi | - |
dc.contributor.author | Camprodon-Rosanas, Ester | - |
dc.date.accessioned | 2024-06-19T22:41:55Z | - |
dc.date.issued | 2024-03-01 | - |
dc.identifier.issn | 0340-6199 | - |
dc.identifier.uri | https://hdl.handle.net/2445/213435 | - |
dc.description.abstract | The patient’s perspective is an essential component of understanding the individual experience of suffering in children with palliative needs, but it is a perspective that is often overlooked. The aim of this study was to compare the perception of quality of life (QoL) of children with life-limiting and life-threatening conditions expressed by the children themselves and their parents. Through a cross-sectional study, the responses of 44 parent–child dyads were obtained and the analysis was performed with the statistics based on Student’s t distribution and non-parametric tests | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Springer Verlag | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1007/s00431-023-05330-4 | - |
dc.relation.ispartof | European Journal of Pediatrics, 2024, vol. 183, num.3, p. 1305-1314 | - |
dc.relation.uri | https://doi.org/10.1007/s00431-023-05330-4 | - |
dc.rights | cc by (c) Toro et al., 2024 | - |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.source | Articles publicats en revistes (Econometria, Estadística i Economia Aplicada) | - |
dc.subject.classification | Tractament pal·liatiu | - |
dc.subject.classification | Infants malalts | - |
dc.subject.classification | Qualitat de vida | - |
dc.subject.other | Palliative treatment | - |
dc.subject.other | Sick children | - |
dc.subject.other | Quality of life | - |
dc.title | Evaluating quality of life in pediatric palliative care: a cross-sectional analysis of children’s and parents’ perspectives | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.identifier.idgrec | 747802 | - |
dc.date.updated | 2024-06-19T22:42:00Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
Appears in Collections: | Articles publicats en revistes (Econometria, Estadística i Economia Aplicada) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
858415.pdf | 964.38 kB | Adobe PDF | View/Open |
This item is licensed under a
Creative Commons License