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dc.contributor.authorHogstad, Ingrid Johnsen
dc.contributor.authorLeer-Salvesen, Kjartan
dc.date.accessioned2023-10-12T11:25:51Z
dc.date.available2023-10-12T11:25:51Z
dc.date.created2020-09-08T09:30:21Z
dc.date.issued2020
dc.identifier.citationEuropean Journal of Oncology Nursing. 2020, 49 (December), 1-8.en_US
dc.identifier.issn1462-3889
dc.identifier.urihttps://hdl.handle.net/11250/3096069
dc.description.abstractPurpose: The Norwegian Health Personnel Act (HPA §10a) obliges health professionals to contribute to meeting minor children's need for information about their parents' illness and prognosis. Previous research has shown that many parents withhold information about illness and anticipated death from their children. This study explored main considerations for palliative health-care professionals in these situations, and how they negotiate conflicting considerations of confidentiality and child involvement. Method: This qualitative exploratory study involved semi-structured interviews with 11 palliative health-care professionals. Hermeneutics informed the data analysis. Results: The health professionals' main considerations were sustaining patients' hope and building trust in the professional–patient relationship. Both concerns were grounded in respect for patient autonomy. The health professionals negotiated patient autonomy and child involvement in different ways, defined in the present analysis on a continuum ranging from granting full patient autonomy to going directly against patients’ will. Conclusions: The professional–patient relationship is the primary consideration in the health care context, and decision making on the degree of children's involvement happens in a dialogical process between health professionals and patients. Close professional–patient relationships might increase the emotional impacts on health professionals, who consequently might give greater relative weight to patients' will. We propose that procedures for initiating collaboration with professionals in the child's everyday life context help health professionals involving the child without threatening trust. Keywords: children as relatives, children as next of kin, patient autonomy, hermeneutics, palliative care, confidentiality, health professionals, moral problem, decision-makingen_US
dc.language.isoengen_US
dc.relation.urihttps://doi.org/10.1016/j.ejon.2020.101839
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleGoing against patients’ will? : a qualitative study of how palliative health-care professionals handle competing considerations when children are excluded from parental illness and deathen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-8en_US
dc.source.volume49en_US
dc.source.journalEuropean Journal of Oncology Nursingen_US
dc.source.issueDecemberen_US
dc.identifier.doi10.1016/j.ejon.2020.101839
dc.identifier.cristin1827960
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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