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dc.contributor.authorStrøm, Anita
dc.contributor.authorDreyer, Anne
dc.date.accessioned2018-12-19T13:37:16Z
dc.date.available2018-12-19T13:37:16Z
dc.date.created2018-12-18T08:55:14Z
dc.date.issued2019
dc.identifier.citationJournal of Multidisciplinary Healthcare. 2019, 12 (1), 1-8.nb_NO
dc.identifier.issn1178-2390
dc.identifier.urihttp://hdl.handle.net/11250/2578344
dc.description.abstractBackground: Next of kin are considered a resource for both the patient and the health service. Need for information varies with severity and duration of health changes. A clear requirement is about what to expect upon homecoming, and what supportive services are available. The picture of relatives’ access to involvement and information is still somewhat unclear. Objective: To investigate what information, knowledge, and involvement next of kin considered important for managing their caring role and collaboration with their close relatives who experienced events that led to chronic illness. Design, setting, and methods: A qualitative exploratory design. Seventeen informants were recruited through various courses offered to relatives. Data were collected in 2017 from individual interviews, analyzed in an interpretative tradition, and involved qualitative content analysis. Results: The results reflect a long intervening period in between the activating incident and a clarification of the situation. This period was characterized by unpreparedness for duration of anxiety and amount of energy involved in balancing the relationship. Further, the interviewees saw retrospectively that information about disease and treatment was available, but they had to find such resources themselves. Information about how to handle the situation was almost absent. Ultimately, they were disappointed over not being involved. Conclusion: Previously provided prospective information about the embedded anxiety in the situation and consequences for relationships, involvement in patients’ services, and better communication about existing services seem to be significant. Health care professionals, especially in outpatient care, may improve their services by debating how they can implement family-oriented care in personalized treatment as usual. Focus on prospective information, early involvement, and relevant information about existing resources may empower relatives and relieve the experience of care burden.nb_NO
dc.language.isoengnb_NO
dc.publisherDove Medical Pressnb_NO
dc.subjectnext of kinnb_NO
dc.subjectchronic illnessnb_NO
dc.subjectinformationnb_NO
dc.subjectinvolvementnb_NO
dc.subjectcare burdennb_NO
dc.subjectinformal carenb_NO
dc.subjectrelativesnb_NO
dc.subjectpårørendenb_NO
dc.subjectkroniske sykdommernb_NO
dc.subjectomsorgsbyrdenb_NO
dc.titleNext of kin’s protracted challenges with access to relevant information and involvement opportunitiesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.rights.holderOpen Accessnb_NO
dc.source.pagenumber1-8nb_NO
dc.source.volume12nb_NO
dc.source.journalJournal of Multidisciplinary Healthcarenb_NO
dc.source.issue1nb_NO
dc.identifier.doihttp://dx.doi.org/10.2147/JMDH.S183946
dc.identifier.cristin1644605
cristin.unitcode251,3,0,0
cristin.unitnameFakultet for helsefag
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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