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dc.contributor.authorJanda, Monikaen_US
dc.contributor.authorChambers, Suzanneen_US
dc.contributor.authorDunn, Jeffen_US
dc.contributor.authorLangbecker, Danetteen_US
dc.contributor.authorWalker, Daviden_US
dc.contributor.authorEakin, Elizabethen_US
dc.contributor.editorDr. L S Wissow (Editor-in-Chief), A Finset (Editor-in-Chief)en_US
dc.date.accessioned2017-04-24T14:52:47Z
dc.date.available2017-04-24T14:52:47Z
dc.date.issued2008en_US
dc.date.modified2014-04-01T05:32:19Z
dc.identifier.issn0738-3991en_US
dc.identifier.doi10.1016/j.pec.2008.01.020en_US
dc.identifier.urihttp://hdl.handle.net/10072/23234
dc.description.abstractObjectives: To assess the supportive care needs and interest in related services among brain tumour patients and their carers and to compare the level of unmet needs to other cancer populations. Methods: A cross-sectional survey was posted to 363 households who were subscribed to the Queensland Cancer Fund Brain Tumour Support Service in 2005. Overall, 75 patients and 70 carers (response rate 29.8%) returned completed questionnaires. Measures were the Supportive Care Needs Survey (SCNS-34) and a brain tumour specific subscale for patients and carers, as well as the Hospital Anxiety and Depression Scale (HADS). Results: Patients most frequently reported requiring support to overcome fatigue, uncertainty about the future and not being able to do the things they used to do. Carers wanted help dealing with fears about the patients mental or physical deterioration, with the impact caring had on their own life, and with reducing stress in the patient's life. Among patients, 30% reported anxious mood and 17% depressed mood on the HADS, while corresponding numbers for carers were 40% and 10%, respectively. Patients and/or carers with higher than average supportive care needs expressed greater interest in support services, such as those to improve physical activity, using community services more effectively and to manage stress. Greater emotional distress predicted higher supportive care needs (e.g. odds ratio depressed patients = 2.11; (95% confidence interval 1.10-4.03), while no association was detected between patients' or carers' demographic characteristics, or patients' self-reported medical status and higher than average supportive care needs. Conclusion: The level of unmet supportive care needs observed among patients with a brain tumour and their carers is similar to that observed among cancer populations with metastatic disease. Practice implications: Interventions for this group should integrate lifestyle, coping support, and neuropsychological rehabilitation. 頲008 Elsevier Ireland Ltd. All rights reserved.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.language.isoen_US
dc.publisherElsevier Ireland Ltden_US
dc.publisher.placeIrelanden_US
dc.relation.ispartofstudentpublicationNen_US
dc.relation.ispartofpagefrom251en_US
dc.relation.ispartofpageto258en_US
dc.relation.ispartofissue2en_US
dc.relation.ispartofjournalPatient Education and Counselingen_US
dc.relation.ispartofvolume71en_US
dc.rights.retentionYen_US
dc.subject.fieldofresearchPublic Health and Health Services not elsewhere classifieden_US
dc.subject.fieldofresearchcode111799en_US
dc.titleUnmet supportive care needs and interest in services among patients with a brain tumour and their carersen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2008
gro.hasfulltextNo Full Text


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