Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/18333
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dc.contributor.authorLang, Heidi-
dc.contributor.authorFrance, Emma-
dc.contributor.authorWilliams, Brian-
dc.contributor.authorHumphris, Gerry-
dc.contributor.authorWells, Mary-
dc.date.accessioned2014-09-15T10:55:58Z-
dc.date.issued2013-12-
dc.identifier.urihttp://hdl.handle.net/1893/18333-
dc.description.abstractObjective: To summarise patients' experiences of head and neck cancer (HNC) by examining the findings of existing qualitative studies Methods: We undertook a systematic review and meta-synthesis of qualitative studies in 29 published articles using Noblit and Hare's ‘meta-ethnography' approach to synthesise findings. The inclusion criteria were primary qualitative studies, focusing on HNC patients' experience and an English abstract. Seven databases were systematically searched. Results: The articles focused on the experience of having HNC, the experience of treatments and the role of information. Our synthesis identified six core concepts-uncertainty and waiting, disruption to daily life, the diminished self, making sense of the experience, sharing the burden and finding a path. People experienced significant disruption to normal daily activities, because of the physical and emotional effects of HNC and its treatment. Day-to-day challenges were compounded by social and existential changes and a palpable loss of the individual's sense of self and future. In order to find a way through the considerable uncertainty and daily challenge of living with and beyond HNC, patients made continual efforts to make sense of their experience. Supportive relationships with their social network, HNC peers and healthcare professionals were particularly important, but support following treatment completion was sometimes limited. Perceptions of the future were affected by whether they saw life as diminished, merely changed or even enhanced by the experience of cancer. Conclusions: This review supports further specific research into these emerging themes and provides a context for future work, informing interventions to improve patients' experiences.en_UK
dc.language.isoen-
dc.publisherWiley-Blackwell-
dc.relationLang H, France E, Williams B, Humphris G & Wells M (2013) The psychological experience of living with head and neck cancer: A systematic review and meta-synthesis, Psycho-Oncology, 22 (12), pp. 2648-2663.-
dc.rightsThe publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.-
dc.subjecthead and neck canceren_UK
dc.subjectoncologyen_UK
dc.subjectqualitative researchen_UK
dc.subjectpsychosocialen_UK
dc.subjectexperienceen_UK
dc.subjectmeta-synthesisen_UK
dc.titleThe psychological experience of living with head and neck cancer: A systematic review and meta-synthesisen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2999-12-31T00:00:00Z-
dc.rights.embargoreasonThe publisher does not allow this work to be made publicly available in this Repository therefore there is an embargo on the full text of the work.-
dc.identifier.doihttp://dx.doi.org/10.1002/pon.3343-
dc.citation.jtitlePsycho-Oncology-
dc.citation.issn1057-9249-
dc.citation.volume22-
dc.citation.issue12-
dc.citation.spage2648-
dc.citation.epage2663-
dc.citation.publicationstatusPublished-
dc.citation.peerreviewedRefereed-
dc.type.statusPublisher version (final published refereed version)-
dc.author.emailmary.wells@stir.ac.uk-
dc.contributor.affiliationUniversity of Dundee-
dc.contributor.affiliationNMAHP Research-
dc.contributor.affiliationNMAHP Research-
dc.contributor.affiliationUniversity of St Andrews-
dc.contributor.affiliationNMAHP Research-
dc.rights.embargoterms2999-12-31-
dc.rights.embargoliftdate2999-12-31-
dc.identifier.isi000327823800002-
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles

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