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dc.contributor.authorHoare, Sarahen
dc.contributor.authorMorris, Zoë Sloteen
dc.contributor.authorKelly, Mikeen
dc.contributor.authorKuhn, Islaen
dc.contributor.authorBarclay, Stephenen
dc.date.accessioned2015-11-02T10:29:05Z
dc.date.available2015-11-02T10:29:05Z
dc.date.issued2015-11-10en
dc.identifier.citationPLoS ONE 2015, 10(11): e0142723. doi:10.1371/journal.pone.0142723en
dc.identifier.issn1932-6203
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/252483
dc.description.abstractBackground – End-of-life care policy has a focus on enabling patients to die in their preferred place; this is believed for most to be home. This review assesses patient preferences for place of death examining: the extent of unreported preferences, the importance of patient factors (place of care and health diagnosis) and who reports preferences. Methods and findings – Systematic literature review of 7 electronic databases, grey literature, backwards citations from included studies and Palliative Medicine hand search. Included studies published between 2000-2015, reporting original, quantifiable results of adult UK preferences for place of death. Of 10826 articles reviewed, 61 met the inclusion criteria. Summary charts present preferences for place of death by health diagnosis, where patients were asked and who reported the preference. These charts are recalculated to include ‘missing data,’ the views of those whose preferences were not asked, expressed or reported or absent in studies. Missing data were common. Across all health conditions when missing data were excluded the majority preference was for home: when missing data were included, it was not known what proportion of patients with cancer, non-cancer or multiple conditions preferred home. Patients, family proxies and public all expressed a majority preference for home when missing data were excluded: when included, it was not known what proportion of patients or family proxies preferred home. Where patients wished to die was related to where they were asked their preference. Missing data calculations are limited to ‘reported’ data. Conclusions – It is unknown what proportion of patients prefers to die at home or elsewhere. Reported preferences for place of death often exclude the views of those with no preference or not asked: when ‘missing data’ are included, they supress the proportion of preferences for all locations. Caution should be exercised if asserting that most patients prefer to die at home.
dc.languageEnglishen
dc.language.isoenen
dc.publisherPLoS
dc.rightsCreative Commons Attribution 4.0 International License
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleDo patients want to die at home? A systematic review of the UK literature, focused on missing preferences for place of deathen
dc.typeArticle
dc.description.versionThis is the final version of the article. It was first available from PLOS via http://dx.doi.org/10.1371/journal.pone.0142723en
prism.numbere0142723en
prism.publicationDate2015en
prism.publicationNamePLoS ONEen
prism.volume10en
dc.rioxxterms.funderNIHR
dcterms.dateAccepted2015-10-25en
rioxxterms.versionofrecord10.1371/journal.pone.0142723en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2015-11-10en
dc.contributor.orcidHoare, Sarah [0000-0002-8933-217X]
dc.contributor.orcidKelly, Mike [0000-0002-2029-5841]
dc.contributor.orcidKuhn, Isla [0000-0002-2879-4020]
dc.contributor.orcidBarclay, Stephen [0000-0002-4505-7743]
dc.identifier.eissn1932-6203
rioxxterms.typeJournal Article/Reviewen


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Creative Commons Attribution 4.0 International License
Except where otherwise noted, this item's licence is described as Creative Commons Attribution 4.0 International License