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dc.contributor.authorSolberg, Carl Tollefen_US
dc.contributor.authorNorheim, Ole Frithjofen_US
dc.contributor.authorBarra, Mathiasen_US
dc.date.accessioned2018-08-28T09:41:11Z
dc.date.available2018-08-28T09:41:11Z
dc.date.issued2018
dc.PublishedSolberg CT, Norheim OF, Barra M. The disvalue of death in the global burden of disease. Journal of Medical Ethics. 2018;44:192-198eng
dc.identifier.issn1473-4257
dc.identifier.issn0306-6800
dc.identifier.urihttps://hdl.handle.net/1956/18289
dc.description.abstractIn the Global Burden of Disease study, disease burden is measured as disability-adjusted life years (DALYs). The paramount assumption of the DALY is that it makes sense to aggregate years lived with disability (YLDs) and years of life lost (YLLs). However, this is not smooth sailing. Whereas morbidity (YLD) is something that happens to an individual, loss of life itself (YLL) occurs when that individual’s life has ended. YLLs quantify something that involves no experience and does not take place among living individuals. This casts doubt on whether the YLL is an individual burden at all. If not, then YLDs and YLLs are incommensurable. There are at least three responses to this problem, only one of which is tenable: a counterfactual account of harm. Taking this strategy necessitates a re-examination of how we count YLLs, particularly at the beginning of life.en_US
dc.language.isoengeng
dc.publisherBMJeng
dc.rightsAttribution CC BY-NCeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/eng
dc.titleThe disvalue of death in the global burden of diseaseen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2018-03-07T10:17:10Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2018 The Author(s)
dc.identifier.doihttps://doi.org/10.1136/medethics-2017-104365
dc.identifier.cristin1521908
dc.source.journalJournal of Medical Ethics
dc.relation.projectNorges forskningsråd: 218694


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