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dc.contributor.authorHall, Brendaen
dc.contributor.authorKadetz, Paulen
dc.contributor.editorCrawford, Paulen
dc.contributor.editorBrown, Brianen
dc.contributor.editorCharise, Andreaen
dc.date.accessioned2022-07-06T09:58:13Z
dc.date.available2022-07-06T09:58:13Z
dc.date.issued2020-02-28
dc.identifier.citationHall, B. and Kadetz, P. (2020) 'Finding the subject in the objectified: Problematizing the dependence on metrics for patient care in the United States', in P. Crawford, B. Brown and A. Charise (eds.) The Routledge Companion to Health Humanities. Abingdon: Routledge, pp. 196-203.en
dc.identifier.isbn9781138579903en
dc.identifier.urihttps://doi.org/10.4324/9780429469060-26
dc.identifier.urihttps://eresearch.qmu.ac.uk/handle/20.500.12289/12406
dc.descriptionPaul I. Kadetz - ORCID: 0000-0002-2824-1856 https://orcid.org/0000-0002-2824-1856en
dc.descriptionItem not available in this repository.
dc.description.abstractThe US Patient Self Determination Act of 1990 sought to provide the legal rights of patients to document their wishes concerning their current and future care. However, nearly 30 years after this legislation went into effect many individuals and families still struggle with end-of-life care planning, receive a lack of continuity of care, and experience insufficient communication with health-care practitioners concerning their treatment wishes for end-of-life care. Although numerous studies have linked age, sex, race, and/or ethnicity with the completion of advance directives, this research does not support any such correlations, but instead suggests that other, often overlooked, variables may influence the completion of advance directives. These variables include the differential treatment of patients based on the caregiver’s assumptions of linkages between patient compliance and demographic groupings, as well as the likelihood that caregivers will engage in dialogue that facilitates an understanding of the concerns and meanings patients attribute to end-of-life decision making; and the inherent difficulties that caregivers experience in approaching the increasingly quantified patient as a subjective individual. Reducing the understanding of why patients do not complete advance directives to aggregated groupings to which the patient purportedly belongs not only perpetuates stereotypes that can potentially foster inequitable health care, but more so may also prohibit any exploration into the actual reasons that compromise the completion of advance directives and, thereby, thwart the ability to resolve these issues and improve patient care.en
dc.description.urihttps://doi.org/10.4324/9780429469060-26en
dc.format.extent196-203en
dc.language.isoenen
dc.publisherRoutledgeen
dc.relation.ispartofThe Routledge Companion to Health Humanitiesen
dc.titleFinding the subject in the objectified: Problematizing the dependence on metrics for patient care in the United Statesen
dc.typeBook chapteren
dcterms.accessRightsnone
dc.description.ispublishedpub
rioxxterms.typeBook chapteren
rioxxterms.publicationdate2020-02-28
refterms.depositExceptionNAen
refterms.accessExceptionNAen
refterms.technicalExceptionNAen
refterms.panelUnspecifieden
qmu.authorKadetz, Paulen
qmu.centreInstitute for Global Health and Developmenten
dc.description.statuspub
refterms.versionNAen


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