Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/26872
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dc.contributor.authorMoon F.en
dc.contributor.authorPoon P.en
dc.contributor.authorMooney C.en
dc.contributor.authorMcDermott F.en
dc.contributor.authorMiller A.en
dc.date.accessioned2021-05-14T08:57:56Zen
dc.date.available2021-05-14T08:57:56Zen
dc.date.copyright2021en
dc.date.created20210326en
dc.date.issued2021-03-26en
dc.identifier.citationBMJ supportive & palliative care. (no pagination), 2021. Date of Publication: 15 Mar 2021.en
dc.identifier.issn2045-4368 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/26872en
dc.description.abstractBACKGROUND: Family involvement in decision making for hospitalised patients is associated with improved end-of-life care. Yet, these discussions can be challenging for physicians and families and associated with distress, confusion and conflict. There is a need to understand how best to support families involved in decisions regarding the transition from active to palliative treatment in hospital settings. AIM: To explore bereaved families' experiences of end-of-life decision making for general medicine patients. DESIGN: A qualitative exploratory study framed by social constructionism using semistructured interviews and thematic analysis. SETTING AND PARTICIPANTS: The general medicine units of one large public hospital in Melbourne, Australia. We recruited 28 bereaved family members of patients who had received end-of-life care. FINDINGS: Patients and families depended on physicians to explain clinical complexity and treatment beneficence; however, trust in medical judgement was mediated by participant's own interpretations of clinical progress. Families sought to be respected as advocates and experienced distress if physicians disregarded their perspectives and insight concerning patient preferences. Ideally, families supported patients to express their preferences to physicians. Otherwise, families contextualised treatment decisions through their knowledge of patient's values and quality of life. Families often felt burdened by or excluded from medical decision making and experienced distress and confusion regarding their rights to request or refuse treatment. CONCLUSION(S): Our study highlights how families contribute to decision making to ensure end-of-life care treatments reflect patient preferences. Physicians can ease families' distress around treatment withdrawal by providing a meaningful explanation of complex clinical issues, clarifying decision-making roles and acknowledge families' desire to protect and advocate for their loved one.Copyright © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.en
dc.languageEnglishen
dc.languageenen
dc.publisherNLM (Medline)en
dc.relation.ispartofBMJ Supportive & Palliative Care-
dc.titleBereaved families' experiences of end-of-life decision making for general medicine patients.en
dc.typeArticleen
dc.identifier.affiliationSocial Worken
dc.identifier.affiliationGeneral Medicineen
dc.identifier.affiliationAllied Health-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/bmjspcare-2020-002743en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid33722814 [http://www.ncbi.nlm.nih.gov/pubmed/?term=33722814]en
dc.identifier.source634577243en
dc.identifier.institution(Moon) Department of Social Work, Monash Health, Clayton, VIC, Australia (Moon, McDermott) Department of Social Work, Monash University, Caulfield East, VIC, Australia (Mooney, Poon) Department of Supportive & Palliative Care, Monash Health, Clayton, VIC, Australia (Miller) Department of General Medicine, Monash Health, Clayton, VIC, Australiaen
dc.description.publicationstatusArticle-in-Pressen
dc.rights.statementThis record is sourced from MEDLINE/PubMed, a database of the U.S. National Library of Medicineen
dc.subect.keywordsclinical decisions communication hospital care terminal careen
dc.identifier.authoremailMoon F.; Felicity.moon@monash.eduen
dc.identifier.affiliationext(Moon, McDermott) Department of Social Work, Monash University, Caulfield East, VIC, Australia-
dc.identifier.affiliationmh(Moon) Department of Social Work, Monash Health, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Mooney, Poon) Department of Supportive & Palliative Care, Monash Health, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Miller) Department of General Medicine, Monash Health, Clayton, VIC, Australia-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptSupportive and Palliative Care-
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