Care considerations in a patient-and family-centered medical assistance in dying program

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dc.contributor.authorBrown, Janine
dc.contributor.authorGoodridge, Donna
dc.contributor.authorHarrison, Averi
dc.contributor.authorKemp, Jordan
dc.contributor.authorThorpe, Lilian
dc.contributor.authorWeiler, Robert
dc.date.accessioned2023-04-17T22:03:27Z
dc.date.available2023-04-17T22:03:27Z
dc.date.issued2020
dc.description© The Author(s) 2020. Reuse is restricted to non-commercial use and no derivative use. This is the accepted manuscript version of the article. The final version is available from SAGE Publications at: https://journals.sagepub.com/doi/10.1177/0825859720951661.en_US
dc.description.abstractMedical Assistance in Dying (MAID) became legal in Canada in June 2016. As part of a project designed to improve end-of-life care for those requesting MAID, qualitative data from patients, families, and providers were used to assess opportunities to enhance patient-and family-centered care (PFCC) in this program.en_US
dc.description.authorstatusFacultyen_US
dc.description.peerreviewyesen_US
dc.identifier.citationBrown, J., Goodridge, D., Harrison, A., Kemp, J., Thorpe, L., & Weiler, R. (2020). Care considerations in a patient-and family-centered medical assistance in dying program. Journal of Palliative Care, 37(3): 341-351en_US
dc.identifier.doi10.1177/0825859720951661
dc.identifier.urihttps://hdl.handle.net/10294/15859
dc.language.isoenen_US
dc.publisherSAGE Publicationsen_US
dc.subjectPatient-and-family centered careen_US
dc.subjectMedical assistance in dyingen_US
dc.subjectquality improvementen_US
dc.subjectend-of-life careen_US
dc.subjectinterdisciplinary careen_US
dc.subjectqualitative researchen_US
dc.titleCare considerations in a patient-and family-centered medical assistance in dying programen_US
dc.typeArticleen_US
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