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Palliative Care Services Utilization and Location of Death

dc.contributor.authorCameron, Barbara
dc.contributor.supervisorCragg, Catherine
dc.date.accessioned2012-06-19T07:07:56Z
dc.date.available2012-06-19T07:07:56Z
dc.date.created2012
dc.date.issued2012
dc.degree.disciplineSciences de la santé / Health Sciences
dc.degree.levelmasters
dc.degree.nameMSc
dc.description.abstractIn this study, the utilization of palliative care services, acute care services, and location of death for clients who were palliative and receiving services from Champlain Community Care Access Centre (CCAC) in Ontario during their last month of life were investigated. An adaptation of Andersen?s Behavioral Model of Health Services Utilization provided context and structure to this study. This is an historical, quantitative descriptive study using chart audits for data collection. The data on CCAC clients who were palliative and who died during the month of July 2009 were tracked during their last month of life. Collection of socio-demographic data, services provided through CCAC, emergency department visits, hospital admissions, and location of death provided the data for this study. The clients who died at home used more CCAC services than those who died at other locations and frequently community palliative care physicians provided their medical care. The findings of this study included: 1) The majority of the clients, who expressed a preference, died in their preferred location. 2) The role of community palliative care physicians was an important component of the services that supported the clients to die in their location of choice. 3) Over 25% of the study sample died in a hospital and the clients used a large number of in-patient hospital days with one quarter of the hospital deaths taking place in an emergency department or an intensive care unit. 4) During the last month of life, 25% of the clients received chemotherapy and/or radiation therapy. 5) The clients who died at home used more CCAC services than those who died in other locations and who used institutional resources. The implications for practice, policy, research, and education are discussed.
dc.embargo.termsimmediate
dc.faculty.departmentSciences infirmières / Nursing
dc.identifier.urihttp://hdl.handle.net/10393/22907
dc.identifier.urihttp://dx.doi.org/10.20381/ruor-5836
dc.language.isoen
dc.publisherUniversité d'Ottawa / University of Ottawa
dc.subjectPalliative Care
dc.subjectLocation of Death
dc.subjectCommunity Palliative Care
dc.subjectCommunity Care Access Centres
dc.subjectAndersen's Behavioral Model of Health Services Utilization
dc.subjectChart Audits
dc.subjectCommunity Palliative Care Physicians
dc.subjectLast Month of Life
dc.subjectChemotherapy and Radiation During Last Month of Life
dc.subjectHome Care
dc.subjectHealth Services Utilization
dc.subjectHospital Use During the Last Month of Life
dc.subjectEmergency Department Use During Last Month of Life
dc.subjectEnd-of-Life Care
dc.subjectTerminally Ill
dc.subjectCancer Deaths
dc.titlePalliative Care Services Utilization and Location of Death
dc.typeThesis
thesis.degree.disciplineSciences de la santé / Health Sciences
thesis.degree.levelMasters
thesis.degree.nameMSc
uottawa.departmentSciences infirmières / Nursing

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