about
The uses of provincial administrative health databases for research on palliative care: Insights from British Columbia, CanadaExamining the process of community development.Situated/being situated: Client and co-worker roles of family caregivers in hospice palliative care.Embedding a Palliative Approach in Nursing Care Delivery: An Integrated Knowledge Synthesis.Canada's Compassionate Care Benefit: is it an adequate public health response to addressing the issue of caregiver burden in end-of-life care?The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial.Cultural influences on palliative family caregiving: service recommendations specific to the Vietnamese in Canada.Conceptual foundations of a palliative approach: a knowledge synthesis.Balancing dual roles in end-of-life research.Supporting lay carers in end of life care: current gaps and future priorities.Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008).Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008).A systematic review of instruments related to family caregivers of palliative care patients.Family caregivers' ideal expectations of Canada's Compassionate Care Benefit.Exposing barriers to end-of-life communication in heart failure: an integrative review.Applying research into practice: a guide to determine the next palliative home care nurse visit.Time-related communication skills from the cancer patient perspective.Patient perceptions of communications on the threshold of cancer survivorship: implications for provider responses.Gendered Processes in Hospice Palliative Home Care for Seniors With Cancer and Their Family Caregivers.Registered nurses' involvement in advance care planning: an integrative review.Identifying socio-environmental factors that facilitate resilience among Canadian palliative family caregivers: a qualitative case study.Structural impact on gendered expectations and exemptions for family caregivers in hospice palliative home care.'Close to' a palliative approach: nurses' and care aides' descriptions of caring for people with advancing chronic life-limiting conditions.Articulating the role of relationships in access to home care nursing at the end of life.Use of palliative care services in a semirural program in British Columbia.End of life in residential care from the perspective of care aides.The information transfer and knowledge acquisition geographies of family caregivers: an analysis of Canada's Compassionate Care Benefit.Contrasting stories of life-threatening illness: a narrative inquiry.Thyroid cancer: patients' experiences of receiving iodine-131 therapy.Death at home: challenges for families and directions for the future.Loss and bereavement: HIV/AIDS family caregiving experiences.OA8 Caring for the family caregiver: working with volunteers to implement and improve a service to enable family caregivers to maintain their own wellbeing.Enabling a family caregiver-led assessment of support needs in home-based palliative care: Potential translation into practice.Palliative approach education for rural nurses and health-care workers: a mixed-method study.Findings on Advance Care Plans among Cognitively Impaired Older Adults.Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial.Analysis and proposed model of family caregivers' relationships with home health providers and perceptions of the quality of formal services.Defining and measuring a palliative approach in primary care.Burdens of family caregiving at the end of life.Legitimising and rationalising in talk about satisfaction with formal healthcare among bereaved family members.
P50
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P50
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P106
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2000-01-01T00:00:00Z