Is It Feasible and Desirable to Collect Voluntarily Quality and Outcome Data Nationally in Palliative Oncology Care?

Is It Feasible and Desirable to Collect Voluntarily Quality and Outcome Data Nationally in Palliative Oncology Care?

Hospice/palliative care is a critical component of cancer care. In Australia, more than 85% ofpeople referred to specialized hospice/palliative care services (SHPCS) have a primary diagnosis ofcancer, and 60% of people who die from cancer will be referred to SHPCS. The Palliative CareOutcomes Collab...

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Bibliographic Details
Main Authors: Currow, D., Eagar, K., Aoun, Samar, Fildes , D., Yates, P., Kristjanson, Linda
Format: Journal Article
Published: American Society of Clinical Oncology 2008
Subjects:
Quality and Outcome Data
Voluntarily
Palliative Oncology
Online Access:http://hdl.handle.net/20.500.11937/32382

Internet

http://hdl.handle.net/20.500.11937/32382

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