Who are consumers?
A consumer is a person who has used or may potentially use, any type of health care service. It includes their family and caregivers. A palliative care consumer is someone with lived experience of a life-limiting illness, either directly or as a family member or carer of someone who has received palliative care.
About Consumer Engagement in PCOC
The Palliative Care Outcomes Collaboration (PCOC) is a national program funded by the Australian Government Department of Health and Ageing. PCOC is based at the University of Wollongong. Participation in PCOC is voluntary.
PCOC is responsible for supporting Palliative Care Services and clinicians in the acute (hospital and hospice) and primary care (community and general practice) settings, to improve palliative care patient, carer and family outcomes.
Measuring patient outcomes is critical for quality and safe care, and for the accountability of a service to its patients, families and carers. PCOC aims to improve palliative care patient, carer and family outcomes. PCOC uses a cycle of routine assessment, measurement of patient outcomes, reporting and benchmarking through Communities of Practice, to support care planning and drive improvements in palliative care in Australia.
For more information about PCOC, see About PCOC.
How have consumers contributed to the work of PCOC?
Consumers have contributed in many ways to strengthen and improve the PCOC program, and ensuring the PCOC program continues to contribute to the provision of quality palliative care across Australia. Some of the projects that consumers have been involved with include:
For more information about ESAS, see Clinical Tools and Assessments.
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To contact PCOC for more information, email pcoc@uow.edu.au