The Australian Palliative Care Outcomes Collaboration (PCOC) : measuring the quality and outcomes of palliative care on a routine basis
Eagar, Kathy, Watters, Prue, Currow, David, Aoun, Samar, & Yates, Patsy (2010) The Australian Palliative Care Outcomes Collaboration (PCOC) : measuring the quality and outcomes of palliative care on a routine basis. Australian Health Review, 34(2), pp. 186-192.
Australia is leading the way in establishing a national system (the Palliative Care Outcomes Collaboration –
PCOC) to measure the outcomes and quality of specialist palliative care services and to benchmark services across the country. This article reports on analysis of data collected routinely at point-of-care on 5939 patients treated by the first fifty one services that voluntarily joined PCOC. By March 2009, 111 services have agreed to join PCOC, representing more than 70% of services and more than 80% of specialist palliative care patients nationally. All states and territories are involved in this unique process that has involved extensive consultation and infrastructure and close collaboration between health services and researchers.
The challenges of dealing with wide variation in outcomes and practice and the progress achieved to date are described.
PCOC is aiming to improve understanding of the reasons for variations in clinical outcomes between specialist palliative care patients and differences in service outcomes as a critical step in an ongoing process to improve both service quality and patient outcomes.
What is known about the topic? Governments internationally are grappling with how best to provide care for people
with life limiting illnesses and how best to measure the outcomes and quality of that care. There is little international evidence on how to measure the quality and outcomes of palliative care on a routine basis.
What does this paper add? The Palliative Care Outcomes Collaboration (PCOC) is the first effort internationally to
measure the outcomes and quality of specialist palliative care services and to benchmark services on a national basis
through an independent third party.
What are the implications for practitioners? If outcomes and quality are to be measured on a consistent national
basis, standard clinical assessment tools that are used as part of everyday clinical practice are necessary.
Citation countsare sourced monthly fromand citation databases.
These databases contain citations from different subsets of available publications and different time periods and thus the citation count from each is usually different. Some works are not in either database and no count is displayed. Scopus includes citations from articles published in 1996 onwards, and Web of Science generally from 1980 onwards.
Citations counts from theindexing service can be viewed at the linked Google Scholar™ search.
|Item Type:||Journal Article|
|Keywords:||palliative care, quality, health services|
|Subjects:||Australian and New Zealand Standard Research Classification > MEDICAL AND HEALTH SCIENCES (110000) > NURSING (111000)|
|Divisions:||Current > QUT Faculties and Divisions > Faculty of Health|
Current > Institutes > Institute of Health and Biomedical Innovation
Current > Schools > School of Nursing
|Deposited On:||08 Dec 2010 13:52|
|Last Modified:||01 Mar 2012 00:25|
Repository Staff Only: item control page