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Western Australia, patient outcomes in palliative care, July – December 2014

Report


Type Of Work


  • Report

Abstract


  • The Palliative Care Outcomes Collaboration (PCOC) is a national program that utilises standardised clinical assessment tools to measure and benchmark patient

    outcomes in palliative care. Participation in PCOC is voluntary and can assist palliative care service providers to improve practice and meet the Palliative Care Australia

    (PCA) Standards for Providing Quality Palliative Care for all Australians. This is achieved via the PCOC dataset; a multi-purpose framework designed to:

    * provide clinicians with an approach to systematically assess individual patient experiences,

    * define a common clinical language to streamline communication between palliative care providers and

    * facilitate the routine collection of national palliative care data to drive quality improvement through reporting and benchmarking.

Publication Date


  • 2014

Citation


  • A. M. Connolly, S. Bird, S. P. Clapham, T. Pidgeon, K. Quinsey, S. F. Allingham & L. M. Foskett, Western Australia, patient outcomes in palliative care, July – December 2014 (Australian Health Services Research Institute, University of Wollongong, 2014). http://ahsri.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow192010.pdf

Url


  • http://ahsri.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow192010.pdf

Place Of Publication


  • University of Wollongong

Type Of Work


  • Report

Abstract


  • The Palliative Care Outcomes Collaboration (PCOC) is a national program that utilises standardised clinical assessment tools to measure and benchmark patient

    outcomes in palliative care. Participation in PCOC is voluntary and can assist palliative care service providers to improve practice and meet the Palliative Care Australia

    (PCA) Standards for Providing Quality Palliative Care for all Australians. This is achieved via the PCOC dataset; a multi-purpose framework designed to:

    * provide clinicians with an approach to systematically assess individual patient experiences,

    * define a common clinical language to streamline communication between palliative care providers and

    * facilitate the routine collection of national palliative care data to drive quality improvement through reporting and benchmarking.

Publication Date


  • 2014

Citation


  • A. M. Connolly, S. Bird, S. P. Clapham, T. Pidgeon, K. Quinsey, S. F. Allingham & L. M. Foskett, Western Australia, patient outcomes in palliative care, July – December 2014 (Australian Health Services Research Institute, University of Wollongong, 2014). http://ahsri.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow192010.pdf

Url


  • http://ahsri.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow192010.pdf

Place Of Publication


  • University of Wollongong