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Patient Outcomes in Palliative Care in Australia: National report for July – December 2018

Report


Type Of Work


  • Report

Abstract


  • The Australian palliative care sector is a world leader in using routine clinical assessment information to guide patient centred care and measure patient and family outcomes. Providers of palliative care are commended for their commitment to excellence in delivering evidence-based, patient-centred care by using the routine Palliative Care Outcomes Collaboration (PCOC) assessment framework and contributing patient data toward national outcome measurement and benchmarking. PCOC acknowledges the dedication and willingness of clinicians to improve the care of patients, their families and caregivers. The information collected is not just data - it represents the real-life outcomes of over 40,000 Australians who die an expected death every year.

    While the focus of this report is on the most recent information relating to July to December 2018, results over the last three years are also presented to highlight achievements and improvement in outcomes. The most recent information corresponds to 23,333 patients, having 29,931 episodes of care and 70,135 palliative care phases from 127 services who provide palliative care in hospital / hospice or in the person’s home.

    The purpose of benchmarking is to drive improvement and palliative care service innovation.

Publication Date


  • 2019

Citation


  • A. Connolly, S. Burns, S. Allingham, L. Foskett & S. Clapham, Patient Outcomes in Palliative Care in Australia: National report for July – December 2018 (Palliative Care Outcomes Collaboration, Australian Health Services Research Institute, University of Wollongong, 2019).

Place Of Publication


  • University of Wollongong

Type Of Work


  • Report

Abstract


  • The Australian palliative care sector is a world leader in using routine clinical assessment information to guide patient centred care and measure patient and family outcomes. Providers of palliative care are commended for their commitment to excellence in delivering evidence-based, patient-centred care by using the routine Palliative Care Outcomes Collaboration (PCOC) assessment framework and contributing patient data toward national outcome measurement and benchmarking. PCOC acknowledges the dedication and willingness of clinicians to improve the care of patients, their families and caregivers. The information collected is not just data - it represents the real-life outcomes of over 40,000 Australians who die an expected death every year.

    While the focus of this report is on the most recent information relating to July to December 2018, results over the last three years are also presented to highlight achievements and improvement in outcomes. The most recent information corresponds to 23,333 patients, having 29,931 episodes of care and 70,135 palliative care phases from 127 services who provide palliative care in hospital / hospice or in the person’s home.

    The purpose of benchmarking is to drive improvement and palliative care service innovation.

Publication Date


  • 2019

Citation


  • A. Connolly, S. Burns, S. Allingham, L. Foskett & S. Clapham, Patient Outcomes in Palliative Care in Australia: National report for July – December 2018 (Palliative Care Outcomes Collaboration, Australian Health Services Research Institute, University of Wollongong, 2019).

Place Of Publication


  • University of Wollongong