Literature DB >> 20497731

The Australian Palliative Care Outcomes Collaboration (PCOC)--measuring the quality and outcomes of palliative care on a routine basis.

Kathy Eagar1, Prue Watters, David C Currow, Samar M Aoun, Patsy Yates.   

Abstract

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.

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Mesh:

Year:  2010        PMID: 20497731     DOI: 10.1071/AH08718

Source DB:  PubMed          Journal:  Aust Health Rev        ISSN: 0156-5788            Impact factor:   1.990


  27 in total

1.  How to implement quality indicators successfully in palliative care services: perceptions of team members about facilitators of and barriers to implementation.

Authors:  Kathleen Leemans; Lieve Van den Block; Robert Vander Stichele; Anneke L Francke; Luc Deliens; Joachim Cohen
Journal:  Support Care Cancer       Date:  2015-04-02       Impact factor: 3.603

2.  Multisite studies offer a solution to recruitment challenges in palliative care studies.

Authors:  Christine S Ritchie; David C Currow; Amy P Abernethy; Jean S Kutner
Journal:  J Palliat Med       Date:  2013-03       Impact factor: 2.947

3.  Development of the Quality Data Collection Tool for Prospective Quality Assessment and Reporting in Palliative Care.

Authors:  Arif H Kamal; Janet Bull; Dio Kavalieratos; Jonathan M Nicolla; Laura Roe; Martha Adams; Amy P Abernethy
Journal:  J Palliat Med       Date:  2016-06-27       Impact factor: 2.947

Review 4.  Challenges and facilitators in delivering optimal care at the End of Life for older patients: a scoping review on the clinicians' perspective.

Authors:  Samantha Fien; Emily Plunkett; Claudia Fien; Sally Greenaway; Daren K Heyland; Justin Clark; Magnolia Cardona
Journal:  Aging Clin Exp Res       Date:  2021-03-13       Impact factor: 3.636

Review 5.  The Impact of Measuring Patient-Reported Outcome Measures on Quality of and Access to Palliative Care.

Authors:  Deborah Dudgeon
Journal:  J Palliat Med       Date:  2018-01       Impact factor: 2.947

6.  Palliative care in australia.

Authors:  Geoffrey Keith Mitchell
Journal:  Ochsner J       Date:  2011

Review 7.  Palliative Care for the Seriously Ill.

Authors:  Amy S Kelley; R Sean Morrison
Journal:  N Engl J Med       Date:  2015-08-20       Impact factor: 91.245

8.  The selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.

Authors:  Catherine J Evans; Hamid Benalia; Nancy J Preston; Gunn Grande; Marjolein Gysels; Vicky Short; Barbara A Daveson; Claudia Bausewein; Chris Todd; Irene J Higginson
Journal:  J Pain Symptom Manage       Date:  2013-04-28       Impact factor: 3.612

9.  Prevalence and severity of sleep difficulty in patients with a CNS cancer receiving palliative care in Australia.

Authors:  Megan S Jeon; Haryana M Dhillon; Joseph Descallar; Lawrence Lam; Samuel Allingham; Eng-Siew Koh; David C Currow; Meera R Agar
Journal:  Neurooncol Pract       Date:  2019-02-19

10.  Towards a standardized method of developing quality indicators for palliative care: protocol of the Quality indicators for Palliative Care (Q-PAC) study.

Authors:  Kathleen Leemans; Joachim Cohen; Anneke L Francke; Robert Vander Stichele; Susanne Jj Claessen; Lieve Van den Block; Luc Deliens
Journal:  BMC Palliat Care       Date:  2013-02-08       Impact factor: 3.234

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