Outcomes in Palliative Care, Report 12 (July - December 2011) - Queensland

PCOC aims to assist services to improve the quality of the palliative care they provide through the analysis and benchmarking of patient outcomes. In this, the twelfth PCOC report, data submitted for the July - December 2011 period are summarised and patient outcomes benchmarked to enable participating services to assess their performance and identify areas in which they may improve. This report is broken into three sections: Section 1 summarises each of the four major benchmark measures and subsets and presents national benchmarking results for these benchmarks Section 2 presents additional analysis for each of the sixteen benchmarks Section 3 provides descriptive analysis of the data items at each of the patient, episode and phase levels In each of the three sections, data and analysis for QLD is presented alongside the national figures for comparative purposes. The national figures reflect all palliative care services who submitted data for the July - December 2011 period. A full list of these services can be found at www.pcoc.org.a

Outcomes in Palliative Care, Report 12 (July - December 2011) - New South Wales

Introduction PCOC aims to assist services to improve the quality of the palliative care they provide through the analysis and benchmarking of patient outcomes. In this, the twelfth PCOC report, data submitted for the July - December 2011 period are summarised and patient outcomes benchmarked to enable participating services to assess their performance and identify areas in which they may improve. This report is broken into three sections: Section 1 summarises each of the four major benchmark measures and subsets and presents national benchmarking results for these benchmarks Section 2 presents additional analysis for each of the sixteen benchmarks Section 3 provides descriptive analysis of the data items at each of the patient, episode and phase levels In each of the three sections, data and analysis for NSW is presented alongside the national figures for comparative purposes. The national figures reflect all palliative care services who submitted data for the July - December 2011 period. A full list of these services can be found at www.pcoc.org.a

PCOC National Report on Outcomes in Palliative Care in Australia July to December 2011

The Palliative Care Outcomes Collaboration (PCOC) was established in mid-2005 and is funded under the National Palliative Care Program supported by the Australian Government Department of Health and Ageing. The goal of the PCOC is to use standardised, validated, clinical assessment tools to benchmark and measure outcomes in palliative care; and assist palliative care services to improve the quality of care. Further information on the tools can be found at www.pcoc.org.au. Each service involved in PCOC submits data every six months. The data are then collated and fed back to services to inform service improvement. Participation in PCOC is voluntary. There are three levels of data items - patient, episode and phase. The broad detail is found at the patient level, where the data items look at patient demographics. At the episode level, the items focus on characterising each setting of palliative care. They also describe the reasons behind why and how palliative care episodes start/end, the level of support patients receive both before and after an episode and (where applicable) the setting in which the patient died. The clinical focus of the data is at the phase level. The items at this level describe the patient\u27s stage of illness, functional impairment as well as their levels of pain and symptom distress. The items at the phase level are used to quantify patient outcomes, and are the focus of the PCOC benchmarks. The current PCOC data set (Version 2) was introduced in July 2007 following consultation with palliative care services and approval by PCOC\u27s Scientific and Clinical Advisory Committee. The data set includes five clinical assessment tools: Phases of Care, Palliative Care Problem Severity Score (PCPSS), Symptom Assessment Scale (SAS), Australia-modified Karnofsky Performance Status Scale (AKPS) and Resource Utilisation Groups - Activities of Daily Living (RUG-ADL). The items included in the PCOC data set serve the dual purpose of: - defining a common clinical language to allow communication between palliative care providers - facilitating the routine collection of national palliative care data for the purpose of reporting and benchmarking to drive quality improvement. Revised phase definitions were implemented in January 2012 but the data in this report does not reflect the revised definitions

Body Mass Index and persistent pain in Australia: Patient characteristics and treatment outcomes

Body mass index (BMI) is calculated using a person’s weight by the square of their height (kg/m2), and is used to broadly categorise a person as underweight, normal weight, overweight or obese. This paper will explore the association of patient characteristics and outcomes by BMI category using data collected by the electronic Persistent Pain Outcomes Collaboration (ePPOC)

Body Mass Index and persistent pain in New Zealand: Patient characteristics and treatment outcomes

Body mass index (BMI), calculated using a person’s weight by the square of their height (kg/m2), is used to broadly categorise weight as underweight, normal weight, overweight and obese. This paper will explore the association of patient characteristics and outcomes by BMI category using data collected by the electronic Persistent Pain Outcomes Collaboration (ePPOC)

Patient Outcomes in Palliative Care, Report 13 (January - June 2012) - Western Australia

PCOC aims to assist services to improve the quality of the palliative care they provide through the analysis and benchmarking of patient outcomes. In this, the thirteenth PCOC report, data submitted for the January - June 2012 period are summarised and patient outcomes benchmarked to enable participating services to assess their performance and identify areas in which they may improve. This report is broken into four sections: Section 1 provides a summary of the data included in this report. Section 2 summarises each of the four outcome measures and presents national benchmarking results for a selection of these measures. Section 3 presents a more detailed analysis of the outcome measures and benchmarks. Section 4 provides descriptive analysis at each of the patient, episode and phase data levels. In each of the four sections, data and analysis for services in WA is presented alongside the national figures for comparative purposes. The national figures reflect all palliative care services who submitted data for the January - June 2012 period. A full list of these services can be found at www.pcoc.org.au The four outcome measures included in this report were first introduced in the reporting period January to June 2009 (Report 7). There is strong sectoral support for national benchmarks and a consensus that such benchmarks can drive service innovation regardless of model of care. Benchmarking provides opportunities to understand the services that are provided, the outcomes patients experience and also to generate research opportunities focused on how to demonstrate variations in practice and outcomes

Western Australia: patient outcomes in palliative care: July - December 2013: report 16

The Palliative Care Outcomes Collaboration (PCOC) assists services to improve the quality of the palliative care they provide through the analysis and benchmarking of patient outcomes. In this, the sixteenth PCOC report, data submitted for the July to December 2013 period are summarised and patient outcomes benchmarked to enable participating services to assess their performance and identify areas in which they may improve

Patient Outcomes in Palliative Care - South Australia, July - December 2018

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\u27s home

National report on patient outcomes in palliative care in Australia: January - June 2014: report 17

The Palliative Care Outcomes Collaboration (PCOC) assists services to improve the quality of the palliative care they provide through the analysis and benchmarking of patient outcomes. In this, the seventeenth PCOC report, data submitted for the January to June 2014 period are summarised and patient outcomes benchmarked to enable participating services to assess their performance and identify areas in which they may improve

A profile of patients receiving palliative care in Queensland for January - June 2019

The Palliative Care Outcomes Collaboration (PCOC) is a national program that aims to improve the quality and outcomes of palliative care in Australia. This is achieved via a standardised clinical language that supports a national data collection. This report provides a high level profile of 4,625 patients who received palliative care in Queensland during January to June 2019 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care