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Patient Outcomes In Pain Management: Enterprise One Pain Management Service, 2018 Annual Report For 1 January To 31 December 2018, Megan B. Blanchard, Janelle M. White, Meredith P. Bryce, Julie A. Blacklock, Karen Quinsey, Hilarie Tardif Jan 2019

Patient Outcomes In Pain Management: Enterprise One Pain Management Service, 2018 Annual Report For 1 January To 31 December 2018, Megan B. Blanchard, Janelle M. White, Meredith P. Bryce, Julie A. Blacklock, Karen Quinsey, Hilarie Tardif

Australian Health Services Research Institute

ePPOC aims to assist services to improve the quality of the pain management they provide through the analysis and benchmarking of patient outcomes. In this report, data submitted for patients active during the period 1 January to 31 December 2018 are summarised to enable participating services to assess their performance and compare this with outcomes achieved by other services.


Electronic Persistent Pain Outcomes Collaboration Annual Data Report 2018, Hilarie Tardif, Megan B. Blanchard, Karen Quinsey, Meredith P. Bryce, Janelle M. White, Julie A. Blacklock, Kathy Eagar Jan 2019

Electronic Persistent Pain Outcomes Collaboration Annual Data Report 2018, Hilarie Tardif, Megan B. Blanchard, Karen Quinsey, Meredith P. Bryce, Janelle M. White, Julie A. Blacklock, Kathy Eagar

Australian Health Services Research Institute

ePPOC is a program that aims to improve services and outcomes for people experiencing persistent pain. It involves specialist pain services collecting a standard set of information to measure outcomes for their patients as a result of treatment. Pain services use the information to triage, monitor and plan treatment for individual clients, and also send non-identifiable information to ePPOC for analysis. The results of these analyses are fed back to participating services every six months, allowing pain management services to assess their results, and compare their patients, services and outcomes to other pain management services. ePPOC also uses the information …


A Profile Of Patients Receiving Palliative Care In Australia For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Linda M. Foskett, Sabina P. Clapham Jan 2019

A Profile Of Patients Receiving Palliative Care In Australia For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 23,333 patients who received palliative care during July to December 2018 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care.


A Profile Of Patients Receiving Palliative Care In Nsw And Act For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Gaye L. Bishop, Linda M. Foskett, Sabina P. Clapham Jan 2019

A Profile Of Patients Receiving Palliative Care In Nsw And Act For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Gaye L. Bishop, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 5,588 patients who received palliative care in NSW and ACT during July to December 2018 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care.


A Profile Of Patients Receiving Palliative Care In Western Australia For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham Jan 2019

A Profile Of Patients Receiving Palliative Care In Western Australia For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 3,813 patients who received palliative care in Western Australia during July to December 2018 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care.


Patient Outcomes In Palliative Care In Australia: National Report For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care In Australia: National Report For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …


Patient Outcomes In Palliative Care - Victoria, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Jane F. Healey, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care - Victoria, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Jane F. Healey, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …


Patient Outcomes In Palliative Care - South Australia, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care - South Australia, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …


Patient Outcomes In Pain Management: Enterprise One Paediatric Pain Management Service, 2018 Annual Report For 1 January To 31 December 2018, Megan B. Blanchard, Meredith P. Bryce, Janelle M. White, Julie A. Blacklock, Karen Quinsey, Hilarie Tardif Jan 2019

Patient Outcomes In Pain Management: Enterprise One Paediatric Pain Management Service, 2018 Annual Report For 1 January To 31 December 2018, Megan B. Blanchard, Meredith P. Bryce, Janelle M. White, Julie A. Blacklock, Karen Quinsey, Hilarie Tardif

Australian Health Services Research Institute

ePPOC aims to assist services to improve the quality of the pain management they provide through the analysis and benchmarking of patient outcomes. In this report, data submitted for patients active during the period 1 January to 31 December 2018 are summarised to enable participating services to assess their performance and compare this with outcomes achieved by other services.


Environmental Effects And Interactions Of Stratospheric Ozone Depletion, Uv Radiation, And Climate Change. 2018 Assessment Report, Paul W. Barnes, Craig E. Williamson, Robyn M. Lucas, Sasha Madronich, Sharon A. Robinson, Nigel D. Paul, Janet F. Bornman, Alkiviadis F. Bais, Barbara Sulzberger, Stephen R. Wilson, Anthony L. Andrady, Patrick Neale, Amy T. Austin, Germar H. Bernhard, Richard L. Mckenzie, Keith R. Solomon, Rachel E. Neale, Paul J. Young, Mary Norval, L E. Rhodes, Samuel Hylander, Kevin C. Rose, Janice Longstreth, Pieter J. Aucamp, Carlos L. Ballare, Rose M. Cory, Stephan D. Flint, Frank R. De Gruijl, Donat -P Hader, Anu Heikkila, Marcel A.K Jansene, Krishna K. Pandey, T Matthew Robson, C A. Sinclair, Robert Worrest, S Yazar, Antony R. Young, Richard G. Zepp Jan 2019

Environmental Effects And Interactions Of Stratospheric Ozone Depletion, Uv Radiation, And Climate Change. 2018 Assessment Report, Paul W. Barnes, Craig E. Williamson, Robyn M. Lucas, Sasha Madronich, Sharon A. Robinson, Nigel D. Paul, Janet F. Bornman, Alkiviadis F. Bais, Barbara Sulzberger, Stephen R. Wilson, Anthony L. Andrady, Patrick Neale, Amy T. Austin, Germar H. Bernhard, Richard L. Mckenzie, Keith R. Solomon, Rachel E. Neale, Paul J. Young, Mary Norval, L E. Rhodes, Samuel Hylander, Kevin C. Rose, Janice Longstreth, Pieter J. Aucamp, Carlos L. Ballare, Rose M. Cory, Stephan D. Flint, Frank R. De Gruijl, Donat -P Hader, Anu Heikkila, Marcel A.K Jansene, Krishna K. Pandey, T Matthew Robson, C A. Sinclair, Robert Worrest, S Yazar, Antony R. Young, Richard G. Zepp

Faculty of Science, Medicine and Health - Papers: Part B

Executive Summary: Thirty-four years ago, an unprecedented thinning of stratospheric ozone was reported over Antarctica.The risk of a consequent increase in exposure to solar UV-B radiation (UV-B; wavelengths 280-315 nm) raised concerns about potentially disastrous effects on human health and the Earth's environment. In response, the international community mobilised and worked together to understand the causes and find a solution to this dramatic change in the Earth's atmosphere. In 1985, the Vienna Convention for the Protection of the Ozone Layer was signed, which provided the framework for the Montreal Protocol on Substances that Deplete the Ozone Layer, signed in 1987. …


A Profile Of Patients Receiving Palliative Care In Queensland For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Claire Christiansen, Anna Mcpherson, Linda M. Foskett, Sabina P. Clapham Jan 2019

A Profile Of Patients Receiving Palliative Care In Queensland For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Claire Christiansen, Anna Mcpherson, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 4,237 patients who received palliative care in Queensland during July to December 2018 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care.


Patient Outcomes In Palliative Care - Nsw And Act, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Gaye L. Bishop, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care - Nsw And Act, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Gaye L. Bishop, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …


A Profile Of Patients Receiving Palliative Care In Victoria For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Jane F. Healey, Linda M. Foskett, Sabina P. Clapham Jan 2019

A Profile Of Patients Receiving Palliative Care In Victoria For July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Jane F. Healey, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 7,189 patients who received palliative care in Victoria during July to December 2018 and had their pain, symptom, family / carer and psychological / spiritual issues assessed as part of routine clinical care.


Patient Outcomes In Palliative Care - Queensland, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Claire Christiansen, Anna Mcpherson, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care - Queensland, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Claire Christiansen, Anna Mcpherson, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …


Patient Outcomes In Palliative Care - Western Australia, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham Jan 2019

Patient Outcomes In Palliative Care - Western Australia, July - December 2018, Alanna M. Connolly, Samuel J. Burns, Samuel F. Allingham, Tanya Pidgeon, Natalie Joseph, Linda M. Foskett, Sabina P. Clapham

Australian Health Services Research Institute

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 …