CareSearch Blog: Palliative Perspectives

The views and opinions expressed in our blog series are those of the authors and are not necessarily supported by CareSearch, Flinders University and/or the Australian Government Department of Health.
 

Why the Palliative Care Service Development Guidelines are important and what were the biggest changes from the previous guidelines

A guest blog post by Jane Fischer, President of Palliative Care Australia, Calvary Health Care Bethlehem

  • 30 May 2018
  • Author: CareSearch
  • Number of views: 3103
  • 0 Comments
Why the Palliative Care Service Development Guidelines are important and what were the biggest changes from the previous guidelines
In 2017 Palliative Care Australia undertook a review and update of the reference documents A Guide to Palliative Care Service Development: A population based approach and Palliative Care Service Provision in Australia: A planning guide. Together these key reference documents have provided a framework for the ongoing development of palliative care policy within the health care system for the last fifteen years.
 

Three things to do about health professionals’ knowledge of end of life law

A guest blog post by Professors Ben White and Lindy Willmott, Directors, Australian Centre for Health Law Research, Faculty of Law, QUT

  • 9 December 2016
  • Author: CareSearch
  • Number of views: 6288
  • 1 Comments
Three things to do about health professionals’ knowledge of end of life law
Health professionals need to know the law that governs withholding and withdrawing life-sustaining treatment. Law is not at the centre of the clinical encounter, but it is part of the regulatory framework that governs these decisions. Failure to know and follow the law puts health professionals and their patients at risk. But we know there are gaps in health professionals’ legal knowledge in this area and this is not surprising either, given how complex and difficult this field of law is.

 

Now there is specialised support and training for Australian GP nurses to provide better care at a very difficult time

A guest blog post by Associate Professor Josephine Clayton, Specialist Physician in Palliative Medicine at HammondCare’s Greenwich Hospital in Sydney, Associate Professor of Palliative Care at the University of Sydney and Director of the Advance Project

  • 2 December 2016
  • Author: CareSearch
  • Number of views: 3865
  • 0 Comments
Now there is specialised support and training for Australian GP nurses to provide better care at a very difficult time
As a young doctor I spent some time working in a palliative care hospital in the early 90’s.  It was such a privilege to be working with people at end of life - with the opportunity to make a difference to quality of life and well-being of patients, and their family members. That experience made me decide to devote my career to Palliative Medicine.
 
I had some experiences at that time that stayed with me.
 
I had a patient, Marion, who had been a school principal. Marion had suffered a severe stroke. She had survived but was very incapacitated, confined to bed and unable to communicate. She was being kept alive, surviving on a feeding tube, and facing a life of care and dependence. Her specialist was very committed to her survival.

 

‘What is needed to improve care planning for people living with dementia?’

A guest blog post from Tim Luckett PhD, Senior Research Fellow, University of Technology Sydney and Ingrid Duff, Research Assistant, Centre for Cardiovascular and Chronic Care

  • 19 July 2016
  • Author: CareSearch
  • Number of views: 7391
  • 2 Comments
‘What is needed to improve care planning for people living with dementia?’
During National Palliative Care Week, the University of Technology Sydney (UTS) hosted a forum on dementia care planning facilitated by the Director of The Centre for Cardiovascular and Chronic Care, Faculty of Health, Professor Jane Phillips. Imelda Gilmore, an Alzheimer’s Australia NSW Dementia Advocate and wife of a person with dementia, opened the forum by highlighting the importance of “getting the word out to have conversations about end of life early on”. A recurring theme at the forum was the need for care decisions to be person-centred and focused on what the person with dementia would have wanted were they able to speak for themselves, rather than the wishes of surrogate decision-makers. Lynn Chenoweth (Professor of Nursing at the Centre for Healthy Brain Ageing, The University of New South Wales) defined person-centredness as respecting the person with dementia’s “values, beliefs, history, likes and dislikes … all of the things that make them unique”.

Four easy steps to help GPs use the palliative care resources on CareSearch

A guest blog post from Dr Christine Sanderson, Staff Specialist, Neringah Community Palliative Care Service, NSW

  • 22 February 2016
  • Author: CareSearch
  • Number of views: 5112
  • 0 Comments
Four easy steps to help GPs use the palliative care resources on CareSearch


CareSearch is an online resource for palliative care. It has evidence-based resources for both clinicians and for patients, and their families and friends. As it is now a very large repository of evidence-based information, I would like to point you to four of the best sections for GPs to start off in.

These sections include the GP Hub, the Clinical Evidence pages, the Finding and Using Evidence pages, and the Education pages. You can also find information specially written for your patients in the Patients, Carers, and Families section. 

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About our Blog

The CareSearch blog Palliative Perspectives informs and provides a platform for sharing views, tips and ideas related to palliative care from community members and health professionals. 
 

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