Palliative Care Australia

Click to expand navigation

Print Page Print this page

National health statistics highlight inequitable access to palliative care

People living outside of major cities have less access to community-based palliative care options.

Where people live and their socioeconomic status has significant bearing on whether they need to rely on hospitals to receive palliative care, or are able to access it within the community, new national statistics suggest.

The 2014-15 statistics, released today by the Australian Institute of Health and Welfare, show that regional areas have a higher rate of palliative-care related hospitalisations than major cities.

Palliative Care Australia CEO Liz Callaghan said this reflects that people living outside of major cities have less access to community-based palliative care options, which leaves them more reliant on hospitals.

“We know that 70% of Australians would rather die at home than in hospital, but dying at home often requires access to outreach services and community-based support,” she said.

“People living outside of major cities don’t get to exercise the same choice about where they die because they have less access to residential aged care, 24-hour community-based services and hospice services.

“People should be able to access the same level of care regardless of their location.”

Palliative Care Australia CEO Liz Callaghan.

It seems capacity to pay also affects choice, with the statistics showing a strong correlation between and palliative care hospitalisations and socioeconomic status.

Ms Callaghan said the most disadvantaged Australians had double the rate of palliative care-related hospitalisations within the public system compared to people in the highest socioeconomic group.

This reflects their capacity to pay for private home-based services or out-of-pocket costs not covered by Medicare.

“To put it simply, being able to pay gives you more options,” Ms Callaghan said.

“Compounding that, hospices are located in higher socioeconomic areas of major cities, so people in lower socioeconomic groups don’t have physical or financial access to them.”

Nationally there had been a small increase in specialist palliative medicine physicians, relative to the population, which Ms Callaghan said was pleasing. However the number of employed palliative care nurses had remained stagnant, despite population growth.

Concerning too was that there were only 80 full-time-equivalent palliative care nurses working in residential health care facilities, which service more than 192,000 people.

Ms Callaghan said the statistics painted a valuable but limited picture of palliative care delivery.


  • My husband passed in november 2017 from brain cancer, my girls and i have since set up a foundation to help those patients who wish to die at home be cared for at home until the end. We launch the foundation with a gala ball in August 19th, i would like to be able to work with within the Palliative Care who my husband had and were beautiful i may add, we would like to help in any way we can.

    - Heather Roberts

Comments are closed.

« Back to Palliative Matters

Search articles

Suggest a story

If you have any stories or ideas to share with us, send us an email.