Dying in Australian hospitals: will a separate national clinical standard improve the delivery of quality care?
Katherine Clark A B D , Aileen Collier C and David C. Currow CA Department of Palliative Care, Calvary Mater Newcastle, Edith Street, Waratah, NSW 2298, Australia.
B The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
C Discipline, Supportive and Palliative Care, Flinders University, Bedford Park, Adelaide, SA 5041, Australia. Email: aileen.collier@flinders.edu.au; david.currow@health.sa.gov.au
D Corresponding author. Email: katherine.clark@calvarymater.org.au
Australian Health Review 39(2) 202-204 https://doi.org/10.1071/AH14175
Submitted: 2 October 2014 Accepted: 19 October 2014 Published: 17 December 2014
Abstract
While it is commonly stated that for most people the preferred place of death is their own homes, the actual reality is that most people will die in hospitals. This is both by choice and necessity. However, for many, the care that they receive would not necessarily align with their expectations. The need to improve the quality of health care at the end of life has been acknowledged by the Australian Commission for Safety and Quality in Healthcare with the release of a recent discussion paper. It is presumed this is a prelude to the release of another quality standard specifically for end of life care. The aim of this paper is to question whether such a standard is likely to result in the hoped for improvements in care.
What is known about the topic? Numerous reports highlight that the care received by people dying predictably in hospital would not always be considered of sufficient quality to reliably and safely address their needs. As the numbers of people dying in Australian hospitals is likely to exponentially rise over the next decade there is a real need to address this care gap.
What does this paper add? The need to address this care gaps has been highlighted by the Australian Commission for Safety and Quality in Healthcare. While this focus is welcomed, this paper questions whether any changes can be made without considering the fundamental issues precluding the delivery of quality health care as would be expected by any other patient cohort.
What are the implications for practitioners? As with care at any point, patients and their families expect care to be delivered in a quality paradigm: patient-centred, evidence-based and safe. Care at the end of life is no different.
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