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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.
There is a need for more research led by nurses working in clinical environments. In the last of our blog series for International Year of the Nurse and Midwife, Dr Caroline Phelan of Flinders University and academic at the Research Centre for Palliative Care, Death and Dying (RePadd) discuss the important role of research nurses in developing evidence, and her personal experience.
To continue our celebration of the International Year of Nurses and Midwife, we are featuring blogs on nurses and their critical role in providing palliative care and how they can be supported further. Kylie Ash, National Project Manager for PCC4U and Melissa Slattery, Head of Discipline for Nursing at EQUALS International, discuss the need for a nationally consistent palliative care education for enrolled nurses, and how the PCC4U EN Toolkit and EQUALs Diploma of Nursing can help.
Art therapy is used in palliative care to compliment a holistic approach to care and to augment traditional clinical and medical approaches. In this blog, Estelle Chapple, an Art Therapist for Central Adelaide Palliative Care, and Michelle Cripps, Director for Centre for Creative Health, discuss the impact of art therapy in palliative care settings.
Discussions about CPR (Cardiopulmonary Resuscitation) are difficult because they confront the person with death. However, when cardiac arrest occurs there is no time to ponder the pros and cons of CPR or to discuss this with the person’s substitute medical treatment decision-maker. Dr Barbara Hayes, Clinical Lead in Advance Care Planning and Palliative Care Consultant at Northern Health, discusses the importance of increasing awareness of CPR decision-making prior to acute illness and why discussions and decisions are a necessary part of medical treatment planning.
Informing people with vastly different backgrounds, literacy levels and capacity, as well as roles is a challenge. This is why in the 2017-2020 project period, CareSearch and palliAGED began the Engagement Project working with specific groups (allied health, aged care and patients, carers, and families) to learn more about how they find and use health care information and what information about end of life and palliative care they need. Dr Katrina Erny-Albrecht, Senior Research Fellow for CareSearch discusses some key findings from the project and the central importance of context.