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Palliative Care 2030 outlines guiding principles to assist the health, disability and aged care sectors, governments and the general community, to plan and prepare for the future where Australians will live longer, demand an improved quality of life, and access to high quality palliative care when living with a life-limiting illness.

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  • Palliative care is defined as comprehensive, interdisciplinary care of patients and families facing a terminal illness, focusing primarily on comfort and support.1 Key aspects include meticulous symptom control; psychosocial and spiritual care; a personalised management plan that maximises patient-determined quality of life; family oriented care that extends through the time of bereavement

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The new edition of this book has been updated to incorporate recent advances in both the approach to, and treatment of, the terminally ill. Based on many years of monitoring clinical practice and research at St Christophers Hospice, the author presents practical, balanced advice on the general ethical and medical principles of caring for dying patients.

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Family carers in palliative care: A guide for health and social care professionals (Edited by Peter Hudson and Sheila Payne) Oxford University Press (2009) Palliative Care Journals Acta Oncologica - a journal for clinical oncologists on all fields of clinical cancer research.

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  • 2021-1-6 · For years, humanitarian relief efforts have focused primarily on saving lives. Traditional methods of triage have been employed, and those thought likely to die have been placed in an “expectant” tent or area. Recently however there has been increasing recognition that palliative care should play an essential role in relief efforts. The goal of humanitarian aid really shouldn’t just be

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