The World Health Organization defines palliative care as an approach to care that improves quality of life of patients facing life-threatening illness and their families, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial, and spiritual.1 In contemporary discussions of healthcare, the topics of palliative care and end-of-life care are prominent. Although palliative medicine specialists have become more widely available for consultation, the care of seriously ill and dying patients is central to the entire practice of medicine, including surgery. However, fear of treating patients at end of life is experienced by many healthcare providers. Providers are generally not formally prepared to manage dying as a normal process. Caring for this population entails complex decisions that may seem to contradict the intent to cure. However, it is recognized that the essential goal of medicine is to relieve suffering, and that caring well for these patients and their families can be a hopeful and healing process. © 2008 Springer New York.
CITATION STYLE
Weinstein, S. M., & Walton, O. (2008). Palliative and end-of-life care. In Surgery: Basic Science and Clinical Evidence: Second Edition (pp. 737–740). Springer New York. https://doi.org/10.1007/978-0-387-68113-9_40
Mendeley helps you to discover research relevant for your work.