Editorial
Building a Simple Way of Knowledge in Palliative Care
Antonio Rozzi1*and Margherita Salerno21Clinical Oncology Unit, Istituto Neurotraumatologico Italiano (I.N.I) Grottaferrata (Rome), Italy
2Palliative Care Center “S. Antonio da Padova”, Rome, Italy
- *Corresponding Author:
- Dr. Antonio Rozzi
Clinical Oncology Unit, I.N.I. Grottaferrata
via di S.Annasnc 00046 Grottaferrata (Rome), Italy
E-mail: antoniorozzi@virgilio.it
Received date: January 03, 2012; Accepted date: January 04, 2012; Published date: January 10, 2012
Citation: Rozzi A, Salerno M (2012) Building a Simple Way of Knowledge in Palliative Care. J Palliative Care Med 2:e110. doi:10.4172/2165-7386.1000e110
Copyright: © 2013 Jung YG. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
The dramatic advances in clinical therapy and nutrition have produced a progressive increase in life expectancy. Due to the ageing of population, a growing proportion of persons may develop, during their life-time, progressive chronic illnesses (cancer, cardiovascular diseases, dementia, debilitating arthritis, infective diseases) with a consequential greater need for social and economic support. Palliative care recognizes the responsibility of attending to the needs of these patients with their families. Physicians involved in palliative care should relieve pain and the other symptoms: they have expertise in symptoms management and in the communication skills to improve discussion with patients and their families about treatment possibilities, preferences and goals of care. Palliative care focuses primarily in diagnosing and treating symptoms experienced by patients with progressive incurable diseases. The ultimate goal of palliative careis to improve quality of life for both the patient and the family, regardless of diagnosis. Moreover, palliative care reduces the need of hospitalization, diagnostic and treatment interventions and nonbeneficial intensive care [1]. The mandatory aim of palliative care is the relief of the “total pain” of a dying person and his family. What is the “total pain”? As firstly described by Cecily Saunders, total pain is the sum of patient’s physical, psychological, social and spiritual pain.
