Ethical Aspects of the Non-Resuscitation Discussion with the Patient and Its Family in Palliative Care

Authors

  • Nicoleta Dima "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Elena Rezuș "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Roxana Gănceanu Rusu "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Codruţa Bădescu "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Daniela Tănase "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Anca Ouatu "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Andreea Clim "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Ana-Maria Pop Clinical Rehabilitation Hospital, 1st Rheumatology Clinic, Iasi, Romania
  • Minela Aida Mărănducă "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania
  • Ciprian Rezuș "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania

DOI:

https://doi.org/10.35478/jime.2020.1.08

Keywords:

palliative care, quality of life, non-resuscitation, death

Abstract

The role of palliative care is to ensure the highest quality of life for the terminally-ill patients and their families. It is vital to integrate and develop palliative care programs within the structure of the community healthcare network under the conditions of demographic dynamics and due to the increase in mortality from oncological or non-oncological conditions. The patient's right to health is based on his/her state of well-being or health care that is judged by professionals with the right expertise. The principles of medical ethics, the limits of medical science, and the religious beliefs of medical staff, patients and their families, influence the individual decision of cardiopulmonary resuscitation

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Published

2020-03-31

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Section

Articles