6360abefb0d6371309cc9857
Keywords: palliative care; oncology; empathy; pain
Introduction
According to the world health organization (who), as
defined in 1990 and updated in 2002, "palliative care consists of
assistance provided by a multidisciplinary team, aimed at improving the quality
of life of patients and their families, in the face of a life-threatening
disease, through the prevention and relief of suffering, early identification,
impeccable assessment and treatment of pain and other physical, social,
psychological and spiritual symptoms" (who, 2002). Illness places individuals
face-to-face with existential questions rarely addressed in daily life. Our
role is to help patients confront these questions, enabling them to experience
and overcome suffering by organizing their internal concerns as closely as
possible to life's realities. Cicely saunders (2006) defines the essence of
palliative care by stating that suffering becomes intolerable only when no one
provides care5. This highlights the
importance of caregiving, even in the presence of life-threatening diseases or
those beyond remission6.
Objectives
This study aims to promote
awareness, training and humanization of palliative care among healthcare
professionals, students and the general community7.
It seeks to enhance the quality of life for patients with severe illnesses and
their families through approaches prioritizing relief from suffering, emotional
support and respect for human dignity.
Materials and methods
The review was conducted through a
bibliographic search in the pubmed and scielo databases, including articles
published over the past 10 years8.
Discussion
This work is essential to addressing this gap, providing
healthcare professionals and the community with a deeper understanding of the
importance of palliative care-not just to prolong life, but to ensure it is
lived with quality and dignity until the end9.
Moreover, the study seeks to demystify misconceptions about palliative care,
showing that it is not limited to end-of-life situations but involves a
comprehensive approach that can begin from the diagnosis of a serious chronic
illness10.
Conclusion
Palliative care plays a crucial role in the healthcare
system, particularly for patients with severe or terminal illnesses. However, a
lack of knowledge and inadequate training in this field often result in
insufficient management of pain and other symptoms, along with poor
communication with patients and their families during challenging times11. It is essential to understand family dynamics, pain and
suffering and to act in ways that provide support during the most difficult
moments-not only during the crisis but also with multidisciplinary support
after the period of anguish and distress12.
References
1. Organização
mundial da saúde (oms). Recursos para avaliação de cuidados paliativos 2024.
2. Scielo.
Cuidados paliativos no sus. Disponível em 2024.
3. Onu
brasil. Relatório sobre acesso a cuidados paliativos. Disponível em 2024.
4. Organização pan-americana da saúde
(ops/oms). Cuidados paliativos: perspectivas na américa latina. Disponível em 2024.
5. Scielo.
Revisão integrativa sobre cuidados paliativos no brasil. Disponível em 2024.
6.
Associação mundial de cuidados paliativos. Atlas global. Disponível em 2024.
7. Organização mundial da saúde (oms).
Cuidados paliativos pediátricos: conceitos e práticas. Disponível em 2024.
8. Scielo.
Cuidados paliativos: ciência e proteção. Disponível em 2024.
9. Palliative care toolkit.
Diretrizes internacionais. Disponível em 2024.
10. Ministério da saúde (brasil).
Diretrizes para cuidados paliativos no sus. Disponível em 2024.
11. Eclac. Panorama dos cuidados
paliativos na américa latina. Disponível em 2024.
12. Revista
brasileira de enfermagem. Impacto dos cuidados paliativos na qualidade de vida.
Disponível em 2024.