Resumen
Background: Low-prevalence diseases (LPDs), previously referred to as orphan diseases or rare diseases, entail a substantial potential for mortality and impose a remarkable burden of symptoms for patients.The process of diagnosing these diseases is often lengthy, and viable treatment options for such conditions are scarce, or in some cases, non-existent. Methods: A narrative review was carried out following the Scale for the Assessment of Narrative Review Articles (SANRA) methodology to establish the role of palliative care in the treatment and follow-up of patients with LPDs. A search was carried out by a multidisciplinary team in EMBASE, PUBMED, Web of Science, CINHAL and OVID. Peer-reviewed articles reporting on the role of palliative care in the multidisciplinary treatment of LPDs were included. Results: The review identified significant areas where palliative care specialists play a crucial role in caring for LPDs.These areas include addressing complex physical and emotional symptoms, assisting patients in adjusting their expectations through genetic counselling, facilitating decision-making across short, medium and long-term perspectives based on disease prognosis, and offering support with care transitions, advanced planning and the grieving process for families. Conclusion: Patients with LPDs and their caregivers experience complex care needs that should be assessed by a palliative care specialist and supported by a multidisciplinary medical group.
| Idioma original | Inglés |
|---|---|
| Páginas (desde-hasta) | 181-188 |
| Número de páginas | 8 |
| Publicación | International Journal of Palliative Nursing |
| Volumen | 31 |
| N.º | 4 |
| DOI | |
| Estado | Publicada - 21 abr. 2025 |
Focos Estratégicos
- Vida Humana Plena (Vita)
Clasificación de Articulo
- Artículo completo de investigación
Indexación Internacional (Artículo)
- ISI Y SCOPUS
Scopus-Q Quartil
- Q3
ISI- Q Quartil
- Q3
Categoría Publindex
- A2