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- Title
ESTUDIO PILOTO EN CUIDADORES DE PACIENTES CON ENFERMEDADES NEUROLÓGICAS, SOBRE EL SIGNIFICADO Y CONOCIMIENTO DE CUIDADOS PALIATIVOS.
- Authors
de los Santos, Zoila Trujillo; Paz-Rodríguez, Francisco; Sánchez Guzmán, María Alejandra; Nava García, Guadalupe; Zamora R., Patricia; García Pastrana, Claudia; Ochoa Morales, Adriana; Medina Durán, María del Refugio
- Abstract
Aim. To describe the meaning attributed to palliative care (PC) by caregivers, as well as their preference with respect to informing the patient and their satisfaction in their caring role. Methodology: Study descriptive transversal, sample intended of 40 caregivers of neurologic patients needing PC. A questionnaire about knowledge of the topic and their burnout status was applied. A descriptive-comparative analysis was carried out with 95% (p<0.05) confidence interval. Results: Patients: 52.6% men, average age 57.9 years, duration of disease: 5 years, average of 2 children. Caregivers: 77.5% women, 25.0% married, average age: 49.3 years, daily caring 18.5 hours, 62.5% with high School or university studies, 40% alone as caregivers, 16.7% do not count with support nets and 42.5% present high burn out status. Of them 70% did not have previous information about PC. Meaning: 50% mentioned "to give help" (physical or emotional), 20% "to enhance quality of life". 87.5% would like to be informed with detail if they were the patients, 86.1% would like to be informed by the physician and 62.5% were in favor to inform with detail to their family member. Conclusions: It is important to disseminate PC to caregivers and to stimulate the right of patients to receive information about the prognosis of their disease.
- Publication
Acta Bioéthica, 2015, Vol 21, Issue 2, p191
- ISSN
0717-5906
- Publication type
Article
- DOI
10.4067/S1726-569X2015000200005