En la presente investigación, se busca conocer las percepciones sociales de los pacientes adultos con epilepsia. Se realizó un estudio cualitativo fenomenológico. La muestra estuvo conformada por 8 participantes (6 varones y 2 mujeres) entre los 22 y 60 años, diagnosticados con epilepsia. Se realizó una entrevista semiestructurada para la cual se elaboraron nueve preguntas. Se construyó una guía con cuatro ejes: a) la percepción del sí mismo de la persona con epilepsia, b) percepción de las personas con epilepsia sobre sus relaciones interpersonales, c) percepciones de epilepsia en su interacción socio laboral d) percepción de la epilepsia sobre su atención y acceso a los servicios de salud. Los hallazgos demuestran que los participantes presentan auto concepto negativo frente a su condición. Perciben que son incluidos socialmente, no obstante, tienden a aislarse. Algunos consideran el cuidado de su clan como sobreprotección familiar, y otros participantes lo valoran como soporte familiar. Los participantes manifiestan ser capaces de reconocer los posibles potenciales episodios desencadenantes de su enfermedad. / In the present investigation, we seek to know the social perceptions of adult patients with epilepsy. A qualitative phenomenological study was carried out. The sample consisted of 8 participants (6 men and 2 women) between 22 and 60 years old, diagnosed with epilepsy. A semi-structured interview was conducted for which nine questions were prepared. A guide was built with four axes: a) the perception of the self of the person with epilepsy, b) perception of people with epilepsy about their interpersonal relationships, c) perceptions of epilepsy in their social-professional interaction and d) perception of epilepsy about their attention and access to Health services. The findings show that the participants have a negative self-concept about their condition. They perceive that they are included socially, however, they tend to isolate themselves. Some consider the care of their clan as family overprotection, and other participants value it as family support. The participants declare that they are able to recognize the possible potential episodes that trigger their illness. / Tesis
| Identifer | oai:union.ndltd.org:PERUUPC/oai:repositorioacademico.upc.edu.pe:10757/626312 |
| Date | 16 August 2019 |
| Creators | Fernandini de la Rosa, Paola María |
| Contributors | Ráez Saavedra, María Cecilia |
| Publisher | Universidad Peruana de Ciencias Aplicadas (UPC) |
| Source Sets | Universidad Peruana de Ciencias Aplicadas (UPC) |
| Language | Spanish |
| Detected Language | English |
| Type | info:eu-repo/semantics/bachelorThesis |
| Format | application/pdf, application/epub, application/msword |
| Source | Universidad Peruana de Ciencias Aplicadas (UPC), Repositorio Académico - UPC |
| Rights | info:eu-repo/semantics/openAccess, Attribution-NonCommercial-ShareAlike 3.0 United States, http://creativecommons.org/licenses/by-nc-sa/3.0/us/ |
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