Bibliographic citations
Luna, K., (2018). Relatos fenomenológicos del autocuidado que determinan la calidad de vida de los pacientes sometidos a hemodiálisis del Hospital Antonio Lorena, Cusco-2018. [Tesis, Universidad Andina del Cusco]. https://hdl.handle.net/20.500.12557/2186
Luna, K., Relatos fenomenológicos del autocuidado que determinan la calidad de vida de los pacientes sometidos a hemodiálisis del Hospital Antonio Lorena, Cusco-2018. [Tesis]. : Universidad Andina del Cusco; 2018. https://hdl.handle.net/20.500.12557/2186
@misc{sunedu/3041916,
title = "Relatos fenomenológicos del autocuidado que determinan la calidad de vida de los pacientes sometidos a hemodiálisis del Hospital Antonio Lorena, Cusco-2018.",
author = "Luna Espinoza, Karem Lucero",
publisher = "Universidad Andina del Cusco",
year = "2018"
}
Thesis entitled “Phenomenological stories of self-care that determine the quality of life of patients in a hemodialysis at the Antonio Hospital Lorena Cusco-2018“. The objective was to: Describe the phenomenological accounts of self-care thatdetermine the quality of life of patients undergoing hemodialysis at the Hospital Antonio Lorena, Cusco 2018. The methodological design was qualitative, the population consisted of 49 patients attending hemodialysis therapy of which 15 patients were randomly chosen; using as a tool, a guide of open questions; as a technique, the in-depth interview; and to record the expressions expressed by patients a recorder. Conclusion: On “self-care in patients undergoing hemodialysis“ different opinions were obtained where the level of knowledge is regular, the patients are not correctly oriented about self-care in its different dimensions, the family, friends, work and circle amical is affected by the changes that the disease imposes, they refer that being sick limits them to many activities and interpersonal relationships.witnessed that patients are in an inadequate psychological and psychological state many of them are in depression, despair, concern that prevent the disease, most patients have support by their relatives or caregivers who are involved in the development of the disease and the changes it imposes on their lives, patients feel uncomfortable in their family relationships feeling like a burden to them, some relatives and caregivers expressed fatigue for having them in charge.
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