¿Como viven su enfermedad las personas en diálisis? una mirada cualitativa a la experiencia del paciente

Translated title of the contribution: How do patients on dialysis experience their disease? A qualitative approach

Mirliana Ramírez-Pereira, Natalie Figueredo-Borda, Pamela Zapata-Sepúlveda, Mónica Ferrada-Muñoz, Luz Angélica Muñoz González

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background: End-stage chronic kidney disease is a severe public health problem due to the poor quality of life of patients on dialysis and the costs associated with renal replacement treatment. Aim: To understand the social representations of kidney disease of people on dialysis. Material and Methods: In a qualitative study under the post-positivist paradigm, eighteen patients in peritoneal or hemodialysis participated in an in-depth interview. The analysis was performed using content analysis. Results: Eight categories were identified: Friends, Health Care Team, Spirituality and Disease, Family, Health Support System, Physical Consequences, Psychosocial Consequences, Self-Care of Continuous Health-Disease. Conclusions: Health care of people on dialysis should take into consideration the experience of kidney disease from the perspective of the patient, including his beliefs and feelings and involving the family, community, and the state.

Translated title of the contributionHow do patients on dialysis experience their disease? A qualitative approach
Original languageSpanish
Pages (from-to)289-294
Number of pages6
JournalRevista Medica de Chile
Volume150
Issue number3
DOIs
StatePublished - Mar 2022

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