Literature DB >> 26060242

Lived experiences and illness representation of Taiwanese patients with late-stage chronic kidney disease.

Chia-Chen Wu1,2, Chiu-Chu Lin3, Hsiu-Fang Hsieh2, Shu-Chen Chang4.   

Abstract

This qualitative study was designed to identify patients' experiences and perceptions related to living with late-stage chronic kidney disease. Interviews were held for 15 patients with late-stage chronic kidney disease from two medical centers in Taiwan. Five themes were identified using content analysis: experiencing moderate to severe symptoms and signs; tracing back to causes; realizing the long-term, irreversible nature of the disease; facing the consequence of unavoidable deterioration; and coping with the disease. The findings present the special lived experiences of Taiwanese chronic kidney disease patients and highlight the need for healthcare providers to assess patients' illness representation before offering interventions for patients coping with chronic kidney disease.
© The Author(s) 2015.

Entities:  

Keywords:  chronic kidney disease; illness representation; lived experiences; nursing; qualitative methods

Mesh:

Year:  2015        PMID: 26060242     DOI: 10.1177/1359105315587134

Source DB:  PubMed          Journal:  J Health Psychol        ISSN: 1359-1053


  7 in total

Review 1.  Patient's perceptions of chronic kidney disease and their association with psychosocial and clinical outcomes: a narrative review.

Authors:  Amy L Clarke; Thomas Yates; Alice C Smith; Joseph Chilcot
Journal:  Clin Kidney J       Date:  2016-05-10

2.  Through the Patients' Eyes: The Experience of End-Stage Renal Disease Patients Concerning the Provided Nursing Care.

Authors:  Areti Stavropoulou; Maria G Grammatikopoulou; Michail Rovithis; Konstantina Kyriakidi; Andriani Pylarinou; Anastasia G Markaki
Journal:  Healthcare (Basel)       Date:  2017-07-21

Review 3.  Patient-Centered Self-Management in Patients with Chronic Kidney Disease: Challenges and Implications.

Authors:  Chiu-Chu Lin; Shang-Jyh Hwang
Journal:  Int J Environ Res Public Health       Date:  2020-12-16       Impact factor: 3.390

4.  Illness perceptions predict mortality in patients with predialysis chronic kidney disease: a prospective observational study.

Authors:  Priscilla Muscat; John Weinman; Emanuel Farrugia; Liberato Camilleri; Joseph Chilcot
Journal:  BMC Nephrol       Date:  2020-12-10       Impact factor: 2.388

5.  Person centred care provision and care planning in chronic kidney disease: which outcomes matter? A systematic review and thematic synthesis of qualitative studies : Care planning in CKD: which outcomes matter?

Authors:  Ype de Jong; Esmee M van der Willik; Jet Milders; Yvette Meuleman; Rachael L Morton; Friedo W Dekker; Merel van Diepen
Journal:  BMC Nephrol       Date:  2021-09-13       Impact factor: 2.388

6.  Lived experiences of patients on hemodialytic treatment: A discursive perspective on fatigue and motivational issues.

Authors:  Laura Angioletti; Maurizio Bossola; Daniela De Filippis; Michela Balconi
Journal:  Health Psychol Open       Date:  2018-11-03

7.  Work of being an adult patient with chronic kidney disease: a systematic review of qualitative studies.

Authors:  Javier Roberti; Amanda Cummings; Michelle Myall; Jonathan Harvey; Kate Lippiett; Katherine Hunt; Federico Cicora; Juan Pedro Alonso; Carl R May
Journal:  BMJ Open       Date:  2018-09-04       Impact factor: 2.692

  7 in total

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