Literature DB >> 23471760

A qualitative study of treatment burden among haemodialysis recipients.

Christina Karamanidou1, John Weinman, Rob Horne.   

Abstract

This study aims to explore the experience of renal patients undergoing dialysis treatment focusing on beliefs about their illness, prescribed treatment and the challenge of adherence. Interpretative phenomenological analysis was used to analyse the accounts of seven haemodialysis patients. Patients have a range of beliefs about their illness and their treatment consistent with the self-regulatory model of illness, that is, identity, cause, consequences, timeline and cure. Patients sometimes consciously did not act in accordance to advice when they considered an aspect of treatment less important or less easy to adhere to. Psychological factors like beliefs might play a role in non-adherence behaviour.

Entities:  

Keywords:  end-stage renal disease; illness perceptions; interpretative phenomenological analysis; self-regulation model; treatment burden

Mesh:

Year:  2013        PMID: 23471760     DOI: 10.1177/1359105313475898

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


  12 in total

Review 1.  A Thematic Synthesis of the Experiences of Adults Living with Hemodialysis.

Authors:  Claire Reid; Julie Seymour; Colin Jones
Journal:  Clin J Am Soc Nephrol       Date:  2016-05-31       Impact factor: 8.237

2.  Patients' experience one year after dialysis initiation: a lexicometric analysis.

Authors:  Lucile Montalescot; Nicole Rascle; Christian Combe; Aurélie Untas
Journal:  Health Psychol Behav Med       Date:  2021-04-30

Review 3.  Living with, managing and minimising treatment burden in long term conditions: a systematic review of qualitative research.

Authors:  Sara Demain; Ana-Carolina Gonçalves; Carlos Areia; Rúben Oliveira; Ana Jorge Marcos; Alda Marques; Ranj Parmar; Katherine Hunt
Journal:  PLoS One       Date:  2015-05-29       Impact factor: 3.240

Review 4.  Measuring the burden of treatment for chronic disease: implications of a scoping review of the literature.

Authors:  Adem Sav; Asiyeh Salehi; Frances S Mair; Sara S McMillan
Journal:  BMC Med Res Methodol       Date:  2017-09-12       Impact factor: 4.615

5.  Reserve-building activities attenuate treatment burden in chronic illness: The mediating role of appraisal and social support.

Authors:  Carolyn E Schwartz; Jie Zhang; Wesley Michael; David T Eton; Bruce D Rapkin
Journal:  Health Psychol Open       Date:  2018-05-14

6.  Adherence to medication in patients with chronic kidney disease: a systematic review of qualitative research.

Authors:  Trine Mechta Nielsen; Metha Frøjk Juhl; Bo Feldt-Rasmussen; Thordis Thomsen
Journal:  Clin Kidney J       Date:  2017-12-25

7.  Understanding the impact of haemodialysis on UK National Health Service patients' well-being: A qualitative investigation.

Authors:  Daniel Jw Jones; Kate Harvey; John P Harris; Laurie T Butler; Emma C Vaux
Journal:  J Clin Nurs       Date:  2017-07-03       Impact factor: 3.036

8.  Illness Perceptions, Self-Care Management, and Clinical Outcomes According to Age-Group in Korean Hemodialysis Patients.

Authors:  Sisook Kim; Eunhye Kim; Eunjung Ryu
Journal:  Int J Environ Res Public Health       Date:  2019-11-13       Impact factor: 3.390

9.  Medication Adherence, Burden and Health-Related Quality of Life in Adults with Predialysis Chronic Kidney Disease: A Prospective Cohort Study.

Authors:  Wubshet H Tesfaye; Charlotte McKercher; Gregory M Peterson; Ronald L Castelino; Matthew Jose; Syed Tabish R Zaidi; Barbara C Wimmer
Journal:  Int J Environ Res Public Health       Date:  2020-01-06       Impact factor: 3.390

10.  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

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