Exploring Patients' Perceptions About Chronic Kidney Disease and Their Treatment: A Qualitative Study

Yvette Meuleman*, Yvonne van der Bent, Leandra Gentenaar, Fergus J. Caskey, Hans A. J. Bart, Wanda S. Konijn, Willem Jan W. Bos, Marc H. Hemmelder, Friedo W. Dekker

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BackgroundUnhelpful illness perceptions can be changed by means of interventions and can lead to improved outcomes. However, little is known about illness perceptions in patients with chronic kidney disease (CKD) prior to kidney failure, and no tools exist in nephrology care to identify and support patients with unhelpful illness perceptions. Therefore, this study aims to: (1) identify meaningful and modifiable illness perceptions in patients with CKD prior to kidney failure; and (2) explore needs and requirements for identifying and supporting patients with unhelpful illness perceptions in nephrology care from patients' and healthcare professionals' perspectives.MethodsIndividual semi-structured interviews were conducted with purposive heterogeneous samples of Dutch patients with CKD (n = 17) and professionals (n = 10). Transcripts were analysed using a hybrid inductive and deductive approach: identified themes from the thematic analysis were hereafter organized according to Common-Sense Model of Self-Regulation principles.ResultsIllness perceptions considered most meaningful are related to the seriousness (illness identity, consequences, emotional response and illness concern) and manageability (illness coherence, personal control and treatment control) of CKD. Over time, patients developed more unhelpful seriousness-related illness perceptions and more helpful manageability-related illness perceptions, caused by: CKD diagnosis, disease progression, healthcare support and approaching kidney replacement therapy. Implementing tools to identify and discuss patients' illness perceptions was considered important, after which support for patients with unhelpful illness perceptions should be offered. Special attention should be paid towards structurally embedding psychosocial educational support for patients and caregivers to deal with CKD-related symptoms, consequences, emotions and concerns about the future.ConclusionsSeveral meaningful and modifiable illness perceptions do not change for the better by means of nephrology care. This underlines the need to identify and openly discuss illness perceptions and to support patients with unhelpful illness perceptions. Future studies should investigate whether implementing illness perception-based tools will indeed improve outcomes in CKD.
Original languageEnglish
Number of pages13
JournalInternational Journal of Behavioral Medicine
DOIs
Publication statusE-pub ahead of print - 1 May 2023

Keywords

  • Chronic kidney disease (CKD)
  • Illness perceptions
  • Patient-reported outcome measures (PROMs)
  • Person-centered healthcare
  • Qualitative research
  • Self-regulation theory
  • ILLNESS PERCEPTION
  • OF-LIFE
  • PREDIALYSIS CARE
  • INTERVENTION
  • ASSOCIATIONS
  • SYMPTOMS
  • MANAGEMENT
  • SURVIVAL
  • DIALYSIS

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