Department of Clinical Epidemiology, Leiden University Medical Centre, Leiden, the Netherlands.
Population Health Sciences, University of Bristol, Bristol, UK.
Int J Behav Med. 2024 Apr;31(2):263-275. doi: 10.1007/s12529-023-10178-x. Epub 2023 May 24.
Unhelpful 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.
Individual 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.
Illness 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.
Several 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.
通过干预可以改变无益的疾病观念,从而改善预后。然而,在肾衰竭之前,对于慢性肾脏病(CKD)患者的疾病观念知之甚少,肾脏病护理中也没有工具可以识别和支持那些无益的疾病观念的患者。因此,本研究旨在:(1)确定肾衰竭前 CKD 患者有意义且可改变的疾病观念;(2)从患者和医疗保健专业人员的角度探讨识别和支持肾脏病护理中无益疾病观念患者的需求和要求。
采用目的抽样法对荷兰 CKD 患者(n=17)和专业人员(n=10)进行了个体半结构式访谈。采用混合归纳和演绎的方法对转录本进行分析:主题分析中确定的主题随后根据自我调节的常识模型原则进行组织。
认为最有意义的疾病观念与 CKD 的严重性(疾病身份、后果、情绪反应和疾病担忧)和可管理性(疾病一致性、个人控制和治疗控制)有关。随着时间的推移,患者对 CKD 的严重性相关的疾病观念变得更加无益,而对可管理性相关的疾病观念变得更加有益,这是由 CKD 诊断、疾病进展、医疗保健支持和接近肾脏替代治疗引起的。被认为重要的是,实施识别和讨论患者疾病观念的工具,然后应为无益疾病观念的患者提供支持。应特别注意为患者及其照顾者提供结构性的社会心理教育支持,以应对与 CKD 相关的症状、后果、情绪和对未来的担忧。
在肾脏科护理中,一些有意义且可改变的疾病观念并没有向好的方向改变。这强调了识别和公开讨论疾病观念以及为无益疾病观念的患者提供支持的必要性。未来的研究应探讨实施基于疾病观念的工具是否确实能改善 CKD 的预后。