Patients’ experiences and perspectives on sleep assessment and management in chronic kidney disease: A multicentre mixed-methods study

 

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Patients’ experiences and perspectives on sleep assessment and management in chronic kidney disease: A multicentre mixed-methods study

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Ginger
Chu
Ginger Chu g.chu@newcastle.edu.au University of Newcastle School of Nursing and Midwifery Callaghan Australia * John Hunter Hospital Nephrology Department New Lambton Height Australia
Andrea Viecelli andrea.viecelli@health.qld.gov.au University of Queensland Australasian Kidney Trials Network Brisbane Australia -
Ritin Fernandez ritin.fernandez@newcastle.edu.au University of Newcastle School of Nursing and Midwifery Callaghan Australia -
Sarah Russo sarah.russo@health.nsw.gov.au John Hunter Hospital Nephrology Department New Lambton Height Australia -
Vasif Abdul Latheef vasif.abdullatheef@health.nsw.gov.au Gosford Hospital Nephrology Department Gosford Australia -
Benjamin Lazarus benjamin.lazarus@health.qld.gov.au Princess Alexandra Hospital Nephrology Department Brisbane Australia - University of Queensland Australasian Kidney Trials Network Brisbane Australia University of Queensland Faculty of Medicine Brisbane Australia
Lisa Matricciani lisa.matricciani@unisa.edu.au University of South Australia Clinical and Health Sciences Adelaide Australia -
Cassandra Foster cassandra.foster@health.nsw.gov.au Gosford Hospital Nephrology Department Gosford Australia -
Catherine Blackamore catherine.blackamore@health.nsw.gov.au Gosford Hospital Nephrology Department Gosford Australia -
Richard Le Leu richard.leleu@sa.gov.au Royal Adelaide Hospital Central Northern Adelaide Renal and Transplantation Service Adelaide Australia - University of South Australia Clinical and Health Sciences Adelaide Australia
Shilpanjali Jesudason shilpa.jesudason@sa.gov.au Royal Adelaide Hospital Central Northern Adelaide Renal and Transplantation Service Adelaide Australia -
 
 
 
 

Sleep is closely linked to kidney health and has a significant impact on quality of life. Screening and managing poor sleep are highly recommended for people with chronic kidney disease (CKD). However, limited studies have examined how sleep concerns among people living with CKD are assessed and managed in clinical practice. This study aims to examine the experiences and perspectives of sleep assessments and management among people living with CKD. 

We obtained ethical approval to conduct a mixed-methods study incorporating a cross-sectional survey and semi-structured interviews to collect data from adults with CKD in four nephrology units across three Australian states between 1 August 2024 and 31 April 2025. We used a convenience sampling strategy, inviting eligible participants to complete the survey either online or on paper and to participate in an online 1:1 interview. Quantitative data were analysed descriptively, and qualitative data were analysed using narrative analysis. 

We analysed 214 surveys and 11 interviews, with 68% male respondents and a mean age of 63 years. Most individuals received haemodialysis (61%). Based on self-reported Pittsburgh Sleep Quality Index (PSQI) scores, 72% of participants were classified as “poor sleepers” (PSQI >5) (Table 1). Sleep disturbances were commonly attributed to broken sleep, nocturia, and other symptoms such as restless legs and pain (Fig. 1). Qualitative data revealed that nocturia was prevalent among participants with CKD not requiring kidney replacement therapy, while machine noise and restricted sleep positions were problematic for peritoneal dialysis participants. Haemodialysis participants reported broken sleep, difficulty initiating sleep, itch, and pain. Transplant recipients also reported poor sleep quality.

Over a third of participants indicated that their nephrologists never inquired about sleep, and only 41% of participants reported sleep issues to their nephrologist. A quarter of participants felt they should manage sleep independently, while 11% did not report sleep disturbances due to other competing symptoms. Only 8% used a wearable sleep tracker, while 51% expressed no interest in using one (Table 1).

Sleep concerns were often not managed. When they were managed, medication was the most common management strategy (19%), followed by sleep education and supportive care (Fig. 2). However, qualitative data revealed that medication burden, such as “not wanting to take more medications”, was a reason for not seeking medical help for sleep issues (Fig. 3). Non-pharmacological interventions were preferred, as participants felt empowered by these strategies. 

Table 1

Figure 1

Figure 2

Sleep problems were infrequently screened or reported. Patients reported a preference for non-pharmacological sleep management strategies, despite the common use of medication. Over a third of participants did not report sleep issues due to a perception of expected self-management or the presence of competing symptoms. These insights underscore the need for routine sleep health assessments and the management of other symptoms, such as pain and restless legs, to improve sleep in people with CKD.

Kewords