Currently submitted to: Interactive Journal of Medical Research
Date Submitted: May 1, 2026
Open Peer Review Period: May 6, 2026 - Jul 1, 2026
(currently open for review)
Warning: This is an author submission that is not peer-reviewed or edited. Preprints - unless they show as "accepted" - should not be relied on to guide clinical practice or health-related behavior and should not be reported in news media as established information.
Chronic Kidney Disease and the Silent Struggles: Loneliness, Uncertainty, and Emotional Burden
ABSTRACT
Background:
Chronic kidney disease (CKD) affects more than 850 million people worldwide, yet the emotional and psychosocial burdens remain underrecognized in nephrology practice. This review explores the overlooked dimensions of loneliness, uncertainty, and emotional suffering in CKD, drawing attention to their implications for both patients and caregivers.
Objective:
The objective of the current review article is to elucidate the mechanisms of the distresses experienced by the hemodialysis patients and their carers
Methods:
We conducted a narrative synthesis of qualitative and quantitative studies across pediatric, adult, and elderly populations, with additional perspectives from culturally and linguistically diverse groups and caregivers
Results:
Loneliness and social isolation affect more than 40% of dialysis patients and are consistently linked with depression, reduced adherence, hospitalization, and increased mortality. Uncertainty about disease trajectory and treatment outcomes generates chronic psychological strain, particularly in older adults. Caregivers report high emotional burden, social withdrawal, and diminished well-being. Despite growing recognition of these issues, systematic psychosocial screening and targeted interventions remain rare in routine nephrology.
Conclusions:
This review highlights loneliness and uncertainty as silent but modifiable risk factors in CKD, on par with traditional biomedical markers. We argue that nephrology urgently requires a shift toward a biopsychosocial model of care that includes structured emotional screening, culturally responsive interventions, and caregiver support. By reframing psychosocial suffering as a clinical priority rather than a secondary concern, nephrology can move toward more person-centered and equitable care.
Citation
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Copyright
© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.