Caregiver Burden and Quality of Life in Chronic Kidney Disease Systems

Summary

Chronic kidney disease (CKD) imposes a progressive loss of renal function that often culminates in end-stage renal failure and the need for renal replacement therapies such as haemodialysis. As patients navigate complex treatment regimens, family members and close associates assume the role of primary caregivers. The demands of caregiving extend beyond mere assistance with medical tasks to encompass emotional support, coordination of care, financial management and adaptation of personal routines. These responsibilities give rise to caregiver burden, a multidimensional construct reflecting physical strain, psychological stress and social disruption. In turn, caregiver burden exerts a direct influence on quality of life, affecting mental well-being, social relationships and general health perception. Globally, the prevalence of CKD continues to rise, heightening the number of informal carers and underscoring the need for structured support mechanisms. Current discourse emphasises routine screening for caregiver distress, targeted educational interventions to foster health-promoting behaviours, and psychosocial strategies to alleviate fatigue and enhance coping. Evidence suggests that approaches tailored to the caregiver’s context—whether focused on skills development, stress-reduction techniques or peer support—can attenuate burden and preserve quality of life. Integrating these measures into clinical pathways and health-policy frameworks is essential to sustain both patient outcomes and caregiver welfare.

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Caregiver Burden and Quality of Life in Chronic Kidney Disease Systems publication trend

The graph below shows the total number of articles in caregiver burden and quality of life in chronic kidney disease systems across all publications each year (not limited to Nature Index journals).

Technical terms

Caregiver burden: The multidimensional strain—physical, psychological and social—experienced by individuals providing unpaid care to patients with chronic conditions.

Quality of life: A subjective measure encompassing an individual’s appraisal of their physical health, psychological state, social relationships and overall life satisfaction.

Chronic kidney disease (CKD): A progressive condition characterised by irreversible decline in kidney function over months or years.

Haemodialysis: A renal replacement therapy in which blood is filtered extracorporeally through a dialyser to remove toxins and excess fluid.

Health-promoting behaviours: Actions and lifestyle choices aimed at maintaining or improving physical and mental well-being, such as balanced nutrition, exercise and stress management techniques.

References

  1. Effect of teaching health-promoting behaviors on the care burden of family caregivers of hemodialysis patients: a four-group clinical trial. BMC Nursing (2023).
  2. Factors Associated with Burden in Caregivers of Patients with End-Stage Kidney Disease (A Systematic Review). Healthcare (2021).
  3. The relationship between care burden and quality of life in caregivers of hemodialysis patients. BMC Nephrology (2018).
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