Quality of life in children with end-stage renal disease based on a PedsQL ESRD module

Ki-Soo Park1, Young Ju Hwang, Min Hyun Cho

  • 1Department of Preventive Medicine and Institute of Health Sciences, Gyeongsang National University Hospital, Jinju, Republic of Korea.

Insights

Children with end-stage renal disease (ESRD) report better quality of life after kidney transplantation compared to dialysis. Self-reports indicate higher quality of life than parent proxy reports for children with ESRD.

Area of Science:

  • Pediatric Nephrology
  • Quality of Life Research
  • Chronic Kidney Disease

Background:

  • Health-related quality of life (HRQOL) is crucial for pediatric patients with end-stage renal disease (ESRD) and their families.
  • ESRD significantly impacts the daily lives and well-being of affected children.

Purpose of the Study:

  • To investigate and compare HRQOL in children with ESRD undergoing different renal replacement therapies.
  • To evaluate the utility of the PedsQL 3.0 ESRD module for assessing HRQOL in this population.

Main Methods:

  • A cross-sectional study involving 92 children (aged 2-18) with ESRD from four Korean university hospitals.
  • Utilized the 34-item Pediatric Quality of Life Inventory 3.0 End-Stage Renal Disease (PedsQL 3.0 ESRD) module for assessment.
  • Compared HRQOL scores between children on dialysis (hemodialysis and peritoneal dialysis) and those who received renal transplantation.

Main Results:

  • Renal transplant recipients reported better HRQOL than dialysis patients in specific domains, including 'About my kidney disease' and 'Worry' (parent proxy), and 'Treatment problems' (child self-report).
  • Children on peritoneal dialysis (PD) reported significantly higher quality of life than those on hemodialysis (HD).
  • Children's self-reports generally indicated higher HRQOL than parent proxy reports, particularly in domains like 'General fatigue,' 'Family & peer interaction,' and 'Worry.'

Conclusions:

  • The PedsQL 3.0 ESRD module demonstrates potential as a valuable, disease-specific tool for evaluating HRQOL in pediatric ESRD patients.
  • Further research with larger sample sizes and longitudinal designs is recommended to confirm these findings and understand long-term HRQOL trajectories.
Abstract

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