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Variation in estimated glomerular filtration rate at dialysis initiation in children
Allison B Dart1, Michael Zappitelli2, Manish M Sood3
1Department of Pediatrics and Child Health, Section of Nephrology and Children's Hospital Research Institute of Manitoba, University of Manitoba, FE009-840 Sherbrook Street, Winnipeg, Manitoba, Canada, R3A 1S1. adart@hsc.mb.ca.
Insights
One-third of pediatric dialysis patients in Canada initiated treatment with a higher estimated glomerular filtration rate (eGFR), indicating variation in dialysis timing. Further research is needed to understand the clinical impact of these practices.
Area of Science:
- Pediatric Nephrology
- Renal Replacement Therapy
- Chronic Kidney Disease
Background:
- Limited data exists on the optimal timing for initiating dialysis in pediatric patients.
- Current practices and trends in dialysis initiation timing based on estimated glomerular filtration rate (eGFR) in Canadian children are not well-defined.
Purpose of the Study:
- To determine current practices and secular trends in the timing of dialysis initiation for children in Canada.
- To analyze dialysis initiation based on estimated glomerular filtration rate (eGFR) levels.
Main Methods:
- An observational study of incident chronic dialysis patients aged 21 years or younger in Canada (2001-2010).
- Patients were categorized into higher (eGFR ≥10.5 ml/min/1.73 m²) or lower (eGFR <10.5 ml/min/1.73 m²) eGFR groups using CKiD Schwartz eGFR.
- Examined differences by treatment facility and region, and analyzed secular trends.
Main Results:
- The median eGFR at dialysis initiation was 8.1 ml/min/1.73 m².
- 29% of pediatric patients started dialysis with an eGFR ≥10.5 ml/min/1.73 m².
- The proportion of children starting dialysis with a higher eGFR increased from 27.3% in 2001 to 35.4% in 2010 (p=0.04), with significant variation across treatment facilities (12-70%, p=0.0001).
- Female sex, genetic cause of end-stage kidney disease, and living ≥50 km from a treatment facility were associated with higher eGFR at initiation.
Conclusions:
- Approximately one-third of children initiated dialysis with an eGFR ≥10.5 ml/min/1.73 m².
- Significant practice variations exist regarding the timing of dialysis initiation among Canadian treatment facilities.
- More research is necessary to evaluate the clinical implications of this observed practice variation.
Background:
Data guiding the timing of dialysis initiation in children are limited. We sought to determine current practice and secular trends in Canada with respect to the timing of dialysis initiation in children based on estimated glomerular filtration rate (eGFR).
Methods:
This observational study included incident chronic dialysis patients aged ≤21 years identified from the Canadian Organ Replacement Register who started dialysis in Canada between January 2001 and December 2010 at any of the nine participating Canadian centers (n = 583). Youth were categorized utilizing CKiD Schwartz eGFR into ≥10.5 (higher) or <10.5 ml/min/1.73 m2 (lower) eGFR groups. Differences at dialysis initiation by facility and region were examined, and secular trends were determined.
Results:
Median eGFR at dialysis initiation was 8.1 (interquartile range 5.4-11.0) ml/min/1.73 m2. Overall, 29 % of the patients started dialysis with an eGFR of ≥10.5 ml/min/1.73 m2. The proportion of children starting with higher eGFR increased from 27.3 % in 2001 to 35.4 % in 2010 (p = 0.04) and differed by treatment facility (12-70 %; p = 0.0001). Factors associated with higher eGFR at dialysis initiation in the adjusted regression model were female sex [odds ratio (OR) 1.48; 95 % confidence interval (CI) 1.02-2.14], genetic cause of end-stage kidney disease (OR 2.77; 95 % CI 1.37-5.58) and living ≥50 km from treatment facility (OR 1.47; 95 % CI 1.01-2.14).
Conclusions:
One-third of the children were found to have initiated dialysis with an eGFR ≥10.5 ml/min/1.73 m2, however significant practice variation exists with respect to timing of dialysis initiation by treatment facility. More data is required to evaluate the clinical implications of this practice variation.
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