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Alternatives for the Bedside Schwartz Equation to Estimate Glomerular Filtration Rate in Children
Hans Pottel1, Laurence Dubourg1, Karolien Goffin1
1Department of Public Health and Primary Care, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium; Exploration Fonctionnelle Rénale, Groupement Hospitalier Edouard Herriot, Hospices Civils de Lyon, Lyon, France; Department of Nuclear Medicine & Molecular Imaging, University Hospital Leuven, Leuven, Belgium; and Nephrology-Dialysis-Transplantation, University of Liège, CHU Sart Tilman, Liège, Belgium.
Insights
The Schwartz equation is not optimal for estimating glomerular filtration rate (GFR) in most children. Alternative equations, like the Full Age Spectrum (FAS), offer better accuracy, especially when combining biomarkers for pediatric kidney function assessment.
Area of Science:
- Pediatric Nephrology
- Clinical Chemistry
- Biomarker Research
Background:
- The Schwartz equation is the standard for estimating glomerular filtration rate (GFR) in children.
- This equation is less accurate for children with GFR >75 mL/min/1.73 m² and requires height, hindering automated reporting.
- Most children, including those in nephrology clinics, have higher GFRs, necessitating alternative estimation methods.
Purpose of the Study:
- To evaluate alternative equations for estimating GFR in children beyond the limitations of the Schwartz equation.
- To explore the utility of the Full Age Spectrum (FAS) equation as a height-independent alternative.
- To assess the impact of combining standardized biomarkers on eGFR prediction performance.
Main Methods:
- Comparison of the Schwartz equation with alternative pediatric eGFR equations, including the FAS equation.
- Evaluation of the FAS equation with and without height as a variable.
- Analysis of prediction performance (P10, P30) using combined biomarkers (serum creatinine, cystatin C) with height.
Main Results:
- The Schwartz equation is suboptimal for children with GFR >75 mL/min/1.73 m².
- The FAS equation provides a height-independent alternative for automated eGFR reporting.
- Combining serum creatinine, serum cystatin C, and height in complex equations yields the highest accuracy and precision for eGFR estimation.
Conclusions:
- Simpler alternatives to the Schwartz equation exist for pediatric eGFR estimation.
- More complex equations incorporating serum creatinine, cystatin C, and height offer superior accuracy for pediatric eGFR.
- The limitations of the Schwartz equation highlight the need for advanced eGFR estimation methods in pediatric care.
Abstract:
The bedside Schwartz equation has long been and still is the recommended equation to estimate glomerular filtration rate (GFR) in children. However, this equation is probably best suited to estimate GFR in children with chronic kidney disease (reduced GFR) but is not optimal for children with GFR >75 mL/min/1.73 m2. Moreover, the Schwartz equation requires the height of the child, information that is usually not available in the clinical laboratory. This makes automatic reporting of estimated glomerular filtration rate (eGFR) along with serum creatinine impossible. As the majority of children (even children referred to nephrology clinics) have GFR >75 mL/min/1.73 m2, it might be interesting to evaluate possible alternatives to the bedside Schwartz equation. The pediatric form of the Full Age Spectrum (FAS) equation offers an alternative to Schwartz, allowing automatic reporting of eGFR since height is not necessary. However, when height is involved in the FAS equation, the equation is essentially equal to the Schwartz equation for children, but there are large differences for adolescents. Combining standardized biomarkers increases the prediction performance of eGFR equations for children, reaching P10 ≈ 45% and P30 ≈ 90%. There are currently good and simple alternatives to the bedside Schwartz equation, but the more complex equations combining serum creatinine, serum cystatin C, and height show the highest accuracy and precision.
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