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Saudi Journal of Kidney Diseases and Transplantation
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ORIGINAL ARTICLE Table of Contents   
Year : 2012  |  Volume : 23  |  Issue : 3  |  Page : 453-460
Comparison of equations to estimate the glomerular filtration rate in post-renal transplant chronic kidney disease patients


1 National Liver Institute, Menoufiya University, Egypt
2 Nephrology Unit, Department of Medicine, Menoufiya University Hospital, Menoufiya University, Egypt
3 Saskatchewan Transplant Program, St. Paul's Hospital, Saskatoon, Canada

Correspondence Address:
Ahmed Shoker
Director of Transplant Program, Department of Medicine, Division of Nephrology, University of Saskatchewan, 103 Hospital Drive, Saskatoon, SK S7N 0W8
Canada
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We determined the performance of estimated glomerular filtration rate equations (eGFR) including MDRD2-Isotope Dilution Mass Spectrometry (MDRD2-IDMS), Cockcroft-Gault (CG) and Virga to measure post-transplant chronic kidney disease (CKD) stages 1-4, using simultaneous isotope GFR (iGFR) measurement. The study was conducted in 97 patients. The eGFR results measured by CG and Virga were normalized to 1.73 m 2 . Analysis of relative and absolute bias, error, scatter, correlation coefficient of variance and accuracy within the 30% range from the reference iGFR result was performed using standard techniques. There were 135, 242, 314 and 82 scans, respectively, in CKD stages 1-4. Bias and accuracy of GFR estimators varied significantly across the CKD stages. In stages 1 and 2, CG had the best error of -12.7 and 0.2 mL/min/1.73 m 2 , respectively, while Virga had the highest accuracy of 74.3% and 85.5, respectively. In stages 3 and 4, MDRD2-IDMS had the best error of -0.52 and 5.8, respectively. Accuracy was the best at 75.1% for Virga in stage 3, while it was the highest of 70.7% for MDRD2-IDMS in stage 4. Virga had the highest accuracy of 75.2% in stage 4. The worst bias was for MDRD2-IDMS in stage 2 (-36.8 mL/min/1.73 m 2 ) and the best bias was for CG in stage 2 (-0.33 mL/min/1.73 m 2 ). The eGFR estimators have inconsistent performances in the various stages of CKD and, thus, another limitation is added to their validity to substitute for the gold standard methods.


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