Comparison of Cystatin C-Based and Serum Creatinine-Based Renal Function Estimates Against Timed Urine Collection in

Sung Jin Jeong1, Andrew J Webb1, Kristy M Phillips2

  • 1Massachusetts General Hospital, Boston, MA, USA.

Hospital Pharmacy
|June 1, 2026
PubMed

Insights

The cystatin C-based eGFRcr-cys calculation showed less bias than the Cockcroft-Gault equation for estimating renal function in critically ill patients. Further research is needed to understand its clinical implications.

Area of Science:

  • Nephrology
  • Critical Care Medicine
  • Clinical Chemistry

Background:

  • Creatinine-based equations for estimating renal function, like Cockcroft-Gault (CG-CrCL), can be inaccurate in critically ill patients.
  • Accurate renal function assessment is crucial for medication dosing and patient management in intensive care units (ICUs).

Purpose of the Study:

  • To compare the accuracy of a cystatin C-based estimated glomerular filtration rate (eGFRcr-cys) calculation against measured creatinine clearance (mCrCL).
  • To evaluate if eGFRcr-cys offers improved renal function estimation compared to CG-CrCL in critically ill adult patients.

Main Methods:

  • A retrospective cohort study included 45 adult ICU patients with concurrent creatinine and cystatin C measurements within 24 hours of timed urine collection.
  • Measured creatinine clearance (mCrCL) from timed urine collection served as the reference standard.
  • Bias was calculated as the mean difference between estimated glomerular filtration rates (eGFRcr-cys and CG-CrCL) and mCrCL, with eGFR adjusted for body surface area (BSA).

Main Results:

  • The mean bias between CG-CrCL and mCrCL was 23.8 mL/min.
  • The mean bias between eGFRcr-cys and mCrCL was 3.3 mL/min.
  • The difference in bias between the two methods was statistically significant (20.5 mL/min, P=.001), favoring eGFRcr-cys.

Conclusions:

  • The cystatin C-based eGFRcr-cys calculation demonstrated significantly less bias than the CG-CrCL equation in estimating renal clearance in critically ill patients.
  • Further investigation is warranted to explore the clinical utility of eGFRcr-cys over CG-CrCL, especially for medication-related decisions in this patient population.
Abstract

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