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Predictive performance of glomerular filtration rate equations based on cystatin C, creatinine and their combination in critically ill patients
  1. Marta Albanell-Fernández1,
  2. Carla Bastida1,
  3. Ángel Marcos Fendian1,
  4. Jordi Mercadal2,
  5. Pedro Castro-Rebollo3,4,
  6. Dolors Soy-Muner4,5,6
  1. 1Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain
  2. 2Anesthesiology Department, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain
  3. 3Medical Intensive Care Unit, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain
  4. 4August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain
  5. 5Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Spain
  6. 6Department of Pharmacology, Toxicology and Therapeutic Chemistry. School of Pharmacy and Food Science, Universitat de Barcelona, Barcelona, Catalunya, Spain
  1. Correspondence to Dr Carla Bastida, Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain; cbastida{at}clinic.cat

Abstract

Objective 24-hour urine creatinine clearance (ClCr 24 hours) remains the gold standard for estimating glomerular filtration rate (GFR) in critically ill patients; however, simpler methods are commonly used in clinical practice. Serum creatinine (SCr) is the most frequently used biomarker to estimate GFR; and cystatin C, another biomarker, has been shown to reflect GFR changes earlier than SCr. We assess the performance of equations based on SCr, cystatin C and their combination (SCr-Cyst C) for estimating GFR in critically ill patients.

Methods Observational unicentric study in a tertiary care hospital. Patients with cystatin C, SCr and ClCr 24 hours measurements in ±2 days admitted to an intensive care unit were included. ClCr 24 hours was considered the reference method. GFR was estimated using SCr-based equations: Chronic Kidney Disease Epidemiology Collaboration based on creatinine (CKD-EPI-Cr) and Cockcroft-Gault (CG); cystatin C-based equations: CKD-EPI-CystC and CAPA; and Cr-CystC-based equations: CKD-EPI-Cr-CystC. Performance of each equation was assessed by calculating bias and precision, and Bland-Altman plots were built. Further analysis was performed with stratified data into CrCl 24 hours <60, 60–130 and ≥130 mL/min/1.73 m2.

Results We included 275 measurements, corresponding to 186 patients. In the overall population, the CKD-EPI-Cr equation showed the lowest bias (2.6) and best precision (33.1). In patients with CrCl 24 hours <60 mL/min/1.73 m2, cystatin-C-based equations showed the lowest bias (<3.0) and CKD-EPI-Cr-CystC was the most accurate (13.6). In the subgroup of 60≤ CrCl 24 hours <130mL/min/1.73 m2, CKD-EPI-Cr-CystC was the most precise (20.9). However, in patients with CrCl 24 hours ≥130mL/min/1.73 m2, cystatin C-based equations underestimated GFR, while CG overestimated it (22.7).

Conclusions Our study showed no evidence of superiority of any equation over the others for all evaluated parameters: bias, precision and Lin’s concordance correlation coefficient. Cystatin C-based equations were less biased in individuals with impaired renal function (GFR <60 mL/min/1.73 m2). CKD-EPI-Cr-CystC performed properly in patients with GFR from 60–130 mL/min/1.73 m2 and none of them were accurate enough in patients ≥130 mL/min/1.73 m2.

  • Critical Care
  • PHARMACY SERVICE, HOSPITAL
  • Kidney Failure, Chronic
  • RESEARCH DESIGN
  • STATISTICS

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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