Predictive performance of glomerular filtration rate equations based on cystatin C, creatinine and their combination in critically ill patients.

Marta Albanell-Fern��ndez, Carla Bastida, ��ngel Marcos Fendian, Jordi Mercadal, Pedro Castro-Rebollo, Dolors Soy-Muner
Author Information
  1. Marta Albanell-Fern��ndez: Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain. ORCID
  2. Carla Bastida: Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain cbastida@clinic.cat. ORCID
  3. ��ngel Marcos Fendian: Pharmacy Service, Division of Medicines, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain.
  4. Jordi Mercadal: Anesthesiology Department, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain.
  5. Pedro Castro-Rebollo: Medical Intensive Care Unit, Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain.
  6. Dolors Soy-Muner: August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Hospital Clinic de Barcelona, Barcelona, Catalunya, Spain.

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���m.
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���m, 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���m, CKD-EPI-Cr-CystC was the most precise (20.9). However, in patients with CrCl 24 hours ���130mL/min/1.73���m, 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���m). CKD-EPI-Cr-CystC performed properly in patients with GFR from 60-130���mL/min/1.73���m and none of them were accurate enough in patients ���130���mL/min/1.73���m.

Keywords

MeSH Term

Humans
Cystatin C
Glomerular Filtration Rate
Creatinine
Critical Illness
Male
Female
Middle Aged
Aged
Biomarkers
Predictive Value of Tests
Aged, 80 and over
Kidney Function Tests

Chemicals

Cystatin C
Creatinine
Biomarkers

Word Cloud

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