Author/Authors :
Abbasi Larki, Rozina Department of Internal Medicine - Yasuj University of Medical Sciences, Yasuj, Iran , Jamali, Bahareh Department of Internal Medicine - Yasuj University of Medical Sciences, Yasuj, Iran , Meidani, Mohsen Department of Infectious Diseases - Al‐Zahra Hospital - Isfahan University of Medical Sciences, Isfahan, Iran , Mousavi, Sarah Department of Clinical Pharmacy and Pharmacy Practice - Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
Objective: Recent studies have shown that serum cystatin C (Cys C) is a better
marker for measuring the glomerular filtration rate and may rise more quickly with
acute kidney injury (AKI). The purpose of this study was to evaluate the clinical
application of serum Cys C to predict colistin‐induced nephrotoxicity in comparison
with serum creatinine (SCr). Methods: Thirty‐two adult patients with no history of
acute or chronic kidney injury having been planned to receive intravenous colistin
for an anticipated duration of at least 1 week for any indication were recruited.
At baseline and 5 days after colistin treatment, serum Cys C as well as creatinine
levels were measured. The incidence of colistin‐induced acute renal failure was
defined according to the AKIN criteria for SCr. Rise in concentration of Cys C
by more than 10% from baseline considered as AKI. Findings: Colistin‐induced
nephrotoxicity (defined as SCr ≥0.3 mg/dl) occurred in 6 patients (18.8%). A Cys
C increase concentration ≥10% after 5 days of colistin treatment was detected
in 15 patients (46.9%). There was a poor agreement between the presence and
absence of any SCr-AKI and Cys C-AKI (κ = 0.28, P = 0.04). Conclusion: Serum
Cys C is a better marker of renal function in early stages of AKI and predictive of
persistent AKI on colistin treatment.
Keywords :
Colistin , cystatin C , nephrotoxicity , serum creatinine