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Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
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Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
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Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery

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Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery
Journal Article

Using Serum Cystatin C to Predict Acute Kidney Injury Following Infant Cardiac Surgery

2023
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Overview
Acute kidney injury (AKI) following cardiopulmonary bypass (CPB) is associated with increased morbidity and mortality. Serum Cystatin C (CysC) is a novel biomarker synthesized by all nucleated cells that may act as an early indicator of AKI following infant CPB. Prospective observational study of infants (< 1 year) requiring CPB during cardiac surgery. CysC was measured at baseline and 12, 24, 48, and 72 h following CPB initiation. Each post-op percent difference in CysC (e.g. %CysC 12h ) from baseline was calculated. Clinical variables along with urine output (UOP) and serum creatinine (SCr) were followed. Subjects were divided into two groups: AKI and non-AKI based upon the Kidney Disease Improving Global Outcomes (KDIGO) classification. AKI occurred in 41.9% (18) of the 43 infants enrolled. Patient demographics and baseline CysC levels were similar between groups. CysC levels were 0.97 ± 0.28 mg/L over the study period, and directly correlated with SCr ( R  = 0.71, p  < 0.0001). Although absolute CysC levels were not significant between groups, the %CysC 12h was significantly greater in the AKI group (AKI: − 16% ± 22% vs. Non-AKI − 28% ± 9% mg/L; p  = 0.003). However, multivariate analysis demonstrated that a lower UOP (Odds Ratio:0.298; 95% CI 0.073, 0.850; p  = 0.02) but not %CysC 12h was independently associated with AKI. Despite a significant difference in the %CysC 12h , only UOP was independently associated with AKI. Larger studies of a more homogenous population are needed to understand these results and to explore the variability in this biomarker seen across institutions.