Usefulness of serum cystatin C to determine the dose of vancomycin in neonate

• Published in: Clinical and experimental pediatrics Vol. 58; no. 11; pp. 421 - 426
• Main Authors: Shin, Jeong Eun, Lee, Soon Min, Eun, Ho Seon, Park, Min Soo, Park, Kook In, Namgung, Ran
• Format: Journal Article
• Language: English
• Published: Korea (South) Clinical and Experimental Pediatics / Korean Pediatric Society 01.11.2015; The Korean Pediatric Society; Korean Pediatric Society; 대한소아청소년과학회
• Subjects: Antibiotics; Birth weight; Clearance; Creatinine; Cystatin C; Drug dosages; Laboratories; Original; Pharmacokinetics; Regression analysis; Staphylococcus infections; Vancomycin; 소아과학; United States > US; Japan; Cystatin C; Clearance; Vancomycin
• ISSN: 1738-1061; 2092-7258; 2713-4148
• DOI: 10.3345/kjp.2015.58.11.421

The vancomycin dosage regimen is regularly modified according to the patient's glomerular filtration rate (GFR). In the present study, we aimed to assess the usefulness of serum cystatin C (Cys-C) concentration, compared with serum creatinine (SCr) concentration, for predicting vancomycin clearance (CLvcm) in neonates. We retrospectively analyzed the laboratory data of 50 term neonates who were admitted to the neonatal intensive care unit and received intravenous vancomycin, and assessed the pharmacokinetic profiles. Creatinine clearance (CLcr) and GFR based on Cys-C (GFRcys-c) were estimated using the Schwartz and Larsson formulas, respectively. The mean CLvcm (±standard deviation) was 74.52±31.17 L/hr, the volume of distribution of vancomycin was 0.67±0.14 L, and vancomycin half-life was 9.16±17.42 hours. The SCr was 0.46±0.25 mg/dL and serum Cys-C was 1.43±0.34 mg/L. The peak and trough concentrations of vancomycin were 24.65±14.84 and 8.10±5.35 mcg/mL, respectively. The calculated GFR based on serum creatinine concentration (GFR-Cr) and GFRcys-c were 70.2±9.45 and 63.6±30.18 mL/min, respectively. The correlation constant for CLvcm and the reciprocal of Cys-C (0.479, P=0.001) was significantly higher than that for CLvcm and the reciprocal of SCr (0.286, P=0.044). GFRcys-c was strongly correlated with CLvcm (P=0.001), and the correlation constant was significantly higher than that for CLvcm and CLcr (0.496, P=0.001). Linear regression analysis showed that only GFRcys-c was independently and positively correlated with CLvcm (F=41.9, P<0.001). The use of serum Cys-C as a marker of CLvcm could be beneficial for more reliable predictions of serum vancomycin concentrations, particularly in neonates.