Shin Jeong Eun, Lee Soon Min, Eun Ho Seon, Park Min Soo, Park Kook In, Namgung Ran
Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.
Korean J Pediatr. 2015 Nov;58(11):421-6. doi: 10.3345/kjp.2015.58.11.421. Epub 2015 Nov 22.
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.
万古霉素给药方案通常会根据患者的肾小球滤过率(GFR)进行调整。在本研究中,我们旨在评估血清胱抑素C(Cys-C)浓度相较于血清肌酐(SCr)浓度在预测新生儿万古霉素清除率(CLvcm)方面的实用性。
我们回顾性分析了50名入住新生儿重症监护病房并接受静脉注射万古霉素的足月儿的实验室数据,并评估了其药代动力学特征。分别使用施瓦茨公式和拉尔森公式估算基于肌酐的肌酐清除率(CLcr)和基于Cys-C的GFR(GFRcys-c)。
平均CLvcm(±标准差)为74.52±31.17L/小时,万古霉素的分布容积为0.67±0.14L,万古霉素半衰期为9.16±17.42小时。SCr为0.46±0.25mg/dL,血清Cys-C为1.43±0.34mg/L。万古霉素的峰浓度和谷浓度分别为24.65±14.84和8.10±5.35mcg/mL。基于血清肌酐浓度计算的GFR(GFR-Cr)和GFRcys-c分别为70.2±9.45和63.6±30.18mL/分钟。CLvcm与Cys-C倒数的相关常数(0.479,P = 0.001)显著高于CLvcm与SCr倒数的相关常数(0.286,P = 0.044)。GFRcys-c与CLvcm密切相关(P = 0.001),且相关常数显著高于CLvcm与CLcr的相关常数(0.496,P = 0.001)。线性回归分析表明只有GFRcys-c与CLvcm独立且呈正相关(F = 41.9,P < 0.001)。
使用血清Cys-C作为CLvcm的标志物可能有助于更可靠地预测血清万古霉素浓度,尤其是在新生儿中。