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

PurposeThe 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 vancomyci...

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Main Authors: Jeong Eun Shin, Soon Min Lee, Ho Seon Eun, Min Soo Park, Kook In Park, Ran Namgung
Format: Article
Language:English
Published: Korean Pediatric Society 2015-11-01
Series:Korean Journal of Pediatrics
Subjects:
Online Access:http://kjp.or.kr/upload/pdf/kjped-58-421.pdf
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author Jeong Eun Shin
Soon Min Lee
Ho Seon Eun
Min Soo Park
Kook In Park
Ran Namgung
author_facet Jeong Eun Shin
Soon Min Lee
Ho Seon Eun
Min Soo Park
Kook In Park
Ran Namgung
author_sort Jeong Eun Shin
collection DOAJ
description PurposeThe 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.MethodsWe 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.ResultsThe 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).ConclusionThe use of serum Cys-C as a marker of CLvcm could be beneficial for more reliable predictions of serum vancomycin concentrations, particularly in neonates.
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spelling doaj.art-91bbf4022a3a41f688f8c3a8777471b52022-12-22T01:03:53ZengKorean Pediatric SocietyKorean Journal of Pediatrics1738-10612092-72582015-11-01581142142610.3345/kjp.2015.58.11.4212014600075Usefulness of serum cystatin C to determine the dose of vancomycin in neonateJeong Eun Shin0Soon Min Lee1Ho Seon Eun2Min Soo Park3Kook In Park4Ran Namgung5Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.PurposeThe 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.MethodsWe 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.ResultsThe 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).ConclusionThe use of serum Cys-C as a marker of CLvcm could be beneficial for more reliable predictions of serum vancomycin concentrations, particularly in neonates.http://kjp.or.kr/upload/pdf/kjped-58-421.pdfVancomycinCystatin CClearance
spellingShingle Jeong Eun Shin
Soon Min Lee
Ho Seon Eun
Min Soo Park
Kook In Park
Ran Namgung
Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
Korean Journal of Pediatrics
Vancomycin
Cystatin C
Clearance
title Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
title_full Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
title_fullStr Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
title_full_unstemmed Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
title_short Usefulness of serum cystatin C to determine the dose of vancomycin in neonate
title_sort usefulness of serum cystatin c to determine the dose of vancomycin in neonate
topic Vancomycin
Cystatin C
Clearance
url http://kjp.or.kr/upload/pdf/kjped-58-421.pdf
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