External evaluation of population pharmacokinetic models of vancomycin in neonates: the transferability of published models to different clinical settings. (15th March 2013)

• Record Type: Journal Article
• Authors: Zhao, Wei; Kaguelidou, Florentia; Biran, Valérie; Zhang, Daolun; Allegaert, Karel; Capparelli, Edmund V.; Holford, Nick; Kimura, Toshimi; Lo, Yoke‐Lin; Peris, José‐Esteban; Thomson, Alison; van den, John N.; Fakhoury, May; Jacqz‐Aigrain, Evelyne
• Is Part Of: British journal of clinical pharmacology. Volume 75:Number 4(2013:Apr.)
• Page Start: 1068
• Page End: 1080
• Publication Date: 2013-03-15
• Subjects: Pharmacology -- Periodicals; Drugs -- Periodicals; 615.1
• DOI: 10.1111/j.1365-2125.2012.04406.x
• Languages: English
• ISSNs: 0306-5251

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bcp4406-sec-0001" sec-type="section"> <title>Aims</title> <p>Vancomycin is one of the most evaluated antibiotics in neonates using modeling and simulation approaches. However no clear consensus on optimal dosing has been achieved. The objective of the present study was to perform an external evaluation of published models, in order to test their predictive performances in an independent dataset and to identify the possible study‐related factors influencing the transferability of pharmacokinetic models to different clinical settings.</p> </sec> <sec id="bcp4406-sec-0002" sec-type="section"> <title>Method</title> <p>Published neonatal vancomycin pharmacokinetic models were screened from the literature. The predictive performance of six models was evaluated using an independent dataset (112 concentrations from 78 neonates). The evaluation procedures used simulation‐based diagnostics [visual predictive check (VPC) and normalized prediction distribution errors (NPDE)].</p> </sec> <sec id="bcp4406-sec-0003" sec-type="section"> <title>Results</title> <p>Differences in predictive performances of models for vancomycin pharmacokinetics in neonates were found. The mean of NPDE for six evaluated models were 1.35, −0.22, −0.36, 0.24, 0.66 and 0.48, respectively. These differences were explained, at least partly, by taking into account the method used to measure serum creatinine concentrations. The adult conversion factor of 1.3 (enzymatic to Jaffé) was tested with an improvement in the VPC and NPDE, but it still needs to be evaluated and validated in neonates. Differences were also identified between analytical methods for vancomycin.</p> </sec> <sec id="bcp4406-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The importance of analytical techniques for serum creatinine concentrations and vancomycin as predictors of vancomycin concentrations in neonates have been confirmed. Dosage individualization of vancomycin in neonates should consider not only patients' characteristics and clinical conditions, but also the methods used to measure serum creatinine and vancomycin.</p> </sec> </abstract>