Skip to main content
Top
Published in: Clinical Pharmacokinetics 10/2018

01-10-2018 | Review Article

Clinical Pharmacokinetics of Amikacin in Pediatric Patients: A Comprehensive Review of Population Pharmacokinetic Analyses

Authors: Sílvia M. Illamola, Catherine M. Sherwin, J. G. Coen van Hasselt

Published in: Clinical Pharmacokinetics | Issue 10/2018

Login to get access

Abstract

Amikacin plays a key role in the treatment of severe hospital-acquired infections with Gram-negative bacteria. Therapeutic use of amikacin is challenged by high inter-individual variability (IIV) combined with a narrow therapeutic spectrum. Pediatric patients represent a particularly fragile population where adequate dosing is crucial yet challenging to achieve due significant IIV associated with developmental processes and other factors. The current review provides an overview of parametric population pharmacokinetic analyses of amikacin in pediatric patients and associated patient-specific determinants of IIV. We searched PubMed for parametric population pharmacokinetic analyses of amikacin in pediatric patients. Information on patient population, study design, pharmacokinetic model characteristics, and identified patient-specific predictors of IIV was collected. Comparative analyses across studies were conducted to characterize quantitative differences reported for different studies and patient populations. Eight eligible publications were identified, of which six analyses involved neonates up to 3 months of age and two studies investigated older pediatric patients (age 2–17 years). Most commonly included covariates were current body weight for both clearance and volume of distribution, followed by age-related covariates on clearance in neonatal studies (four of six models). Quantitative comparisons of different models reported generally showed similar developmental effects in neonatal populations. The present review provides a comprehensive overview of parametric population pharmacokinetic studies for amikacin. Future studies could address the knowledge gap of patients between 3 months and 2 years of age. Furthermore, systematic studies of additional potential predictors for IIV (e.g., sepsis, inflammatory markers, renal function biomarkers) could be of relevance to address the significant IIV remaining after inclusion of the most commonly identified covariates.
Literature
1.
go back to reference Boehr DD, Draker KA, Wright GD. Aminoglycoside and aminocyclitols. In: Finch RG, Greenwood D, Norrby SR, Whitley RJ, editors. Antibiotic and chemotherapy: anti-infective agents and their use in therapy. New York: Churchill Livingstone; 2003. pp. 155–84. Boehr DD, Draker KA, Wright GD. Aminoglycoside and aminocyclitols. In: Finch RG, Greenwood D, Norrby SR, Whitley RJ, editors. Antibiotic and chemotherapy: anti-infective agents and their use in therapy. New York: Churchill Livingstone; 2003. pp. 155–84.
3.
go back to reference BMS. Amikacin. Summary of product characteristics. Princeton, NJ: BMS; 2014. BMS. Amikacin. Summary of product characteristics. Princeton, NJ: BMS; 2014.
8.
go back to reference Zaske D. Applied pharmacokinetics. Principles of therapeutic drug monitoring. 3rd ed. Vancouver: Applied Therapeutics; 1992. Zaske D. Applied pharmacokinetics. Principles of therapeutic drug monitoring. 3rd ed. Vancouver: Applied Therapeutics; 1992.
13.
go back to reference Wang J, Liang WQ, Wu JJ, Pan CM. Population pharmacokinetic analysis of amikacin and validation on neonates using Monte Carlo method. Acta Pharmacol Sin. 2000;21(10):954–60.PubMed Wang J, Liang WQ, Wu JJ, Pan CM. Population pharmacokinetic analysis of amikacin and validation on neonates using Monte Carlo method. Acta Pharmacol Sin. 2000;21(10):954–60.PubMed
14.
go back to reference Padovani EM, Pistolesi C, Fanos V, Messori A, Martini N. Pharmacokinetics of amikacin in neonates. Dev Pharmacol Therap. 1993;20(3–4):167–73.CrossRef Padovani EM, Pistolesi C, Fanos V, Messori A, Martini N. Pharmacokinetics of amikacin in neonates. Dev Pharmacol Therap. 1993;20(3–4):167–73.CrossRef
15.
go back to reference Golenz MR, Wilson WD, Carlson GP, Craychee TJ, Mihalyi JE, Knox L. Effect of route of administration and age on the pharmacokinetics of amikacin administered by the intravenous and intraosseous routes to 3-day-old and 5-day-old foals. Equine Vet J. 1994;26(5):367–73.CrossRefPubMed Golenz MR, Wilson WD, Carlson GP, Craychee TJ, Mihalyi JE, Knox L. Effect of route of administration and age on the pharmacokinetics of amikacin administered by the intravenous and intraosseous routes to 3-day-old and 5-day-old foals. Equine Vet J. 1994;26(5):367–73.CrossRefPubMed
16.
go back to reference Petersen PO, Wells TG, Kearns GL. Amikacin dosing in neonates - evaluation of a dosing chart based on population pharmacokinetic data. Dev Pharmacol Ther. 1991;16(4):203–11.PubMed Petersen PO, Wells TG, Kearns GL. Amikacin dosing in neonates - evaluation of a dosing chart based on population pharmacokinetic data. Dev Pharmacol Ther. 1991;16(4):203–11.PubMed
22.
go back to reference De Cock RFW, Allegaert K, Schreuder MF, Sherwin CMT, de Hoog M, van den Anker JN, et al. Maturation of the glomerular filtration rate in neonates, as reflected by amikacin clearance. Clin Pharmacokinet. 2012;51(2):105–17.CrossRefPubMed De Cock RFW, Allegaert K, Schreuder MF, Sherwin CMT, de Hoog M, van den Anker JN, et al. Maturation of the glomerular filtration rate in neonates, as reflected by amikacin clearance. Clin Pharmacokinet. 2012;51(2):105–17.CrossRefPubMed
24.
go back to reference Allegaert K, Scheers I, Cossey V, Anderson BJ. Covariates of amikacin clearance in neonates: the impact of postnatal age on predictability. Drug Metab Lett. 2008;2(4):286–9.CrossRefPubMed Allegaert K, Scheers I, Cossey V, Anderson BJ. Covariates of amikacin clearance in neonates: the impact of postnatal age on predictability. Drug Metab Lett. 2008;2(4):286–9.CrossRefPubMed
26.
go back to reference Karlsson MO, Sheiner LB. The importance of modeling interoccasion variability in population pharmacokinetic analyses. J Pharmacokinet Biopharm. 1993;21(6):735–50.CrossRefPubMed Karlsson MO, Sheiner LB. The importance of modeling interoccasion variability in population pharmacokinetic analyses. J Pharmacokinet Biopharm. 1993;21(6):735–50.CrossRefPubMed
29.
go back to reference Garraffo R, Drugeon HB, Dellamonica P, Bernard E, Lapalus P. Determination of optimal dosage regimen for amikacin in healthy-volunteers by study of pharmacokinetics and bactericidal activity. Antimicrob Agents Chemother. 1990;34(4):614–21.CrossRefPubMedPubMedCentral Garraffo R, Drugeon HB, Dellamonica P, Bernard E, Lapalus P. Determination of optimal dosage regimen for amikacin in healthy-volunteers by study of pharmacokinetics and bactericidal activity. Antimicrob Agents Chemother. 1990;34(4):614–21.CrossRefPubMedPubMedCentral
30.
33.
go back to reference Boucher BA, Kuhl DA, Hickerson WL. Pharmacokinetics of systemically administered antibiotics in patients with thermal-injury. Clin Infect Dis. 1992;14(2):458–63.CrossRefPubMed Boucher BA, Kuhl DA, Hickerson WL. Pharmacokinetics of systemically administered antibiotics in patients with thermal-injury. Clin Infect Dis. 1992;14(2):458–63.CrossRefPubMed
34.
go back to reference Jaehde L, Sorgel F. Clinical pharmacokinetics in patients with burns. Clin Pharmacokinet. 1995;29(1):15–28.CrossRefPubMed Jaehde L, Sorgel F. Clinical pharmacokinetics in patients with burns. Clin Pharmacokinet. 1995;29(1):15–28.CrossRefPubMed
Metadata
Title
Clinical Pharmacokinetics of Amikacin in Pediatric Patients: A Comprehensive Review of Population Pharmacokinetic Analyses
Authors
Sílvia M. Illamola
Catherine M. Sherwin
J. G. Coen van Hasselt
Publication date
01-10-2018
Publisher
Springer International Publishing
Published in
Clinical Pharmacokinetics / Issue 10/2018
Print ISSN: 0312-5963
Electronic ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-018-0641-x

Other articles of this Issue 10/2018

Clinical Pharmacokinetics 10/2018 Go to the issue