Population Pharmacokinetic Characteristics of Amikacinin Suspected Cases of Neonatal Sepsisina Low-Resource African Setting: A Prospective Nonrandomized Single-SiteStudy

Abstract

Background: Amikacin exhibits marked pharmacokinetic (PK) variability and is commonly used in Combination with other drugs in the treatment of neonatal sepsis. There is a paucity of amikacin PK Information in neonates from low-resource settings. Objectives: To determine the PK parameters of amikacin, and explore the influence of selected covariates, including coadministration with aminophylline, on amikacin disposition in neonates of African origin. Methods: Neonates with suspected sepsis admitted to an intensive care unit in Accra, Ghana, and treated with amikacin (15mg/kg loading followed by 7.5mg/kg every 12 hours), were recruited. Serum amikacin Concentration was measured at specified times after treatment initiation and analysed using a population PK modelling approach. Results: A total of 419 serum concentrations were available for 247 neonates. Mean (SD) trough amikacin concentration (from samples collected 30 minutes before the fourth dose) among term (n ¼ 25), and preterm (< 37weeks’ gestation n ¼ 36) neonates were 6.2 (3.4) and 9.2 (5.7) mg/mL, respectively (P ¼ 0.02). A 1-compartment model best fitted amikacin disposition, and birth weight was the most important predictor of amikacin clearance (CL) and distribution (V). The population CL and V of amikacin were related as CL (L/h) ¼ 0.153 (birthweight/2.5) 1.31, V(L) ¼ 2.94 (birthweight/2.5)1.18. There was a high between-subject variability (58.9% and 50.7% ) in CL and V, respectively. CL and V were 0.058L/h/kg and 1.15L/kg, respectively, for a mean birth weight of 2.1kg, and the mean half-life (based on 1-compartmentmodel), was 13.7hours. Conclusions: The V and half-life of amikacin in this cohort varied from that reported in non-African populations, and the high trough and low peak amikacin concentrations in both term and preterm neonates suggest strategies to optimize amikacin dosing are required in this population.

Description

Article

Keywords

aminoglycoside, clearance, distribution, sepsis

Citation

Endorsement

Review

Supplemented By

Referenced By