N. Krivoy et al., Pharmacokinetic analysis of amikacin twice and single daily dosage in immunocompromised pediatric patients, INFECTION, 26(6), 1998, pp. 396-398
Ten children received amikacin twice daily and 13 were treated using the si
ngle daily protocol, All had fever and neutropenia on admission, and receiv
ed a total daily dose of 20 mg/kg when included in the study, Individual ph
armacokinetic parameters were calculated using a one-compartment model for
two blood amikacin samples, The mean (+/- SD) of elimination half-life (h),
amikacin clearance (l/h/kg), volume of distribution (l/kg), peak concentra
tion (mu g/ml) and trough concentration (mu g/ml) were: 2.51 (0.74) and 2.8
5 (0.32) h; 0.26 (0.16) and 0.115 (0.02) l/h/kg; 0.74 (0.44) and 0.47 (0.11
) l/kg; 19.1 (12.3) and 42.6 (12.6) mu g/ml; 0.85 (0.74) and 0.18 (0.24) mu
g/ml with twice and single daily dosage schedules, respectively. A single
daily dose of amikacin had a significantly longer elimination half-life, lo
wer clearance, higher peak concentration and lower trough concentration in
comparison to the twice-daily schedule. The use of amikacin 20 mg/kg daily
delivered in a single daily dose is recommended for immunocompromised pedia
tric patients with fever and neutropenia, in spite of the measured pharmaco
kinetic differences.