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Antimicrobial Agents and Chemotherapy, January 2001, p. 150-157, Vol. 45, No. 1
Pharmacie and Centre de Recherche en
Pathologie Infectieuse et Tropicale, Hopital Avicenne, Bobigny
93009,1 Service de Pharmacologie,
Centre René Huguenin, Saint
Cloud,2 Glaxo-Wellcome,
Marly-le-Roi,3 and
Néonatalogie, Hôpital Robert Debré,
Paris,4 France
Received 18 November 1999/Returned for modification 4 July
2000/Accepted 26 September 2000
Acyclovir is approved for the treatment of herpes simplex virus
(HSV) and varicella-zoster virus (VZV) infections in children by the
intravenous and oral routes. However, its use by the oral route in
children younger than 2 years of age is limited due to a lack of
pharmacokinetic data. The objectives of the present study were to
determine the typical pharmacokinetics of an oral suspension of
acyclovir given to children younger than 2 years of age and the
interindividual variabilities in the values of the pharmacokinetic
parameters in order to support the proposed dosing regimen (24 mg/kg of
body weight three times a day for patients younger than 1 month of
age or four times a day otherwise). Children younger than age 2 years
with HSV or VZV infections were enrolled in a multicenter study.
Children were treated for at least 5 days with an acyclovir oral
suspension. Plasma samples were obtained at steady state, before
acyclovir administration, and at 2, 3, 5, and 8 h after acyclovir
administration. Acyclovir concentrations were measured by
radioimmunoassay. The data were analyzed by a population approach. Data
for 79 children were considered in the pharmacokinetic study (212 samples, 1 to 5 samples per patient). Acyclovir clearance was related
to the estimated glomerular filtration rate, body surface area, and
serum creatinine level. The volume of distribution was related to body
weight. The elimination half-life decreased sharply during the first
month after birth, from 10 to 15 h to 2.5 h. Bioavailability
was 0.12. The interindividual variability was less pronounced when the
parameters were normalized with respect to body weight. Hence, dosage
adjustment by body weight is recommended for this population.
Simulations showed that the length of time that acyclovir remains above
the 50% inhibitory concentration during a 24-h period was more than
12 h for HSV but not for VZV. The proposed dosing regimen seems
adequate for the treatment of HSV infections, while for the treatment
of VZV infections, a twofold increase in the dose seems necessary for children older than age 3 months.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.1.150-157.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Pharmacokinetics of Oral Acyclovir in Neonates and
in Infants: a Population Analysis
*
Corresponding author. Mailing address: Pharmacie,
Hôpital Avicenne, 125 route de Stalingrad, 93009 Bobigny, France.
Phone: 33 1 48 95 56 61. Fax: 33 1 48 95 56 59. E-mail:
michel.tod{at}avc.ap-hop-paris.fr.
The Acyclovir Pediatric French Group consists of Y. Aujard, C. Bouille, J. P. Carrière, G. Cheron, J. P. Dommergues, D. Floret, P. François, D. Gendrel, F. Guillot, H. Haas, P. Labrune, J. B. Lobut, E. Mallet, A. Mouzard, M. Odièvre, C. Olivier, P. Reinert, and F. de la Rocque.
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