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PEDIATRICS |
From the Department of Rheumatology, Hospital General de Mexico, Mexico (Dr. Burgos-Vargas); the Pediatric Rheumatology Clinic, Allgemeines Krankenhaus Eilbek, Hamburg, Germany (Dr. Foeldvari); the Department of Pediatric Rheumatology, University Children Hospital, Hannover, Germany (Dr. Thon); and the Department of Clinical Research, Boehringer Ingelheim Pharma KG (Dr. Linke) and the Department of Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharma KG, Biberach, Germany (Dr. Tuerck).
The pharmacokinetics of a meloxicam suspension were studied in 18 children with juvenile rheumatoid arthritis. Children received a single 0.25-mg/kg dose up to a maximum of 15 mg. Pharmacokinetic parameters after the first dose were calculated by noncompartmental methods. Geometric mean (percent coefficient of variation for geometric mean [gCV]) Cmax, AUC0-
, apparent clearance, apparent volume of distribution, and elimination half-life values were 1.24 µg/mL (47% gCV), 25.6 µgh/mL (81% gCV), 0.17 mL/min/kg (83% gCV), 0.19 L/kg (63% gCV), and 13.4 hours (54% gCV) in the younger group and 1.89 µg/mL (25% gCV), 35.8 µgh/mL (21% gCV), 0.12 mL/min/kg (23% gCV), 0.13 L/kg (22% gCV), and 12.7 hours (21% gCV) for the older group, respectively. Area under the curve, volume of distribution, and clearance tended to be higher in the younger group, whereas elimination half-lives were similar. A post hoc comparison to pharmacokinetic data in adults revealed no relevant differences. Thus, a common body weight-normalized dose is considered appropriate for children older than 2 years.
Key Words: Meloxicam pediatrics pharmacokinetics juvenile rheumatoid arthritis (JRA)
Address for reprints: Dr. Dietrich Tuerck, Boehringer Ingelheim Pharma KG, Department of Drug Metabolism and Pharmacokinetics, Birkendorfer Strasse 65, 88397 Biberach an der Riss, Germany.
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