| Autor: |
Trenque, T., Simon, N., Villena, I., Chemla, C., Quereux, C., Leroux, B., Jaussaud, R., Rémy, G., Dupouy, D., Millart, H., Pinon, J.-M., Urien, S. |
| Předmět: |
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| Zdroj: |
British Journal of Clinical Pharmacology; Jun2004, Vol. 57 Issue 6, p735-741, 7p |
| Abstrakt: |
To develop a population pharmacokinetic model for pyrimethamine (PYR) and sulfadoxine (SDX) in children with congenital toxoplasmosis. Children were treated with PYR (1.25 mg kg−1) and SDX (25 mg kg−1) (Fansidar®) plus folinic acid (Lederfoline® 5 mg). Plasma concentrations, available from a therapeutic drug monitoring database, were determined by high-performance liquid chromatogrphy. Population pharmacokinetic analysis was performed using a nonlinear mixed effects model. Eighty-nine children, aged 1 week to 14 years and weighing 2.9–59 kg, were available for evaluation. Both PYR and SDX concentration-time profiles were best described by a one-compartment open model. Volume of plasma distribution ( V) and clearance (CL) were significantly related to body weight (BW) using an allometric function. Typical CL and V estimates (95% confidence interval), for a child weighing 11 kg were 5.50 (5.28, 5.73) l day−1 and 36 (33, 39) l for PYR and 0.26 (0.25, 0.27) l day−1 and 2.1 (1.9, 2.3) l for SDX. For BW between 3.5 and 60 kg, plasma half-lives were predicted to vary from 4.0 to 5.2 days for PYR, and from 5.0 to 7.5 days for SDX. This study indicated that body weight influences PYR and SDX pharmacokinetics in children. To optimize PYR/SDX combination treatment in congenital toxoplasmosis, short dosing intervals in very young low-wight children are probably appropriate. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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