0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessObjective Our objective was to characterize the pharmacokinetic properties of sulfadoxine-pyrimethamine in African adults and children with acute falciparum malaria. Despite decades of widespread use, there are few data to inform dose recommendations. Methods In a prospective multicenter pharmacokinetic study in 307 patients with acute falciparum malaria, capillary blood concentrations of sulfadoxine and pyrimethamine were determined at 9 visits over a period of 42 days by mass spectrometry. Results After adjustment for dose, the area under the concentration-time curves (AUCs) of sulfadoxine and pyrimethamine in children aged 2 to 5 years were half of those in adults (median AUC, 410 μg/mL · d [interquartile range (IQR), 126-705 μg/mL · d] versus 816 μg/mL · d [IQR, 536-1150 μg/mL · d] [P = .0001] for sulfadoxine and 620 ng/mL · d [IQR, 229-1399 ng/mL · d] versus 1518 ng/mL · d [IQR, 1117-2013 ng/mL · d] for pyrimethamine). The effect of age on the AUC of sulfadoxine and pyrimethamine reflected higher clearance rates and larger apparent volumes of distribution in children aged 2 to 5 years when compared with adults (median clearance, 64.5 mL · kg−1 · d−1 [IQR, 46.2-132.6 mL · kg−1 · d−1] versus 32.7 mL · kg−1 · d−1 [IQR, 22.3-52.2 mL · kg−1 · d−1] for sulfadoxine [P = .0001] and 1.77 L · kg−1 · d−1 [IQR, 1.0-3.0 L · kg−1 · d−1] versus 0.85 L · kg−1 · d−1 [IQR, 0.62-1.21 L · kg−1 · d−1] for pyrimethamine [P = .0001]; median volume of distribution, 413 mL/kg [IQR, 299-711 mL/kg] versus 372 mL/kg [IQR, 267-488 mL/kg] for sulfadoxine [P = .0021] and 6.28 L/kg [IQR, 3.83-11.24 L/kg] versus 3.83 L/kg [IQR, 2.73-5.11 L/kg] for pyrimethamine [P = .0001]). Day 7 concentrations of both sulfadoxine and pyrimethamine provided good surrogate measures (R2 ≥ 0.72) of their respective AUCs. Conclusions Pharmacokinetic factors may contribute to the increased risk of sulfadoxine-pyrimethamine antimalarial treatment failure in young children. The current dose recommendations need revision. We predict that children aged 2 to 5 years should be treated with 1 g sulfadoxine/50 mg pyrimethamine to achieve drug concentrations equivalent to those in adults. Clinical Pharmacology & Therapeutics (2006) 80, 582–596; doi: 10.1016/j.clpt.2006.08.016
Karen I. Barnes, Francesca Little, Peter G. Smith, Allan M. Evans, W.M. Watkins, Sir Nicholas White (2006). Sulfadoxine-pyrimethamine pharmacokinetics in malaria: Pediatric dosing implications. Clinical Pharmacology & Therapeutics, 80(6), pp. 582-596, DOI: 10.1016/j.clpt.2006.08.016.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2006
Authors
6
Datasets
0
Total Files
0
Language
English
Journal
Clinical Pharmacology & Therapeutics
DOI
10.1016/j.clpt.2006.08.016
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access