Intravenous voriconazole therapy in a preterm infant
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Updated: Aug 17, 2026

Intravenous Injections in Neonatal Mice
Published on: November 11, 2014
Kendre'a M Muldrew1, Holly D Maples, Cindy D Stowe
1Department of Pharmacy Practice, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Insights
A preterm infant with fluconazole-resistant Candida infection received voriconazole treatment. Higher doses achieved therapeutic serum concentrations, resolving the infection safely alongside phenobarbital.
Area of Science:
- Neonatal Medicine
- Infectious Diseases
- Pharmacology
Background:
- Disseminated fluconazole-resistant Candida albicans infections pose a significant challenge in preterm infants.
- Standard antifungal treatment regimens may require adjustments in neonates due to altered pharmacokinetics.
Observation:
- A preterm infant presented with a severe Candida albicans infection resistant to fluconazole.
- Initial treatment with liposomal amphotericin B was followed by combination therapy including intravenous voriconazole.
- Concomitant phenobarbital therapy was administered throughout the infant's hospitalization.
Findings:
- Initial high-dose intravenous voriconazole (6 mg/kg every 12 hours) resulted in sub-therapeutic serum concentrations in the infant.
- Increasing the voriconazole dosage to 6 mg/kg every 8 hours achieved therapeutic serum concentrations comparable to adult levels.
- The infection resolved following the dose escalation of voriconazole, and the regimen was safely tolerated with phenobarbital.
Implications:
- Optimized dosing of intravenous voriconazole is crucial for achieving therapeutic efficacy in preterm infants with invasive fungal infections.
- Pharmacokinetic considerations, including developmental changes in drug metabolism and excretion, must guide voriconazole dosing in neonates.
- This case highlights the successful use of adjusted-dose voriconazole in treating resistant fungal infections in a vulnerable preterm population.
Abstract:
A preterm infant younger than 3 months developed a disseminated fluconazole-resistant Candida albicans infection that was treated with liposomal amphotericin B for 52 days, followed by the combination of intravenous voriconazole and liposomal amphotericin B for an additional 19 days. The infant received concomitant phenobarbital throughout the hospital stay. The infection resolved after addition of voriconazole to the treatment regimen. Intravenous voriconazole was begun at a high dosage, 6 mg/kg every 12 hours, for anticipated developmental and drug-induced changes in volume of distribution and clearance. On day 4 of therapy, serum concentrations of voriconazole were 3.27 microg/ml immediately after infusion and 0.33 microg/ml 6 hours after infusion. These levels were significantly lower than those achieved in adult pharmacokinetic and safety studies. After the infant's dosage was increased to 6 mg/kg every 8 hours, serum concentrations were 5.33 microg/ml 30 minutes after infusion and 2.67 microg/ml 6 hours after infusion. These levels were similar to those observed in adults. Intravenous voriconazole 6 mg/kg every 8 hours was administered safely, with concomitant phenobarbital therapy, in this preterm infant with developmentally diminished renal function.
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