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An Optimized Voriconazole Dosing Strategy to Achieve Therapeutic Serum Concentrations in Children Younger than 2
Tracy N Zembles1, Nathan E Thompson2, Peter L Havens3
1Department of Pharmacy, Children's Hospital and Health System, Milwaukee, Wisconsin. tzembles@chw.org.
Insights
Higher initial doses and more frequent administration of voriconazole are recommended for children under two years. Intensive therapeutic drug monitoring (TDM) is crucial for optimizing voriconazole dosing in this young population.
Area of Science:
- Pediatric Pharmacology
- Infectious Diseases
- Clinical Pharmacy
Background:
- Voriconazole is an important antifungal medication.
- Dosing in young children (<2 years) requires careful consideration due to pharmacokinetic differences.
- Optimizing voriconazole therapy in this age group necessitates therapeutic drug monitoring (TDM).
Observation:
- A case series involving three pediatric patients under two years old receiving voriconazole.
- An optimized dosing strategy incorporating intensive TDM was implemented.
- Initial voriconazole doses (9 mg/kg IV q12h or 9 mg/kg enteral BID) were often insufficient.
Findings:
- Multiple dose escalations and more frequent dosing were required to achieve target voriconazole trough concentrations (2-6 μg/ml).
- Final adjusted dosages varied significantly, including 12 mg/kg IV q8h and enteral doses up to 17.7 mg/kg TID.
- No visual, neurologic, or hepatic toxicities were observed during treatment.
Implications:
- Higher initial voriconazole doses and potentially thrice-daily dosing may be necessary for pediatric patients under two.
- Clinical practice guidelines and pharmacist involvement in TDM are essential for safe and effective voriconazole use in young children.
- This approach supports individualized voriconazole therapy to achieve therapeutic targets and minimize toxicity.
Study Objective:
To describe our experience with voriconazole in three patients younger than 2 years using an optimized dosing strategy for voriconazole that incorporates intensive therapeutic drug monitoring (TDM).
Design:
Case series.
Setting:
Large pediatric hospital.
Patients:
Three patients younger than 2 years who received voriconazole therapy and had serum trough concentrations measured between January 1, 2010, and October 31, 2015.
Measurements And Main Results:
A clinical practice guideline developed at our institution was used to standardize initial dosing, appropriate use and timing of TDM, and dosage modifications based on TDM. TDM was used to guide dosing to achieve a target voriconazole serum trough concentration of 2-6 μg/ml. Voriconazole samples were assayed by using a high-performance liquid chromatography analytical method with solid-phase extraction. Initial dosages for the three patients were 9 mg/kg intravenously every 12 hours (one patient) and 9 mg/kg enterally twice/day (two patients). Multiple dose escalations and a more frequent dosing interval were required to achieve trough concentrations within the target range. The final dosages were 12 mg/kg intravenously every 8 hours, 17.7 mg/kg enterally 3 times/day, and 8.5 mg/kg enterally 3 times/day, respectively. In addition to voriconazole trough concentrations, TDM included evaluations for drug toxicities. Visual, neurologic, or hepatic adverse effects were not encountered in the three patients.
Conclusion:
Our data support higher initial doses and perhaps a 3 times/day dosing schedule to achieve voriconazole serum concentrations in the target range for children younger than 2 years. Implementation of a clinical practice guideline with the participation of pharmacists specializing in pharmacokinetics allows for effective use of voriconazole in young children.
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