An Optimized Voriconazole Dosing Strategy to Achieve Therapeutic Serum Concentrations in Children Younger than 2 Years Old

被引:18
作者
Zembles, Tracy N. [1 ]
Thompson, Nathan E. [2 ]
Havens, Peter L. [3 ]
Kaufman, Bruce A. [4 ]
Huppler, Anna R. [3 ]
机构
[1] Childrens Hosp & Hlth Syst, Dept Pharm, POB 1997,Mail Stn 730, Milwaukee, WI 53210 USA
[2] Childrens Hosp & Hlth Syst, Dept Pediat, Crit Care Med, Med Coll Wisconsin,Childrens Res Inst, Milwaukee, WI USA
[3] Childrens Hosp & Hlth Syst, Dept Pediat, Infect Dis, Med Coll Wisconsin,Childrens Res Inst, Milwaukee, WI USA
[4] Childrens Hosp & Hlth Syst, Dept Neurosurg, Med Coll Wisconsin, Milwaukee, WI USA
来源
PHARMACOTHERAPY | 2016年 / 36卷 / 10期
关键词
voriconazole; pediatrics; therapeutic drug monitoring; guideline; dosing; POPULATION PHARMACOKINETIC ANALYSIS; IMMUNOCOMPROMISED CHILDREN; SAFETY; ADOLESCENTS;
D O I
10.1002/phar.1829
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study ObjectiveTo 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). DesignCase series. SettingLarge pediatric hospital. PatientsThree 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 ResultsA 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 g/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. ConclusionOur 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.
引用
收藏
页码:1102 / 1108
页数:7
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