Phenobarbital population pharmacokinetics across the pediatric age spectrum.

ObjectivePhenobarbital is frequently used in pediatric patients for treatment and prophylaxis of seizures. Pharmacokinetic data for this patient population is lacking and would assist in dosing decisions. MethodsA retrospective population pharmacokinetic analysis was designed for all pediatric patients <19years of age initiated on phenobarbital at our institution from January 2011 to June 2017. Patients were included if they were initiated on intravenous or enteral phenobarbital for treatment or prophylaxis of seizures and had a serum phenobarbital concentration monitored while an inpatient. Data collection included the following: age, weight, height, gestational age, core body temperature, serum creatinine, blood urea nitrogen, aspartase aminotransferase, alanine aminotransferase, urine output over the prior 12hours, phenobarbital doses and serum concentrations, and potential drug-drug interactions. Descriptive statistical methods were used to summarize the data. Pharmacokinetic analysis was performed with NONMEM and simulation was performed for doses of 10, 20, 30, and 40mgkg(-1)dose(-1), iv, followed by enteral doses of 3, 4, 5, and 6mgkg(-1)d(-1). ResultsA total of 355 patients (50.3% male, median gestational age 39weeks (interquartile range [IQR] 35, 40), median age 0.28years (IQR 0.06, 0.82). Median phenobarbital dose was enteral = 2.6 (IQR 1.9, 3.9) mgkg(-1)dose(-1); intravenous = 2.6 (IQR 2.2, 4.9) mgkg(-1)dose(-1)) and mean serum concentration was 41.123.9mg/L at median 6.5 (IQR 2.9, 11.1) hours after a dose. A one-compartment proportional error model best fit the data where clearance and volume of distribution were allometrically scaled using fat-free mass. Significant covariates included serum creatinine, postmenstrual age, and drug-drug interactions on clearance, and age in years on volume of distribution. SignificancePhenobarbital dosing of 30mgkg(-1)dose(-1),iv, followed by 4mgkg(-1)d(-1) had the highest probability of attaining a therapeutic concentration at 7days. Postmenstrual age and drug-drug interactions should be incorporated into dosing decisions.