Population pharmacokinetics of levetiracetam in neonates with seizures
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What is known and objective: This study developed a population pharmacokinetic (PK) model of levetiracetam (LEV) for treating neonatal seizures (NS) and determined the influence of clinically relevant covariates to explain the interindividual variability and residual error. Methods: Twenty newborns admitted to the Neonatal Intensive Care Unit at the Hospital Central “Dr. Ignacio Morones Prieto” were included. LEV doses were administered by intermittent infusion. Blood samples were drawn 3 times post-infusion. Levetiracetam was quantified by a chromatographic technique. NONMEM software was used to determine the population PK model of LEV in neonates and the influence of clinical covariates on drug disposition. Results and discussion: The LEV PK in neonates is described by a one-compartment open model with first-order elimination. The influence of creatinine clearance (CRCL) and body weight (BW) on clearance (CL[L/h] = 0.47*CRCL), as well as the volume of the distribution (Vd[L] = 0.65*BW) of LEV, were confirmed, considering interindividual variabilities of 36%25 and 22%25, respectively, and a residual error of 13%25. What is new and Conclusion: Based on the PK of LEV in neonates and the influence of the final PK model, a priori dosing guidelines are proposed considering CRCL, BW and LEV plasma concentrations between 6 and 20 mg/L for NS treatment. © 2017 John Wiley %26 Sons Ltd
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What is known and objective: This study developed a population pharmacokinetic (PK) model of levetiracetam (LEV) for treating neonatal seizures (NS) and determined the influence of clinically relevant covariates to explain the interindividual variability and residual error. Methods: Twenty newborns admitted to the Neonatal Intensive Care Unit at the Hospital Central “Dr. Ignacio Morones Prieto” were included. LEV doses were administered by intermittent infusion. Blood samples were drawn 3 times post-infusion. Levetiracetam was quantified by a chromatographic technique. NONMEM software was used to determine the population PK model of LEV in neonates and the influence of clinical covariates on drug disposition. Results and discussion: The LEV PK in neonates is described by a one-compartment open model with first-order elimination. The influence of creatinine clearance (CRCL) and body weight (BW) on clearance (CL[L/h] = 0.47*CRCL), as well as the volume of the distribution (Vd[L] = 0.65*BW) of LEV, were confirmed, considering interindividual variabilities of 36%25 and 22%25, respectively, and a residual error of 13%25. What is new and Conclusion: Based on the PK of LEV in neonates and the influence of the final PK model, a priori dosing guidelines are proposed considering CRCL, BW and LEV plasma concentrations between 6 and 20 mg/L for NS treatment. © 2017 John Wiley & Sons Ltd
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levetiracetam; neonatal seizures; population pharmacokinetics creatinine; levetiracetam; anticonvulsive agent; creatinine; etiracetam; piracetam; Article; blood sampling; body weight; clinical article; controlled study; creatinine clearance; data analysis software; drug blood level; drug clearance; drug disposition; drug distribution; drug elimination; error; female; hospital admission; human; interindividual variability; male; neonatal intensive care unit; newborn; population research; prospective study; residual error; seizure; statistical parameters; analogs and derivatives; biological model; dose response; seizure; tissue distribution; Anticonvulsants; Creatinine; Dose-Response Relationship, Drug; Female; Humans; Infant, Newborn; Male; Models, Biological; Piracetam; Prospective Studies; Seizures; Tissue Distribution
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