TY - JOUR
T1 - Population Pharmacokinetics and Exploratory Exposure-Response Relationships of Diazepam in Children Treated for Status Epilepticus
AU - On behalf of the Best Pharmaceuticals for Children Act - Pediatric Trials Network Steering Committee
AU - Ku, Lawrence C.
AU - Hornik, Christoph P.
AU - Beechinor, Ryan J.
AU - Chamberlain, James M.
AU - Guptill, Jeffrey T.
AU - Harper, Barrie
AU - Capparelli, Edmund V.
AU - Martz, Karen
AU - Anand, Ravinder
AU - Cohen-Wolkowiez, Michael
AU - Gonzalez, Daniel
AU - Furda, Gary
AU - Benjamin, Danny
AU - Kearns, Gregory L.
AU - Paul, Ian M.
AU - Sullivan, Jan
AU - Hornik, Christoph P.
AU - Wade, Kelly
AU - Siegel, David
AU - Taylor-Zapata, Perdita
AU - Zajicek, Anne
AU - Ren, Zhaoxia
AU - Tsilou, Ekaterini
AU - Pagan, Alice
AU - Simone, Gina
AU - Ku, Lawrence
AU - Mills, Mary
AU - Watt, Kevin
N1 - Publisher Copyright:
© 2018 The Authors CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics
PY - 2018/11
Y1 - 2018/11
N2 - Diazepam is labeled for status epilepticus (SE) in children, but there are limited data characterizing its disposition in pediatric patients. We developed a population pharmacokinetic (PK) model of i.v. diazepam in children with SE. We evaluated relationships between PK parameters and both safety and efficacy, and simulated exposures using dosing regimens from the product label and clinical practice. The model was developed using prospective data from a pediatric clinical trial comparing diazepam to lorazepam for treatment of SE. Altogether, 87 patients aged ≥ 3 months to < 18 years contributed 162 diazepam concentrations. Diazepam PKs were well characterized by a two-compartment model scaled by body size. No significant or clinically important relationships were observed between diazepam PKs and safety or efficacy. Simulations demonstrated that, compared with label dosing, the study dose (0.2 mg/kg i.v., maximum 8 mg) resulted in greater frequency in rapidly achieving the target therapeutic range of 200–600 ng/mL.
AB - Diazepam is labeled for status epilepticus (SE) in children, but there are limited data characterizing its disposition in pediatric patients. We developed a population pharmacokinetic (PK) model of i.v. diazepam in children with SE. We evaluated relationships between PK parameters and both safety and efficacy, and simulated exposures using dosing regimens from the product label and clinical practice. The model was developed using prospective data from a pediatric clinical trial comparing diazepam to lorazepam for treatment of SE. Altogether, 87 patients aged ≥ 3 months to < 18 years contributed 162 diazepam concentrations. Diazepam PKs were well characterized by a two-compartment model scaled by body size. No significant or clinically important relationships were observed between diazepam PKs and safety or efficacy. Simulations demonstrated that, compared with label dosing, the study dose (0.2 mg/kg i.v., maximum 8 mg) resulted in greater frequency in rapidly achieving the target therapeutic range of 200–600 ng/mL.
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U2 - 10.1002/psp4.12349
DO - 10.1002/psp4.12349
M3 - Article
C2 - 30267478
AN - SCOPUS:85054077759
SN - 2163-8306
VL - 7
SP - 718
EP - 727
JO - CPT: Pharmacometrics and Systems Pharmacology
JF - CPT: Pharmacometrics and Systems Pharmacology
IS - 11
ER -