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 - Funding Information:
Source of Funding. This work was funded under National Institute of Child Health and Human Development (NICHD) contract HHSN275201000003I for the Pediatric Trials Network (Principal Investigator Daniel K. Benjamin, Jr.). Research reported in this publication was also supported by the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH) under award number UL1TR001117. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Funding Information:
Conflicts of Interest. L.C.K. received support from NIH grants T32GM086330, 5T32HD043029, and 4K12HD043494. R.J.B. is supported by the National Institute of General Medical Sciences (NIGMS) of the NIH under award T32GM086330.C.P.H.receives salary support for research from NICHD (K23HD090239),the US government for his work in pediatric and neonatal clinical pharmacology (Government Contract HHSN267200700051C, PI: Benjamin, under the Best Pharmaceuticals for Children Act), and industry for drug development in adults and children (www.dcri.duke.edu/ research/coi.jsp). M.C-W. receives support for research from the NIH (1R01-HD076676-01A1), the National Center for Advancing Translational Sciences of the NIH (UL1TR001117), the National Institute of Allergy and Infectious Disease (NIAID; HHSN272201500006I and HHSN272201300017I), NICHD (HHSN275201000003I), the Biomedical Advanced Research and Development Authority (BARDA) (HHSO100201300009C), the nonprofit organization Thrasher Research Fund (www.thrasherresearch.org), and from industry for drug development in adults and children (www.dcri. duke.edu/research/coi.jsp). J.T.G. receives support for research from the National Institute of Neurological Disorders and Stroke (K23NS085049; HHSN27100001), The Patient-Centered Outcomes Research Institute, and industry sponsors (www.dcri.duke.edu/research/coi.jsp). D.G. receives support for research from NICHD (K23HD083465). The remaining authors have no funding to disclose.
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 -