TY - JOUR
T1 - Plasma and cerebrospinal fluid concentrations of ibuprofen in pediatric patients and antipyretic effect
T2 - Pharmacokinetic-pharmacodynamic modeling analysis
AU - Har-Even, Ronly
AU - Stepensky, David
AU - Britzi, Malka
AU - Soback, Stefan
AU - Chaim, Adina Bar
AU - Brandriss, Norit
AU - Goldman, Michael
AU - Berkovitch, Matitiahu
AU - Kozer, Eran
PY - 2014/1/1
Y1 - 2014/1/1
N2 - We aimed to determine the relationship between plasma and cerebrospinal fluid (CSF) concentrations of ibuprofen and the antipyretic effect in pediatric patients. A prospective cohort of infants and children aged 3 months to 15 years and treated with ibuprofen was studied. The patients received ibuprofen (via oral route, median dose of 10.0mg/kg; 3.4-11.4mg/kg range), samples of blood and CSF were collected, and body temperature was measured. Sequential analysis of the pharmacokinetic and pharmacodynamic data from 28 patients was performed using a population modeling approach. The observed concentration versus time data indicated substantial pharmacokinetic variability in absorption and distribution of ibuprofen between the patients. The pharmacokinetic modeling outcomes indicate that following a ∼25-minute lag time, ibuprofen is rapidly absorbed to the central compartment and rapidly equilibrates with the CSF, resulting in the total ibuprofen concentration in the CSF versus plasma (C CSF/Cplasma) of 0.011±0.007. The antipyretic effect of ibuprofen was best described by an indirect response PK-PD model incorporating patient baseline body temperature and ibuprofen concentration in the CSF. We conclude that the pharmacokinetic-pharmacodynamic modeling can be used to predict the time course of ibuprofen plasma and CSF concentrations and of the antipyretic effects in individual pediatric patients.
AB - We aimed to determine the relationship between plasma and cerebrospinal fluid (CSF) concentrations of ibuprofen and the antipyretic effect in pediatric patients. A prospective cohort of infants and children aged 3 months to 15 years and treated with ibuprofen was studied. The patients received ibuprofen (via oral route, median dose of 10.0mg/kg; 3.4-11.4mg/kg range), samples of blood and CSF were collected, and body temperature was measured. Sequential analysis of the pharmacokinetic and pharmacodynamic data from 28 patients was performed using a population modeling approach. The observed concentration versus time data indicated substantial pharmacokinetic variability in absorption and distribution of ibuprofen between the patients. The pharmacokinetic modeling outcomes indicate that following a ∼25-minute lag time, ibuprofen is rapidly absorbed to the central compartment and rapidly equilibrates with the CSF, resulting in the total ibuprofen concentration in the CSF versus plasma (C CSF/Cplasma) of 0.011±0.007. The antipyretic effect of ibuprofen was best described by an indirect response PK-PD model incorporating patient baseline body temperature and ibuprofen concentration in the CSF. We conclude that the pharmacokinetic-pharmacodynamic modeling can be used to predict the time course of ibuprofen plasma and CSF concentrations and of the antipyretic effects in individual pediatric patients.
KW - drug concentrations in plasma and cerebrospinal fluid
KW - ibuprofen antipyretic effect
KW - infants and children
KW - pharmacokinetic-pharmacodynamic modeling
UR - http://www.scopus.com/inward/record.url?scp=84905591556&partnerID=8YFLogxK
U2 - 10.1002/jcph.307
DO - 10.1002/jcph.307
M3 - Article
C2 - 24733245
AN - SCOPUS:84905591556
VL - 54
SP - 1023
EP - 1030
JO - Journal of Clinical Pharmacology
JF - Journal of Clinical Pharmacology
SN - 0091-2700
IS - 9
ER -