Oral bioavailability of clonidine in children
Peter Larsson1, Anders Nordlinder, Henrik T G Bergendahl
1Department of Physiology & Pharmacology, Section of Anaesthesiology & Intensive Care, Karolinska Institutet, Stockholm, Sweden. peter.larsson@karolinska.se
Insights
Oral clonidine bioavailability in children undergoing surgery is 55.4%, which is lower than in adults. Higher pediatric doses are needed for similar therapeutic effects.
Area of Science:
- Pediatric Pharmacology
- Anesthesiology
- Pharmacokinetics
Background:
- Oral clonidine is a common premedication for children.
- Adult oral clonidine bioavailability ranges from 75-100%.
- Bioavailability of oral clonidine in children was previously unknown.
Purpose of the Study:
- To determine the oral bioavailability of clonidine in children.
- To characterize the pharmacokinetic profile of oral clonidine in pediatric patients.
Main Methods:
- Children aged 3-10 years received oral clonidine (4 mcg·kg(-1)) mixed with fruit drink.
- Plasma clonidine concentrations were measured over 18 hours using liquid chromatography-mass spectroscopy.
- Pharmacokinetic parameters were calculated using nonlinear mixed-effects models and pooled with existing IV clonidine data.
Main Results:
- A two-compartment model described the time-concentration profiles.
- Key pharmacokinetic parameters included absorption half-life (0.45 h) and lag time (0.148 h).
- Oral bioavailability was determined to be 55.4% (95% CI 0.469-0.654).
Conclusions:
- Oral clonidine absorption in children is variable and relatively slow (Tmax 1.04 h).
- The oral bioavailability of 55.4% is significantly lower than in adults.
- Higher oral clonidine doses (per kg) are necessary in children to achieve adult-like plasma concentrations.
Background:
Oral clonidine is used as premedication in children. The bioavailability of clonidine given orally in adults is 75-100% but is unknown in children.
Methods:
Children (3-10 years) undergoing adenotonsillectomy were administered oral clonidine 4 mcg·kg(-1) mixed with apple fruit drink as premedication. Intravenous plasma was assayed for clonidine concentration at 5, 15, 30, 45 min and 1, 2, 4, 6, 12, 18 h after administration. Clonidine plasma concentrations were determined by liquid chromatography-mass spectroscopy, and pharmacokinetic parameters were calculated using nonlinear effects mixed-effects models. Current data were pooled with published time-concentration profiles from children (n = 49) administered intravenous clonidine to determine oral bioavailability.
Results:
There were eight children studied (age 3-10 years, weight 10.5-36 kg). A two-compartment model with first-order absorption and elimination was used to describe time-concentration profiles. Population parameter estimates (CV%; 95% CI), standardized to a 70-kg person, were absorption half-life (Tabs), 0.45 (85.1; 0.221-0.884) h, absorption lag time (Tlag), 0.148 (91.2; 0.002-0.316) h, Clearance (CL) 17.9 (30.3; 16-20.3) l·h(-1) per 70 kg, between compartment clearance (Q) 121 (44.3; 80.1-165) l·h(-1) per 70 kg, central volume (V1) 81.2 (71.5; 60.7-105) l·70 kg(-1), peripheral volume of distribution (V2) 113 (33.9; 91-131) l·70 kg(-1). The oral bioavailability was 55.4% (CV 6.4%; 95% CI 0.469, 0.654).
Conclusions:
Clonidine administered with an apple fruit drink displays a variable and relatively slow absorption after oral administration (T(max) 1.04 h, C(max) 0.77 mcg·l(-1)). The oral bioavailability was 55.4%, which is less than reported in adults. Consequently, higher oral doses of clonidine (per kg) are required when this formulation is used to achieve concentrations similar to those reported in adults.
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