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Population Pharmacokinetics of Doxycycline in Children
Elizabeth J Thompson1, Huali Wu2, Chiara Melloni2
1Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
Insights
Doxycycline dosing for children under 8 years old is not well-established. This study found that pharmacokinetic parameters for doxycycline in children are similar to adults, suggesting similar per kg dosing may be appropriate for younger children.
Area of Science:
- Pharmacology
- Pediatric Medicine
- Drug Development
Background:
- Doxycycline is FDA-approved for children over 8 years old.
- Limited pharmacokinetic data exists for doxycycline in children 8 years and younger.
- Off-label use in younger children is common for severe infections despite tooth staining risks.
Purpose of the Study:
- To characterize doxycycline pharmacokinetics (PK) in children aged 0-18 years.
- To evaluate the impact of age, obesity, and fasting on doxycycline PK.
- To inform dosing guidelines for pediatric populations.
Main Methods:
- Developed a population pharmacokinetic model using plasma samples from 47 pediatric patients.
- Included 14 participants aged 8 years and younger.
- Analyzed data from oral and intravenous doxycycline doses.
Main Results:
- A one-compartment PK model showed doxycycline clearance (3.32 L/h/70 kg) and volume (96.8 L/70kg) comparable to adults.
- Estimated bioavailability was 89.6%, consistent with adult data.
- No significant differences in allometrically scaled PK parameters were found between children ≤8 years and >8 to ≤18 years.
Conclusions:
- Pediatric doxycycline pharmacokinetics are similar to adult values.
- Current per kg dosing may be appropriate for children 8 years and younger.
- Obesity and fasting status did not significantly impact doxycycline PK in this cohort.
Abstract:
Doxycycline is a tetracycline-class antimicrobial labeled by the United States (U.S.) Food and Drug Administration for children >8 years of age for many common childhood infections. Doxycycline is not labeled for children ≤8 years of age, due to the association between tetracycline class antibiotics and tooth staining, although doxycycline may be used off-label in severe conditions. Accordingly, there is a paucity of pharmacokinetic (PK) data to guide dosing in children 8 years and younger. We leveraged opportunistically-collected plasma samples after intravenous (IV) and oral doxycycline doses received per standard of care to characterize the PK of doxycycline in children of different ages, and evaluated the effect of obesity and fasting status on PK parameters.We developed a population PK model of doxycycline using data collected from 47 patients 0-18 years of age, including 14 participants ≤8 years. We developed a 1 compartment PK model and found doxycycline clearance to be 3.32 L/h/70 kg and volume to be 96.8 L/70kg for all patients; comparable to values reported in adults. We estimated a bioavailability of 89.6%, also consistent with adult data. Allometrically scaled clearance and volume of distribution did not differ between children 2 to ≤8 years of age and children >8 to ≤18 years of age, suggesting that younger children may be given the same per kg dosing. Obese and fasting status were not selected for inclusion in the final model. Additional doxycycline PK samples collected in future studies may be used to improve model performance and maximize its clinical value.
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