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Published on: February 28, 2012
Response to warfarin therapy in obese pediatric patients dosed according to institutional guidelines
Brady S Moffett1, Lisa R Bomgaars
1*Department of Pharmacy, Texas Children's Hospital †Department of Pediatrics, Hematology Section, Baylor College of Medicine, Houston, TX.
Insights
Obese children require longer to reach a therapeutic warfarin dose compared to non-obese children. Current dosing guidelines may need adjustment for pediatric obesity to ensure safe and effective anticoagulation.
Area of Science:
- Pediatric pharmacology
- Anticoagulation therapy
- Obesity research
Background:
- Current warfarin dosing guidelines do not account for obesity in pediatric patients.
- Adult data suggest obesity impacts warfarin dosing, but this is understudied in children.
- Pediatric obesity is common, necessitating evaluation of current warfarin dosing strategies.
Purpose of the Study:
- To evaluate warfarin dosing requirements and time to therapeutic anticoagulation in obese pediatric patients.
- To compare outcomes between obese and non-obese pediatric patients receiving warfarin.
Main Methods:
- Retrospective cohort study of obese and non-obese pediatric patients (2-18 years) initiated on warfarin.
- Patients were matched by age and sex; obesity defined by CDC guidelines.
- Primary endpoint: time to therapeutic International Normalized Ratio (INR); secondary: supratherapeutic INR rates.
Main Results:
- Obese patients received significantly lower initial and maximum warfarin doses per kg.
- Median time to achieve a therapeutic INR was twice as long in obese patients (6 days vs. 3 days).
- No significant differences in INR monitoring frequency, doses administered, or length of stay were observed.
Conclusions:
- Obese pediatric patients experience delayed achievement of therapeutic anticoagulation with standard warfarin dosing.
- Traditional warfarin dosing guidelines may be inadequate for obese pediatric populations.
- Further research into optimized warfarin dosing for pediatric obesity is warranted.
Background:
Current warfarin dosing guidelines for pediatric patients do not account for obesity. Published data from adults suggest that obesity may affect warfarin dosing requirements. Obesity is prevalent in the pediatric population, and current warfarin dosing methods should be evaluated in obese pediatric patients.
Methods:
Patients aged 2 to 18 years who were obese and initiated on warfarin therapy at our institution as inpatients from 2004 to 2010 were identified and matched in a 1:2 ratio by age and sex with nonobese patients who were initiated on warfarin therapy. Patients were categorized obese per Centers for Disease Control guidelines. Demographic and disease state information, warfarin dosing information, INR values, and interacting medications were collected. Warfarin was dosed according to the institutional guidelines adapted from the published literature. Time to therapeutic INR value was the primary endpoint and percent of patients with supratherapeutic INR values was the secondary endpoint.
Results:
A total of 30 patients met the study criteria (10 obese, 20 nonobese), and baseline demographic variables were similar. No significant differences were noted in the number of INR values drawn, number of warfarin doses administered, or length of stay. Initial and maximum doses of warfarin per kg were significantly lower in obese patients compared with nonobese patients (P<0.05). Median time to therapeutic INR value was twice as long in obese patients as in nonobese patients (median=6 [range, 4 to 28 d] versus median=3 [range, 1 to 10 d]; P<0.01).
Conclusions:
Obese pediatric patients have an increased time to therapeutic INR value when traditional warfarin dosing guidelines are used.
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