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Updated: Jul 11, 2025

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Real-world experience with edoxaban for anticoagulation in children at risk for coronary artery thrombosis
Eyal Sagiv1, David M Newland2, April Slee3
1Division of Pediatric Cardiology, Seattle Children's Hospital, Seattle, WA, USA.
Insights
Edoxaban is a feasible and well-tolerated direct oral anticoagulant for children needing long-term anticoagulation for Kawasaki disease. Weight-based dosing showed promising results in preventing coronary artery thrombosis.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Hematology
Background:
- Direct oral anticoagulants (DOACs) offer potential advantages for pediatric anticoagulation.
- Edoxaban's favorable pharmacokinetics suggest suitability for younger patients.
- However, long-term safety and efficacy data in pediatric populations are limited.
Purpose of the Study:
- To evaluate the single-center experience of using edoxaban in children requiring chronic anticoagulation.
- Focus on patients with large coronary artery aneurysms secondary to Kawasaki disease.
Main Methods:
- Weight-based, once-daily oral edoxaban dosing was used as an alternative to standard anticoagulation.
- Included patients aged 1-18 years.
- Median follow-up of 49 months; pharmacokinetic and pharmacodynamic analyses were performed.
Main Results:
- Sixteen pediatric patients received chronic edoxaban therapy.
- No major bleeding events were reported.
- Two patients experienced coronary artery thrombosis, predicting a 70% event-free rate at 12 years post-diagnosis; adult-like exposure was observed.
Conclusions:
- Edoxaban is feasible and well-tolerated for long-term pediatric use.
- Weight-based, once-daily dosing may provide comparable anticoagulation to standard care for preventing coronary artery thrombosis.
- Larger studies are necessary to confirm long-term safety and efficacy.
Background:
Direct oral anticoagulants have the potential to improve care in children requiring chronic anticoagulation. Edoxaban has favourable pharmacokinetics that could benefit younger patients but data on long-term safety and efficacy for specific paediatric indications are lacking.
Study Aims:
We present a single-centre experience using edoxaban in children who require chronic anticoagulation for large coronary artery aneurysms secondary to Kawasaki disease.
Methods:
Weight-based dosing of once-daily oral edoxaban was offered as alternative to standard anticoagulation for patients aged 1-18 years. Chart review was performed for a median follow-up period of 49 months on edoxaban. Steady-state pharmacokinetics and pharmacodynamics of edoxaban were also explored.
Results:
Sixteen patients on chronic therapy with edoxaban were included. No major bleeding events were reported. Two patients experienced coronary artery thrombosis after 23 and 38 months on edoxaban, 7 and 11 years after diagnosed with Kawasaki disease, respectively. This predicts 70% event-free rate at 12 years from diagnosis. Area under the curve estimates over the dosing interval of 24 hours were similar to those reported in adults.
Conclusions:
Edoxaban use is feasible and well-tolerated for long-term use in paediatric population. We suggest appropriate exposure using weight-based once-daily dosing strategy that may be comparable to standard-of-care anticoagulation in prevention of coronary artery thrombosis. Larger studies are needed to evaluate long-term safety and efficacy of edoxaban in this population.
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