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Published on: October 12, 2012
Low molecular weight heparin in children
Manuela Albisetti1, Maureen Andrew
1Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada. manuela.albisetti@kispi.unizh.ch
Insights
Low molecular weight heparins offer a safe and effective alternative for preventing and treating blood clots in children. These agents provide predictable anticoagulation with fewer complications than traditional treatments.
Area of Science:
- Pediatric Hematology
- Pharmacology
Background:
- Thromboembolic events pose risks in pediatric patients.
- Current anticoagulation options include unfractionated heparin and oral anticoagulants.
Purpose of the Study:
- To evaluate the efficacy and safety of low molecular weight heparins (LMWHs) in pediatric thromboembolism.
- To compare LMWHs with unfractionated heparin and oral anticoagulants in children.
Main Methods:
- Review of available data on LMWH use in pediatric populations.
- Analysis of pharmacokinetic and pharmacodynamic properties of LMWHs versus unfractionated heparin.
Main Results:
- LMWHs demonstrate superior bioavailability and longer half-life compared to unfractionated heparin.
- Subcutaneous administration of LMWHs requires minimal monitoring and dose adjustment.
- Complications like osteoporosis and heparin-induced thrombocytopenia are less frequent with LMWHs.
Conclusions:
- Low molecular weight heparins represent an efficient and safe alternative for anticoagulation in children.
- LMWHs are suitable for both prevention and treatment of thromboembolic events across various pediatric conditions.
Unlabelled:
Low molecular weight heparins potentially have significant advantages over unfractionated heparin and oral anticoagulants for both the prevention and treatment of thromboembolic events in children. Compared to standard heparin, low molecular weight heparins have superior bioavailability, a longer half-life, and a dose-independent clearance, which results in a more predictable anticoagulant response. Low molecular weight heparins are administered subcutaneously and require minimal laboratory monitoring and dose adjustment, offering important benefits to children with poor venous access. In addition, complications including osteoporosis and heparin-induced thrombocytopenia are relatively rare with low molecular weight heparins compared to unfractionated heparin.
Conclusion:
based on the available data, low molecular weight heparins seem to be an efficient and safe alternative to standard anticoagulation therapy with unfractionated heparin and oral anticoagulants for both treatment and prevention of thromboembolic events in children of varying ages and underlying disorders.
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