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Updated: Aug 17, 2026

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
[Congenital cardiopathy: indications for anticoagulant treatment]
J Losay1, A Touchot-Koné, V Lambert
1Hôpital Marie Lannelongue, Le Plessis-Robinson. jlosay@ccml.com
Insights
Children with congenital heart defects and thromboembolic disease often require anticoagulation. Current evidence suggests Vitamin K antagonists are suitable for mechanical valves and post-Fontan procedures, with ongoing research for optimal duration.
Area of Science:
- Pediatric Cardiology
- Hematology
- Thrombosis Research
Context:
- Congenital heart disease (CHD) frequently coexists with thromboembolic disease in children.
- Limited objective clinical data exist for the medium and long-term management of pediatric thromboembolism.
- Vitamin K antagonists (VKAs) are a potential therapeutic option.
Purpose:
- To review current evidence and expert opinion on anticoagulation strategies in pediatric patients with congenital cardiopathy and thromboembolic disease.
- To provide guidance on the use of anticoagulants in specific scenarios such as mechanical valves, post-Fontan procedures, and interventional catheterization.
Summary:
- Children with mechanical heart valves require anticoagulation, mirroring adult guidelines, due to significant thromboembolic risks.
- Anticoagulation is recommended for up to one year post-Fontan procedure due to elevated thromboembolic risk factors.
- In Eisenmenger's syndrome, anticoagulation is generally avoided unless specific indications like pulmonary embolism exist. For intra-atrial prostheses and certain stents, shorter durations of anticoagulation or antiplatelet therapy are considered.
Impact:
- Highlights the need for objective clinical data and prospective studies to refine anticoagulation protocols in pediatric CHD.
- Informs clinical decision-making for managing thromboembolic complications in children with complex congenital heart conditions.
- Emphasizes the importance of individualized anticoagulation strategies based on specific cardiac defects and procedural risks.
Abstract:
Congenital cardiopathy is common in children with thromboembolic disease. There are no objective clinical data for medium and long term treatment. Vitamin K antagonists could be envisaged for this. Children with a mechanical valve should be anticoagulated. This has been validated in adults, there has been no study in children which contradicts this, and the serious nature of thromboembolic complications in this group is significant. In atrial fibrillation, the most frequent indication for oral anticoagulants is after a Fontan procedure, because of the thromboembolic risk factors. Anticoagulation following Fontan or similar procedures relies on the thrombotic factors and their temporal distribution, being more pronounced in the first postoperative year; anticoagulants should be given over this period. In Eisenmenger's syndrome haemorrhage is common: these patients are not anticoagulated unless there is an indication such as recent pulmonary embolus. During interventional catheterisation thromboembolic accidents are rare, occurring early, and more commonly with certain prostheses. In adults with an intra-atrial prosthesis oral anticoagulants are used for three months, and then replaced by antiplatelet drugs. In congenital cardiopathy the stent is often pulmonary or aortic, and the incidence of thromboembolic accident is therefore very low. For a venous channel or in the context of a Fontan procedure, oral anticoagulants are justified for between three and six months. It is to be hoped that prospective studies, of which some are in progress, will provide further guidance for these indications.
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