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Full-root Aortic Valve Replacement by Stentless Aortic Xenografts in Patients with Small Aortic Roots
Published on: May 21, 2017
Antithrombotic therapy in patients undergoing transcatheter aortic valve implantation
Vincent Johan Nijenhuis1, Jorn Brouwer1, Lars Søndergaard2
1Department of Cardiology, St Antonius Hospital, Nieuwegein, The Netherlands.
Insights
Antiplatelet therapy (APT) is often preferred after transcatheter aortic valve implantation (TAVI) due to bleeding risks with anticoagulants. Dual APT or vitamin-K antagonist (VKA) use is reserved for specific high-risk patient groups.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Transcatheter aortic valve implantation (TAVI) is a growing procedure for aortic stenosis.
- Optimal antithrombotic therapy post-TAVI remains debated due to limited robust clinical trial data.
- Current guidelines often extrapolate evidence from other cardiovascular patient populations.
Purpose of the Study:
- To review and synthesize current evidence regarding antithrombotic strategies following TAVI.
- To provide guidance on the use of antiplatelet therapy (APT) and oral anticoagulation (OAC).
- To delineate specific patient scenarios warranting different antithrombotic regimens.
Main Methods:
- Comprehensive literature review of available data on antithrombotic therapy post-TAVI.
- Analysis of clinical practice trends and extrapolation of evidence from other patient cohorts.
- Evaluation of risks and benefits associated with different antithrombotic agents.
Main Results:
- Single antiplatelet therapy (APT) is generally favored over dual APT post-TAVI.
- Dual APT is considered for patients with recent acute coronary syndrome, complex stenting, or specific stroke/atheroma risk factors.
- Vitamin-K antagonist (VKA) monotherapy is indicated for patients with atrial fibrillation or other long-term OAC needs.
- VKA initiation is recommended for clinical valve thrombosis; its role in subclinical leaflet thrombosis is uncertain.
- Direct-acting oral anticoagulants (DOACs) may be used when OAC is indicated and no contraindications exist.
Conclusions:
- Antiplatelet therapy (APT) is a primary consideration post-TAVI, with single APT preferred.
- Specific high-risk conditions may necessitate dual APT or vitamin-K antagonist (VKA) therapy.
- The choice of antithrombotic regimen requires careful patient-specific risk-benefit assessment.
Abstract:
This review provides a comprehensive overview of the available data on antithrombotic therapy after transcatheter aortic valve implantation (TAVI). In the absence of large randomised clinical trials, clinical practice is leaning towards evidence reported in other populations. Due to the greater risk of major bleeding associated with oral anticoagulation using a vitamin-K antagonist (VKA), antiplatelet therapy (APT) may be considered as the first-line treatment of patients undergoing TAVI. Overall, single rather than dual APT is preferred. However, dual APT should be considered in patients with a recent acute coronary syndrome (ie, within 6 months), complex coronary stenting, large aortic arch atheromas or previous non-cardioembolic stroke. Monotherapy with VKA should be considered if concomitant atrial fibrillation or any other indication for long-term oral anticoagulation is present. APT on top of VKA seems only reasonable in patients with recent acute coronary syndrome, extensive or recent coronary stenting or large aortic arch atheromas. A direct-acting oral anticoagulant may be considered if oral anticoagulation is indicated in the absence of contraindications. Initiation of VKA is indicated in clinical valve thrombosis, for example, with high transvalvular gradient, whereas the role of VKA in the case of subclinical leaflet thrombosis is currently uncertain.
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