INR Goal for TAVR Patients
For patients undergoing Transcatheter Aortic Valve Replacement (TAVR), anticoagulation with a vitamin K antagonist (VKA) to achieve an INR of 2.5 may be reasonable for at least 3 months after the procedure in patients at low risk of bleeding. 1
Evidence-Based Recommendations
Anticoagulation After TAVR
- The 2017 AHA/ACC guidelines provide a Class IIb recommendation (Level of Evidence: B-NR) for anticoagulation with a VKA to achieve an INR of 2.5 for at least 3 months after TAVR in patients at low risk of bleeding 1
- This recommendation is based on evidence showing that valve thrombosis may develop in patients after TAVR when assessed by multidetector computerized tomography
- Studies have demonstrated that prosthetic valve thrombosis occurs in patients who received antiplatelet therapy alone but not in those treated with VKA 1
Rationale for Anticoagulation
- The incidence of valve thrombosis after TAVR varies from 7% to 40%, depending on whether patients are from clinical trials or registries and whether they received anticoagulation 1
- Up to 18% of patients with thrombus formation developed clinically overt obstructive valve thrombosis 1
- A post-TAVR antithrombotic regimen without warfarin appears to predispose patients to valve thrombosis 1
Antiplatelet Therapy
- In addition to potential anticoagulation, clopidogrel 75 mg daily may be reasonable for the first 6 months after TAVR, along with lifelong aspirin 75-100 mg daily (Class IIb, Level of Evidence: C) 1
- This recommendation is based on protocols used in prospective randomized controlled trials of balloon-expandable TAVR for treatment of aortic stenosis 1
Important Considerations
Duration of Therapy
- Anticoagulation is typically recommended for at least 3 months after TAVR 1
- This timeframe is intended to decrease the risk of thromboembolism until the prosthetic valve is fully endothelialized
Risk Assessment
- The potential benefit of anticoagulation therapy must be weighed against the risk of bleeding
- Anticoagulation is specifically recommended for patients at low risk of bleeding 1
- The decision should prioritize prevention of valve thrombosis and thromboembolic events, which can significantly impact morbidity and mortality
Direct Oral Anticoagulants (DOACs)
- The utility of DOACs in TAVR patients is unknown at this time 1
- DOACs are contraindicated for mechanical valve prostheses (Class III: Harm, Level of Evidence: B) 1
Clinical Algorithm for TAVR Anticoagulation
- Assess bleeding risk after TAVR
- For patients at low bleeding risk:
- Consider VKA with target INR of 2.5 for at least 3 months
- Add clopidogrel 75 mg daily for 6 months
- Maintain lifelong aspirin 75-100 mg daily
- For patients at high bleeding risk:
- Consider antiplatelet therapy alone (clopidogrel + aspirin)
- Monitor closely for valve thrombosis with imaging
- For all patients:
- Regular follow-up to assess for signs of valve thrombosis or bleeding
- Consider imaging surveillance with echocardiography
By following these evidence-based recommendations, clinicians can help minimize the risk of valve thrombosis and thromboembolic events while maintaining an acceptable bleeding risk profile in patients who have undergone TAVR.