Edoxaban Versus Dual Antiplatelet Therapy for Leaflet Thrombosis and Cerebral Thromboembolism After TAVR: The ADAPT-TAVR Randomized Clinical Trial

• Published in: Circulation (New York, N.Y.) Vol. 146; no. 6; pp. 466 - 479
• Main Authors: Park, Duk-Woo, Ahn, Jung-Min, Kang, Do-Yoon, Kim, Kyung Won, Koo, Hyun Jung, Yang, Dong Hyun, Jung, Seung Chai, Kim, Byungjun, Wong, Yiu Tung Anthony, Lam, Cheung Chi Simon, Yin, Wei-Hsian, Wei, Jeng, Lee, Yung-Tsai, Kao, Hsien-Li, Lin, Mao-Shin, Ko, Tsung-Yu, Kim, Won-Jang, Kang, Se Hun, Yun, Sung-Cheol, Lee, Seung-Ah, Ko, Euihong, Park, Hanbit, Kim, Dae-Hee, Kang, Joon-Won, Lee, Jae-Hong, Park, Seung-Jung
• Format: Journal Article
• Language: English
• Published: United States Lippincott Williams & Wilkins 09-08-2022
• Subjects: Anticoagulants - therapeutic use; Aortic Valve - diagnostic imaging; Aortic Valve - surgery; Aortic Valve Stenosis - complications; Aortic Valve Stenosis - diagnostic imaging; Aortic Valve Stenosis - surgery; Humans; Platelet Aggregation Inhibitors - adverse effects; Pyridines; Risk Factors; Thiazoles; Thromboembolism - diagnostic imaging; Thromboembolism - epidemiology; Thromboembolism - etiology; Thrombosis - diagnostic imaging; Thrombosis - drug therapy; Thrombosis - epidemiology; Transcatheter Aortic Valve Replacement - adverse effects; Transcatheter Aortic Valve Replacement - methods; Treatment Outcome; anticoagulants; aortic valve stenosis; transcatheter aortic valve replacement; thromboembolism; thrombosis
• ISSN: 0009-7322; 1524-4539
• DOI: 10.1161/CIRCULATIONAHA.122.059512

It is unknown whether the direct oral anticoagulant edoxaban can reduce leaflet thrombosis and the accompanying cerebral thromboembolic risk after transcatheter aortic valve replacement. In addition, the causal relationship of subclinical leaflet thrombosis with cerebral thromboembolism and neurological or neurocognitive dysfunction remains unclear.
We conducted a multicenter, open-label randomized trial comparing edoxaban with dual antiplatelet therapy (aspirin plus clopidogrel) in patients who had undergone successful transcatheter aortic valve replacement and did not have an indication for anticoagulation. The primary end point was an incidence of leaflet thrombosis on 4-dimensional computed tomography at 6 months. Key secondary end points were the number and volume of new cerebral lesions on brain magnetic resonance imaging and the serial changes of neurological and neurocognitive function between 6 months and immediately after transcatheter aortic valve replacement.
A total of 229 patients were included in the final intention-to-treat population. There was a trend toward a lower incidence of leaflet thrombosis in the edoxaban group compared with the dual antiplatelet therapy group (9.8% versus 18.4%; absolute difference, -8.5% [95% CI, -17.8% to 0.8%];
=0.076). The percentage of patients with new cerebral lesions on brain magnetic resonance imaging (edoxaban versus dual antiplatelet therapy, 25.0% versus 20.2%; difference, 4.8%; 95% CI, -6.4% to 16.0%) and median total new lesion number and volume were not different between the 2 groups. In addition, the percentages of patients with worsening of neurological and neurocognitive function were not different between the groups. The incidence of any or major bleeding events was not different between the 2 groups. We found no significant association between the presence or extent of leaflet thrombosis with new cerebral lesions and a change of neurological or neurocognitive function.
In patients without an indication for long-term anticoagulation after successful transcatheter aortic valve replacement, the incidence of leaflet thrombosis was numerically lower with edoxaban than with dual antiplatelet therapy, but this was not statistically significant. The effects on new cerebral thromboembolism and neurological or neurocognitive function were also not different between the 2 groups. Because the study was underpowered, the results should be considered hypothesis generating, highlighting the need for further research.
URL: https://www.
gov. Unique identifier: NCT03284827.