No Antithrombotic Therapy After Transcatheter Aortic Valve Replacement Insight From the OCEAN-TAVI Registry

被引:20
|
作者
Kobari, Yusuke [1 ]
Inohara, Taku [1 ]
Tsuruta, Hikaru [1 ]
Yashima, Fumiaki [1 ,2 ]
Shimizu, Hideyuki [1 ]
Fukuda, Keiichi [1 ]
Naganuma, Toru [3 ]
Mizutani, Kazuki [4 ]
Yamawaki, Masahiro [5 ]
Tada, Norio [6 ]
Yamanaka, Futoshi [7 ]
Shirai, Shinichi [8 ]
Tabata, Minoru [9 ]
Ueno, Hiroshi [10 ]
Takagi, Kensuke [11 ]
Watanabe, Yusuke [12 ]
Yamamoto, Masanori [13 ,14 ]
Hayashida, Kentaro [1 ]
机构
[1] Keio Univ, Sch Med, Tokyo, Japan
[2] Saiseikai Utsunomiya Hosp, Tochigi, Japan
[3] New Tokyo Hosp, Matsudo, Chiba, Japan
[4] Osaka City Gen Hosp, Osaka, Japan
[5] Saiseikai Yokohama City Eastern Hosp, Yokohama, Kanagawa, Japan
[6] Sendai Kousei Hosp, Sendai, Miyagi, Japan
[7] Shonan Kamakura Gen Hosp, Kamakura, Kanagawa, Japan
[8] Kokura Mem Hosp, Kokura, Japan
[9] Tokyo Bay Urayasu Ichikawa Med Ctr, Chiba, Japan
[10] Toyama Univ Hosp, Toyama, Japan
[11] Ogaki Municipal Hosp, Gifu, Japan
[12] Teikyo Univ, Sch Med, Tokyo, Japan
[13] Toyohashi Heart Ctr, Toyohashi, Aichi, Japan
[14] Nagoya Heart Ctr, Nagoya, Aichi, Japan
关键词
antithrombotics; bleeding; transcatheter aortic valve replacement; RISK; IMPLANTATION; MANAGEMENT; THROMBOSIS; OUTCOMES;
D O I
10.1016/j.jcin.2022.10.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Several trials demonstrated that aspirin monotherapy compared with aspirin plus clopidogrel is associated with a lower incidence of bleeding without an increased risk of ischemic events in patients after transcatheter aortic valve replacement (TAVR); however, there remains a paucity of data to prove the necessity of even aspirin monotherapy. OBJECTIVES This study aimed to compare clinical outcomes and valve performance of the 3 different antithrombotic strategies post-TAVR from the OCEAN-TAVI (Optimized transCathEter vAlvular iNtervention) registry. METHODS Patients who received anticoagulation or had procedural complications were excluded. The remaining patients were classified into 3 groups according to the antithrombotic regimen at discharge: 1) nonantithrombotic therapy (None); 2) single-antiplatelet therapy (SAPT); and 3) dual-antiplatelet therapy (DAPT). The primary outcome was the incidence of net adverse clinical events (NACEs) (ie, cardiovascular death, stroke, myocardial infarction, and life-threatening or major bleeding). RESULTS Overall, 3,575 TAVR patients were included (None, 293; SAPT, 1,354; DAPT, 1,928). The median follow-up period was 841 days (IQR: 597-1,340 days). The incidence of NACEs did not differ between the groups (None vs SAPT: adjusted HR [aHR]: 1.18; P = 0.45; None vs DAPT: aHR: 1.09; P = 0.67). There was a lower incidence of all bleeding in patients with no antithrombotics (None vs SAPT: aHR: 0.63; P = 0.12; None vs DAPT: aHR: 0.51; P = 0.04). The valve performance was similar among the groups. Leaflet thrombosis was detected in 8.5% of the nonantithrombotic group. CONCLUSIONS Compared with SAPT/DAPT, the nonantithrombotic strategy was not associated with an increased risk of NACEs and potentially reduced the risk of bleeding events. The nonantithrombotic strategy may be an acceptable alternative to SAPT/DAPT in selected patients with TAVR. (c) 2023 by the American College of Cardiology Foundation.
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收藏
页码:79 / 91
页数:13
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