Can TAVI patients receive aspirin monotherapy as patients after surgical aortic bioprosthesis implantation? Data from the Polish Registry - POL-TAVI

被引:25
作者
Czerwinska-Jelonkiewicz, Katarzyna [1 ]
Zembala, Marian [2 ]
Dabrowski, Maciej [3 ]
Witkowski, Adam [3 ]
Ochala, Andrzej [4 ]
Kochman, Janusz [5 ]
Dudek, Dariusz [6 ]
Kubler, Piotr [7 ]
Jagielak, Dariusz [8 ]
Stepinska, Janina [1 ]
机构
[1] Inst Cardiol, Intens Cardiac Therapy Dept, Alpejska 42 Str, PL-04628 Warsaw, Poland
[2] Silesian Ctr Heart Dis, Dept Cardiac Surg & Trausplantol, Zabrze, Poland
[3] Inst Cardiol, Dept Intervent Cardiol & Angioi, Warsaw, Poland
[4] Silesian Med Univ, Publ Hosp 7, Katowice, Poland
[5] Med Univ Warsaw, Dept Carcliol 1, Warsaw, Poland
[6] Jagiellonian Univ, Coll Med, Krakow, Poland
[7] Wroclaw Med Univ, Mil Hosp, Wroclaw, Poland
[8] Med Univ, Dept Cardiac & Vasc Surg, Gdansk, Poland
关键词
Transcatheter aortic valve implantation; Bleeding; Vascular complications; Dual antiplatelet therapy; ANTITHROMBOTIC THERAPY; ATRIAL-FIBRILLATION; VALVE IMPLANTATION; ANTICOAGULANT-THERAPY; CLOPIDOGREL; WARFARIN; RISK; SINGLE; OLDER;
D O I
10.1016/j.ijcard.2016.11.095
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: This observational analysis investigated in-hospital safety and efficacy of periprocedural antithrombotic/antiplatelet therapy used in TAVI patients included into the Polish Nationwide Cardiac Surgical and Cardiology Registry of Transcatheter Aortic Valve Implantation (POL-TAVI). Methods and results: All patients who underwent TAVI in the participating centers between 2013 and 2014 were included. The primary endpoints were: severe bleeding, vascular complications, thromboembolic events, myocardial infarction, 30-days mortality, defined according to Valve Academic Research Consortium scale 2. A total of 827 patients were included; 35-93 years old (79.31 +/- 7.53); 457 (55.29%) women. Endpoints noted: severe bleeding -130 (15.72%) pts, vascular complications -135 (16.32%) pts, thromboembolic events -29 (3.5%) pts, myocardial infarction -24 (2.90%) pts, deaths -58 (7.01%) pts. Aspirin premedication, resulted in the least number of vascular complications (OR 0.56 95% CI [0.345-0.938]; p = 0.027). Aspirin after TAVI reduced the risk of vascular complications (OR 0.089 95% CI [0.0217-0.372]; p = 0.001) and bleeding (OR 0.138 95% CI [0.043-0.447]; p = 0.001) with no adverse impact on efficacy endpoints. Beneficial safety profile of postprocedural aspirin monotherapy remained significant in comparison to all other types of prophylaxis also in propensity score analysis: OR 0.068 95% CI[0.009-0.529]; p = 0.01 for vascular complications, OR 0.176 95% CI [0.049-0.627]; p = 0.007 for bleeding. NNT for vascular complications and bleeding with postprocedural aspirin prophylaxis was 5.5 and 6.42, respectively. Conclusion: Aspirin after TAVI appears to be beneficial than currently recommended dual antiplatelet therapy; therefore, it might be considered as TAVI antithrombotic prophylaxis. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:305 / 311
页数:7
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