Transapical aortic valve implantation using a new self-expandable bioprosthesis (ACURATE TA™): 6-month outcomes†

被引:55
作者
Kempfert, Joerg [1 ]
Treede, Hendrik [2 ]
Rastan, Ardawan J. [3 ]
Schoenburg, Markus [1 ]
Thielmann, Matthias [4 ]
Sorg, Stefan [5 ]
Mohr, Friedrich-W. [3 ]
Walther, Thomas [1 ]
机构
[1] Kerckhoff Clin Bad Nauheim, Dept Cardiac Surg, D-61231 Bad Nauheim, Germany
[2] Univ Hamburg, Dept Cardiac Surg, Heartctr, Hamburg, Germany
[3] Univ Leipzig, Dept Cardiac Surg, Heartctr, Leipzig, Germany
[4] Univ Duisburg Essen, West German Heart Ctr Essen, Dept Cardiac Surg, Essen, Germany
[5] Univ Freiburg, Dept Cardiac Surg, Clin Cardiac Surg, D-79106 Freiburg, Germany
关键词
Aortic valve implantation; Minimally invasive; Transapical; HIGH-RISK PATIENTS; OUTCOME SOURCE REGISTRY; EDWARDS SAPIEN VALVE; EUROPEAN REGISTRY; TRANSCATHETER; REPLACEMENT; EXPERIENCE; STENOSIS; PROSTHESIS; PREDICTORS;
D O I
10.1093/ejcts/ezs139
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ACURATE TA((TM)) Aortic Bioprosthesis and Delivery System (Symetis S.A., Ecublens, Switzerland) is a new transcatheter aortic valve designed for transapical implantation. The six-month results from the completed first-in-man study are reported. The Symetis ACURATE TA((TM)) is composed of a porcine biological tissue valve attached to a self-expandable nitinol stent. It allows for anatomical orientation and facilitates intuitive implantation providing tactile feedback. Since November 2009, a total of 40 high-risk elderly patients have been treated. The mean age of enrolled patients was 83.2 +/- 4.0; 60.0% were female, with a mean logistic EuroSCORE of 21.2 +/- 10.8% and a mean Society of Thoracic Surgeons (STS) score of 9.0 +/- 4.7%. All implants were delivered successfully in the intra-annular and subcoronary position. One patient was converted to conventional surgery due to coronary impingement (after valve-in-valve implantation). One additional patient received valve-in-valve treatment (SAPIEN THV TA((TM))). Five patients expired within 30 days and two additional patients expired during the 6-month follow-up due to non-valve-related causes resulting in a mid-term survival rate of 82.5%. Two patients suffered a stroke and another three required new onset pacemaker implantation. The mean aortic gradient significantly improved and remained stable throughout the follow-up (baseline: 51.9 +/- 14.3 mmHg, 30 days: 12.3 +/- 5.1 mmHg, 6 months: 11.9 +/- 5.8 mmHg). At the 6-month follow-up, 96.7% of patients demonstrated either none/trace or mild (1+/4) paravalvular leakage only. According to the Valve Academic Research Council the device's success rate was 92.5%, with a 30-day safety profile of 25%. At the 6-month follow-up, the ACURATE TA((TM)) device showed stable valve function with low rates of paravalvular leakages. The cohort of high-risk patients demonstrated good clinical outcomes and 6-month survival.
引用
收藏
页码:52 / 57
页数:6
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