Outcomes for the Commercial Use of Self-Expanding Prostheses in Transcatheter Aortic Valve Replacement A Report From the STS/ACC TVT Registry

被引:52
作者
Sorajja, Paul [1 ]
Kodali, Susheel [2 ]
Reardon, Michael J. [3 ]
Szeto, Wilson Y. [4 ]
Chetcuti, Stanley J. [5 ]
Hermiller, James [6 ]
Chenoweth, Sharla [7 ]
Adams, David H. [8 ]
Popma, Jeffrey J. [9 ]
机构
[1] Minneapolis Heart Inst Fdn, Valve Sci Ctr, Minneapolis, MN USA
[2] Columbia Univ, Med Ctr, New York, NY USA
[3] Houston Methodist DeBakey Heart & Vasc Ctr, Houston, TX USA
[4] Univ Penn, Philadelphia, PA 19104 USA
[5] Univ Michigan, Ann Arbor, MI 48109 USA
[6] St Vincents Heart Ctr Indiana, Indianapolis, IN USA
[7] Medtronic, Minneapolis, MN USA
[8] Mt Sinai Med Ctr, New York, NY 10029 USA
[9] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
aortic stenosis; CoreValve; Evolut R; outcomes; transcatheter; CLINICAL-OUTCOMES; EVOLUT R; 2-YEAR OUTCOMES; EXTREME RISK; STENOSIS; BIOPROSTHESIS; IMPLANTATION; MANAGEMENT;
D O I
10.1016/j.jcin.2017.07.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The authors sought to compare the outcomes of commercial transcatheter aortic valve replacement (TAVR) with the repositionable Evolut R platform to those observed with the CoreValve device in the Society of Thoracic Surgeons (STS)/American College of Cardiology (ACC) Transcatheter Valve Therapy (TVT) Registry. BACKGROUND TAVR continues to evolve, with rapid adoption of iterative changes for commercial practice. Insight into the outcomes of this adoption is needed. METHODS Patients in the TVT Registry who had TAVR using a 23-,26-, or 29-mm self-expanding prosthesis were enrolled. Site-reported events for procedural, in-hospital, and 30-day outcomes were examined. RESULTS Between January 2014 and April 2016, 9,616 patients underwent TAVR with a self-expanding prosthesis with data entered in the TVT Registry. Compared with patients treatedwith CoreValve TAVR, those who received Evolut R TAVR had a lower STS-PROM score (8.0 +/- 5.4% vs. 8.7 +/- 5.3%; p < 0.001), more iliofemoral access (91.6% vs. 89.2%; p < 0.001), and more frequently had conscious sedation (27.4% vs. 12.7%; p<0.001). With Evolut R TAVR, there was less need for a second prosthesis (2.2% vs. 4.5%; p<0.001), less device migration (0.2% vs. 0.6%; p = 0.01), a lower incidence of moderate/severe paravalvular regurgitation (post-procedure, 4.4% vs. 6.2%; p < 0.001), and shorter median hospital stay (4.0 vs. 5.0 days; p < 0.001). Patients treatedwith Evolut R TAVR had greater device success (96.3% vs. 94.9%; p = 0.001). At 30 days, Evolut R patients had both lower mortality (3.7% vs. 5.3%; p < 0.001) and less need for a pacemaker (18.3% vs. 20.1%; p = 0.03). CONCLUSIONS Commercial adoption of the Evolut R platform is associated with significant improvements in acute outcomes for patients undergoing TAVR for aortic stenosis. (C) 2017 by the American College of Cardiology Foundation.
引用
收藏
页码:2090 / 2098
页数:9
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