One-year outcomes after rapid-deployment aortic valve replacement

被引:18
|
作者
Young, Christopher [1 ]
Laufer, Guenther [2 ]
Kocher, Alfred [2 ]
Solinas, Marco [3 ]
Alamanni, Francesco [4 ]
Polvani, Gianluca [4 ]
Podesser, Bruno K. [5 ]
Aramendi, Jose Ignacio [6 ]
Arribas, Jose [7 ]
Bouchot, Olivier [8 ]
Livi, Ugolino [9 ]
Massetti, Massimo [10 ]
Terp, Kim [11 ]
Giot, Christophe [12 ]
Glauber, Mattia [13 ]
机构
[1] St Thomas Hosp, Dept Cardiac Surg, London, England
[2] Allgemeines Krankenhaus Wien, Dept Cardiac Surg, Vienna, Austria
[3] Osped Cuore G Pasquinucci, Cardiac Surg Dept, Massa, Italy
[4] Ctr Cardiol Monzino, Dept Cardiac Surg, Milan, Italy
[5] Landesklinikum St Polten, Dept Cardiac Surg, St Polten, Austria
[6] Ctr Sanitario Hosp Univ Cruces, Dept Cardiac Surg, Baracaldo, Spain
[7] Hosp Univ Virgen de La Arrixaca, Dept Cardiac Surg, Murcia, Spain
[8] CHU Bocage, Dept Cardiac Surg, Dijon, France
[9] Santa Maria della Misericordia, Dept Cardiac Surg, Udine, Italy
[10] Policlin Univ Agostino Gemelli, Dept Cardiac Surg, Rome, Italy
[11] Aarhus Univ Hosp Skejby, Cardiac Surg Dept, Aarhus, Denmark
[12] Edwards Lifesci SA, Nyon, Switzerland
[13] Ist Clin San Ambrogio, Dept Cardiac Surg, Milan, Italy
来源
关键词
aortic valve replacement; bioprosthesis; heart valve; hemodynamics; PROSPECTIVE MULTICENTER; PATIENT MISMATCH; SURGERY; TRIAL; IMPLANTATION; PERFORMANCE; EXPERIENCE; STENOSIS; ERA;
D O I
10.1016/j.jtcvs.2017.09.133
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The goals of rapid-deployment aortic valve replacement include facilitation of minimally invasive surgery and reduced aortic crossclamp time. We report the short-term outcomes of a series of 493 patients undergoing rapid-deployment aortic valve replacement with the EDWARDS INTUITY valve system (Edwards Lifesciences, LLC, Irvine, Calif). Methods: Assessing Standard oF Care and Clinical Outcomes UsiNg the EDWARDS INTUITY VAlve SysTem in a European multI-center, Active, pOstmarket surveillaNce Study was a prospective, multicenter (n = 26) European registry designed to evaluate the safety and performance of the valve system. During rapid-deployment aortic valve replacement, device technical success and crossclamp time were assessed. Procedural outcomes, hemodynamic performance, and various adverse events and clinical outcomes were evaluated up to 2 years. Results: Between 2012 and 2014, 493 of 517 enrolled patients successfully received implants with the study valve (95.4% technical success). Mean crossclamp times for 163 full sternotomies, 128 mini-upper sternotomies, and 36 right anterior thoracotomies isolated aortic valve replacements were 47.3, 52.0, and 73.3 minutes, respectively. Mean follow-up was 1.8 years, with 870 total patient-years of follow-up. Mean effective orifice area increased from 0.72 (baseline) to 1.88 cm 2, and mean pressure gradient decreased from 47.6 to 9.6 mm Hg (1 year). Mean effective orifice area index increased (0.39-1.01 cm(2)/m(2)), and 28 of 287 patients (9.8%) exhibited severe prosthesis-patient mismatch at 1 year. After 1 year, 68.1% and 21.7% of patients were in New York Heart Association class I and II, respectively. Freedom from death, major bleeding, major perivalvular leak, reoperation, and device explant at 1 year were 0.935, 0.939, 0.976, 0.975, and 0.983, respectively. Conclusions: These results demonstrate commendable safety and performance of the test valve system over the short term in a broad European setting.
引用
收藏
页码:575 / 585
页数:11
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