Haemodynamic benefits of rapid deployment aortic valve replacement via a minimally invasive approach: 1-year results of a prospective multicentre randomized controlled trialaEuro

被引:77
作者
Borger, Michael A. [1 ]
Dohmen, Pascal M. [2 ]
Knosalla, Christoph [3 ]
Hammerschmidt, Robert [3 ]
Merk, Denis R. [2 ]
Richter, Markus [4 ]
Doenst, Torsten [4 ]
Conradi, Lenard [5 ]
Treede, Hendrik [5 ]
Moustafine, Vadim [6 ]
Holzhey, David M. [2 ]
Duhay, Francis [7 ]
Strauch, Justus [6 ]
机构
[1] Columbia Univ, Med Ctr, 177 Ft Washington Ave,Milstein 7 GN-435, New York, NY 10032 USA
[2] Leipzig Heart Ctr, Leipzig, Germany
[3] German Heart Inst Berlin, Berlin, Germany
[4] Jena Univ Hosp, Jena, Germany
[5] Univ Med Ctr Hamburg Eppendorf, Hamburg, Germany
[6] Ruhr Univ Bochum, Univ Hosp, Bochum, Germany
[7] Edwards Lifesci LLC, Irvine, CA USA
关键词
Aortic valve replacement; Heart valve; Bioprosthesis; Haemodynamics; Minimally invasive; PERMANENT PACEMAKER IMPLANTATION; RISK-FACTORS; OUTCOMES; GUIDELINES; EXPERIENCE; MINISTERNOTOMY; STERNOTOMY; OPERATIONS; MORTALITY; SURGERY;
D O I
10.1093/ejcts/ezw042
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aortic valve replacement (AVR) via minimally invasive surgery (MIS) may provide clinical benefits in patients with aortic valve disease. A new class of bioprosthetic valves that enable rapid deployment AVR (RDAVR) may facilitate MIS. We here report the 1-year results of a randomized, multicentre trial comparing the outcomes for MIS-RDAVR with those for conventional AVR via full sternotomy (FS) with a commercially available stented aortic bioprosthesis. A total of 100 patients with aortic stenosis were enrolled in a prospective, multicentre, randomized comparison trial (CADENCE-MIS). Key exclusion criteria included AVR requiring concomitant procedures, ejection fraction of < 25% and recent myocardial infarction or stroke. Patients were randomized to undergo MIS-RDAVR via upper hemisternotomy (EDWARDS INTUITY) or AVR via FS with a commercially available stented valve. Procedural, early and late clinical outcomes were assessed for both groups. Haemodynamic performance was evaluated by an echocardiography CoreLaboratory. Technical success was achieved in 94% of MIS-RDAVR patients. MIS-RDAVR was associated with significantly reduced cross-clamp times compared with FS (41.3 +/- 20.3 vs 54.0 +/- 20.3 min, P < 0.001). Clinical and functional outcomes were similar at 30 days and 1 year postoperatively for both groups. While both groups received a similarly sized implanted valve (22.9 +/- 2.1 mm MIS-RDAVR vs 23.0 +/- 2.1 mm FS-AVR; P = 0.91), MIS-RDAVR patients had significantly lower peak gradients 1 year postoperatively (16.9 +/- 5.3 vs 21.9 +/- 8.6 mmHg; P = 0.033) and a trend towards lower mean gradients (9.1 +/- 2.9 vs 11.5 +/- 4.3 mmHg; P = 0.082). In addition, MIS-RDAVR patients had a significantly larger effective orifice area 1 year postoperatively (1.9 +/- 0.5 vs 1.7 +/- 0.4 cm(2); P = 0.047). Paravalvular leaks, however, were significantly more common in the MIS-RDAVR group (P = 0.027). MIS-RDAVR is associated with a significantly reduced cross-clamp time and better valvular haemodynamic function than FS-AVR. However, paravalvular leak rates are higher with MIS-RDAVR.
引用
收藏
页码:713 / 720
页数:8
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