Percutaneous Repair or Surgery for Mitral Regurgitation

被引:1590
作者
Feldman, Ted [1 ]
Foster, Elyse [2 ]
Glower, Donald G. [3 ]
Kar, Saibal [5 ]
Rinaldi, Michael J. [4 ]
Fail, Peter S. [6 ]
Smalling, Richard W. [7 ]
Siegel, Robert [5 ]
Rose, Geoffrey A. [4 ]
Engeron, Eric [6 ]
Loghin, Catalin [7 ]
Trento, Alfredo [5 ]
Skipper, Eric R. [4 ]
Fudge, Tommy [6 ]
Letsou, George V. [7 ]
Massaro, Joseph M. [8 ]
Mauri, Laura [9 ]
机构
[1] NorthShore Univ Hlth Syst, Evanston Hosp, Div Cardiol, Evanston, IL 60201 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Duke Univ, Med Ctr, Durham, NC 27706 USA
[4] Carolinas Med Ctr, Sanger Heart & Vasc Inst, Charlotte, NC 28203 USA
[5] Cedars Sinai Med Ctr, Inst Heart, Los Angeles, CA 90048 USA
[6] Terrebonne Gen Med Ctr, Houma, LA USA
[7] UT Hlth, Mem Hermann Heart & Vasc Inst, Houston, TX USA
[8] Boston Univ, Sch Publ Hlth, Harvard Clin Res Inst, Boston, MA 02215 USA
[9] Harvard Univ, Brigham & Womens Hosp, Sch Med, Harvard Clin Res Inst, Boston, MA 02115 USA
关键词
DOUBLE-ORIFICE TECHNIQUE; TO-EDGE TECHNIQUE; VALVE REPAIR; EVALVE MITRACLIP; MANAGEMENT; SEVERITY; DISEASE; UPDATE; TRIAL;
D O I
10.1056/NEJMoa1009355
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Mitral-valve repair can be accomplished with an investigational procedure that involves the percutaneous implantation of a clip that grasps and approximates the edges of the mitral leaflets at the origin of the regurgitant jet. METHODS We randomly assigned 279 patients with moderately severe or severe (grade 3+ or 4+) mitral regurgitation in a 2: 1 ratio to undergo either percutaneous repair or conventional surgery for repair or replacement of the mitral valve. The primary composite end point for efficacy was freedom from death, from surgery for mitral-valve dysfunction, and from grade 3+ or 4+ mitral regurgitation at 12 months. The primary safety end point was a composite of major adverse events within 30 days. RESULTS At 12 months, the rates of the primary end point for efficacy were 55% in the percutaneous-repair group and 73% in the surgery group (P = 0.007). The respective rates of the components of the primary end point were as follows: death, 6% in each group; surgery for mitral-valve dysfunction, 20% versus 2%; and grade 3+ or 4+ mitral regurgitation, 21% versus 20%. Major adverse events occurred in 15% of patients in the percutaneous-repair group and 48% of patients in the surgery group at 30 days (P<0.001). At 12 months, both groups had improved left ventricular size, New York Heart Association functional class, and quality-of-life measures, as compared with baseline. CONCLUSIONS Although percutaneous repair was less effective at reducing mitral regurgitation than conventional surgery, the procedure was associated with superior safety and similar improvements in clinical outcomes.
引用
收藏
页码:1395 / 1406
页数:12
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