Five-year comparison of clinical and echocardiographic outcomes of pure aortic stenosis with pure aortic regurgitation or mixed aortic valve disease in the COMMENCE trial

被引:0
作者
Thourani, Vinod H. [1 ]
Puskas, John D. [2 ]
Griffith, Bartley [3 ]
Svensson, Lars G. [4 ]
Pibarot, Philippe [5 ]
Borger, Michael A. [6 ]
Heimansohn, David [7 ]
Beaver, Thomas [8 ]
Blackstone, Eugene H. [4 ]
Antonio, Anna Liza M. [9 ]
Bavaria, Joseph E. [10 ]
机构
[1] Piedmont Heart Inst, Marcus Valve Ctr, Dept Cardiovasc Surg, 95 Collier Rd,Ste 5015, Atlanta, GA 30309 USA
[2] Emory Univ, Sch Med, Div Cardiothorac Surg, Atlanta, GA USA
[3] Univ Maryland, Med Ctr, Dept Surg, Baltimore, MD USA
[4] Cleveland Clin, Dept Thorac & Cardiovasc Surg, Cleveland, OH USA
[5] Laval Univ, Quebec Heart & Lung Inst, Dept Cardiol, Quebec City, PQ, Canada
[6] Heart Ctr Leipzig, Univ Dept Cardiac Surg, Leipzig, Germany
[7] St Vincent Heart Ctr Indiana, Dept Cardiothorac Surg, Indianapolis, IN USA
[8] Univ Florida Hlth, Div Cardiovasc Surg, Gainesville, FL USA
[9] Edwards Lifesci, Irvine, CA USA
[10] Jefferson Hlth, Dept Cardiovasc Surg, Philadelphia, PA USA
来源
JTCVS OPEN | 2024年 / 22卷
关键词
aortic stenosis; aortic regurgitation; mixed aortic valve disease; aortic valve replacement; clinical outcomes;
D O I
10.1016/j.xjon.2024.08.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To compare outcomes of aortic valve replacement (AVR) in patients with pure aortic stenosis (Pure AS) and those with pure aortic regurgitation (Pure AR) or mixed AS and AR (MAVD) in the COMMENCE trial. Methods: Of 689 patients who underwent AVR in the COMMENCE trial, patients with moderate or severe AR with or without AS (Pure AR + MAVD; n = 135) or Pure AS (n = 323) were included. Inverse probability of treatment weighting Kaplan-Meier survival curves were used for time-to-event endpoints, and longitudinal changes in hemodynamics were evaluated using mixed-effects models. Echocardiographic outcomes were assessed by an echo core laboratory and clinical outcomes adjudicated by a clinical events committee. The mean duration of follow-up was 5.3 +/- 2.2 years. Results: At 5 years, adjusted safety endpoints were not statistically different between groups; no structural valve deterioration (SVD) event occurred in either group. After adjustment, the Pure AR + MAVD group had a greater change in body surface area-corrected left ventricular (LV) mass reduction (P = .03) compared to the Pure AS patients. Those patients with a baseline LV ejection fraction (LVEF) >55% continued to demonstrate preserved contractility compared to patients with an LVEF <= 55% at baseline (P < .0001). No significant difference in mean gradient (P = .07) or effective orifice area (P = .96) at 5 years was evident between the groups. Conclusions: Patients with Pure AR + MAVD demonstrated similar clinical safety and freedom from SVD at 5 years compared to those with Pure AS. There was a significant difference in LV reverse remodeling in the Pure AR + MAVD group compared to the Pure AS group at 5 years. These favorable outcomes in patients with AR may reinforce the need for treatment before irreversible changes occur.
引用
收藏
页码:160 / 173
页数:14
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