Acker Michael A, Bolling Steven, Shemin Richard, Kirklin James, Oh Jae K, Mann Douglas L, Jessup Mariell, Sabbah Hani N, Starling Randall C, Kubo Spencer H
Department of Surgery, University of Pennsylvania, Philadelphia, PA 19104-6070, USA.
J Thorac Cardiovasc Surg. 2006 Sep;132(3):568-77, 577.e1-4. doi: 10.1016/j.jtcvs.2006.02.062. Epub 2006 Jul 31.
The study objective was to evaluate in a prospective, randomized, multicenter trial the safety and efficacy of mitral valve surgery with and without the CorCap cardiac support device (Acorn Cardiovascular, St Paul, Minn) in patients with New York Heart Association Class II to IV heart failure.
Although mitral valve surgery has been performed successfully in patients with heart failure, the safety and long-term efficacy have not been established in a multicenter prospective trial. Cardiac support devices that reduce ventricular wall stress and promote beneficial reverse remodeling have been proposed as a new treatment option as a stand-alone procedure and as an adjunct to mitral valve surgery.
A subgroup of 193 patients were enrolled in the mitral valve repair or replacement stratum of the Acorn Clinical Trial; 102 patients were randomized to the mitral valve surgery alone group (control) and 91 patients were randomized to mitral valve surgery with implantation of the CorCap cardiac support device. Patients were followed for a median duration of 22.9 months.
For the entire mitral valve surgery group, the 30-day operative mortality rate was only 1.6% at 30 days. Mitral surgery was associated with progressive reductions in left ventricle end-diastolic volume, left ventricle end-systolic volume, and left ventricular mass, and increases in left ventricle ejection fraction and sphericity index, all consistent with reverse remodeling. Recurrence of clinically significant mitral regurgitation was uncommon. Quality of life, exercise performance, and New York Heart Association functional class were all improved. Finally, the addition of the CorCap cardiac support device led to greater decreases in left ventricular end-diastolic volume and left ventricular end-systolic volume, a more elliptical shape, and a trend for a reduction in major cardiac procedures and improvement in quality of life compared with mitral surgery alone.
These findings suggest that there is clear benefit to the surgical elimination of mitral regurgitation and that there is additional benefit with the CorCap cardiac support device. Given the improvement in left ventricle structure and function, along with a low mortality rate, physicians should strongly consider offering mitral valve surgery in combination with the CorCap cardiac support device to patients with heart failure who are on an optimal medical regimen.
本研究目的是在一项前瞻性、随机、多中心试验中,评估在纽约心脏协会II至IV级心力衰竭患者中,使用和不使用CorCap心脏支持装置(Acorn Cardiovascular公司,明尼苏达州圣保罗)进行二尖瓣手术的安全性和有效性。
尽管二尖瓣手术已在心力衰竭患者中成功实施,但多中心前瞻性试验尚未确定其安全性和长期疗效。已提出可减少心室壁应力并促进有益逆向重构的心脏支持装置,作为一种独立手术及二尖瓣手术辅助手段的新治疗选择。
193名患者被纳入Acorn临床试验的二尖瓣修复或置换层;102名患者被随机分配至单纯二尖瓣手术组(对照组),91名患者被随机分配至植入CorCap心脏支持装置的二尖瓣手术组。患者的中位随访时间为22.9个月。
对于整个二尖瓣手术组,30天手术死亡率仅为1.6%。二尖瓣手术与左心室舒张末期容积、左心室收缩末期容积和左心室质量的逐渐降低,以及左心室射血分数和球形指数的增加相关,所有这些均与逆向重构一致。具有临床意义的二尖瓣反流复发并不常见。生活质量、运动能力和纽约心脏协会功能分级均得到改善。最后,与单纯二尖瓣手术相比,添加CorCap心脏支持装置导致左心室舒张末期容积和左心室收缩末期容积进一步降低,形状更呈椭圆形,并且有减少主要心脏手术和改善生活质量的趋势。
这些发现表明,手术消除二尖瓣反流有明显益处,并且CorCap心脏支持装置有额外益处。鉴于左心室结构和功能的改善以及低死亡率,医生应强烈考虑为接受最佳药物治疗方案的心力衰竭患者提供二尖瓣手术联合CorCap心脏支持装置的治疗。