Reyes V P, Raju B S, Wynne J, Stephenson L W, Raju R, Fromm B S, Rajagopal P, Mehta P, Singh S, Rao D P
Division of Cardiology, Harper Hospital, Wayne State University School of Medicine, Detroit, MI 48201.
N Engl J Med. 1994 Oct 13;331(15):961-7. doi: 10.1056/NEJM199410133311501.
Percutaneous balloon mitral valvuloplasty has been proposed as an alternative to open surgical commissurotomy for the treatment of rheumatic mitral-valve stenosis.
We enrolled 60 patients with severe mitral stenosis and favorable valvular anatomy in a prospective, randomized trial comparing the two procedures. All patients underwent cardiac catheterization before the procedure and one week, six months, and three years thereafter. Hemodynamic data were analyzed by investigators who were blinded to the patients' treatment assignments.
Mitral-valve areas improved initially in both groups, from a mean (+/- SD) of 0.9 +/- 0.3 cm2 to 2.1 +/- 0.6 cm2 in the balloon-valvuloplasty group (30 patients; P < 0.01) and from 0.9 +/- 0.3 cm2 to 2.0 +/- 0.6 cm2 in the surgical group (30 patients; P < 0.001). Although improvement was maintained in both groups, mitral-valve areas were greater in the patients in the balloon-valvuloplasty group at three years (2.4 +/- 0.6 cm2, vs. 1.8 +/- 0.4 cm2 in the surgery group, P < 0.001). Restenosis occurred in three patients in the balloon-valvuloplasty group and four in the surgery group. One patient in the balloon-valvuloplasty group died of an apparent stroke after 2.5 years; four patients in the balloon-valvuloplasty group had residual atrial septal defects, and three patients (two in the balloon-valvuloplasty group and one in the surgery group) were judged to have severe mitral regurgitation. Seventy-two percent of the patients who underwent balloon valvuloplasty and 57 percent of the surgically treated patients were in New York Heart Association functional class I (i.e., they had no cardiovascular symptoms) at three years. No patient was lost to follow-up.
In the treatment of mitral stenosis, balloon valvuloplasty and open surgical commissurotomy have comparable initial results and low rates of restenosis, and both produce good functional capacity for at least three years. The potential complications associated with balloon valvuloplasty should be noted. The better hemodynamic results at three years, lower cost, and elimination of the need for thoracotomy suggest that balloon valvuloplasty should be considered for all patients with favorable mitral-valve anatomy.
经皮气囊二尖瓣成形术已被提议作为治疗风湿性二尖瓣狭窄的开胸手术交界切开术的替代方法。
我们将60例重度二尖瓣狭窄且瓣膜解剖结构良好的患者纳入一项前瞻性随机试验,比较这两种手术方法。所有患者在手术前以及术后1周、6个月和3年都接受了心导管检查。血流动力学数据由对患者治疗分配不知情的研究人员进行分析。
两组患者二尖瓣面积最初均有改善,气囊成形术组(30例患者)从平均(±标准差)0.9±0.3 cm²增至2.1±0.6 cm²(P<0.01),手术组(30例患者)从0.9±0.3 cm²增至2.0±0.6 cm²(P<0.001)。尽管两组的改善情况均得以维持,但气囊成形术组患者在3年时的二尖瓣面积更大(2.4±0.6 cm²,而手术组为1.8±0.4 cm²,P<0.001)。气囊成形术组有3例患者发生再狭窄,手术组有4例。气囊成形术组有1例患者在2.5年后死于明显的中风;气囊成形术组有4例患者存在残余房间隔缺损,3例患者(气囊成形术组2例,手术组1例)被判定有严重二尖瓣反流。3年时,接受气囊成形术的患者中有72%以及接受手术治疗的患者中有57%处于纽约心脏协会心功能I级(即他们没有心血管症状)。没有患者失访。
在二尖瓣狭窄的治疗中,气囊成形术和开胸手术交界切开术的初始结果相当,再狭窄率低,并且两者至少在3年内都能产生良好的心功能。应注意与气囊成形术相关的潜在并发症。3年时更好的血流动力学结果、更低的成本以及无需开胸提示,对于所有二尖瓣解剖结构良好的患者都应考虑气囊成形术。