Gonzalez Manuel A, Ben-Dor Itsik, Maluenda Gabriel, Pichard Augusto D, Satler Lowell F, Waksman Ron
Division of Cardiology, Cardiovascular Research Institute at Washington Hospital Center, 110 Irving Street, NW, Suite 4B-1, Washington, DC 20010, USA.
J Heart Valve Dis. 2012 Nov;21(6):724-31.
Severe aortic regurgitation (AR) is a contraindication for balloon aortic valvuloplasty (BAV). As the effects of mild and moderate AR are unknown, the study aim was to determine the effects of BAV in patients with mild and moderate AR.
A total of 263 consecutive patients with symptomatic severe aortic stenosis (AS) who underwent BAV was included in the study. The patients were stratified into three groups according to their pre-procedural degree of AR, as assessed echocardiographically.
The study groups included pre-BAV with no AR (n = 76; 28.9%), mild AR (n = 180; 68.4%), and moderate AR (n = 7; 2.7%). There were no differences in the baseline characteristics of the groups, with a mean age of 81.9 +/- 9.0 years and a Society of Thoracic Surgeons score of 12.9 +/- 6.0. Among patients with no AR pre-BAV, 48.7% developed mild AR post-BAV, while 4.5% of those with mild AR pre-BAV developed moderate AR (p < 0.001). The majority of patients (93%) had mild AR both pre- and post-BAV. Only two patients developed severe AR post-BAV. A good agreement existed between the categories of AR pre- and post-BAV (weighted kappa = 0.54, 95% CI, 0.43-0.65). The degree of AR post-BAV did not impact on the mortality rates of mild AR (41.1%), moderate AR (46.9%), or severe AR (63.6%) (p = 0.31).
It is safe to perform BAV in patients with mild and moderate AR. About half of all patients with no AR may develop mild AR, the majority will remain in mild AR, and a small percentage will develop moderate or severe AR.
重度主动脉瓣反流(AR)是球囊主动脉瓣成形术(BAV)的禁忌证。由于轻度和中度AR的影响尚不清楚,本研究的目的是确定BAV对轻度和中度AR患者的影响。
本研究纳入了263例连续接受BAV治疗的有症状重度主动脉瓣狭窄(AS)患者。根据术前经超声心动图评估的AR程度,将患者分为三组。
研究组包括BAV术前无AR的患者(n = 76;28.9%)、轻度AR患者(n = 180;68.4%)和中度AR患者(n = 7;2.7%)。各组基线特征无差异,平均年龄为81.9±9.0岁,胸外科医师协会评分12.9±6.0。BAV术前无AR的患者中,48.7%在BAV术后发生轻度AR,而BAV术前轻度AR患者中有4.5%发展为中度AR(p < 0.001)。大多数患者(93%)在BAV术前和术后均为轻度AR。仅2例患者在BAV术后发生重度AR。BAV术前和术后AR类别之间存在良好的一致性(加权kappa = 0.54,95%CI,0.43 - 0.65)。BAV术后AR程度对轻度AR(41.1%)、中度AR(46.9%)或重度AR(63.6%)的死亡率无影响(p = 0.31)。
对轻度和中度AR患者进行BAV是安全的。所有无AR的患者中约一半可能发展为轻度AR,大多数仍为轻度AR,一小部分将发展为中度或重度AR。