Nijhoff Freek, Abawi Masieh, Agostoni Pierfrancesco, Ramjankhan Faiz Z, Doevendans Pieter A, Stella Pieter R
From the Departments of Cardiology (F.N., M.A., P.A., P.A.D., P.R.S.) and Cardiothoracic Surgery (F.Z.R.), University Medical Center Utrecht, Utrecht, Netherlands.
Circ Cardiovasc Interv. 2015 Jun;8(6):e002408. doi: 10.1161/CIRCINTERVENTIONS.115.002408.
The new balloon-expandable Sapien 3 transcatheter heart valve (S3-THV) incorporates new features to reduce aortic regurgitation (AR) and vascular complications in transcatheter aortic valve implantation. Aim of this study is to compare the outcomes of the S3-THV with the preceding Sapien XT THV (SXT-THV) in patients who underwent transcatheter aortic valve implantation for symptomatic severe native aortic stenosis.
Eligible patients were retrospectively identified in our institutional database and periprocedural clinical and imaging data were collected. Non-parsimonious one-to-many propensity score matching was performed to account for differences in baseline characteristics. Between November 2011 and December 2014, 167 patients underwent balloon-expandable transcatheter aortic valve implantation with either the S3-THV (n=49) or SXT-THV (n=118). Forty-four (89.8%) S3-THV patients were matched to 66 (55.9%) SXT-THV patients (mean age 80.3±8.4 and 80.5±7.8 years, median EuroSCORE 15.8 and 16.5%, respectively). In the S3-THV and SXT-THV groups, transfemoral approach (77.3% versus 78.8%) and postdilatation rates (15.9% versus 12.1%) were similar. Predischarge echocardiography demonstrated a lower incidence of ≥mild AR (15.9% versus 46.2%, P=0.003) for the S3-THV, despite reduced annulus area to prosthesis oversizing (8.2±5.1 versus 18.2±10.7%, P=0.001). Transfemoral access site-related life-threatening or major bleedings and vascular complications were absent in the S3-THV group (0% versus 7.7%, P=0.15). No differences were observed in pacemaker implantation rate (9.8% versus 8.8%, P=0.94) and 30-day mortality (both 5%).
In this retrospective, propensity score-matched analysis, the S3-THV performed superiorly to the SXT-THV, as demonstrated by improved valve patency and increased transfemoral access safety.
新型球囊扩张式Sapien 3经导管心脏瓣膜(S3 - THV)具备新特性,可减少经导管主动脉瓣植入术中的主动脉瓣反流(AR)及血管并发症。本研究旨在比较S3 - THV与前代Sapien XT经导管心脏瓣膜(SXT - THV)在因有症状的重度原发性主动脉瓣狭窄而接受经导管主动脉瓣植入术患者中的治疗效果。
在我们机构的数据库中对符合条件的患者进行回顾性识别,并收集围手术期临床和影像数据。采用非简约一对多倾向评分匹配法以考虑基线特征的差异。2011年11月至2014年12月期间,167例患者接受了球囊扩张式经导管主动脉瓣植入术,其中使用S3 - THV的患者有49例,使用SXT - THV的患者有118例。44例(89.8%)使用S3 - THV的患者与66例(55.9%)使用SXT - THV的患者进行了匹配(平均年龄分别为80.3±8.4岁和80.5±7.8岁,EuroSCORE中位数分别为15.8%和16.5%)。在S3 - THV组和SXT - THV组中,经股动脉入路(77.3%对78.8%)和后扩张率(15.9%对12.1%)相似。出院前超声心动图显示,S3 - THV组≥轻度AR的发生率较低(15.9%对46.2%,P = 0.003),尽管瓣环面积与人工瓣膜尺寸不匹配程度降低(8.2±5.1%对18.2±10.7%,P = 0.001)。S3 - THV组未出现经股动脉入路相关的危及生命或严重出血及血管并发症(0%对7.7%,P = 0.15)。在起搏器植入率(9.8%对8.8%,P = 0.94)和30天死亡率(均为5%)方面未观察到差异。
在这项回顾性、倾向评分匹配分析中,S3 - THV的表现优于SXT - THV,瓣膜通畅性改善和经股动脉入路安全性提高证明了这一点。