Filip Grzegorz, Litwinowicz Radoslaw, Kapelak Boguslaw, Piatek Jacek, Bartus Magdalena, Konstanty-Kalandyk Janusz, Brzezinski Maciej, Bartus Krzysztof
Department of Cardiovascular Surgery and Transplantology, Jagiellonian University, John Paul II Hospital, Krakow, Poland.
Department of Experimental Pharmacology, Jagiellonian University, Krakow, Poland.
J Thorac Dis. 2018 Nov;10(11):6128-6136. doi: 10.21037/jtd.2018.10.10.
Aortic stenosis (AS) is the most common valve disease in the adult population and its prevalence increases with age. Unfortunately, older age and comorbidities significantly increase mortality, operative risk and worsen prognosis. In recent years, sutureless bioprosthesis [sutureless-aortic valve replacement (SU-AVR)] has become an alternative to standard AVR or TAVI in high-risk patients. Compared to standard AVR, the advantages of SU-AVR include shorter valve implantation, shorter aortic cross clamp (ACC) and cardiopulmonary bypass (CPB) times and higher valve EOA with more favorable hemodynamic parameters. Good early clinical and hemodynamic outcomes have been reported in several studies. However, although early SU-AVR results reported in the literature are encouraging, there are few results of long term follow-up. The aim of this study is to present long term echocardiographic hemodynamic outcomes of the Enable sutureless bioprosthesis.
The first human implantation of the Enable sutureless bioprosthesis was performed on the 13th January, 2005 by the authors of this manuscript. From that time until July 2008, 25 patients underwent isolated SU-AVR implantation. The median preoperative logistic EuroSCORE was 1.92±0.17 [standard deviation (SD)] and the STS score was 2.96±2.73. Preoperatively, 65.4% of patients were in NYHA class III or IV, the peak/mean gradient transaortic gradient was 84.6/52.1 mmHg.
After the SU-AVR procedure, the average peak/mean aortic gradients were respectively: 12.9/7.1 mmHg at the intraoperative time; 18.1/9.5 mmHg at 3-6 months; 18.3/9.6 mmHg at 11-14 months; 16.9/9.3 mmHg at 2 years; 15.3/8 mmHg at 3 years; 13.4/7.1 mmHg at 4 years; 16.7/8.9 mmHg at 5 years follow-up. Other hemodynamic echocardiographic parameters such as LVOT diameter, LVOT peak velocity, LVOT TVI, valve peak velocity and valve TVI were stable during the follow-up period.
In summary, sutureless bioprostheses are safe and effective treatments for valve stenosis with excellent outcomes and hemodynamic profile which remained stable during the follow-up period. The peak and mean gradients were 16.7 and 8.9 mmHg, respectively, over a 5-year follow-up period.
主动脉瓣狭窄(AS)是成年人群中最常见的瓣膜疾病,其患病率随年龄增长而增加。不幸的是,高龄和合并症会显著增加死亡率、手术风险并使预后恶化。近年来,无缝合生物假体[无缝合主动脉瓣置换术(SU-AVR)]已成为高危患者标准AVR或TAVI的替代方案。与标准AVR相比,SU-AVR的优势包括瓣膜植入时间更短、主动脉交叉钳夹(ACC)和体外循环(CPB)时间更短,以及瓣膜有效开口面积(EOA)更大,血流动力学参数更有利。多项研究报告了良好的早期临床和血流动力学结果。然而,尽管文献中报道的早期SU-AVR结果令人鼓舞,但长期随访结果却很少。本研究的目的是展示Enable无缝合生物假体的长期超声心动图血流动力学结果。
本手稿的作者于2005年1月13日首次对人类植入Enable无缝合生物假体。从那时起到2008年7月,25例患者接受了单纯SU-AVR植入。术前逻辑EuroSCORE中位数为1.92±0.17[标准差(SD)],STS评分为2.96±2.73。术前,65.4%的患者为纽约心脏协会(NYHA)III或IV级,经主动脉峰值/平均压差为84.6/52.1 mmHg。
SU-AVR手术后,平均峰值/平均主动脉压差分别为:术中12.9/7.1 mmHg;3至6个月时18.1/9.5 mmHg;11至14个月时18.3/9.6 mmHg;2年时16.9/9.3 mmHg;3年时15.3/8 mmHg;4年时13.4/7.1 mmHg;5年随访时16.7/8.9 mmHg。其他超声心动图血流动力学参数,如左心室流出道直径、左心室流出道峰值速度、左心室流出道TVI、瓣膜峰值速度和瓣膜TVI在随访期间保持稳定。
总之,无缝合生物假体是治疗瓣膜狭窄的安全有效方法,具有优异的结果和血流动力学特征,在随访期间保持稳定。在5年的随访期内,峰值和平均压差分别为16.7和8.9 mmHg。