Department of Cardiology, Changhai Hospital, Second Military Medical University, Shanghai, 200433, China.
Department of Cardiology, ShangRao Hospital of Traditional Chinese Medicine, Shangrao, 334000, Jiangxi, China.
J Cardiothorac Surg. 2020 Sep 29;15(1):276. doi: 10.1186/s13019-020-01327-4.
In this study, we sought to evaluate the feasibility of improved transcatheter aortic valve implantation (TAVI) in noncalcified aortic valve by using the novel concept of double-layer ChenValve prosthesis. TAVI was initially considered as an alternative treatment for high-risk patients with aortic stenosis. However, non noncalcified aortic valve disease was considered as a contraindication to TAVI.
ChenValve prosthesis, which consisted of a self-expanding Nitinol ring, a balloon-expandable cobalt-chromium alloy stent and a biological valve, was implanted at the desired position under fluoroscopic guidance in a transapical approach through a 20F sheath in 10 goats. Aortic angiography was performed to measure the diameter of the aotic annulus and assess the performance of the artificial valve. The ultrasound was used to evaluate the regurgitation or paravalvular leakage and trans-prosthetic vascular flow velocity postoperatively. The aortogram and transthoracic echocardiography were applied to observe whether the valve stent was implanted at the desired position.
ChenValve prosthesis was successfully transppical implanted in all animals. The aortogram and transthoracic echocardiography performed immediately after implantation revealed that the valve stent was implanted at the desired position. There was no significant paravalvular leakage, obstruction of coronary artery ostia, stent malpositioning or dislodgement occurred.
This preliminary trial with the novel double-layer ChenValve prosthesis demonstrated the feasibility of improved TAVI in noncalcified aortic valve. The mechanism of Nitinol ring-guided locating the aortic sinus enables us to anatomically correct position the artifact valve. This improved strategy seems to make the TAVI process more safe and repeatable in noncalcified aortic valve.
本研究旨在通过新型双层 ChenValve 人工瓣膜的新概念,评估经导管主动脉瓣植入术(TAVI)在非钙化主动脉瓣中的可行性。TAVI 最初被认为是高危主动脉瓣狭窄患者的替代治疗方法。然而,非钙化主动脉瓣疾病被认为是 TAVI 的禁忌症。
在 10 只山羊中,经心尖途径,在 20F 鞘管下,在荧光透视引导下,将 ChenValve 人工瓣膜(由自膨式 Nitinol 环、球囊扩张钴铬合金支架和生物瓣组成)植入所需位置。进行主动脉造影以测量主动脉瓣环的直径,并评估人工瓣膜的性能。超声心动图用于评估术后瓣周漏或瓣周漏和跨瓣血流速度。主动脉造影和经胸超声心动图用于观察瓣膜支架是否植入到所需位置。
ChenValve 人工瓣膜在所有动物中均成功经心尖植入。植入后即刻行主动脉造影和经胸超声心动图检查显示,瓣膜支架植入到所需位置。无明显瓣周漏、冠状动脉开口阻塞、支架定位不当或移位。
本研究初步探讨了新型双层 ChenValve 人工瓣膜在非钙化主动脉瓣中的可行性。Nitinol 环引导定位主动脉窦的机制使我们能够在解剖学上正确定位人工瓣膜。这种改良策略似乎使 TAVI 过程在非钙化主动脉瓣中更加安全和可重复。