Ueno Hiroshi, Hida Yuki, Ueno Yohei, Tanaka Shuhei, Ushijima Ryuichi, Sobajima Mitsuo, Fukuda Nobuyuki, Imamura Teruhiko, Kameyama Akiyo, Komiya Ryosuke, Ito Hisakatsu, Yokoyama Shigeki, Doi Toshio, Fukahara Kazuaki, Kinugawa Koichiro
Cardiovascular Center, Toyama University Hospital, Toyama, Japan.
J Cardiol Cases. 2020 Sep 25;23(1):49-52. doi: 10.1016/j.jccase.2020.09.003. eCollection 2021 Jan.
A 76-year-old woman had received surgical mitral valve replacement with Magna Mitral Ease (Edwards Lifesciences, Irvine, CA, USA) 25 mm for functional severe mitral regurgitation 6 years previously. She presented recurrence of heart failure due to severe stenotic and moderate regurgitant degeneration of the implanted mitral bioprosthesis. Considering her comorbidities and left ventricular systolic dysfunction, our heart valve team eventually decided to perform percutaneous transseptal transcatheter mitral valve-in-valve replacement instead of surgical redo mitral valve replacement, using a 26 mm SAPIEN 3 valve (Edwards Lifesciences) via trans-femoral approach. Post-procedural course was uneventful and she was discharged on post-procedural day 2. This is, to the best of our knowledge, the first case of successful percutaneous transseptal transcatheter mitral valve-in-valve replacement in Japan. Further large-scale prospective studies are warranted to validate its long-term safety and efficacy, particularly by comparing with the redo surgery. < We experienced an off-label transseptal mitral valve-in-valve replacement using SAPIEN 3 to treat degenerative mitral bioprosthesis for the first time in Japan. Although further large-scale prospective studies are warranted, this procedure should be a promising therapeutic alternative to conventional redo-surgery, particularly for elderly patients with multiple comorbidities.>.
一名76岁女性6年前因功能性严重二尖瓣反流接受了使用美国加利福尼亚州尔湾市爱德华兹生命科学公司生产的25毫米Magna Mitral Ease人工二尖瓣进行的二尖瓣置换手术。她因植入的二尖瓣生物瓣膜严重狭窄和中度反流性退变而出现心力衰竭复发。考虑到她的合并症和左心室收缩功能障碍,我们的心脏瓣膜团队最终决定采用经皮经间隔经导管二尖瓣瓣中瓣置换术,而不是再次进行二尖瓣置换手术,通过经股动脉途径使用26毫米的SAPIEN 3瓣膜(爱德华兹生命科学公司)。术后过程顺利,她在术后第2天出院。据我们所知,这是日本首例成功的经皮经间隔经导管二尖瓣瓣中瓣置换术。有必要进行进一步的大规模前瞻性研究,以验证其长期安全性和有效性,特别是与再次手术进行比较。<我们在日本首次使用SAPIEN 3进行了非标签经间隔二尖瓣瓣中瓣置换术,以治疗退变的二尖瓣生物瓣膜。尽管有必要进行进一步的大规模前瞻性研究,但该手术对于传统再次手术而言应是一种有前景的治疗选择,特别是对于患有多种合并症的老年患者。>