Assistance Publique-Hôpitaux de Paris, Bichat-Claude Bernard Hospital, Paris, France.
Eur J Cardiothorac Surg. 2013 Jul;44(1):e8-15. doi: 10.1093/ejcts/ezt155. Epub 2013 Mar 25.
Redo surgery after failed mitral valve repair may be high risk, or contraindicated in patients with comorbidities. Because of this high risk, other interventional possibilities like transcatheter valve implantation might be of benefit. We report our experience with transcatheter mitral valve-in-ring implantation (TVIR) in high-risk patients after failure of surgical ring annuloplasty.
From January 2010 to February 2012, following a multidisciplinary discussion, 17 high-risk patients underwent TVIR using Edwards SAPIEN XT prostheses, via either a transvenous transseptal (n = 8), or a transapical approach (n = 9).
Patients were aged 70 ± 16 years, in New York Association classes III/IV. Their mean logistic EuroSCORE was 36 ± 17% and mean Society of Thoracic Surgeons risk score 13 ± 9%. The mean time interval between surgery and repair failure was 7 ± 3 years. Annuloplasty rings were semi-rigid in 14 cases, flexible in 2, and rigid in 1. Manufacturers ring diameters were 26 mm in 4 patients, 27 mm in 1, 28 mm in 9, 30 mm, 31 mm and 34 mm in 1. The predominant failure mode was regurgitation in 12 cases and stenosis in 5. SAPIEN XT diameters were 26 mm in 15 patients, 23 mm and 29 mm in 1. Procedural success rate was 88% (15/17). Emergency surgery was needed in 1 patient due to acute dislodgement of the ring. The degree of mitral regurgitation was reduced to none or mild in all but 2 patients; final mean gradient was 7 ± 3 mmHg. Thirty-day survival was 82% (14/17 patients). At last follow-up (13 ± 5 months), survival rate was 71% (12/17).
These preliminary results suggest that TVIR is feasible, with low operative risk, and may provide short-term clinical and haemodynamic improvement in selected high-risk patients with failure of mitral ring annuloplasty.
二尖瓣修复术后再手术风险可能很高,或合并症患者禁忌。由于这种高风险,其他介入治疗方法,如经导管瓣膜植入术可能有益。我们报告了在外科环瓣环成形术失败后,对高危患者进行经导管二尖瓣环中瓣植入术(TVIR)的经验。
从 2010 年 1 月至 2012 年 2 月,经过多学科讨论,17 名高危患者采用 Edwards SAPIEN XT 假体通过经静脉经间隔(n=8)或经心尖入路(n=9)进行 TVIR。
患者年龄 70±16 岁,纽约协会分类为 III/IV 级。平均逻辑 EuroSCORE 为 36±17%,平均胸外科医生协会风险评分 13±9%。手术和修复失败之间的平均时间间隔为 7±3 年。瓣环成形环在 14 例中为半刚性,在 2 例中为柔性,在 1 例中为刚性。制造商的环直径为 4 例患者 26mm,1 例患者 27mm,9 例患者 28mm,1 例患者 30mm、31mm 和 34mm。主要失败模式为 12 例反流和 5 例狭窄。SAPIEN XT 直径为 15 例患者 26mm,1 例患者 23mm 和 29mm。手术成功率为 88%(17/17)。1 例患者因环急性移位而紧急手术。除 2 例患者外,所有患者的二尖瓣反流程度均减轻至无或轻度;最终平均梯度为 7±3mmHg。30 天生存率为 82%(17/17 例患者)。最后一次随访(13±5 个月)时,生存率为 71%(17/24 例)。
这些初步结果表明,TVIR 是可行的,手术风险低,并可能为二尖瓣环瓣环成形术失败的高危患者提供短期临床和血液动力学改善。