Cardiac Catheterisation Laboratory, Cardiothoracic Department, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
EuroIntervention. 2010 Nov;6(5):568-74. doi: 10.4244/EIJV6I5A96.
Transcatheter aortic valve implantation (TAVI) is a new option for patients with severe aortic stenosis at high surgical risk. We compared the clinical outcome of patients referred for TAVI and subsequently treated with TAVI, surgical aortic valve replacement (SAVR), balloon aortic valvuloplasty (BAV), or medical management (MM).
All consecutive patients (n=166, EuroSCORE 24.9 ± 13.9%) referred for TAVI to our two centres were enrolled in a prospective registry and were assigned to SAVR (n=21), TAVI with the CoreValve prosthesis (n=75), BAV (n=20), or MM (n=50) by a multi-specialty team. The primary endpoint was 6-month cardiac mortality. Patients undergoing BAV had a significantly higher EuroSCORE (33.6 ± 15.9%; p=0.01). Median follow-up time was nine months (interquartile range 4.5-12.4 months). Six-month freedom from cardiac death was 81.0 ± 8.6%, 92.0 ± 3.1%, 72.9 ± 10.5%, and 72.7 ± 6.5% for SAVR, TAVI, BAV, and MM groups, respectively. Freedom from major cardiac and cerebrovascular events was 76.2 ± 9.3%, 83.9 ± 4.3%, 72.9 ± 10.5%, and 65.6 ± 6.8% for SAVR, TAVI, BAV, and MM groups, respectively.
With respect to medical management and BAV, TAVI was associated with lower cardiac mortality at six months. Clinical outcome after TAVI was similar to that of less sick patients undergoing SAVR.
经导管主动脉瓣植入术(TAVI)是高危外科手术的严重主动脉瓣狭窄患者的新选择。我们比较了 TAVI 转归患者,并将其随后接受 TAVI、外科主动脉瓣置换术(SAVR)、球囊主动脉瓣成形术(BAV)或药物治疗(MM)的临床结果。
我们对两个中心的所有连续 TAVI 转归患者(n=166,欧洲心脏手术风险评估系统评分 24.9±13.9%)进行了前瞻性登记,并由多学科团队分配至 SAVR(n=21)、CoreValve 瓣膜 TAVI(n=75)、BAV(n=20)或 MM(n=50)。主要终点为 6 个月心脏死亡率。行 BAV 的患者欧洲心脏手术风险评估系统评分明显更高(33.6±15.9%;p=0.01)。中位随访时间为 9 个月(四分位间距 4.5-12.4 个月)。SAVR、TAVI、BAV 和 MM 组的 6 个月无心脏死亡生存率分别为 81.0±8.6%、92.0±3.1%、72.9±10.5%和 72.7±6.5%。SAVR、TAVI、BAV 和 MM 组的 6 个月无重大心脏和脑血管事件生存率分别为 76.2±9.3%、83.9±4.3%、72.9±10.5%和 65.6±6.8%。
与药物治疗和 BAV 相比,TAVI 在 6 个月时的心脏死亡率较低。TAVI 的临床结果与接受 SAVR 的病情较轻患者相似。