McGill University Health Centre, Montreal, Canada.
EuroIntervention. 2017 Nov 20;13(10):1149-1156. doi: 10.4244/EIJ-D-16-00303.
Transcatheter aortic valve implantation for a failing surgical bioprosthesis (TAV-in-SAV) has become an alternative for patients at high risk for redo surgical aortic valve replacement (redo-SAVR). Comparisons between these approaches are non-existent. This study aimed to compare clinical and echocardiographic outcomes of patients undergoing TAV-in-SAV versus redo-SAVR after accounting for baseline differences by propensity score matching.
Patients from seven centres in Europe and Canada who had undergone either TAV-in-SAV (n=79) or redo-SAVR (n=126) were identified. Significant independent predictors used for propensity scoring were age, NYHA functional class, number of prior cardiac surgeries, urgent procedure, pulmonary hypertension, and COPD grade. Using a calliper range of ±0.05, a total of 78 well-matched patient pairs were found. All-cause mortality was similar between groups at 30 days (6.4% redo-SAVR vs. 3.9% TAV-in-SAV; p=0.49) and one year (13.1% redo-SAVR vs. 12.3% TAV-in-SAV; p=0.80). Both groups also showed similar incidences of stroke (0% redo-SAVR vs. 1.3% TAV-in-SAV; p=1.0) and new pacemaker implantation (10.3% redo-SAVR vs. 10.3% TAV-in-SAV; p=1.0). The incidence of acute kidney injury requiring dialysis was numerically lower in the TAV-in-SAV group (11.5% redo-SAVR vs. 3.8% TAV-in-SAV; p=0.13). The TAV-in-SAV group had a significantly shorter median total hospital stay (12 days redo-SAVR vs. 9 days TAV-in-SAV; p=0.001).
Patients with aortic bioprosthesis failure treated with either redo-SAVR or TAV-in-SAV have similar 30-day and one-year clinical outcomes.
对于外科生物瓣(SAV)功能障碍的患者,经导管主动脉瓣植入术(TAV-in-SAV)已成为再次行主动脉瓣置换术(redo-SAVR)的替代方法。目前尚未对这两种方法进行比较。本研究旨在通过倾向评分匹配来比较 TAV-in-SAV 与 redo-SAVR 治疗后患者的临床和超声心动图结果。
从欧洲和加拿大的 7 个中心确定了行 TAV-in-SAV(n=79)或 redo-SAVR(n=126)的患者。用于倾向评分的独立预测因子包括年龄、NYHA 心功能分级、先前心脏手术次数、紧急手术、肺动脉高压和 COPD 分级。使用 0.05 的卡尺范围,共找到 78 对匹配良好的患者。30 天和 1 年时两组的全因死亡率相似(redo-SAVR 组为 6.4%,TAV-in-SAV 组为 3.9%;p=0.49)和(redo-SAVR 组为 13.1%,TAV-in-SAV 组为 12.3%;p=0.80)。两组的卒中发生率(redo-SAVR 组为 0%,TAV-in-SAV 组为 1.3%;p=1.0)和新植入起搏器的发生率(redo-SAVR 组为 10.3%,TAV-in-SAV 组为 10.3%;p=1.0)也相似。需要透析治疗的急性肾损伤发生率在 TAV-in-SAV 组中略低(redo-SAVR 组为 11.5%,TAV-in-SAV 组为 3.8%;p=0.13)。TAV-in-SAV 组的中位总住院时间明显缩短(redo-SAVR 组为 12 天,TAV-in-SAV 组为 9 天;p=0.001)。
对于外科生物瓣功能障碍的患者,行 redo-SAVR 或 TAV-in-SAV 治疗的患者 30 天和 1 年的临床结局相似。