Division of Cardiology, CAST, Policlinico G. Rodolico-Vittorio Emanuele Hospital, University of Catania, Catania, Italy.
Catheter Cardiovasc Interv. 2020 Feb 15;95(3):398-407. doi: 10.1002/ccd.28524. Epub 2019 Oct 14.
To evaluate outcomes of transfemoral transcatheter aortic valve implantation (TF-TAVI) using three different new-generation devices.
Although new generation transcatheter aortic valves (TAVs) have demonstrated to improve procedural outcomes, to date few head-to-head comparisons are available among these devices.
This is a single center, retrospective study. From September 2014 to February 2018, 389 patients underwent elective TF-TAVI for native, severe aortic stenosis using a new-generation transcatheter aortic valve (TAV) with a preprocedural multi-detector computed tomography assessment. Among these, 346 patients received an Edwards SAPIEN 3 (n = 134), Medtronic Evolut R (n = 111), or Boston ACURATE neo (n = 101) prosthesis. Differences in baseline clinical characteristics between groups were accounted using the propensity score weighting method.
The mean age for the entire study cohort was 81.4 ± 5.2 years while the Society of Thoracic Surgery predicted risk of mortality was 4.0 ± 2.5%. After propensity score weighting adjustment, TAVs did not differently impact on 30-day all-cause and cardiovascular mortality. Evolut R device showed an increased risk of permanent pacemaker implantation (PPI) after the procedure (8.3% for SAPIEN 3 vs. 16.7% for Evolut R vs. 2.1% for ACURATE neo, p < .05). At 30 days, patients treated with SAPIEN 3 valve showed a higher mean transvalvular gradient (9.7 ± 7.5 mmHg vs. 6.1 ± 2.4 mmHg vs. 8.4 ± 3.5 mmHg for SAPIEN 3, Evolut R, and ACURATE neo, respectively, p < .01) and a lower rate of more-than-trace paravalvular regurgitation (PVR) (18.8 vs. 47.9 vs. 45.8%, for SAPIEN 3, Evolut R, and ACURATE neo, respectively, p < .01). At 1 year, SAPIEN 3, Evolut R, and ACURATE neo TAVs showed excellent and comparable outcomes with no difference in terms of freedom from major adverse cardiovascular and cerebrovascular event (MACCE) (p = 0.534).
TAVI using new-generation prostheses was associated with high device success (97.0% vs. 92.8% vs. 95.0% for SAPIEN 3, Evolut R and ACURATE neo, respectively) and low complications rates up to 1 year. Evolut R valve was associated with a higher rate of PPI whereas SAPIEN 3 valve was associated with a higher mean transvalvular gradient and lower rate of more-than-trace PVR. At 1-year, MACCE rates were similar among the three groups.
评估使用三种不同新一代器械经股动脉行主动脉瓣置换术(TF-TAVI)的结果。
尽管新一代经导管主动脉瓣(TAVs)已被证明可改善手术结果,但迄今为止,这些器械之间的头对头比较很少。
这是一项单中心回顾性研究。2014 年 9 月至 2018 年 2 月,389 例因原发性严重主动脉瓣狭窄而接受择期 TF-TAVI 的患者使用经导管主动脉瓣前的多探测器计算机断层扫描评估接受新一代经导管主动脉瓣治疗。其中,346 例患者接受了爱德华兹 SAPIEN 3(n=134)、美敦力 Evolut R(n=111)或波士顿 ACURATE neo(n=101)瓣膜。使用倾向评分加权法对各组间的基线临床特征差异进行了校正。
整个研究队列的平均年龄为 81.4±5.2 岁,而胸外科协会预测的死亡率为 4.0±2.5%。在进行倾向评分加权调整后,TAV 对 30 天全因和心血管死亡率没有不同的影响。Evolut R 装置在手术后有更高的永久性起搏器植入(PPI)风险(SAPIEN 3 为 8.3%,Evolut R 为 16.7%,ACURATE neo 为 2.1%,p<.05)。在 30 天时,SAPIEN 3 瓣膜治疗的患者平均跨瓣梯度更高(9.7±7.5mmHg 比 6.1±2.4mmHg 比 Evolut R 为 8.4±3.5mmHg,p<.01),而微量以上的瓣周漏(PVR)发生率较低(18.8%比 Evolut R 为 47.9%,比 ACURATE neo 为 45.8%,p<.01)。在 1 年时,SAPIEN 3、Evolut R 和 ACURATE neo TAVs 的结果均优异且相当,在主要不良心血管和脑血管事件(MACCE)无差异的情况下,MACCE 发生率(p=0.534)。
使用新一代瓣膜的 TAVI 与高器械成功率(SAPIEN 3 为 97.0%,Evolut R 为 92.8%,ACURATE neo 为 95.0%)和 1 年以下的低并发症发生率相关。Evolut R 瓣膜与更高的 PPI 发生率相关,而 SAPIEN 3 瓣膜与更高的平均跨瓣梯度和较低的微量以上 PVR 发生率相关。在 1 年时,三组的 MACCE 发生率相似。