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比较 Sapien 3 与 ACURATE neo 瓣膜系统:倾向评分分析。

Comparison of the Sapien 3 versus the ACURATE neo valve system: A propensity score analysis.

机构信息

Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.

Department of Cardiology, Thoraxcenter, Erasmus Medical Centre, Rotterdam, the Netherlands.

出版信息

Catheter Cardiovasc Interv. 2021 Mar;97(4):E597-E606. doi: 10.1002/ccd.29240. Epub 2020 Sep 4.

Abstract

OBJECTIVES

To compare the outcomes of transfemoral ACURATE neo (NEO) and Sapien 3 (S3) patients in terms of device success and clinical safety outcomes using a propensity score analysis.

BACKGROUND

Differences in clinical outcomes between the latest-generation balloon-expandable S3 and self-expanding NEO in a "real-world transfemoral TAVI population" are still unclear.

METHODS

We compared up to 6 months clinical outcomes using a propensity score analysis (inverse probability of treatment weighting [IPTW]) to account for differences in baseline characteristics.

RESULTS

A total of 345 patients underwent transfemoral transcatheter aortic valve implantation (TAVI) with either NEO or S3 at two centers in the Netherlands. Composite device success and early safety endpoints were comparable between NEO and S3 (Device success: IPTW-adjusted OR: 0.35 [95% CI: 0.12-1.18], and early safety: IPTW-adjusted OR: 0.51 [95% CI: 0.19-1.38]). Six-months mortality was 5.3 versus 3.6%, stroke was 2.8 versus 3.3%, and pacemaker rate was 6.1 versus 8.6%, respectively with p = NS. Mean aortic gradient was lower in the NEO group (5.72 ± 2.47 vs. 9.05 ± 3.48; p = <.001), with a comparable rate of moderate or severe paravalvular leak (0 versus 2.1%; p = NS).

CONCLUSIONS

Device success and clinical safety outcomes were comparable for both valves. Up to 6-months follow-up clinical outcomes and mortality rate remained excellent. Mean aortic gradient was lower after ACURATE neo implantation.

摘要

目的

使用倾向评分分析比较经股动脉 ACURATE neo(NEO)和 Sapien 3(S3)患者在器械成功和临床安全结局方面的差异。

背景

在“真实世界经股动脉 TAVI 人群”中,最新一代球囊扩张 S3 和自膨式 NEO 之间的临床结局差异仍不清楚。

方法

我们使用倾向评分分析(逆概率治疗加权[IPTW])比较了长达 6 个月的临床结局,以考虑基线特征的差异。

结果

共有 345 名患者在荷兰的两个中心接受了经股动脉经导管主动脉瓣植入术(TAVI),分别使用 NEO 或 S3。NEO 和 S3 的复合器械成功率和早期安全性终点相当(器械成功率:IPTW 调整后的 OR:0.35[95%CI:0.12-1.18],早期安全性:IPTW 调整后的 OR:0.51[95%CI:0.19-1.38])。6 个月死亡率分别为 5.3%和 3.6%,卒中发生率分别为 2.8%和 3.3%,起搏器使用率分别为 6.1%和 8.6%,p 值均无统计学意义。NEO 组的平均主动脉梯度较低(5.72±2.47 vs. 9.05±3.48;p<.001),中重度瓣周漏发生率相当(0% vs. 2.1%;p=NS)。

结论

两种瓣膜的器械成功率和临床安全性结局相当。6 个月的随访临床结局和死亡率仍然良好。ACURATE neo 植入后平均主动脉梯度较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de4/7984444/6e776cbc9522/CCD-97-E597-g005.jpg

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