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ASSURED 试验中房间隔缺损封堵器的长期结果:联合关键/持续入路队列。

Long-Term Results of the Atrial Septal Defect Occluder ASSURED Trial for Combined Pivotal/Continued Access Cohorts.

机构信息

The Lillie Frank Abercrombie Division of Cardiology, Texas Children's Hospital, Houston, Texas, USA; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

Columbia University of New York, New York, New York, USA.

出版信息

JACC Cardiovasc Interv. 2024 Oct 14;17(19):2274-2283. doi: 10.1016/j.jcin.2024.07.013. Epub 2024 Sep 18.

Abstract

BACKGROUND

The GORE CARDIOFORM ASD Occluder (GCA, W. L. Gore & Associates) was approved in 2019 for ostium secundum atrial septal defect (ASD) closure.

OBJECTIVES

This study sought to report the combined pivotal and continued access cohorts of the ASSURED (Safety and Efficacy Study of Transcatheter Closure of Ostium Secundum ASDs) trial results through 36 months.

METHODS

This prospective, multicenter, single-arm trial evaluated procedural and clinical outcomes of ASD closure with the GCA. The primary endpoints were 6-month closure success following device implantation and composite clinical success (deployment/retention of device, safety, and closure). Technical and procedure success, safety, clinically significant new arrhythmia (CSNA) secondary endpoints, and wire frame fracture (WFF, with fluoroscopy) at 6 and 36 months were evaluated.

RESULTS

Of 569 patients (median age of 10.4 years and median weight of 35.0 kg) who underwent attempted secundum ASD closure, 526 were technical successes. The mean stop-flow ASD diameter was 17.6 ± 5.3 mm. All 478 patients with 6-month imaging achieved closure success. Composite clinical success at 6 and 36 months was achieved in 87.6% (468/534) and 84.0% (351/418) of patients, respectively. Technical failure occurred in 8.1% (43/548), 30-day device- or procedure-related serious adverse event in 3.9% (21/534), and 6-month device events in 2.8% (15/534) of patients. At 30 days, 21 of 569 patients (3.7%) had CSNA. At 6 months, 138 of 436 (31.7%) patients had WFFs and 105 of 185 (56.8%) at 36 months (without sequelae).

CONCLUSIONS

In this large congenital ASD device trial, the GCA had acceptable results. WFFs, although common, did not result in any clinical sequelae. The unique features, size range, and safety profile expand the options for secundum ASD closure. (Safety and Efficacy Study of Transcatheter Closure of Ostium Secundum ASDs [ASSURED]; NCT02985684).

摘要

背景

戈尔心血管 FORM ASD 封堵器(GCA,戈尔联合公司)于 2019 年获准用于治疗继发孔型房间隔缺损(ASD)。

目的

本研究旨在报告经导管关闭继发孔 ASD 的 ASSURED(经导管关闭继发孔 ASD 的安全性和疗效研究)试验的主要和持续访问队列结果,随访时间为 36 个月。

方法

这是一项前瞻性、多中心、单臂试验,评估了 GCA 用于 ASD 封堵的手术和临床结果。主要终点为植入装置后 6 个月的封堵成功率和复合临床成功率(装置的植入/保留、安全性和封堵)。评估了技术和程序成功率、安全性、临床显著新心律失常(CSNA)次要终点,以及 6 个月和 36 个月时的线框骨折(WFF,透视)。

结果

在 569 例尝试进行继发孔 ASD 封堵的患者中(中位年龄为 10.4 岁,中位体重为 35.0kg),526 例患者技术成功。平均停流 ASD 直径为 17.6±5.3mm。所有 478 例有 6 个月影像学结果的患者均达到了封堵成功。6 个月和 36 个月的复合临床成功率分别为 87.6%(468/534)和 84.0%(351/418)。技术失败率为 8.1%(43/548),30 天内与器械或手术相关的严重不良事件发生率为 3.9%(21/534),6 个月时器械事件发生率为 2.8%(15/534)。30 天时,569 例患者中有 3.7%(21 例)出现 CSNA。6 个月时,436 例患者中有 31.7%(138 例)发生 WFF,185 例患者中有 56.8%(105 例)发生 WFF(无后遗症)。

结论

在这项大型先天性 ASD 器械试验中,GCA 结果可接受。尽管 WFF 很常见,但并未导致任何临床后遗症。其独特的特征、尺寸范围和安全性特征为继发孔 ASD 封堵提供了更多选择。(经导管关闭继发孔 ASD 的安全性和疗效研究[ASSURED];NCT02985684)。

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