The Zena and Michael A. Weiner Cardiovascular Institute and the Marie-Josée and Henry R. Kravis Cardiovascular Health Center, Department of Medicine/Cardiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J Interv Cardiol. 2021 Jun 1;2021:9047596. doi: 10.1155/2021/9047596. eCollection 2021.
To compare the safety and efficacy between the SpiderFX EPD and Emboshield NAV6 filter in the collection of embolic debris created from lower limb atherectomy procedures in patients with PAD.
Between January 2014 and October 2015, 507 patients with symptomatic peripheral artery disease were treated with directional atherectomy (SilverHawk), rotational atherectomy (JetStream), or laser atherectomy (Turbo Elite) based on operator discretion. Emboshield NAV6 ( = 161) and SpiderFX ( = 346) embolic protection devices were used with each of the 3 atherectomy devices. The primary study endpoint was 30-day freedom from major adverse events (MAEs). An MAE was defined as death, MI, TVR, thrombosis, dissection, distal embolization, perforation at the level of the filter, and unplanned amputation. A descriptive comparison of the MAE rates between Emboshield NAV6 and SpiderFX embolic protection devices was conducted.
The freedom from major adverse event (MAE) rate was 92.0% (CI: 86.7%, 95.7%) in patients who received an Emboshield NAV6 filter compared to 91.6% (CI: 88.2%, 94.3%) in patients who received the SpiderFX filter (=0.434). The lower limit of 86.7% freedom from major adverse event rate in the Emboshield NAV6 group was above the performance goal of 83% ( < 0.0008).
There were no significant clinical outcome differences between Emboshield NAV6 and SpiderFX EPD filters in the treatment of lower extremities. This evaluation indicates the safety and efficacy to use either filter device to treat PAD patients with lower extremity lesions.
比较 SpiderFX EPD 和 Emboshield NAV6 过滤器在下肢动脉成形术治疗外周动脉疾病(PAD)患者中收集栓塞碎片的安全性和疗效。
2014 年 1 月至 2015 年 10 月,507 例有症状的外周动脉疾病患者根据操作者的判断接受了定向旋切术(SilverHawk)、旋转旋切术(JetStream)或激光旋切术(Turbo Elite)治疗。3 种旋切术设备均分别使用了 Emboshield NAV6( = 161)和 SpiderFX( = 346)栓塞保护装置。主要研究终点是 30 天免于主要不良事件(MAE)。MAE 定义为死亡、心肌梗死、TVR、血栓形成、夹层、远端栓塞、过滤器水平穿孔和计划外截肢。对 Emboshield NAV6 和 SpiderFX 栓塞保护装置的 MAE 发生率进行了描述性比较。
接受 Emboshield NAV6 过滤器的患者 MAE 发生率为 92.0%(CI:86.7%,95.7%),而接受 SpiderFX 过滤器的患者为 91.6%(CI:88.2%,94.3%)(=0.434)。Emboshield NAV6 组的 MAE 发生率下限为 86.7%,高于 83%的性能目标(<0.0008)。
在治疗下肢疾病方面,Emboshield NAV6 和 SpiderFX EPD 过滤器之间没有明显的临床结果差异。该评估表明,使用这两种过滤器装置治疗下肢病变的 PAD 患者是安全有效的。