Section of Vascular Surgery, Department of Surgery, Washington University, St. Louis, Mo.
North Carolina Heart and Vascular, Rex Hospital, Raleigh, NC.
J Vasc Surg. 2021 Mar;73(3):918-929.e5. doi: 10.1016/j.jvs.2020.08.135. Epub 2020 Sep 18.
No vascular implant is commercially available in the United States to treat post-angioplasty dissections in below-the-knee (BTK) arteries. The Tack Endovascular System (Intact Vascular, Wayne, Pa) is purpose-built to repair postpercutaneous transluminal angioplasty (PTA) BTK dissections. A trial was conducted to investigate the safety and efficacy of the first-of-a-kind implantable BTK device to treat post-PTA dissections in the setting of critical limb ischemia.
The present prospective, single-arm, multicenter study evaluated the Tack Endovascular System for treating post-PTA dissections in the mid/distal popliteal, tibial, and peroneal arteries. The primary safety endpoint was major adverse limb events (MALE) plus perioperative death (POD), assessed at 30 days after the index procedure. The primary efficacy endpoint was a composite of MALE at 6 months and POD. The unpowered secondary endpoint was primary patency at 6 months. With no available on-label comparator, the primary endpoints of the present trial were determined using objective performance goals from a systematic literature search. The secondary endpoints included Tacked segment patency and target limb salvage at 6 months. The 6-month results are reported.
Of the 233 patients enrolled, 117 (50.2%) had Rutherford class 5 and 78 (33.5%) had Rutherford class 4. A total of 341 post-PTA dissections were treated. Each patient received at least one Tack implant, and 100% of the dissections resolved according to the angiographic core laboratory findings. The primary safety and efficacy endpoints were both met. The rate of MALE plus POD at 30 days was 1.3% (3 of 228) and freedom from MALE at 6 months plus POD at 30 days was 95.6% (196 of 205). The 6-month Tacked segment patency was 82.1% (247 of 301) and target limb salvage was 98.5% (202 of 205). The Kaplan-Meier freedom from clinically driven target lesion revascularization and amputation-free survival at 6 months was 92.0% and 95.7%, respectively. Rutherford improvement was reported in 79.4% (158 of 199). Most (90 of 122; 73.8%) preexisting wounds had healed or were improving.
The Tack Endovascular System is safe and effective for treating post-PTA BTK dissections through 6 months, with favorable rates of MALE plus POD, patency, clinically driven target lesion revascularization, limb salvage, and wound healing.
目前美国尚无血管植入物可用于治疗膝下(BTK)动脉经皮腔内血管成形术后的夹层。Tack 血管内系统(完整血管,宾夕法尼亚州韦恩)是专门为修复经皮腔内血管成形术后 BTK 夹层而设计的。进行了一项试验,以研究首例可植入 BTK 装置在严重肢体缺血情况下治疗经皮腔内血管成形术后(PTA)夹层的安全性和有效性。
本前瞻性、单臂、多中心研究评估了 Tack 血管内系统治疗中/远段腘动脉、胫动脉和腓动脉 PTA 后夹层的情况。主要安全性终点是 30 天后指数手术后的主要不良肢体事件(MALE)加围手术期死亡(POD)。主要疗效终点是 6 个月时 MALE 和 POD 的复合。无动力次要终点是 6 个月时的原发性通畅率。由于没有可用的上市对照物,本试验的主要终点是通过系统文献检索的客观绩效目标确定的。次要终点包括 6 个月时的 Tacked 节段通畅率和目标肢体存活率。报告了 6 个月的结果。
在 233 名入组患者中,有 117 名(50.2%)为 Rutherford 5 级,78 名(33.5%)为 Rutherford 4 级。共有 341 例 PTA 后夹层接受治疗。每位患者至少接受了一次 Tack 植入,根据血管造影核心实验室的结果,所有夹层均得到解决。主要安全性和疗效终点均达到。30 天的 MALE 加 POD 发生率为 1.3%(228 例中的 3 例),30 天的 MALE 加 POD 无发生率为 95.6%(205 例中的 196 例)。6 个月时 Tacked 节段通畅率为 82.1%(301 例中的 247 例),目标肢体存活率为 98.5%(205 例中的 202 例)。6 个月时的 Kaplan-Meier 临床驱动的靶病变血运重建和无截肢生存率分别为 92.0%和 95.7%。199 例中有 79.4%(158 例)报告了 Rutherford 改善。大多数(122 例中的 90 例;73.8%)先前存在的伤口已愈合或正在改善。
Tack 血管内系统在治疗膝下(BTK)动脉经皮腔内血管成形术后 6 个月时是安全有效的,其主要不良肢体事件(MALE)加 POD、通畅率、临床驱动的靶病变血运重建、肢体存活率和伤口愈合率均较好。