Randomized clinical Trial Comparing drug Eluting Stent Zilver PTX® Versus Bare Metal Stent Zilver Flex® for Treatment of Lesions in Femoral and Popliteal Arteries in Chronic Limb Threatening Ischemia.

IF 0.7 4区 医学 Q4 PERIPHERAL VASCULAR DISEASE Vascular and Endovascular Surgery Pub Date : 2023-10-01 Epub Date: 2023-04-21 DOI:10.1177/15385744231171746
Torbjörn Fransson, Anders Gottsäter, Mohammad Abdulrasak, Martin Malina, Timothy Resch
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Abstract

Objective: Drug eluting stents (DES) might improve the results of stenting in the femoropopliteal (FP) segment, but randomized data between DES and BMS in the treatment of patients with chronic limb threatening ischemia (CLTI) is lacking. The aim of this study was to perform a randomized comparison, between DES and bare metal stent (BMS) implantation in a subgroup of CLTI patients with lesions in the superficial femoral artery (SFA) and the P1-P2 portion of the popliteal artery.

Methods: Patients presenting with CLTI scheduled for endovascular treatment of FP lesions were randomly assigned by blinded envelopes 1:1 in a single blinded, parallel group design to DES or BMS after lesion crossing. Primary endpoints were target lesion revascularization (TLR) at 12 and 24 months and primary patency at 12 and 24 months. Secondary endpoints were technical success (TS), clinical success, secondary patency at 12 and 24 months, limb salvage, serious adverse events (SAE) at 24 month and survival at five years.

Results: A total of 48 CLTI patients and 49 limbs, were enrolled, 22 in the BMS group and 27 in the DES group. Demographics, comorbidities, and Rutherford class were similar in both treatment arms. The overall rate of total occlusions was 96% and the corresponding overall median lesion length was 240 mm. No patients were lost to follow up. No significant differences were detected between groups regarding TLR and primary patency. The overall primary patency at 12 and 24 months was 42.9% and 36.7% respectively and the overall freedom from TLR was 67.3% and 61.2% respectively. The results in the two groups were also similar regarding secondary outcomes.

Conclusions: This single centre, randomized study could not demonstrate superiority of DES compared to BMS when treating long FP lesions in patients with CLTI but was limited by insufficient patient inclusion.

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比较药物洗脱支架Zilver PTX®与裸金属支架Zilver-Flex®治疗慢性肢体威胁性缺血中股动脉和腘动脉病变的随机临床试验。
目的:药物洗脱支架(DES)可以改善股腘段支架植入术的效果,但缺乏DES和BMS治疗慢性肢体威胁性缺血(CLTI)患者的随机数据。本研究的目的是在股浅动脉(SFA)和腘动脉P1-P2部分有病变的CLTI患者亚组中,对DES和裸金属支架(BMS)植入进行随机比较。方法:将计划进行FP病变血管内治疗的CLTI患者通过单盲、平行组设计中的盲信封1:1随机分配到病变交叉后的DES或BMS。主要终点为12个月和24个月时的靶病变血运重建(TLR)以及12个月至24个月的主要通畅性。次要终点为技术成功率(TS)、临床成功率、12个月和24个月的次要通畅率、肢体挽救率、24个月严重不良事件(SAE)和5年生存率。结果:共有48名CLTI患者和49条肢体入选,其中22例在BMS组,27例在DES组。两个治疗组的人口学、合并症和Rutherford分类相似。总闭塞率为96%,相应的总中位病变长度为240mm。没有患者失访。两组之间在TLR和初次通畅性方面没有发现显著差异。12个月和24个月时的总体初次通畅率分别为42.9%和36.7%,TLR的总体自由度分别为67.3%和61.2%。两组的次要结果也相似。结论:这项单中心随机研究在治疗CLTI患者的长FP病变时,不能证明DES与BMS相比的优越性,但受患者纳入不足的限制。
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来源期刊
Vascular and Endovascular Surgery
Vascular and Endovascular Surgery SURGERY-PERIPHERAL VASCULAR DISEASE
CiteScore
1.70
自引率
11.10%
发文量
132
审稿时长
4-8 weeks
期刊介绍: Vascular and Endovascular Surgery (VES) is a peer-reviewed journal that publishes information to guide vascular specialists in endovascular, surgical, and medical treatment of vascular disease. VES contains original scientific articles on vascular intervention, including new endovascular therapies for peripheral artery, aneurysm, carotid, and venous conditions. This journal is a member of the Committee on Publication Ethics (COPE).
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