Clinic for Vascular Surgery, St. Franziskus Hospital and University Clinic of Muenster, Muenster, Germany.
Clinic for Vascular Surgery, St. Franziskus Hospital and University Clinic of Muenster, Muenster, Germany.
JACC Cardiovasc Interv. 2018 May 28;11(10):957-966. doi: 10.1016/j.jcin.2018.03.046.
The aim of this study was to assess the performance of the fluoropolymer-based paclitaxel-eluting stent (PES) in long femoropopliteal lesions.
The new-generation fluoropolymer-based PES showed promising outcomes in short femoropopliteal lesions. The main feature of the stent is its controlled and sustained paclitaxel release over 12 months. However, the safety and efficacy of this technology in longer femoropopliteal lesions remain unclear.
Between March 2016 and March 2017, 62 patients were included in this analysis. Indications for fluoropolymer-based PES deployment were insufficient luminal gain or flow-limiting dissection after plain old balloon angioplasty in a femoropopliteal lesion. Primary patency, freedom from target lesion revascularization, amputation-free survival, and paclitaxel-related adverse events were retrospectively analyzed for up to 1 year of follow-up.
Lesions were de novo in 84% of patients. Mean lesion length was 20 ± 12 cm, and 79% of the lesions (n = 49) were chronic total occlusions. Moderate or severe calcification was present in 42% of the lesions (n = 26). Stent implantation involved the distal superficial femoral artery and the proximal popliteal artery in 76% (n = 47) and 44% (n = 27) of patients, respectively. The Kaplan-Meier estimate of primary patency and freedom from target lesion revascularization was 87%. Amputation-free survival was 100% for patients with claudication (n = 32 [52%]) and 87% in patients with critical limb ischemia (n = 30 [48%]) (hazard ratio: 6.3; 95% confidence interval: 1.25 to 31.54; p = 0.052). Five aneurysm formations of the treated segments (8%) were thought to be attributable to paclitaxel.
The fluoropolymer-based PES showed promising 1-year clinical and angiographic outcomes in real-world long femoropopliteal lesions. The long-term impact of aneurysm formation remains to be further investigated.
本研究旨在评估基于氟聚合物的紫杉醇洗脱支架(PES)在长段股腘病变中的表现。
新一代基于氟聚合物的 PES 在短段股腘病变中显示出良好的结果。支架的主要特点是其在 12 个月内持续控制和释放紫杉醇。然而,这种技术在更长的股腘病变中的安全性和疗效尚不清楚。
2016 年 3 月至 2017 年 3 月,共纳入 62 例患者进行本分析。基于氟聚合物的 PES 植入的适应证为股腘病变行单纯球囊血管成形术后管腔获得不足或存在限制血流的夹层。回顾性分析了 1 年随访期间的主要通畅率、免于靶病变血运重建、免于截肢生存率和紫杉醇相关不良事件。
84%的患者病变为初发型。平均病变长度为 20±12cm,79%(n=49)的病变为慢性完全闭塞。42%(n=26)的病变存在中度或重度钙化。支架植入涉及远端股浅动脉和近端腘动脉的患者分别占 76%(n=47)和 44%(n=27)。Kaplan-Meier 估计的主要通畅率和免于靶病变血运重建率分别为 87%。有跛行症状的患者免于截肢生存率为 100%(n=32[52%]),有严重肢体缺血症状的患者为 87%(n=30[48%])(风险比:6.3;95%置信区间:1.25 至 31.54;p=0.052)。认为 5 例(8%)治疗节段的动脉瘤形成与紫杉醇有关。
在真实世界的长段股腘病变中,基于氟聚合物的 PES 显示出有前景的 1 年临床和血管造影结果。动脉瘤形成的长期影响仍需进一步研究。