Department of Radiology, Nara Medical University, Nara, Japan.
Department of Diabetes Care Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.
Eur J Vasc Endovasc Surg. 2022 Oct;64(4):359-366. doi: 10.1016/j.ejvs.2022.05.046. Epub 2022 Jun 6.
Stent grafts (SG) and drug eluting stents (DES) have emerged to combat intimal hyperplasia. It remains unclear which type of stent yields superior outcomes in femoropopliteal (FP) arterial lesions. This study compared the clinical data between the VIABAHN SG and the Eluvia DES two years after endovascular treatment.
In this retrospective multicentre study, 504 cases with a lesion length > 10 cm treated either with SG or DES were analysed. Ankle brachial index (ABI) measurements were conducted before and after the endovascular procedure, and every three months thereafter. When the ABI dropped ≥ 0.15 compared with the baseline value, a duplex ultrasound was conducted to check stent patency. The outcome measures were stent patency rates, freedom from target lesion revascularisation (TLR), stent thrombosis, and acute limb ischaemia (ALI) accompanying loss of patency rates. Propensity score matching (PSM) was performed to adjust for confounding baseline characteristics.
PSM extracted 219 limbs in the SG group and 109 limbs in the DES group. Compared with the SG group, the DES group had statistically significantly higher rates of freedom from TLR (86.0 ± 4.2% vs. 73.1 ± 4.8%, p = .040), and ALI accompanying loss of patency (98.9 ± 1.1% vs. 93.5 ± 1.8%, p = .029) at two years. Primary patency (75.9 ± 5.9% vs. 69.5 ± 5.9%, p = .087) and freedom from stent thrombosis (90.4 ± 3.3% vs. 81.2% ± 3.0%, p = .11) were not statistically significantly different. For lesions ≤ 15 cm, primary patency in the DES group was statistically significantly better than the SG group.
FP lesions treated with Eluvia DES had a higher primary patency rate in lesions ≤ 15 cm, freedom from clinically driven TLR and ALI accompanying loss of patency than the VIABAHN SG.
支架移植物(SG)和药物洗脱支架(DES)的出现是为了对抗内膜增生。在股腘动脉(FP)病变中,哪种支架的效果更好仍不清楚。本研究比较了腔内治疗两年后 VIABAHN SG 和 Eluvia DES 的临床数据。
在这项回顾性多中心研究中,分析了 504 例病变长度> 10 cm 的患者,分别接受 SG 或 DES 治疗。在血管内手术前后及此后每三个月进行踝肱指数(ABI)测量。当 ABI 与基线值相比下降≥0.15 时,进行双功超声检查以检查支架通畅性。主要终点是支架通畅率、免于靶病变血运重建(TLR)、支架血栓形成和急性肢体缺血(ALI)合并通畅丧失率。采用倾向评分匹配(PSM)调整混杂的基线特征。
PSM 提取了 SG 组的 219 条肢体和 DES 组的 109 条肢体。与 SG 组相比,DES 组在免于 TLR(86.0±4.2% vs. 73.1±4.8%,p=0.040)和 ALI 合并通畅丧失(98.9±1.1% vs. 93.5±1.8%,p=0.029)方面的两年无事件率更高。原发性通畅率(75.9±5.9% vs. 69.5±5.9%,p=0.087)和免于支架血栓形成(90.4±3.3% vs. 81.2%±3.0%,p=0.11)无统计学差异。对于≤15 cm 的病变,DES 组的原发性通畅率明显优于 SG 组。
在≤15 cm 的病变中,Eluvia DES 治疗的 FP 病变具有更高的原发性通畅率、免于临床驱动的 TLR 和 ALI 合并通畅丧失。