1 Department of Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia.
2 Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.
J Endovasc Ther. 2018 Dec;25(6):694-701. doi: 10.1177/1526602818799736. Epub 2018 Sep 12.
To investigate the midterm performance of the everolimus-eluting Absorb bioresorbable vascular scaffold (BVS) for the treatment of symptomatic infrapopliteal atherosclerotic disease.
A single-center study prospectively enrolled 48 symptomatic patients (mean age 82.1±8.0 years; 27 men) between September 2013 and February 2018 to evaluate the Absorb everolimus-eluting BVS system in distal popliteal and tibial lesions. Mean lesion length was 20.1±10.8 mm. Following predilation, up to 2 BVS were implanted in target lesions in 55 limbs. Clinical and duplex ultrasound follow-up was performed at 1, 3, 6, 12, 24, 36, and 48 months to determine 30-day morbidity and midterm Kaplan-Meier estimates of binary restenosis, clinically-driven target lesion revascularization (CD-TLR), amputation, and mortality.
Seventy-one scaffolds were implanted to treat 61 lesions. Technical success was achieved in all patients, with no amputation, death, or target limb bypass surgery within 30 days of the index procedure. There was 1 early thrombotic occlusion of 2 BVS in a previously anticoagulated patient not given antiplatelet medication after the procedure. During a mean follow-up of 24.0±15.3 months, 11 (23%) patients died; the remaining 37 were available for follow-up. Binary restenosis (50%-75%) was detected in 6 (8%) scaffolds. Primary patency estimates at 12, 24, and 36 months were 92.2%, 90.3%, and 81.1%; freedom from CD-TLR estimates were 97.2%, 97.2%, and 87.3% at the same time points. No late scaffold thrombosis has been observed. The majority of the 55 limbs (51, 93%) were clinically improved; 4 (7%) were unchanged. Thirty-six (92%) of 39 limbs treated for tissue loss achieved complete wound healing, with no major amputation (limb salvage 100%).
Midterm follow-up demonstrates excellent safety, patency, and freedom from CD-TLR rates using the Absorb bioresorbable vascular scaffold below the knee.
研究依维莫司洗脱 Absorb 生物可吸收血管支架(BVS)治疗有症状的下肢动脉粥样硬化疾病的中期疗效。
本单中心前瞻性研究于 2013 年 9 月至 2018 年 2 月间入组了 48 例有症状的下肢动脉粥样硬化患者(平均年龄 82.1±8.0 岁;男性 27 例),以评估 Absorb 依维莫司洗脱 BVS 系统在治疗腘动脉和胫动脉远端病变中的疗效。平均病变长度为 20.1±10.8mm。预扩张后,55 条肢体的目标病变中最多植入 2 个 BVS。通过临床和超声双功能检查,在术后 1、3、6、12、24、36 和 48 个月评估 30 天内发病率和中期 Kaplan-Meier 估计的二元再狭窄、临床驱动的靶病变血运重建(CD-TLR)、截肢和死亡率。
71 个支架被植入以治疗 61 个病变。所有患者均达到技术成功,在索引手术 30 天内无截肢、死亡或靶肢体旁路手术。1 例先前接受抗凝治疗且术后未给予抗血小板药物的患者,2 个 BVS 中有 1 个发生早期血栓闭塞。平均 24.0±15.3 个月的随访期间,11 例(23%)患者死亡;其余 37 例可进行随访。6 个(8%)支架检测到二元再狭窄(50%-75%)。12、24 和 36 个月时的主要通畅率估计值分别为 92.2%、90.3%和 81.1%;相应时间点的免于 CD-TLR 率分别为 97.2%、97.2%和 87.3%。未观察到晚期支架血栓形成。55 条肢体中的大部分(51,93%)临床改善;4 条(7%)肢体无变化。39 条因组织丢失而接受治疗的肢体中,36 条(92%)完全愈合,无主要截肢(肢体挽救率 100%)。
中期随访结果显示,在膝下使用 Absorb 生物可吸收血管支架治疗有症状的下肢动脉粥样硬化疾病具有良好的安全性、通畅率和免于 CD-TLR 率。