Antoniou George A, Georgakarakos Efstratios I, Antoniou Stavros A, Georgiadis George S
Department of Vascular Surgery, Northern Vascular Centre, Freeman Hospital, Newcastle upon Tyne, UK
Department of Vascular and Endovascular Surgery, Democritus University of Thrace, Alexandroupolis, Greece.
Interact Cardiovasc Thorac Surg. 2014 Aug;19(2):282-5. doi: 10.1093/icvts/ivu093. Epub 2014 Apr 11.
A best evidence topic in vascular and endovascular surgery was developed according to a structured protocol. The question addressed was whether treatment of infra-inguinal arterial occlusive disease with drug-eluting stents (DESs) provides improved outcomes compared with bare metal stents (BMSs) or percutaneous balloon angioplasty (PTA) alone. Altogether, 136 papers were found using the reported searches, of which 5 provided the best evidence to answer the question. All papers represent either level 1 or 2 evidence. The authors, journal, date, country of publication, patient group studied, study type, relevant outcomes and results of these papers are tabulated. Main outcome measures varied among the studies, and included patency, in-stent restenosis, target lesion revascularization, major adverse events, clinical improvement and limb salvage. Evidence on the comparative efficacy of DESs in femoro-popliteal arterial disease is mainly based on two randomized, controlled trials. Paclitaxel-eluting stents were evaluated in the Zilver PTX trial and demonstrated superior 2-year results to either BMSs or PTA, as indicated/shown by patency (DES vs PTA, 74.8 vs 26.5%, P < 0.01), clinical benefit (DES vs PTA, P < 0.01) and event-free survival (DES vs PTA, 86.6 vs 77.9%, P = 0.02). However, the SIROCCO trial found that the sirolimus-eluting stent did not exhibit statistically significant differences in 2-year in-stent restenosis (22.9 vs 21.1%) and target lesion revascularization (6 vs 13%) compared with the BMS. Treatment of infra-politeal arterial disease with DESs was related with superior outcomes to those of BMSs, as indicated/shown by patency, freedom from target lesion revascularization and freedom from major adverse events. Furthermore, the ACHILLES trial, the only published trial comparing the infra-popliteal DES with PTA, revealed lower angiographic restenosis (22.4 vs 41.9%, P = 0.019) and greater vessel patency (75 vs 57.1%, P = 0.025) in the DES group at 1 year. However, data related to clinical parameters in patients with critical limb ischaemia secondary to infrageniculate arterial disease, such as limb salvage and ulcer healing, are insufficient. In conclusion, treatment of infra-inguinal arterial disease with DES is safe and seems to be superior to treatment with PTA alone or BMS. The role of DES in sustained improvement in clinical outcome end-points, such as limb salvage, remains to be elucidated.
根据结构化方案制定了血管和血管内手术的最佳证据主题。所探讨的问题是,与裸金属支架(BMS)或单纯经皮球囊血管成形术(PTA)相比,药物洗脱支架(DES)治疗腹股沟下动脉闭塞性疾病是否能带来更好的疗效。通过报告的检索共找到136篇论文,其中5篇提供了回答该问题的最佳证据。所有论文均代表1级或2级证据。现将这些论文的作者、期刊、日期、出版国家、研究的患者群体、研究类型、相关结局和结果制成表格。各研究的主要结局指标各不相同,包括通畅率、支架内再狭窄、靶病变血管重建、主要不良事件、临床改善情况和肢体挽救情况。关于DES在股腘动脉疾病中比较疗效的证据主要基于两项随机对照试验。在Zilver PTX试验中对紫杉醇洗脱支架进行了评估,结果显示其2年疗效优于BMS或PTA,通畅率(DES组 vs PTA组,74.8% vs 26.5%,P<0.01)、临床获益(DES组 vs PTA组,P<0.01)和无事件生存率(DES组 vs PTA组,86.6% vs 77.9%,P = 0.02)均表明了这一点。然而,SIROCCO试验发现,与BMS相比,西罗莫司洗脱支架在2年支架内再狭窄(22.9% vs 21.1%)和靶病变血管重建(6% vs 13%)方面未显示出统计学显著差异。DES治疗腘下动脉疾病的疗效优于BMS,在通畅率、无靶病变血管重建和无主要不良事件方面均有体现。此外,ACHILLES试验是唯一一项比较腘下DES与PTA的已发表试验,该试验显示DES组在1年时血管造影再狭窄率较低(22.4% vs 41.9%,P = 0.019),血管通畅率更高(75% vs 57.1%,P = 0.025)。然而,关于膝下动脉疾病继发严重肢体缺血患者临床参数的数据,如肢体挽救和溃疡愈合情况,并不充分。总之,DES治疗腹股沟下动脉疾病是安全的,且似乎优于单纯PTA或BMS治疗。DES在持续改善临床结局终点(如肢体挽救)方面的作用仍有待阐明。