Lawaetz Martin, Fisker Lasse, Lönn Lars, Sillesen Henrik, Eiberg Jonas
Department of Vascular Surgery, Rigshospitalet, Denmark.
Department of Vascular Surgery, Rigshospitalet, Denmark; Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Ann Vasc Surg. 2020 Aug;67:437-447. doi: 10.1016/j.avsg.2020.03.035. Epub 2020 Mar 29.
The objective of the study was to compare bypass surgery and endovascular revascularization of the femoropopliteal segment in patients with peripheral arterial disease and critical limb-threatening ischemia (CLTI).
This is a single-center study including patients undergoing first-time lower extremity intervention with peripheral bypass surgery or percutaneous transluminal angioplasty with or without stenting (PTA/S) of the femoropopliteal segment because of CLTI from 2011 to 2015. Based on prospective entered data from the Danish Vascular Registry, the primary end points were amputation-free survival, overall mortality, and reinterventions.
A total of 679 patients with CLTI were included of which 35% (n = 239) were treated with PTA/S, 54% (n = 363) with vein bypass, and 11% (n = 77) with synthetic bypass. After 3 years, amputation-free survival was significantly better with a vein bypass (41.8% [95% CI: 35-48.4]) than both PTA/S (29.7% (95% CI: 22.7-37)) and synthetic bypass (31.7% [95% CI: 19-45.1]). Overall, the endovascular-treated patients faced more than 50% increased risk of major amputation or death than that of a vein bypass, after adjusting for comorbidity and Trans-Atlantic Inter-Society Consensus (TASC) classification (HR: 1.56 [95% CI: 1.21-2.05]). As expected, postoperative complications, length of hospital stay, and reinterventions were more frequent in the bypass groups.
In this nonrandomized study, autologous vein bypass was superior to both PTA/S and synthetic bypass in regard to amputation-free survival and overall mortality. Despite the increased frequency of surgical complications, a vein bypass appears justified in both shorter (TASC B-C) and longer (TASC D) femoropopliteal lesions.
本研究的目的是比较外周动脉疾病和严重肢体缺血(CLTI)患者股腘段的搭桥手术和血管腔内血运重建术。
这是一项单中心研究,纳入了2011年至2015年因CLTI首次接受下肢干预的患者,这些患者接受了外周搭桥手术或股腘段经皮腔内血管成形术(PTA/S),可选择或不选择支架置入。基于丹麦血管登记处的前瞻性录入数据,主要终点为无截肢生存期、总死亡率和再次干预。
共纳入679例CLTI患者,其中35%(n = 239)接受PTA/S治疗,54%(n = 363)接受静脉搭桥治疗,11%(n = 77)接受人工血管搭桥治疗。3年后,静脉搭桥组的无截肢生存期(41.8% [95% CI:35 - 48.4])显著优于PTA/S组(29.7%(95% CI:22.7 - 37))和人工血管搭桥组(31.7% [95% CI:19 - 45.1])。总体而言,在调整合并症和跨大西洋跨学会共识(TASC)分类后,血管腔内治疗的患者面临的主要截肢或死亡风险比静脉搭桥组高50%以上(HR:1.56 [95% CI:1.21 - 2.05])。正如预期的那样,搭桥组术后并发症、住院时间和再次干预更为频繁。
在这项非随机研究中,自体静脉搭桥在无截肢生存期和总死亡率方面优于PTA/S和人工血管搭桥。尽管手术并发症发生率增加,但对于较短(TASC B - C)和较长(TASC D)的股腘段病变,静脉搭桥似乎是合理的。