Division of Vascular and Endovascular Surgery, Boston University, School of Medicine, Boston, Mass.
Division of Vascular and Endovascular Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Mass.
J Vasc Surg. 2018 Jul;68(1):161-167. doi: 10.1016/j.jvs.2017.12.022. Epub 2018 Mar 1.
Retrograde popliteal artery (RPA) access to treat superficial femoral artery and popliteal artery disease is an option when treatment through common femoral artery (CFA) access is not possible. Our goal was to compare the safety and efficacy of RPA access with CFA access for treatment of femoral and popliteal artery lesions.
The Vascular Quality Initiative was queried for all patients undergoing RPA access from 2010 to 2016 for symptomatic peripheral arterial disease. These were compared with standard CFA access. Patients with acute limb ischemia were excluded. Preoperative, operative, and postoperative data were analyzed. Perioperative and 6-month outcomes were analyzed. Multivariable analysis was used to assess the effect of RPA access on amputation or death, major adverse limb event (MALE) or death, patency, and death.
There were 30,074 patients with isolated superficial femoral and popliteal artery disease treated, 148 of whom had RPA access. Indications overall included claudication (56.3%), rest pain (13.9%), and tissue loss (29.8%). RPA access had a significantly lower rate of technical success compared with CFA access (80.4% vs 93.8%; P < .001). RPA access and CFA access were similar for rates of arterial dissection (8.3% vs 6.3%; P = .333), distal embolization (0% vs 1.2%; P = .183), access site hematoma (3.4% vs 3.1%; P = .849), and 30-day mortality (1.4% vs 1.1%; P = .789). There were no differences between RPA access and CFA access for unadjusted 6-month amputation-free survival (94.8% vs 96%; P = .747) or survival (934.3% vs 95.6%; P = .845). MALE-free survival (74.5% vs 83.5%; P = .016) and patency (70.3% vs 83.1%; P < .001) were significantly lower in the RPA access group. Multivariable analysis showed no differences between patients who were successfully treated by RPA access and CFA access for amputation-free survival (hazard ratio [HR], 1.24; 95% confidence interval [CI], 0.46-3.32; P = .669), MALE-free survival (HR, 1.57; 95% CI, 0.99-2.5; P = .057), and survival (HR, 0.86; 95% CI, 0.43-1.73; P = .675). RPA access was independently associated with loss of primary patency (HR, 1.91; 95% CI, 1.24-2.94; P = .003).
RPA access had lower technical success and primary patency compared with antegrade access at 6 months. There were no differences demonstrated between the two access techniques in perioperative morbidity and mortality or 6-month amputation, MALE, and survival. This technique should be considered when CFA access cannot be accomplished.
当经股总动脉(CFA)入路治疗不可行时,逆行腘动脉(RPA)入路是治疗股浅动脉和腘动脉疾病的一种选择。我们的目标是比较 RPA 入路与 CFA 入路治疗股浅动脉和腘动脉病变的安全性和有效性。
通过血管质量倡议(Vascular Quality Initiative)查询了 2010 年至 2016 年期间因症状性外周动脉疾病而行 RPA 入路的所有患者。将这些患者与标准 CFA 入路进行比较。排除急性肢体缺血患者。分析了术前、术中和术后数据。分析了围手术期和 6 个月的结果。采用多变量分析评估 RPA 入路对截肢或死亡、主要肢体不良事件(MALE)或死亡、通畅率和死亡率的影响。
共治疗了 30074 例孤立性股浅动脉和腘动脉疾病患者,其中 148 例行 RPA 入路。总的适应证包括跛行(56.3%)、静息痛(13.9%)和组织缺失(29.8%)。与 CFA 入路相比,RPA 入路的技术成功率明显较低(80.4% vs 93.8%;P<0.001)。RPA 入路和 CFA 入路在动脉夹层发生率(8.3% vs 6.3%;P=0.333)、远端栓塞(0% vs 1.2%;P=0.183)、入路部位血肿(3.4% vs 3.1%;P=0.849)和 30 天死亡率(1.4% vs 1.1%;P=0.789)方面无差异。RPA 入路和 CFA 入路在未经调整的 6 个月无截肢生存率(94.8% vs 96%;P=0.747)或生存率(934.3% vs 95.6%;P=0.845)方面无差异。MALE 无事件生存率(74.5% vs 83.5%;P=0.016)和通畅率(70.3% vs 83.1%;P<0.001)在 RPA 入路组明显较低。多变量分析显示,成功接受 RPA 入路和 CFA 入路治疗的患者在无截肢生存率(风险比[HR],1.24;95%置信区间[CI],0.46-3.32;P=0.669)、MALE 无事件生存率(HR,1.57;95%CI,0.99-2.5;P=0.057)和生存率(HR,0.86;95%CI,0.43-1.73;P=0.675)方面无差异。RPA 入路与原发性通畅率丧失独立相关(HR,1.91;95%CI,1.24-2.94;P=0.003)。
与逆行入路相比,RPA 入路在 6 个月时的技术成功率和原发性通畅率较低。两种入路技术在围手术期发病率和死亡率或 6 个月时的截肢、MALE 和生存率方面无差异。当 CFA 入路无法完成时,应考虑这种技术。