Auda Matthew E, Ratner Molly, Pezold Michael, Rockman Caron, Sadek Mikel, Jacobowitz Glenn, Berland Todd, Siracuse Jeffrey J, Teter Katherine, Johnson William, Garg Karan
Division of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, USA.
Division of Vascular and Endovascular Surgery, Boston Medical Center, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, USA.
Vascular. 2025 Feb;33(1):34-41. doi: 10.1177/17085381241236923. Epub 2024 Feb 28.
Management of acute limb ischemia (ALI) has seen greater utilization of catheter-based interventions over the last two decades. Data on their efficacy is largely based on comparisons of catheter-directed thrombolysis (CDT) and open thrombectomy. During this time, many adjuncts to CDT have emerged with different mechanisms of action, including pharmacomechanical thrombolysis (PMT) and aspiration mechanical thrombectomy (AMT). However, the safety and efficacy of newer adjuncts like AMT have not been well established. This study is a retrospective analysis of the contemporary management of ALI comparing patients treated with aspiration mechanical thrombectomy to patients treated with the more established CDT adjunct, pharmacomechanical thrombolysis.
Patients undergoing peripheral endovascular intervention for ALI using an adjunctive device were identified through query of the Vascular Quality Initiative (VQI) Peripheral Vascular Intervention (PVI) module from 2014 to 2019. Patients with a nonviable extremity (Rutherford ALI Stage 3), prior history of ipsilateral major amputation, popliteal aneurysm, procedures that were deemed elective (>72 h from admission), procedures that did not utilize an endovascular adjunctive device, and patients without short-term follow-up were all excluded from analysis. The primary outcome was a composite outcome of freedom from major amputation and/or death in the perioperative time period.
We identified 528 patients with Rutherford ALI Stage 1 or 2 who were treated with an endovascular adjunct. 433 patients did not undergo aspiration mechanical thrombectomy (no AMT group) and 95 patients did undergo aspiration mechanical thrombectomy (AMT group). The amputation-free survival across all patients was 93.4%. There were significant differences in demographic, comorbidity, and treatment variables between groups (e.g., gender, prior percutaneous coronary intervention (PCI), history of prior peripheral artery disease intervention, and history of prior infra-inguinal PVI), so a propensity score matched analysis was included to account for these group differences. In the propensity score matched analysis, there was no significant difference in major amputation (AMT 7.4% vs no AMT 3.2%, = 0.13) or death (AMT 95.8% survival vs no AMT 98.4% survival, = 0.23) with the use of aspiration mechanical thrombectomy. However, there was significantly worse amputation-free survival with the use of aspiration mechanical thrombectomy (AMT 88.4% vs no AMT 95.3%, = 0.03). On multivariate analysis, prior supra-inguinal bypass (OR 4.85, 1.70-13.84, = 0.003), Rutherford ALI Stage 2B (OR 3.13, 1.47-6.67, = 0.003), and aspiration mechanical thrombectomy (OR 2.71, 1.03-7.17, = 0.05) were associated with the composite outcome.
Short-term amputation-free survival rates of endovascular management of acute limb ischemia are adequate across all modalities. However, aspiration mechanical thrombectomy was associated with significantly worse amputation-free survival compared to other endovascular adjuncts alone (i.e., pharmacomechanical thrombolysis). Severe limb ischemia (Rutherford ALI Stage 2B) and prior supra-inguinal bypass were associated with worse amputation-free survival regardless of the choice of endovascular intervention.
在过去二十年中,急性肢体缺血(ALI)的治疗更多地采用了基于导管的干预措施。关于其疗效的数据主要基于导管定向溶栓(CDT)和开放性血栓切除术的比较。在此期间,许多CDT辅助手段相继出现,其作用机制各不相同,包括药物机械溶栓(PMT)和抽吸机械血栓切除术(AMT)。然而,AMT等新型辅助手段的安全性和疗效尚未得到充分证实。本研究是一项对ALI当代治疗的回顾性分析,比较了接受抽吸机械血栓切除术的患者与接受更成熟的CDT辅助手段即药物机械溶栓治疗的患者。
通过查询2014年至2019年血管质量倡议(VQI)外周血管介入(PVI)模块,确定接受外周血管内介入治疗ALI并使用辅助装置的患者。将肢体无活力(卢瑟福ALI 3期)、同侧大腿截肢既往史、腘动脉瘤、被视为择期手术(入院超过72小时)、未使用血管内辅助装置的手术以及无短期随访的患者全部排除在分析之外。主要结局是围手术期无大截肢和/或死亡的复合结局。
我们确定了528例卢瑟福ALI 1期或2期且接受血管内辅助治疗的患者。433例患者未接受抽吸机械血栓切除术(非AMT组),95例患者接受了抽吸机械血栓切除术(AMT组)。所有患者的无截肢生存率为93.4%。两组在人口统计学、合并症和治疗变量方面存在显著差异(如性别、既往经皮冠状动脉介入治疗(PCI)、既往外周动脉疾病介入治疗史和既往腹股沟下PVI史),因此进行了倾向评分匹配分析以考虑这些组间差异。在倾向评分匹配分析中,使用抽吸机械血栓切除术时,大截肢(AMT组为7.4%,非AMT组为3.2%,P = 0.13)或死亡(AMT组生存率为95.8%,非AMT组生存率为98.4%,P = 0.23)无显著差异。然而,使用抽吸机械血栓切除术时,无截肢生存率显著更差(AMT组为88.4%,非AMT组为95.3%,P = 0.03)。多因素分析显示,既往腹股沟上旁路手术(OR 4.85,1.70 - 13.84,P = 0.003)、卢瑟福ALI 二期B级(OR 3.13,1.47 - 6.67,P = 0.003)和抽吸机械血栓切除术(OR 2.71,1.03 - 7.17,P = 0.05)与复合结局相关。
急性肢体缺血血管内治疗的短期无截肢生存率在所有治疗方式中都较为可观。然而,与单独使用其他血管内辅助手段(即药物机械溶栓)相比,抽吸机械血栓切除术的无截肢生存率显著更差。严重肢体缺血(卢瑟福ALI 二期B级)和既往腹股沟上旁路手术与较差的无截肢生存率相关,无论选择何种血管内干预方式。