Beschorner Ulrich, Boehme Tanja, Noory Elias, Bollenbacher Roaa, Salm Jonas, Mashayekhi Kambis, Westermann Dirk, Zeller Thomas
University Heart Center Freiburg-Bad Krozingen, Faculty of Medicine, University of Freiburg, Südring 15, 79189 Bad Krozingen, Germany.
MediClin Herzzentrum Lahr, Hohbergweg 2, 77933 Lahr, Germany.
J Clin Med. 2024 Sep 26;13(19):5732. doi: 10.3390/jcm13195732.
: To evaluate the safety and efficacy of catheter-directed thrombolysis (CDT) with the recombinant tissue plasminogen activator (rt-PA) in all patients with symptomatic peripheral artery disease in real world practice. Consecutive patients treated with CDT between January 2013 and December 2020 were included in this retrospective analysis. The primary endpoint was the rate of serious adverse events (SAEs) until discharge. Secondary endpoints included interventional success, predictors for SAEs, bleeding and reperfusion edema/compartment syndrome, limb salvage, and clinical outcomes including target lesion revascularization rate (TLR). Overall, 1238 patients were treated with CDT. SAEs occurred in 511 (41.3%) of the patients, 314 (25.4%) being bleeding complications. There were 95 cases of reperfusion edema/compartment syndrome. Forty-two patients underwent amputation and 33 patients (2.7%) died. CDT was successful in 1177 cases (95.1%). Multivariate logistic regression analysis identified age, abciximab and alprostadil usage, and lysis duration as predictors for SAEs and the use of abciximab as a predictor of reperfusion edema/compartment syndrome. Predictors for bleeding were age, alprostadil usage, and lysis duration. At 12 and 24 months, the limb salvage rate was 91.6% and 88.8%, and TLR rate was 46% and 57.2%, respectively. CDT is an effective endovascular method for the treatment of thrombotic peripheral artery occlusions but is associated with a high complication rate. For SAEs in general and bleeding specifically, increasing age, alprostadil use, and lysis duration were independent risk factors.
在真实世界实践中评估重组组织型纤溶酶原激活剂(rt-PA)导管直接溶栓(CDT)治疗所有有症状外周动脉疾病患者的安全性和有效性。纳入2013年1月至2020年12月期间接受CDT治疗的连续患者进行这项回顾性分析。主要终点是出院前严重不良事件(SAE)的发生率。次要终点包括介入成功率、SAE的预测因素、出血和再灌注水肿/骨筋膜室综合征、肢体挽救以及包括靶病变血运重建率(TLR)在内的临床结局。总体而言,1238例患者接受了CDT治疗。511例(41.3%)患者发生了SAE,其中314例(25.4%)为出血并发症。有95例再灌注水肿/骨筋膜室综合征。42例患者接受了截肢手术,33例患者(2.7%)死亡。CDT在1177例(95.1%)中成功。多因素逻辑回归分析确定年龄、阿昔单抗和前列地尔的使用以及溶栓持续时间为SAE的预测因素,阿昔单抗的使用为再灌注水肿/骨筋膜室综合征的预测因素。出血的预测因素为年龄、前列地尔的使用和溶栓持续时间。在12个月和24个月时,肢体挽救率分别为91.6%和88.8%,TLR率分别为46%和57.2%。CDT是治疗血栓性外周动脉闭塞的一种有效血管内方法,但并发症发生率较高。对于一般SAE尤其是出血,年龄增加、前列地尔的使用和溶栓持续时间是独立危险因素。