University Hospital Heidelberg, Germany.
Vascular Center Klinikum Arnsberg, Germany.
Vasa. 2021 Sep;50(5):378-386. doi: 10.1024/0301-1526/a000960. Epub 2021 Jun 22.
Traditionally endarterectomy has been considered as the gold standard technique for the treatment of common femoral artery (CFA) lesions. The aim of this study is to investigate the procedural safety and mid-term outcomes of minimal invasive Phoenix atherectomy for the treatment of CFA lesions. Phoenix atherectomy was used for treatment of 61 consecutive, moderately to heavily calcified CFA lesions in 56 patients. Lesions were classified based on the CFA occlusive disease classification (Type I, II&III lesions). Primary endpoints were technical, procedural, and clinical success rate. Safety endpoints (vessel perforation, peripheral embolization) and clinically driven target lesion revascularization (TLR) were also assessed. Of 61 CFA lesions, 58 (95%) exhibited at least moderate/severe calcification (PACSS3 in 38 (62%) and PACSS4 in 20 (33%) cases). Type III lesions were present in 30 (49%), type I/II lesions in 31 (51%) cases. Technical and procedural success was achieved in 30 (49%) and all 61 (100%) lesions, respectively with low complication rates (0% perforation, 2% embolization). Adjunctive treatment after atherectomy was performed using drug-coated balloon (DCB) in 35 (57%) and bail-out stenting in 6 (10%) cases. Target lesion revascularization (TLR) occurred in 4 (7%) cases during a mean follow-up duration of 11±7months. All patients exhibited clinical improvement at follow-up, showing mean Rutherford category reduction from 3.7±1.1 to 1.5±1.1 (p<0.001). The Phoenix device can be used for the effective endovascular treatment of CFA lesions, due to its reasonable safety profile and mid-term results.
传统上,内膜切除术被认为是治疗股总动脉(CFA)病变的金标准技术。本研究旨在探讨微创凤凰旋切术治疗 CFA 病变的安全性和中期结果。
61 例连续、中度至重度钙化的 CFA 病变患者(56 例)接受了 Phoenix 旋切术治疗。病变根据 CFA 闭塞性疾病分类(I 型、II&III 型病变)进行分类。主要终点是技术、程序和临床成功率。还评估了安全性终点(血管穿孔、外周栓塞)和临床驱动的靶病变血运重建(TLR)。
61 例 CFA 病变中,58 例(95%)至少有中度/重度钙化(PACSS3 38 例(62%),PACSS4 20 例(33%))。III 型病变 30 例(49%),I/II 型病变 31 例(51%)。技术和程序成功率分别为 30 例(49%)和 61 例(100%),并发症发生率低(无穿孔,2%栓塞)。旋切后辅助治疗采用药物涂层球囊(DCB)35 例(57%),紧急支架置入 6 例(10%)。平均随访 11±7 个月,有 4 例(7%)发生靶病变血运重建(TLR)。所有患者在随访时均有临床改善,Rutherford 分类从 3.7±1.1 降至 1.5±1.1(p<0.001)。
由于 Phoenix 装置具有合理的安全性和中期结果,可用于有效治疗 CFA 病变。