Safety and effectiveness of Phoenix atherectomy for endovascular treatment in calcified common femoral artery lesions

Author:

Kronlage Mariya1,Erbel Christian1,Lichtenberg Michael2,Heinrich Ulrike3,Katus Hugo A.1,Frey Norbert1,Giusca Sorin4,Korosoglou Grigorios4ORCID

Affiliation:

1. University Hospital Heidelberg, Germany

2. Vascular Center Klinikum Arnsberg, Germany

3. Practice for Vascular Medicine and Gastroenterology, Weinheim, Germany

4. GRN Hospital Weinheim, Cardiology and Vascular Medicine, Weinheim, Germany

Abstract

Summary: Background: 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. Patients and methods: 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. Results: 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). Conclusions: The Phoenix device can be used for the effective endovascular treatment of CFA lesions, due to its reasonable safety profile and mid-term results.

Publisher

Hogrefe Publishing Group

Subject

Cardiology and Cardiovascular Medicine

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