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- W2912389606 abstract "The aim of this study was to independently evaluate the real-world performances of Eluvia paclitaxel drug-eluting stents (DES) (Boston Scientific, Marlborough, Massachusetts) for the treatment of external iliac and femoropopliteal artery lesions.We prospectively collected, and retrospectively reviewed, data for all patients who underwent an endovascular treatment with an Eluvia DES for the treatment of an external iliac or femoropopliteal lesion. Patient demographics, concomitant procedures, arterial lesions characteristics, procedural details, and follow-up were reviewed.Between April and October 2016, 15 Eluvia DES were placed in 15 consecutive adult patients with a technical success of 100%. The treated lesions had a mean length of 93.9 ±58 mm. Sixty percent of the lesions were total occlusions and 13% were restenosis of previous stents. An additional inflow treatment was performed in 40% of the cases. At six months, two patients were lost at follow-up and one had an occluded stent. We had a primary patency rate and freedom from TLR of 92%. All remaining patients had an improved Rutherford class, improved quality of life and wound healing, and an increase in walking distance. Survival and limb salvage rates were 100%.This study confirms the good result of DES, in general, and of the Eluvia stent, in particular, in the treatment of external iliac and femoropopliteal arterial lesions, with a primary patency rate and a freedom from TLR of 92% at six months. A larger number of patients and longer follow-up will be required to determine the true real-world efficacy of the Eluvia DES, but short-term experience is encouraging." @default.
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- W2912389606 date "2017-11-09" @default.
- W2912389606 modified "2023-09-27" @default.
- W2912389606 title "Short-Term Results of Eluvia Paclitaxel-Eluting Stent in External Iliac and Femoropopliteal Lesions." @default.
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