Randomized controlled study of excimer laser atherectomy for treatment of femoropopliteal in-stent restenosis: initial results from the EXCITE ISR trial (EXCImer Laser Randomized Controlled Study for Treatment of FemoropopliTEal In-Stent Restenosis)
| Autor: | Eric J, Dippel, Prakash, Makam, Richard, Kovach, Jon C, George, Raghotham, Patlola, D Christopher, Metzger, Carlos, Mena-Hurtado, Robert, Beasley, Peter, Soukas, Pedro J, Colon-Hernandez, Matthew A, Stark, Craig, Walker, Daniel, Van Roy |
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| Rok vydání: | 2014 |
| Předmět: |
Male
Atherectomy Time Factors Constriction Pathologic Prosthesis Design Amputation Surgical Peripheral Arterial Disease Recurrence Alloys Humans Popliteal Artery Prospective Studies Vascular Patency Aged Middle Aged Limb Salvage Combined Modality Therapy United States Femoral Artery Treatment Outcome Chronic Disease Female Lasers Excimer Stents Laser Therapy Angioplasty Balloon |
| Zdroj: | JACC. Cardiovascular interventions. 8(1 Pt) |
| ISSN: | 1876-7605 |
| Popis: | The purpose of this study was to evaluate the safety and efficacy of excimer laser atherectomy (ELA) with adjunctive percutaneous transluminal angioplasty (PTA) versus PTA alone for treating patients with chronic peripheral artery disease with femoropopliteal bare nitinol in-stent restenosis (ISR).Femoropopliteal stenting has shown superiority to PTA for lifestyle-limiting claudication and critical limb ischemia, although treating post-stenting artery reobstruction, or ISR, remains challenging.The multicenter, prospective, randomized, controlled EXCITE ISR (EXCImer Laser Randomized Controlled Study for Treatment of FemoropopliTEal In-Stent Restenosis) trial was conducted across 40 U.S. centers. Patients with Rutherford Class 1 to 4 and lesions of target lesion length ≥4 cm, vessel diameter 5 to 7 mm were enrolled and randomly divided into ELA + PTA and PTA groups by a 2:1 ratio. The primary efficacy endpoint was target lesion revascularization (TLR) at 6-month follow up. The primary safety endpoint was major adverse event (death, amputation, or TLR) at 30 days post-procedure.Study enrollment was stopped at 250 patients due to early efficacy demonstrated at a prospectively-specified interim analysis. A total of 169 ELA + PTA subjects (62.7% male; mean age 68.5 ± 9.8 years) and 81 PTA patients (61.7% male; mean age 67.8 ± 10.3 years) were enrolled. Mean lesion length was 19.6 ± 12.0 cm versus 19.3 ± 11.9 cm, and 30.5% versus 36.8% of patients exhibited total occlusion. ELA + PTA subjects demonstrated superior procedural success (93.5% vs. 82.7%; p = 0.01) with significantly fewer procedural complications. ELA + PTA and PTA subject 6-month freedom from TLR was 73.5% versus 51.8% (p0.005), and 30-day major adverse event rates were 5.8% versus 20.5% (p0.001), respectively. ELA + PTA was associated with a 52% reduction in TLR (hazard ratio: 0.48; 95% confidence interval: 0.31 to 0.74).The EXCITE ISR trial is the first large, prospective, randomized study to demonstrate superiority of ELA + PTA versus PTA alone for treating femoropopliteal ISR. (Randomized Study of Laser and Balloon Angioplasty Versus Balloon Angioplasty to Treat Peripheral In-stent Restenosis [EXCITE ISR]; NCT01330628). |
| Databáze: | OpenAIRE |
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