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Short-term Results of the RAPID Randomized Trial of the Legflow Paclitaxel-Eluting Balloon With Supera Stenting vs Supera Stenting Alone for the Treatment of Intermediate and Long Superficial Femoral Artery Lesions.
de Boer, Sanne W; van den Heuvel, Daniel A F; de Vries-Werson, Debbie A B; Vos, Jan Albert; Fioole, Bram; Vroegindeweij, Damnis; Elgersma, Otto E; Tutein Nolthenius, Rudolph P; Heyligers, Jan M M; Bosma, Gerlof P T; de Leeuw, Bernart; Bouwman, Lee H; Böckler, Dittmar; Dovzhanskiy, Dmitriy I; Vos, Floris W F; Vink, Ted W F; Hooijboer, Pieter G A; Hissink, Rutger J; de Vries, Jean-Paul P M.
Afiliação
  • de Boer SW; 1 Department of Interventional Radiology, St Antonius Hospital, Nieuwegein, the Netherlands.
  • van den Heuvel DAF; 1 Department of Interventional Radiology, St Antonius Hospital, Nieuwegein, the Netherlands.
  • de Vries-Werson DAB; 2 Department of Vascular Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.
  • Vos JA; 1 Department of Interventional Radiology, St Antonius Hospital, Nieuwegein, the Netherlands.
  • Fioole B; 3 Department of Vascular Surgery, Maasstad Hospital, Rotterdam, the Netherlands.
  • Vroegindeweij D; 4 Department of Interventional Radiology, Maasstad Hospital, Rotterdam, the Netherlands.
  • Elgersma OE; 5 Department of Interventional Radiology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
  • Tutein Nolthenius RP; 6 Department of Vascular Surgery, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
  • Heyligers JMM; 7 Department of Vascular Surgery, Elisabeth Tweesteden Hospital, Tilburg, the Netherlands.
  • Bosma GPT; 8 Department of Interventional Radiology, Elisabeth Tweesteden Hospital, Tilburg, the Netherlands.
  • de Leeuw B; 9 Department of Interventional Radiology, Zuyderland Medical Centre, Heerlen, the Netherlands.
  • Bouwman LH; 10 Department of Vascular Surgery, Zuyderland Medical Centre, Heerlen, the Netherlands.
  • Böckler D; 11 Clinic for Vascular and Endovascular Surgery, University Hospital Heidelberg, Germany.
  • Dovzhanskiy DI; 11 Clinic for Vascular and Endovascular Surgery, University Hospital Heidelberg, Germany.
  • Vos FWF; 12 Department of Vascular Surgery, Medical Centre Leeuwarden, the Netherlands.
  • Vink TWF; 13 Department of Interventional Radiology, Medical Centre Leeuwarden, the Netherlands.
  • Hooijboer PGA; 14 Department of Interventional Radiology, Scheper Hospital, Emmen, the Netherlands.
  • Hissink RJ; 15 Department of Vascular Surgery, Scheper Hospital, Emmen, the Netherlands.
  • de Vries JPM; 2 Department of Vascular Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.
J Endovasc Ther ; 24(6): 783-792, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28795638
PURPOSE: To report a randomized trial comparing the Legflow paclitaxel-eluting balloon (PEB) + Supera stenting to Supera stenting alone in patients with intermediate to long superficial femoral artery (SFA) lesions. METHODS: The multicenter RAPID trial ( controlled-trials.com ; identifier ISRCTN47846578) randomized (1:1) 160 patients (mean age 67 years; 102 men) with Rutherford category 2-6 ischemia to treatment with Legflow PEB + Supera stent or Supera stent alone in intermediate to long SFA lesions (mean lesion length 15.8±7.4 vs 15.8±7.6 cm, respectively). The efficacy outcome was primary patency, defined as freedom from restenosis on duplex ultrasound or angiography. RESULTS: Baseline characteristics including the percentage of occlusions were similar between groups. In the intention-to-treat analysis, the estimated primary patency at 1 year was 68.3% (95% CI 56.7% to 79.9%) in the PEB + Supera group vs 62.0% (95% CI 49.1% to 74.9%) in the Supera group (p=0.900). Per-protocol analysis showed a 12-month primary patency estimate of 74.7% (95% CI 63.1% to 86.3%) in the PEB + Supera group vs 62.0% (95% CI 49.1% to 74.9%) in the control group (p=0.273). Secondary patency estimates at 12 months (per-protocol analysis) were 89.0% (95% CI 80.6% to 97.4%) vs 98.0% (95% CI 94.1% to 100%; p=0.484); the estimates for freedom from clinically driven target lesion revascularization (CD-TLR) were 83.0% (95% CI 72.8% to 93.2%) and 77.8% (95% CI 66.6% to 89.0%; p=0.277), respectively. CONCLUSION: The short-term results from the multicenter RAPID randomized controlled trial indicate that the Legflow PEB is safe and feasible for the treatment of intermediate to long SFA lesions. In this trial, at least 70% of the patients suffered an occlusion. The PEB group had higher rates of primary patency and freedom from CD-TLR, although there were no statistically significant differences vs controls.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Cardiovasculares / Paclitaxel / Angioplastia com Balão / Materiais Revestidos Biocompatíveis / Artéria Femoral / Doença Arterial Periférica / Dispositivos de Acesso Vascular / Stents Metálicos Autoexpansíveis Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Cardiovasculares / Paclitaxel / Angioplastia com Balão / Materiais Revestidos Biocompatíveis / Artéria Femoral / Doença Arterial Periférica / Dispositivos de Acesso Vascular / Stents Metálicos Autoexpansíveis Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article