Superiority of stent-grafts for in-stent restenosis in the superficial femoral artery: twelve-month results from a multicenter randomized trial

J Endovasc Ther. 2015 Feb;22(1):1-10. doi: 10.1177/1526602814564385.

Abstract

Purpose: To evaluate the short- and midterm outcomes of the Viabahn endoprosthesis with Propaten Bioactive Surface vs. standard balloon angioplasty for treatment of in-stent restenosis in the superficial femoral artery.

Methods: Between June 2010 and February 2012, 83 patients with superficial femoral artery in-stent and Rutherford category 2 to 5 ischemia were enrolled at 7 sites participating in this prospective randomized controlled study (RELINE; ClinicalTrials.gov; identifier NCT01108861). The patients were randomized to treatment with either the heparin-bonded Viabahn endoprosthesis (n = 39: 29 men; mean age 67.7 ± 9.8 years) or a standard angioplasty balloon (n = 44: 32 men; mean age 69.0 ± 9.7 years). The primary effectiveness outcome was primary patency at 12 months, defined as no restenosis/occlusion within the target lesion based on duplex ultrasound and no target lesion revascularization. The primary safety endpoint was the incidence of serious device-related adverse events within 30 days of the procedure.

Results: All patients randomized to receive dilation or the Viabahn stent-graft were treated according to their assignment. The technical success was 100% for the Viabahn group and 81.8% for the angioplasty group (p = 0.002) owing to 9 patients requiring a bailout procedure after unsuccessful angioplasty. The 12-month primary patency rates were 74.8% for the Viabahn group and 28.0% for the angioplasty group (p < 0.001). Excluding the 9 angioplasty patients who received bailout stenting, the primary patency for optimal balloon angioplasty was 37.0% (p < 0.001). Three patients experienced device-related adverse events within 30 days: occlusion of the target lesion (Viabahn group), peripheral embolization (angioplasty group), and reocclusion of the target lesion (angioplasty group).

Conclusion: In this study, the treatment of femoropopliteal in-stent restenosis with a Viabahn endoprosthesis showed significantly better results than treatment with a standard balloon at 1 year.

Keywords: balloon angioplasty; covered stent; endovascular therapy; in-stent restenosis; percutaneous transluminal angioplasty; peripheral artery disease; randomized controlled trial; stent-graft; superficial femoral artery.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Angioplasty, Balloon* / methods
  • Belgium
  • Coated Materials, Biocompatible
  • Constriction, Pathologic
  • Drug-Eluting Stents*
  • Female
  • Femoral Artery*
  • Follow-Up Studies
  • Germany
  • Humans
  • Male
  • Middle Aged
  • Peripheral Arterial Disease / pathology
  • Peripheral Arterial Disease / therapy*
  • Prospective Studies
  • Recurrence
  • Single-Blind Method
  • Stents / adverse effects
  • Time Factors
  • Treatment Outcome
  • Vascular Patency

Substances

  • Coated Materials, Biocompatible

Associated data

  • ClinicalTrials.gov/NCT01108861