Skip to main content

Chronic total SFA occlusions

Consider the complexity of treating chronic total occlusions (CTOs)

  • CTOs can increase the need for provisional stenting1
    • In the Medtronic IN.PACT Global Study, treatment of CTOs increased the rate of provisional stenting by 85%
  • Although a rare complication, the risk of distal embolization has been shown to increase when treating a CTO2-3
  • Limited comparison data exists between newer endovascular technologies compared to surgical bypass, the current recommended treatment for CTOs4 

The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface* has been extensively studied in CTOs5-9 

Proven patency

  • 72% of limbs studied in five multicenter, prospective, randomized or single arm studies were CTOs (302/422) that achieved 75% primary patency5-9

Demonstrated durability

  • 97% three-year secondary patency in complex disease (27 cm average lesion length, 93% CTOs)10
  • Comparable clinical results to above knee surgical bypass (both prosthetic5 and native vein11) 

The GORE® VIABAHN® Endoprosthesis design is uniquely capable of treating CTOs 

  • ePTFE flow lumen covers and seals off residual thrombosis
  • CBAS Heparin Surface, also featured in the GORE® PROPATEN® Vascular Graft, is the proven, lasting heparin bonding technology designed to resist thrombus formation**

Connect with a Gore technical sales associate

* Heparin Bioactive Surface is synonymous with the CBAS Heparin Surface.

** CBAS Heparin Surface.  W. L. Gore & Associates Web site.   https://www.goremedical.com/cbas/references. Accessed July 30, 2018.

 

  1. Brodmann M. Real world value of the In.Pact Admiral DCB (Medtronic) for fem-pop lesions: from the In.Pact Global Registry: what else does it tell us. Presented at the 44th Annual Symposium on Vascular and Endovascular Issues, Techniques, Horizons (VEITH symposium); November 14-18, 2017; New York, NY. 
  2. Wu W, Hua S, Li Y, et al. Incidence, risk factors, treatment and prognosis of popliteal artery embolization in the superficial femoral artery interventions. PLoS One 2014;9(9):e107717. 
  3. Shrikhande GV, Khan SZ, Hussain HG, Dayal R, McKinsey JF, Morrissey N. Lesion types and device characteristics that predict distal embolization during percutaneous lower extremity interventions. Journal of Vascular Surgery 2011;53(2):347-352.
  4. Norgren L, Hiatt WR, Dormandy JA, Nehler MR, Harris KA, Fowkes FG; TASC II Working Group. Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II). Journal of Vascular Surgery 2007;45(1)Supplement:S5-S67.
  5. Reijnen M, van Walraven L, Fritschy W, et al. 1-year results of a multicenter, randomized controlled trial comparing heparin-bonded endoluminal to femoropopliteal bypass. Journal of Cardiovascular Interventions 2017;10(22):2320-2331.
  6. Ohki T, Kichikawa K, Yokoi H, et al. Outcomes of the Japanese multicenter Viabahn trial of endovascular stent grafting for superficial femoral artery lesions. Journal of Vascular Surgery 2017;66(1):130-142.e1.
  7. Saxon RR, Chervu A, Jones PA, et al. Heparin‑bonded, expanded polytetrafluoroethylene‑lined stent graft in the treatment of femoropopliteal artery disease: 1‑year results of the VIPER (Viabahn Endoprosthesis with Heparin Bioactive Surface in the Treatment of Superficial Femoral Artery Obstructive Disease) Trial. Journal of Vascular & Interventional Radiology 2013;24(2):165-173.
  8. Lammer J, Zeller T, Hausegger KA, et al. Sustained benefit at 2 years for covered stents versus bare-metal stents in long SFA lesions: the VIASTAR trial. Cardiovascular & Interventional Radiology 2015;38(1):25-32.
  9. Zeller T, Peeters P, Bosiers M, et al. Heparin‑bonded stent‑graft for the treatment of TASC II C and D femoropopliteal lesions: the Viabahn‑25 cm Trial. Journal of Endovascular Therapy 2014;21(6):765‑774.
  10.   GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface [Instructions for Use]. Flagstaff, AZ: W. L. Gore & Associates, Inc; 2014. MD147177.
  11.   McQuade K, Gable D, Pearl G, Theune B, Black S. Four-year randomized prospective comparison of percutaneous ePTFE/nitinol self-expanding stent graft versus prosthetic femoral-popliteal bypass in the treatment of superficial femoral artery occlusive disease. Journal of Vascular Surgery 2010;52(3):584-591.