Literature DB >> 29285955

Novel Nitinol Stent for Lesions up to 24 cm in the Superficial Femoral and Proximal Popliteal Arteries: 24-Month Results From the TIGRIS Randomized Trial.

John R Laird1, Thomas Zeller2, Christian Loewe3, Jack Chamberlin4, Richard Begg5, Peter A Schneider6, Aravinda Nanjundappa7, Frank Bunch8, Scott Schultz9, Stuart Harlin10, Alexandra Lansky11, Michael R Jaff12.   

Abstract

PURPOSE: To evaluate the safety and effectiveness of the TIGRIS stent for lesions up to 24 cm in the superficial femoral and proximal popliteal arteries (SFA/PPA).
METHODS: This prospective, multicenter, randomized study enrolled 274 subjects at 36 sites in the United States and Europe. Subjects were randomly assigned in a 3:1 ratio to treatment with the TIGRIS stent (n=197; mean age 66.7±9.28 years; 141 men) or LifeStent (n=70; mean age 67.9±8.87 years; 49 men). The primary safety endpoint was 30-day freedom from major adverse events (MAE). The primary efficacy endpoint was primary patency at 12 months. Secondary endpoints included target lesion revascularization (TLR) and stent fracture. Clinical success and quality of life were also assessed.
RESULTS: Mean lesion length (107.6 vs 117.9 mm, p=0.29), procedure success (99.5% vs 97.1%, p=0.17), and freedom from MAE (99.5% vs 100%, p>0.99) were similar for the TIGRIS and control groups, respectively. Likewise, there was no difference in primary patency at 12 months (60.6% vs 63.2%, p=0.73) or 24 months (56.3% vs 50.2%, p=0.60) or in TLR at the same time points (76.6% vs 80.6%, p=0.49; 70.5% vs 67.2%, p=0.85). There were no differences in the changes in Rutherford category or the ankle/brachial index through 24 months. The rate of stent fracture was lower for TIGRIS compared with LifeStent (0% vs 32.7%, p<0.001).
CONCLUSION: The TIGRIS stent and LifeStent were similarly effective for the treatment of lesions in the SFA and PPA. The high flexibility and zero fracture rate associated with the TIGRIS stent make this device favorable for use in high-flexion arteries.

Entities:  

Keywords:  femoropopliteal segment; lesion length; nitinol stent; peripheral artery disease; popliteal artery; randomized trial; stent fracture; superficial femoral artery

Mesh:

Substances:

Year:  2017        PMID: 29285955     DOI: 10.1177/1526602817749242

Source DB:  PubMed          Journal:  J Endovasc Ther        ISSN: 1526-6028            Impact factor:   3.487


  4 in total

1.  State-of-the-Art Endovascular Therapies for the Femoropopliteal Segment: Are We There Yet?

Authors:  Ramya C Mosarla; Ehrin Armstrong; Yonatan Bitton-Faiwiszewski; Peter A Schneider; Eric A Secemsky
Journal:  J Soc Cardiovasc Angiogr Interv       Date:  2022-08-20

2.  Lesion Revascularisation Subsequent to Femoropopliteal Spot Stenting Using the Multi-LOC Stent Delivery System.

Authors:  Martin Sigl; Klaus Amendt; Matthias Waliszewski; Nils Rathmann
Journal:  In Vivo       Date:  2020 Jan-Feb       Impact factor: 2.155

3.  Long-Term Patency and Clinical Outcomes of Nitinol Stenting for Femoropopliteal Atherosclerotic Disease.

Authors:  Sherwin Abdoli; Steven Katz; Christian Ochoa
Journal:  Ann Vasc Surg       Date:  2019-11-06       Impact factor: 1.607

4.  Application of Combined Superficial Femoral Artery Stenting and Deep Femoral Artery Profundoplasty in Chinese Patients With Lower Extremity Artery Disease.

Authors:  Guoqing Chi; Mingchao Ding
Journal:  Front Surg       Date:  2021-12-23
  4 in total

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