Structural-transport finite element models of drug eluting stents in large arteries

2006 ◽  
Vol 39 ◽  
pp. S400
Author(s):  
B. Simon ◽  
J. Vande Geest ◽  
P. Rigby ◽  
T. Newberg ◽  
S. Williams ◽  
...  
2013 ◽  
Vol 479-480 ◽  
pp. 225-229
Author(s):  
Hao Ming Hsiao ◽  
Chun Ting Yeh ◽  
Tsung Yuan Wu ◽  
Li Wei Wu ◽  
Bor Hann Huang ◽  
...  

The effects of micro-sized through-hole drug reservoirs on several key clinical attributes of the drug eluting depot stent were investigated. Finite element models were developed to predict the mechanical integrity of a balloon-expandable stent at various stages such as manufacturing and deployment, as well as the stent radial strength and fatigue life. Results show that (1) creating drug reservoirs on a stent could impact the stent fatigue resistance to certain degrees, and (2) drug reservoirs on the stent crowns led to much greater loss in all key clinical attributes than reservoirs on other locations. Based on these findings, an optimized depot stent was proposed/manufactured and proven to be a feasible design.


2012 ◽  
Vol 45 (14) ◽  
pp. 8
Author(s):  
MICHELE G. SULLIVAN

VASA ◽  
2012 ◽  
Vol 41 (2) ◽  
pp. 90-95 ◽  
Author(s):  
Rastan ◽  
Noory ◽  
Zeller

We have investigated the role of drug-eluting stents on patency rates after treatment of focal infrapopliteal lesions in patients with intermittent claudication and critical limb ischemia. Reports indicate that drug-eluting stents reduce the risk of restenosis after percutaneous infrapopliteal artery revascularization. A Pub Med, EMBASE, Cochrane database review search of non-randomized studies investigating patency rates, target lesion revascularisation rates, limb salvage rates and mortality rates in an up to 3-year follow-up period after drug-eluting stent placement was conducted. In addition, preliminary results of randomized studies comparing drug-eluting stents with bare-metal stents and plain balloon angioplasty in treatment of focal infrapopliteal lesions were included in this review. A total of 1039 patients from 10 non-randomized and randomized studies were included. Most commonly used drug-eluting stents were sirolimus-eluting. The mean follow-up period was 12.6 (range 8 - 24). The mean 1-year primary patency rate was 86 ± 5 %. The mean target lesion revascularization rate and limb salvage rate was 9.9 ± 5 % and 96.6 %±4 %, respectively. Results from non-randomized and preliminary results from prospective, randomized trials show a significant advantage for drug-eluting stents in comparison to plain balloon angioplasty and bare-metal stents concerning target lesion patency and in parts target lesion revascularisation. No trial reveals an advantage for drug-eluting stents with regard to limb salvage and mortality.


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