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Like metal stents, placement of a bioresorbable stent will restore blood flow and support the vessel through the healing process. However, in the case of a bioresorbable stent, the stent will gradually resorb and be benignly cleared from the body, enabling a natural reconstruction of the arterial wall and restoration of vascular function. [6]
The catheter/stent system is introduced into the body by penetrating a peripheral artery (an artery located in the arm or leg) and passed through the arterial system to deliver the DES into the blocked coronary artery. The stent is then expanded to dilate (open) blocked or narrowed coronary arteries (narrowed by plaque buildup), caused by a ...
With further study, [41] the FDA approved the use of the Taxus stent in the United States in March 2004. [ 42 ] By the end of 2004, drug-eluting stents were used in nearly 80 percent of all percutaneous coronary interventions.
The FDA has given Medtronic approval to use longer lengths of the company's Resolute Integrity drug-eluting stent in treating diabetes patients with coronary artery disease who have long coronary ...
Abbott Labs announced in a press release late last week that the Food and Drug Administration has approved the company's next-generation Xience Xpedition drug-eluting coronary stent. The company ...
PES also reduced the need for repeat procedures and improved the outcomes of patients with different types of lesions and risk factors. The paclitaxel-eluting Taxus stent received FDA approval and was launched in the US in 2004, [145] after a series of trials that compared it with a bare metal stent in various settings. The trials showed a ...