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Carotid Stent System Gets FDA Nod, With Conditions


 

The Food and Drug Administration's latest approval of a carotid stent system came with a list of postmarketing study commitments that includes monitoring outcomes in recipients and evaluating training programs for physicians using the device.

In January, the FDA approved the Protégé GPS and Protégé RX carotid stent systems for treating patients with carotid artery disease who are at high risk for adverse events from carotid endarterectomy. The FDA requires use of the embolic protection devices made by the same company, approved by the FDA in February 2006, with the stent.

Candidates for the stent must meet the following criteria:

▸ They must have stenosis of the common or internal carotid artery measuring 50% or greater if they are symptomatic, or 80% or greater if they are asymptomatic (as determined by ultrasound or angiography).

▸ They must have a reference vessel diameter within the range of 4.5 mm and 9.5 mm at the target lesion.

The Protégé carotid stent system, with the embolic protection device, was studied in the prospective, nonrandomized, multicenter Carotid Revascularization With ev3 Inc. Arterial Technology Evolution (CREATE) trial of 419 patients with carotid artery disease who were at risk for stoke and at high risk for adverse events from surgery.

The risk of death, stroke, and MI at 30 days, or any stroke in the area of the blockage at 1 year, was similar to the rate of complications reported in the literature from patients undergoing surgery, according to the FDA. The study also showed that the stent still maintained blood flow to the brain more than 1 year after the procedure.

As part of the approval, the manufacturer, ev3, has agreed to conduct a long-term follow-up study of patients from the CREATE study to evaluate the effectiveness and safety of the stent through 3 years after its implantation, according to the FDA approval letter. This will include performing a clinical exam, carotid duplex ultrasound, and neurologic exam annually. The company also will conduct a postapproval study of at least 1,500 patients from high-, moderate-, and low-volume centers who were treated by physicians with different categories of training. The study will evaluate the composite rate of death, ipsilateral cerebrovascular accident (CVA), procedure-related CVA, or MI 30 days after the procedure in 1,000 patients. This study also will follow these patients and determine the rate of ipsilateral stroke at 12 months.

Plymouth, Minn.-based ev3 Inc. manufactures the stents and the distal filter embolic protection device. The filter is marketed as the SpiderRX Embolic Protection Device.

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