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FDA clears Evolution duodenal stent for treatment of gastric outlet obstructions


Wednesday, 02 Nov 2011 17:04

The Food and Drug Administration has granted 510(k) clearance to Cook Medical for its Evolution Duodenal Controlled-Release stent. This new stent expands palliative care options for patients experiencing issues associated with malignant gastric outlet obstruction, a late stage complication of a variety of gastrointestinal related cancers with pancreatic cancer being the most common cause.


Studies indicate that as many as 50% of the malignancies involving the small intestine, including pancreatic, gastric, duodenal and cholangiocarcinoma, occur in the duodenum. The stent offers these patients a minimally invasive alternative to relieve the symptoms and potentially life-threatening complications resulting from duodenal obstruction, such as abdominal pain, vomiting, malnutrition and aspiration.


The Evolution Duodenal Controlled-Release stent, the only duodenal stent delivery system that allows for controlled release and recapturability, is designed to provide physicians with precise control and maneuverability to ensure proper placement and potentially reduce complications such as migration and perforation. This stent is uniquely designed with 18 crowns at both the distal and proximal ends, which allow the stent to adapt to the natural curvature of the anatomy. The proximal and distal flanges are designed to reduce the risk of stent migration, while the patented Flexor catheter with kink-resistant technology provides trackability and maneuverability for deployment in the difficult anatomy of the duodenum.

“The Evolution duodenal stent includes several product features that are designed to make stent placement easier and more precise for the physician,” said John G Lee, professor of clinical medicine at the HH Chao Comprehensive Digestive Disease Center at University of California Irvine Medical Center. “These features of the stent allow for better wall apposition and potentially reduce the risk of migration, both of which are essential when treating patients with gastric outlet obstructions.”

In a prospective multicentre European study of 23 patients, 21 had significant improvement of symptoms. No early or late complications were recorded after a median follow-up of 8.8 weeks. Twenty-one patients (91.3%) were able to tolerate oral intake with a significant improvement of GOOSS (gastric outlet obstruction scoring system) score. Preliminary conclusions from researchers stated that the Evolution duodenal stent provided effective palliation for malignant gastric outlet obstruction. Additionally, physicians have now completed enrolment of 110 patients in a separate ongoing prospective multicentre study and final analysis of data is presently underway.

“The design of the stent and delivery system with recapturability make it easier to deploy in hard-to-reach areas such as the distal duodenum,” said Willis Parsons, medical director of the Northwest Community Hospital Gastroenterology Center. “The stent platform is designed for optimal trackability and maneuverability in difficult angulations, providing superior stability at crucial points during delivery.”


 




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