Healthcare Industry News: coronary bifurcation
News Release - May 17, 2011
Cappella Medical to Share Data Documenting Benefits of Full Ostial Protection at EuroPCR 2011PARIS--(Healthcare Sales & Marketing Network)-- Cappella, Inc. (Cappella), a medical device company developing dynamic solutions for the treatment of coronary bifurcation disease, today revealed how its innovative Sideguard® coronary sidebranch technology will be featured in several scientific sessions at this week’s EuroPCR Congress in Paris, including a new European survey on the challenges in treating bifurcation disease.
Dr. Farzin Fath-Ordoubadi, Consultant Cardiologist and Cath Lab Director at the Heart Centre, Manchester Royal Infirmary commented, “Treating bifurcation disease has always been a challenge for physicians due to the complex anatomy of the coronary sidebranch. Conventional procedures forced us to treat the bifurcation with either two stents that weren’t intended for this use, or one main vessel stent that has limitations in terms of ostial protection and sidebranch preservation. Now with today’s newer technology, such as the Cappella Sideguard system, we have a technology dedicated to bifurcation disease that scaffolds the ostium reducing plaque and carina shift while preserving the sidebranch. This offers a straightforward approach, minimising the technical limitations associated with conventional treatments. I am confident that dedicated bifurcation solutions will find a place in our practice going forward.”
A recent survey carried out on behalf of Cappella Medical and published in the May/June edition of Coronary Heart magazine, invited clinicians across Europe to share their views on the challenges and opportunities for improvement in the treatment of bifurcation lesion treatment (BLT). David Blossom, Vice President of Commercial Operations at Cappella Medical, said of the results, “It was promising to learn that even though 82% of respondents most frequently used provisional stenting when treating bifurcation disease and an additional 13% used a mixture of the provisional and 2-stent approach, 95% of respondents were open to the idea of treating the sidebranch prior to the main artery.” The survey revealed that clinicians were aware of the limitations of current practice with 83% reporting that up to 30% of provisionally stented patient’s return for sidebranch treatment at which point they may not be able to regain access to the sidebranch. These procedures are costly, so it is clear that a ‘get it right first time’ approach is ideal. David commented, “This survey, added to the growing body of data being presented here at EuroPCR, reinforces our belief that the Sideguard system addresses a currently unmet need for the protection, and preservation, of the coronary sidebranch artery.” The full survey results can be viewed online at www.cardiologyhd.com.
Several new studies have been released comparing the Cappella Sideguard technology to current practice. Dr. Akiko Maehara presented data recently showing that the self-expanding Cappella Sideguard stent is effective in maintaining an adequate lumen volume in the sidebranch and, especially, an adequate lumen area at the sidebranch carina at follow-up. In addition, the study also found that expansion of a balloon-expandable stent in the main vessel of a bifurcation lesion is associated with axial plaque redistribution that is not seen in the corresponding sidebranch treated with the self-expanding Cappella Sideguard stent, concluding that long-term follow-up will determine the impact of this phenomenon on ostial sidebranch restenosis. Dr. Nicolas Foin and colleagues from the Imperial College and Royal Brompton and Harefield NHS Trust, London, UK and the London Chest Hospital will be presenting results from a study comparing the treatment of bifurcations using Sideguard as a first line treatment compared to a conventional two-stent strategy. The study concludes that use of Sideguard appears to offer complete stent scaffolding at the sidebranch ostium while reducing strut malapposition at the bifurcation ostium. The clinical information being presented at EuroPCR continues to validate the unique advantages of the Cappella Sideguard technology. Cappella looks forward to sharing additional data in the coming months.
About Cappella Medical Devices:
Cappella, Inc. is a medical device company that develops novel solutions for the treatment of complex coronary artery disease (CAD) focused on protecting the coronary sidebranch arteries. Cappella’s Sideguard® coronary sidebranch technology offers interventional cardiologists a straightforward, effective, and easy to use solution that preserves the sidebranch of diseased coronary arteries by protecting the ostium while minimizing plaque shift. The Sideguard delivery system features a proprietary split-sheath, balloon released, technology that ensures precise placement on the ostial borderline. The Sideguard self-expanding, nitinol, stent promotes continuous wall apposition and positive remodelling and its unique trumpet-shaped design conforms to varying characteristics of the sidebranch ostium. The Cappella Sideguard system is currently CE mark approved and is being distributed throughout Europe and South America. Cappella Medical Devices Ltd., Galway, Ireland is the R&D and manufacturing subsidiary of Cappella, Inc. For more information, please visit the Cappella Medical Systems website at www.cappella-med.com.
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