Medical Center & Health Care
Stony Brook Heart Institute Evaluates First Dissolvable Stent
Clinical trial compares new device with standard metallic drug-eluting stents and investigates vasomotion, a measure of how much natural motion returns to the vessel
For patients who do not require open heart surgery to open blocked blood vessels, inserting metallic drug-eluting stents is standard therapy. Stony Brook specialists will compare the efficacy and safety of Absorb™, a drug-eluting bioresorbable vascular scaffold (BVS) manufactured by Abbott, to standard metallic drug-eluting stents in two groups of patients. Absorb will only be used in patients whose condition enables them to elect for the dissolvable stent. The Principal Investigator leading the trial at Stony Brook is Luis Gruberg, MD.
“This type of coronary stent that ‘disappears’ is the latest technology to treat vessel blockages,” said Dr. Gruberg, Professor of Medicine, Division of Cardiovascular Medicine, and Director of Research, Interventional Cardiology, at Stony Brook University School of Medicine. “Unlike metallic stents that stay within the vessels permanently, this stent completely dissolves within about two years after implantation and may promote natural vessel motion to the treated tissue.”
The ABSORB III clinical trial will enroll approximately 2,250 patients. At Stony Brook, Dr. Gruberg expects to enroll 30 to 40 patients. Eligibility is based on non-emergency cases with simple blockages in the coronary arteries. Men or women of any age in need of stent implantation may be eligible.
Dr. Gruberg said that the BVS technology and the device acting as a “temporary scaffold” to the vessel is designed to result in more vessel flexibility compared to vessels with permanent metallic stents. He explained that the potential end result is a dissolved stent with a vessel that has enhanced pulsation similar to a normal, unblocked blood vessel. To determine this endpoint, Dr. Gruberg will evaluate vasomotion, a measure of how much natural motion returns to the vessel in patients treated with Absorb once the new device dissolves into arterial tissue.
A unique aspect of the BVS stent is that it is made of polylactide, a naturally dissolvable material derived from products like corn starch, which is commonly used in medical implants such as dissolving sutures. After the drug-eluting stent dissolves only two pairs of tiny metallic markers are left behind to enable a physician to identify where the device was implanted.
For more information about this clinical trial and enrollment at Stony Brook, please call the Stony Brook University Heart Institute Research Office at 631-444-3309.
About Stony Brook University Heart Institute:
Stony Brook University Heart Institute is located within Stony Brook University Hospital as part of Long Island's premier university-based medical center. The Heart Institute offers a comprehensive, multidisciplinary program for the prevention, diagnosis and treatment of cardiovascular disease. The staff includes 50 full-time and community-based, board-certified cardiologists and cardiothoracic surgeons, as well as 350 specially trained anesthesiologists, nurses, physician assistants, nurse practitioners, respiratory therapists, surgical technologists, perfusionists, and other support staff. Their combined expertise provides state-of-the-art interventional and surgical capabilities in 24-hour cardiac catheterization labs and surgical suites. And while the Heart Institute clinical staff offers the latest advances in medicine, its physician-scientists are also actively enhancing knowledge of the heart and blood vessels through basic biomedical studies and clinical research. To learn more, visit www.heart.stonybrookmedicine.edu.
© Stony Brook University 2013