Advances in Intracoronary Diagnostics and Therapeutics

The field of cardiology has experienced impressive progress over the past decades, in part due to improvements in intracoronary diagnostic and therapeutic techniques. However, despite these advances, cardiovascular disease remains the leading cause of death in the developed world. Today’s Forum will focus on emerging intracoronary technologies that may substantially improve management of cardiovascular disease. The first talk will feature a discussion of the problems associated with current stent designs, and strategies to improve them. The second talk will examine the limitation of traditional intracoronary diagnostic methods, and will describe novel approaches that may shift the diagnostic paradigm.

Moderator: Thomas J. Brady, MD, Co-Program Leader, Cardiovascular Disease, Co-Director, Office of Education and Senior Consultant, CIMIT; Director, Cardiovascular Imaging and Intervention and Vice Chairman, Director of Radiology Research, Massachusetts General Hospital; L.L Robbins Professor of Radiology, Harvard Medical School, tom@nmr.mgh.harvard.edu

4:00PM  Introduction: Ahmed Tawakol, MD, Co-Leader: CIMIT Cardiovascular Disease Program; Co-Director, Cardiac MR-PET-CT Program and Associate Director, Nuclear Cardiology, Massachusetts General Hospital, atawakol@partners.org

 

4:10PM  Drug Eluting Stents: Lessons in Biocompatibility
Sahil A. Parikh
, MD, Interventional Cardiology Fellow, Brigham and Women’s Hospital; Clinical and Research Fellow, Harvard Medical School; Research Affiliate, Harvard-MIT Division of Health Sciences and Technology, sparikh1@partners.org 

 

The purpose of placing a stent in an artery is to prevent restenosis (re-narrowing of the artery) without causing thrombosis (the formation of a clot), for both restenosis and thrombosis can lead to heart attacks.  Drug-eluting stents, which limit restenosis, were regarded as a major medical advance when they first appeared, but new evidence suggests that they also confer long-term risks.  In a significant number of cases, particularly in patients who stop taking anti-clotting drugs, the stents have caused fatal thromboses years after their placement in an artery.  To make drug-eluting stents as safe and effective as possible, researchers are seeking to improve the stents’ biocompatibility.      

 

A stent is a foreign object in the body, and the body responds to the stent’s presence in a variety of ways.  Amongst other responses, macrophages accumulate around the stent, and nearby smooth muscle cells proliferate.  These physiological changes, which can cause restenosis, can be limited by drugs released by the stent, but these drugs also limit re-endothelialization.  This lack of healing can make the stent an exposed surface on which a life-threatening clot can form. 

 

The safety and effectiveness of a drug-eluting stent depends on its design and on its materials.  The structure of a stent’s metal backbone, for example, has a significant effect on the amount of endothelial denudation that the stent causes.  When comparing drug-eluting stents to bare-metal stents, one should remember that drug-eluting stents are only beginning to adopt the sophisticated structures that are commonly used in state-of-the-art bare-metal stents.  The properties of the drug used in a drug-eluting stent are also extremely important.  Hydrophobic drugs are more likely to be retained in the arterial wall than hydrophilic drugs, and for all drugs, the concentration varies with wall depth.  Finally, the polymer coating of a drug-eluting stent influences the stent’s tendency to cause a clot. 

In the future, researchers hope to create stents, or at least polymer coatings, that will degrade in the body over time.  This project will require expertise in both materials science and medicine. 

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4:30PM  Advances in Intra-coronary Diagnostic Methods as a means of Matching Type of Therapy with the Type of Plaque Present
James E. Muller, MD , CEO, InfraReDx, Inc., jmuller@infraredx.com

Coronary heart disease is the leading cause of death in the United States, and 1.2 million fatal and non-fatal heart attacks occur each year.  Of these heart attacks, 700,000 occur in patients with no documented history of heart problems.  That more than half of all heart attacks occur without warning represents a major diagnostic failure and implies that new diagnostic techniques are needed.

 

Myocardial infarctions often occur when a lipid-rich plaque ruptures and causes an artery-clogging clot to form.  Unfortunately, current diagnostic methods are largely incapable of identifying lipid-rich plaques before they rupture.  With this problem in mind, researchers are exploring new ways to identify lipid-rich plaques.  Intravascular magnetic resonance imaging (MRI), which uses a magnetic coil small enough to fit inside an artery, presents one possibility; and optical coherence tomography (OCT) provides another.  At the moment, however, both of these techniques are hampered by blood, so both require arterial occlusion.  In contrast, near-infrared (NIR) spectroscopy, which characterizes a chemical mixture based on its absorption of NIR light, works even if the spectroscopic catheter is surrounded by blood.  NIR spectroscopy can differentiate between the fat in plaques and the fat in surrounding tissue, and early results indicate that the technique can be used to effectively identify lipid-rich plaques.  

 

Doctors may soon be able to make treatment decisions, such as whether to use a bare-metal stent or a drug-eluting stent in a given patient, based on the type of plaque that the patient has.  Hopefully, “personalized stenting” based on tissue type will be the method of the future.  Non-invasive molecular imaging techniques will also hopefully be developed to help doctors make informed diagnostic decisions.

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5:00PM  Panel discussion – View this video