CardioSource WorldNews December 2014 | Page 37

The 2014 American Heart Association meeting included a number of clinically important presentations, including several failing to find support for some standard practices. So many negative trials have gathered attention recently that new rules are being considered that would require more such data be available freely to the public. (See the sidebar on Positive News on Negative Trials.) Here’s a collection of some of the most interesting items from this meeting. DAPT Beyond 1 Year Wins in Large Study The optimal duration of dual antiplatelet therapy (DAPT) has been the subject of considerable debate in the last couple years. Supporters of longer-term use got a big shot in the arm from the results of the DAPT Study. Study participants (about 10,000 total from 11 countries) who took aspirin plus a thienopyridine (clopidogrel or prasugrel) for 30 rather than 12 months after stenting • were half as likely to develop in-stent thrombosis than patients who received DAPT for 12 months, followed by aspirin plus placebo for 18 months (placebo group) (FIGURE), and • had about half the risk of a new myocardial infarction (MI) compared to the placebo group. Kirk Garratt, MD, Lenox Hill Heart and Vascular Institute, New York City, said in a press conference, “Thirty months of treatment with prasugrel plus aspirin was associated with important reductions in major adverse cardiovascular and cerebrovascular events and stent thrombosis compared to 12 months of treatment, with no signal of truly dangerous bleeds being increased with longer therapy.” He added, “Withdrawal of prasugrel at 12 months was associated with an important increase in the risk of ischemic events early after drug discontinuation, the principal risk being myocardial infarction, and the impact of drug withdrawal was evident within 90 days of drug cessation.” The study’s principal investigator and lead author, Laura Mauri, MD, said DAPT “was the first and only study comparing durations of treatment with antiplatelet therapy that was adequately powered to detect a benefit on stent-related heart attacks.” The study enrolled “a broadly inclusive population treated with coronary stents.” Dr. Mauri, who is an interventional cardiologist at Brigham and Women’s DAPT: Primary Endpoint – Stent Thrombosis FIGURE CardioSource.org/CSWN Hospital and chief scientific adviser at the Harvard Clinical Research Institute in Boston, Massachusetts, added, “Overall the benefits of longer therapy were very consistent throughout the types of patients we studied, and outweighed the risks.” According to Dominick J. Angiolillo, MD, PhD, director of Cardiovascular Research at the University of Florida College of Medicine, “…the guideline recommendation of one year of dual antiplatelet therapy remains steadfast.” He did add, “We cannot ignore other trials presented this week or earlier trials suggesting shorter durations of dual antiplatelet therapy for some patients. We will continue to follow guideline-based care, while evaluating the findings of DAPT and the forthcoming PEGASUS trial and how best to implement the implications of those results in clinical practice for the benefit of each individual patient.” IMPROVE IT: Ezetimibe/Statin Combination Better After ACS than Statin Alone It has been a decade since Christopher Cannon, MD, Brigham and Women’s Hospital, Boston, Massachusetts, presented the game-changing PROVE IT – TIMI 22 results at ACC.04 comparing intensive versus moderate lipid lowering with statins after acute coronary syndrome (ACS). Now, he is the lead author of IMPROVE-IT. “This is the first trial to demonstrate an incremental clinical benefit when adding a non-statin cholesterol-lowering agent to a statin,” he said, “and we found that even lower was even better, reaffirming the LDL hypothesis that reducing LDL