TCT
PARTNER II Valve-in-Valve registry suggests alternative to reoperation in failed aortic bioprostheses
ISAR DESIRE 4: Paclitaxel-coated balloon is safe in treating in DES restenosis
BIOSOLVE-II: Novel magnesium alloy scaffold shows promise in treating CAD
SAN FRANCISCO — A second-generation drug-eluting bioresorbable scaffold made of magnesium alloy appears to be a feasible treatment in patients with de novo coronary artery lesions, with promising safety and performance outcomes observed at 6 months, according to study results presented at the annual TCT Scientific Symposium and published online in The Lancet.
Comparable outcomes with BVS, EES in ABSORB II interim 'need to be confirmed'
In patients with STEMI and CTO, PCI for CTO is safe, feasible
In patients with STEMI treated with primary percutaneous coronary intervention, undergoing PCI for chronic total occlusion within a week of STEMI appears to be safe and feasible, according to results from the EXPLORE trial presented at the annual TCT Scientific Symposium. However, PCI for CTO does not appear to improve left ventricular ejection fraction or left ventricular diastolic volume at 4 months.
Cryptogenic stroke recurrence less likely with PFO closure than medical management
Patent foramen ovale closure appears to be superior to medical management in preventing the recurrence of cryptogenic stroke, according to extended follow-up results from the RESPECT trial presented at the annual TCT Scientific Symposium. “We conclude, with this long-term, really extensive amount of new data, that treatment with the Amplatzer PFO Occluder is superior to guideline-recommended medical management,” John D. Carroll, MD, of the University of Colorado School of Medicine, said.
PANDA III: Distinct elution, absorption rates with bioresorbable DES offer comparable clinical outcomes
A uniquely-designed, sirolimus-eluting, bioresorbable stent was noninferior to an existing sirolimus-eluting stent for target lesion failure at 1 year, according to results from the PANDA III trial presented at the annual TCT Scientific Symposium. In the prospective, randomized, multicenter trial, Bo Xu, MBBS, of Fu Wai Hospital, Beijing, and colleagues enrolled 2,348 patients with symptomatic CAD, silent ischemia or ACS from 46 centers. All patients were eligible for PCI.