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Edwards Lifesciences announced that its got Europe's CE Mark for transcatheter aortic valve replacement (TAVR) in severe, symptomatic aortic stenosis patients. The Ultra model uses a new delivery system and sheath and adds an "on balloon" design that makes valve alignment unnecessary, the press release said.

TAVR was for short-term survival among low-risk patients with a Society of Thoracic Surgeons score under 4%, according to the German registry. (European Heart Journal)

The first-in-human experience with the transfemoral resulted in underexpansion of the valve during TAVR, although the manufacturer is making changes to the delivery system to fix the issue, according to a case study published in EuroIntervention.

What do you do in the cath lab when someone presents with an acute MI due to saphenous vein graft failure and has a chronic total occlusion in the native coronary artery supplied? , one group suggested with a two-case series. (Catheterization and Cardiovascular Interventions)

Among older acute MI patients in the ACTION registry, were less likely to undergo cardiac catheterization but the ones that did experienced more in-hospital bleeding, according to a report in JACC: Cardiovascular Interventions. There was no such bleeding disadvantage for these patients getting conservative management, however. See 麻豆传媒's full coverage here.

The used in Reva's Fantom bioresorbable scaffold is being used to develop embolic microbeads to target liver cancer, uterine fibroids, and benign prostatic hyperplasia, the company announced.

of failed endovascular thrombectomy with a permanent self-expandable stent yielded a favorable outcome in 43% of patients and death in 21%, according to a meta-analysis in the Journal of NeuroInterventional Surgery.

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