The data thus far suggest fewer repeat interventions with the newly FDA approved resorbable device compared with PTA.

No matter whether patients had CAD or not, the simpler regimen was linked to less mortality and major bleeding at 6 months.

WASHINGTON, DC—For vascular closure after transfemoral TAVI, a strategy that combines suture- and plug-based devices halves ...

WASHINGTON, DC—How patients weigh the opinions of their family and friends when making decisions about PAD varies by sex and ...

Ami Bhatt and Michael Mack explore the ethics of AI use in the detection of subclinical cardiovascular disease.

Ami Bhatt and Michael Mack explain the economics of AI use in the detection of subclinical cardiovascular disease.

With further refinement and defined thresholds for treatment, this technology has the potential to guide treatment decisions.

The inability of QFR to rival FFR for 1-year MACE is a reminder of the need for large studies, even when new tech is enticing ...

Conference news filled our list this month, dominated by TCT 2024, although two EACTS stories also cracked our top 10.

The benefit was confined to symptoms, but in a very sick population with few options, that’s important, say researchers.

The result calls into question the prospects of FDA approval for the Acurate neo2 valve, which is already in use globally.

Several experts argue that AI-QCA is not a replacement for OCT, but could be valuable in low-resource settings.