News | Heart Failure

Medtronic plc announced the results of an analysis that reveals patients increasingly adhere to heart failure medications after they receive cardiac resynchronization therapy (CRT) devices. The analysis of more than 4,500 patients revealed that compliance with their medications increased 67 percent 24 months after receiving their CRT implants, compared to the 24 months prior to implant (p<0.001). The results were presented at the 2016 Heart Failure Society of America (HFSA) Scientific Meeting in Orlando, Fla.

Home September 20, 2016
Home
News | Vascular Access

September 20, 2016 — Teleflex Inc. recently displayed its vascular access technologies and a new educational platform ...

Home September 20, 2016
Home
News | Heart Valve Technology

September 19, 2016 — Edwards Lifesciences received European CE mark to expand use of the Edwards Sapien 3 transcatheter ...

Home September 20, 2016
Home
News | Cath Lab

September 19, 2016 — Shockwave Medical announced positive clinical results from the pooled DISRUPT PAD Study, a single ...

Home September 19, 2016
Home
News | Heart Valve Technology

Valtech Cardio Ltd. announced that it will present the first-in-man data for its Cardioband Tricuspid (TR) system at PCR London Valves 2016, Sept. 18-20. In addition, updated two-year follow-up results of the multi-center Cardioband Mitral study will be presented at the meeting.

Home September 19, 2016
Home
News | Heart Valve Technology

September 19, 2016 — Boston Scientific received European CE mark approval for its Lotus Edge Valve System, the company's ...

Home September 19, 2016
Home
Technology | Drug-Eluting Balloons

Medtronic plc announced that the U.S. Food and Drug Administration (FDA) approved the IN.PACT Admiral drug-coated balloon (DCB) as a treatment for in-stent restenosis (ISR) in patients with peripheral artery disease (PAD). This is the first DCB that has gained approval to treat ISR in the United States. FDA approval was based on ISR data from the IN.PACT Global Study compared to a standard percutaneous balloon angioplasty (PTA) control.

Home September 19, 2016
Home
Technology | Peripheral Artery Disease (PAD)

September 16, 2016 — The U.S. Food and Drug Administration (FDA) has granted market clearance for Shockwave Medical’s ...

Home September 16, 2016
Home
Videos | Peripheral Artery Disease (PAD)

This video, provided by Shockwave Medical, demonstrates the Lithoplasty System. It uses ultrasonic waves to treatment ...

Home September 16, 2016
Home
News | Cardiac Resynchronization Therapy Devices (CRT)

EBR Systems Inc. announced the U.S. Food and Drug Administration (FDA) has granted an Investigational Device Exemption (IDE) for its WiSE (Wireless Stimulation Endocardially) Technology for cardiac resynchronization therapy (CRT). This IDE enables EBR Systems to start a major U.S. study to establish safety and effectiveness in support of U.S. approval.

Home September 15, 2016
Home
VIVA 2016, late breaking trials, cath lab
Feature | Cath Lab

Vascular Interventional Advances (VIVA) 2016 released its list late-breaking research presentations in vascular ...

Home September 14, 2016
Home
News | Cardiac Diagnostics

September 13, 2016 — Results from a new study suggest that small molecules known as microRNAs may be part of the pathway ...

Home September 13, 2016
Home
News | Cardiac Diagnostics

September 13, 2016 — Findings from a small study suggest that people who followed the popular Paleo diet for only eight ...

Home September 13, 2016
Home
bundled payments for cardiology, CMS cardiac reimbursements
Feature | Cardiovascular Business | John W. Meyer, MPH, FACHE

(Editor’s note: This is the first part of a two-part series on the proposed Medicare five-year demonstration for ...

Home September 13, 2016
Home
News | Artificial Heart

August 29, 2016 — SynCardia Systems, manufacturer of the Total Artificial Heart (TAH), announced that the judge ...

Home September 13, 2016
Home
Subscribe Now