News | PET-MRI

March 31, 2017 — Northwestern Memorial Hospital is now home to the Chicago area's first combined magnetic resonance (MRI ...

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News | Stents Bifurcation

Tryton Medical Inc. recently announced that the first U.S. commercial case using the Tryton Side Branch Stent was completed at New York-Presbyterian Hospital/Columbia University Medical Center in New York City. The device was used to treat a coronary bifurcation lesion involving a large side branch (appropriate for a ≥2.5mm stent) in a procedure performed by Martin Leon, M.D., director of the Center for Interventional Vascular Therapy, and Ajay Kirtane, M.D., SM, director of the Cardiac Catheterization Laboratory.

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News | Vascular Access

The U.S. Food and Drug Administration (FDA) announced it has initiated a Class I recall of the Merit Prelude Short Sheath Introducer, warning that a manufacturing defect may cause the tip to separate from the sheath during the separation procedure. The agency said that if this occurs, the tip could enter the patient’s bloodstream. This may result in prolonged procedure times, additional surgery to remove the tip from the patient, blood clots, internal tears and perforation to arteries or veins, excessive bleeding and death.

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Videos | Stents Bioresorbable

Stephen Ellis, M.D., professor of medicine and director of interventional cardiology at Cleveland Clinic, discusses the ...

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News | Radiation Dose Management

The Connecticut Hospital Association (CHA) and Bayer announced an alliance to establish the United States' first-ever statewide radiation dose management repository for patients undergoing certain radiological procedures. The repository will use Bayer’s Radimetrics, a radiation and contrast dose management and analytics tool which provides clinicians with data needed for them to help ensure their patients receive the lowest radiation dosage necessary. The goal is for clinicians to be able to share the data in order to benchmark radiation exposure.

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March 30, 2017 — New late-breaking featured clinical research presented today adds strong clinical support for Abbott's ...

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News | Defibrillator Monitors

Automated external defibrillators (AEDs) are associated with increased survival of sudden cardiac arrest when installed in schools, yet only 17 out of 50 U.S. states require AED installation in at least some of their schools, according to a new analysis. The analysis was published in the Journal of the American College of Cardiology.

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News | Patient Monitors

Acarix AB recently announced the results from a new multi-center trial of its handheld CADScor System for non-invasive, non-radiation acoustic detection of coronary artery disease (CAD). The results were presented at the American College of Cardiology (ACC) 2017 Annual Scientific Meeting, held March 17-19 in Washington, D.C., and showed the handheld CADScor System rules out CAD with 97 percent negative predictive value. The results confirm the company’s previously announced figures which, prior to this study, were unconfirmed.

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Feature | Left Atrial Appendage (LAA) Occluders

March 29, 2017 — For patients with atrial fibrillation (AFib), closing the area of the heart known as the left atrial ...

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Ablation procedure, EP lab, Uninterrupted Dabigatran Etexilate in Comparison to Uninterrupted Warfarin in Pulmonary Vein Ablation
Feature | Atrial Fibrillation

March 29, 2017 — Uninterrupted treatment with dabigatran (Pradaxa), a non-vitamin K, novel antagonist oral anticoagulant ...

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News | Pharmaceuticals

Injection of a novel form of synthetic high-density lipoprotein cholesterol (HDL-C), or good cholesterol, into the arteries of recent heart attack patients did not reduce the volume of plaque in the arteries compared with placebo injections, according to new research. The findings were presented at the American College of Cardiology’s 66th Annual Scientific Sessions, March 17-19 in Washington, D.C.

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News | Chronic Total Occlusion (CTO) | Dave Fornell

March 29, 2017 — In patients with a complete, persistent arterial blockage, medication alone was found to be equal to ...

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Videos | Cath Lab

MDBuyline analyst Tom Watson shares some of the most important trends in cardiac technology he saw at the 2017 American ...

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News | Defibrillator Monitors

Philips and the U.S. Food and Drug Administration (FDA) announced the company has initiated a recall of its HeartStart MRx Monitor/Defibrillator. The Class I recall is due to electrical and battery connection issues that may prevent the device from powering up, charging and delivering electrical shock therapy. The device may also unexpectedly stop pacing. A delay in delivering therapy could result in serious patient injury such as permanent organ damage, brain injury or death.

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News | Pharmaceuticals

When used as a preventive measure during heart surgery, the heart failure drug levosimendan did not significantly reduce rates of death, heart attack, kidney dialysis or use of a mechanical assist device among patients at high risk for low cardiac output syndrome. These findings were part of a study presented at the American College of Cardiology’s 66th Annual Scientific Session, March 17-19 in Washington, D.C.

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