ICE is offered on GE Healthcares Vivid i and Vivid q portable ultrasound systems. Images can be integrated into GEs CardioLab electrophysiology system. Intracardiac echo (ICE) imaging technology advances.
Feature | Dave Fornell

Intracardiac echocardiography (ICE) offers a clearer view of transcatheter devices and electrophysiology (EP) procedures from inside the heart.

Home May 07, 2010
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May 7, 2010 – Findings from the SPIRIT IV trial, one of the largest randomized clinical trials comparing two drug eluting stents with 3,690 U.S.-based patients, were published this week in The New England Journal of Medicine.

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May 6, 2010 – Patients who can postpone noncardiac surgery for at least six weeks after receiving a coronary stent are less likely to suffer reduced blood flow to the heart, heart attack and death than those who have surgery sooner. This was the finding of Scottish researchers in Circulation: Cardiovascular Interventions, an American Heart Association journal.

Home May 06, 2010
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May 6, 2010 – After entered the Japanese drug-eluting stent market earlier this year, Abbott's Xience V and Boston Scientific's Promus stents picked up share from competitors Medtronic and Cordis, according to the market intelligence firm Millennium Research Group (MRG).

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May 5, 2010 - Emergency department use of 256-slice computed tomography angiography (CTA) can help physicians triage patients with indeterminate chest pain without the need for additional diagnostic testing which can be costly and time consuming, according to a study to be presented at the American Roentgen Ray Society (ARRS) 2010 Annual Meeting in San Diego, Calif.

Home May 05, 2010
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May 5, 2010 – A federal jury awarded more than $29.4 million in damages in a patent infringement lawsuit between two interventional cardiology access dressing manufacturers. Marine Polymer Technologies Inc. won its case against HemCon Medical Technologies Inc. April 29 .

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May 5, 2010 – Catheter ablation of ventricular tachycardia (VT) is one of the fastest growing electrophysiology (EP) procedures, but requires the delivery of robust lesions for clinical success. Stereotaxis Inc. is starting a multicenter clinical study on VT treatment outcomes using its Niobe Magnetic Navigation System.

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May 5, 2010 – A new high-definition intravascular imaging system gained U.S. Food and Drug Administration (FDA) clearance today. LightLab Imaging Inc. said its C7-XR optical coherence tomography (OCT) imaging system and companion C7 Dragonfly OCT imaging catheter are now available on the U.S. market.

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May 4, 2010 - Researchers have developed a computer-based system that can automatically track patient-specific radiation dose exposure on every patient that receives a computed tomography (CT) scan, according to a study to be presented at American Roentgen Ray Society (ARRS) 2010 Annual Meeting in San Diego.

Home May 04, 2010
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April 27, 2010 — While repair of large abdominal aortic aneurysms (AAA's) is well accepted, randomized clinical trials have failed to demonstrate benefit for early surgical repair of small aneurysms over surveillance, according to researchers from New York-Presbyterian Hospital in New York.

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April 28, 2010 — The U.S. District Court in Minnesota this week declined to accept the plea agreement between Guidant and the U.S. Justice Department related to its failure to report adverse events from its implantable cardioverter defibrillators (ICDs) in 2005. Boston Scientific acquired Guidant after the incident.

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May 4, 2010 — Including a coronary artery calcium score in a risk assessment for future heart disease events — such as heart attacks — provides a better estimate in some populations than a standard coronary risk factors assessment, according to research supported by the National Heart, Lung, and Blood Institute (NHLBI), part of the National Institutes of Health (NIH).

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May 4, 2010 — New research released this week in the Journal of the American College of Cardiology shows the value of implantable cardiac device diagnostics in identifying worsening heart failure.

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May 4, 2010 – The U.S. District Court in New Hampshire is being asked this week to review and reverse a jury verdict on patent litigation involving two companies with competing hemostasis management technology used in the cath lab.

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May 4, 2010 – A deal has been struck to produce a generic version of Merck & Company’s Zetia (ezetimibe). In the United States, the cholesterol modifying agent has annual U.S. sales of about $1.4 billion, according to IMS Health data.

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