Technology

February 24, 2012 — Simbionix USA Corp. announced that it received U.S. Food and Drug Administration (FDA) clearance for the endovascular aneurysm repair (EVAR) application for the PROcedure Rehearsal Studio (PRS). Last year Simbionix received clearance for the PRS carotid intervention application.

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The U.S. Food and Drug Administration (FDA) granted the first coronary stent indication for use in patients experiencing an acute myocardial infarction (AMI), or heart attack. The Boston Scientific Ion paclitaxel-eluting stent system and Taxus Liberte paclitaxel-eluting stent system are now the only drug-eluting stents (DES) in the United States with an approved indication to treat patients with AMI.

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February 24, 2012 — For the first time in years, information technology (IT) leaders at healthcare organizations did not identify a lack of financial support for IT as an obstacle to implementation; instead, concerns about staffing resources was cited as the key barrier.

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3-D reconstruction of a CT scan of a mummy.
Feature | Advanced Visualization

Computed tomography (CT) and advanced visualization software has allowed researchers to vitually unwrap a 2000-year-old mummy at the National Museums Scotland. Together with a team of radiologists and a forensic pathologist from Edinburgh University, a great deal has been learned about this female mummy, who died when she was in her mid-to-late twenties.

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February 23, 2012 – According to a new survey issued by the Heart Rhythm Society (HRS), the majority of Americans are unaware of two serious and potentially life-threatening heart rhythm disorders, atrial fibrillation (AF) and sudden cardiac arrest (SCA).

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February 23, 2012 — AstraZeneca announced that the American College of Chest Physicians (ACCP) has updated its guidelines on Antithrombotic Therapy and Prevention of Thrombosis to include a recommendation for giving the oral antiplatelet medicine, BRILINTA (ticagrelor) tablets with low-dose aspirin, to patients who suffer from acute coronary syndrome (ACS).

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Teleflex Inc. announced a new agreement with HealthTrust Purchasing Group L.P. (HealthTrust), for its Arrow Intra-Aortic Balloon Pump and Catheter products. The new agreement begins March 1, 2012 and extends through Feb. 28, 2015.

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February 23, 2012 — At the European Congress of Radiology taking place March 1-5, Spellman High Voltage Electronics Corp. and K&S Röntgenwerk will exhibit together for the first time at the Austria Center Vienna under the name Spellman High Voltage GmbH.

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February 22, 2012 — Attendees at the HIMSS 2012 meeting in Las Vegas were given a preview of what will be in the expected proposed rules for Stage 2 meaningful use, certification and standards from officials at the Office of the National Coordinator for Health IT (ONC) and the Centers for Medicare and Medicaid Services (CMS). In a recap featured on its website, HIMSS reported that Farzad Mostashari, National Coordinator for Health Information Technology, told attendees, “We stayed the course.” He also noted that image viewing will be an option for meaningful use (MU).

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U.S. Department of Health and Human Services’ (HHS) Secretary Kathleen Sebelius announced the number of hospitals using health information technology (IT) has more than doubled in the last two years. She also announced new data showing that nearly 2,000 hospitals and more than 41,000 doctors have received $3.1 billion in incentive payments for ensuring meaningful use of health IT, particularly certified electronic health records (EHR).

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February 22, 2012 — HeartWare International Inc. announced that a U.S. Food and Drug Administration (FDA) Circulatory System Devices Panel will review the premarket approval (PMA) application for the HeartWare Ventricular Assist Device system on April 25, 2012.

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February 22, 2012 — Cardiologists are expecting to use fewer imaging modalities per patient case in the future, according to a new report released by market research firm IMV Medical Information Division.

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February 21, 2012 — Circadence, a provider of WAN and network optimization solutions for healthcare, announced a set of solutions for optimizing electronic content delivery to iOS, Android and Windows clients.

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A comparison of HIMSS Analytics data from September 2011 to December 2011 suggests that a number of hospital segments showed increased capability to achieve Stage 1 of meaningful use.

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February 20, 2012 — ReCor Medical announced that its Paradise percutaneous ultrasound renal denervation system for achieving rhas received the CE mark. Paradise is designed to treat patients with resistant hypertension (HTN), a major risk factor for cardiovascular disease.

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