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Led by the launch of the Aplio 500 and Aplio 300 ultrasound systems, Toshiba America Medical Systems Inc. saw a 28 percent U.S. ultrasound business growth in 2012, far exceeding the industry’s 3 percent, according to Klein Biomedical Consultants Inc.’s industry report published in April 2013.

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Extracorporeal membrane oxygenation (ECMO), a procedure traditionally used during cardiac surgeries and in the intensive care unit (ICU) that functions as an artificial replacement for a patient's heart and lungs, has also been used to resuscitate cardiac arrest victims in Japan, Taiwan and South Korea. Now, a novel study of this technique in the United States has been completed by researchers at the Perelman School of Medicine at the University of Pennsylvania, indicating a potential role for this intervention to save patients who are unable to be resuscitated through conventional measures.

Home June 07, 2013
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GE Healthcare has announced that all of its new computed tomography (CT) products meet the Medical Imaging and Technology Alliance (MITA) smart dose standard that raises the bar for CT dose management.

Home June 06, 2013
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Boston Scientific Corporation reported interim data from the REDUCE-HTN clinical program, which demonstrated a significant and sustained reduction in the blood pressure of patients treated with the Vessix Renal Denervation System. Data on the first 41 subjects enrolled in the REDUCE-HTN clinical program were presented today at the annual EuroPCR Scientific Program in Paris by Joachim Schofer, M.D., of the Hamburg University Cardiovascular Center.

Home June 06, 2013
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The American College of Cardiology and the American Heart Association released an expanded clinical practice guideline for the management of patients with heart failure, updating definitions and classifications for heart failure and increasing emphasis on patient-centric outcomes such as quality of life, shared decision making, care coordination, transitions and palliative care.

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Data presented at Heart Rhythm 2013 show that Medtronic Inc. Lead Integrity Alert (LIA) software detected pace/sense lead issues in non-Medtronic leads at a greater rate than standard impedance monitoring alone (impedance monitoring measures the electrical continuity of a lead four times per day). The retrospective analysis, which focused on Endotak leads (Boston Scientific) and was presented by Kenneth Ellenbogen, M.D., shows that for every one Endotak pace/sense lead issue detected by impedance monitoring, the LIA software detected four cases that impedance monitoring alone missed. LIA is not currently FDA approved for use with non-Medtronic leads.

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The National Institutes of Health (NIH), the nation’s medical research agency and the leading supporter of biomedical research in the world, said all of its clinical programs will be effected by $1.55 billion in NIH budget cuts due to sequestration. On March 1, 2013, as required by statute, President Obama signed an order initiating sequestration. This requires NIH to cut 5 percent, or $1.55 billion, of its fiscal year (FY) 2013 budget. NIH must apply the cut evenly across all programs, projects and activities (PPAs), which are primarily NIH institutes and centers.

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Many providers, and even consumers, are now aware of low-dose technologies, such as computed tomography (CT) systems that enable high-quality images with low radiation. Today, a growing number of hospitals are also adopting monitoring technology that takes dose management to the next level.

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Technology

Covidien recently introduced its RapidCross 0.014-inch Rapid Exchange Percutaneous Transluminal Angioplasty (PTA) Balloon, which offers rapid exchange (RX) convenience with kink-resistant pushability for below-the-knee (BTK) interventions.

Home June 04, 2013
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The Medicare trustees have projected that the trust fund that finances Medicare’s hospital insurance coverage will remain solvent until 2026, two years beyond what was projected in last year’s report.

Home June 04, 2013
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The U.S. Department of Health and Human Services (HHS) announced that more than half of all doctors and other eligible providers have received Medicare or Medicaid incentive payments for adopting or meaningfully using electronic health records (EHRs).

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June 4, 2013 — During the 2013 Annual Meeting of the Society for Imaging Informatics in Medicine (SIIM), DR Systems will demonstrate its DR Systems Unity Enterprise Imaging Excellence Solution, e|HR for Meaningful Use and eMix, and electronic medical information exchange

Home June 04, 2013
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Technology

HealthHelp’s MedTree ODS offers a transparent clinical decision support system that allows providers to self-govern the ordering process and receive approval for most decisions in less than one minute, 24 hours a day, seven days a week.

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critical results reporting, CTRM
Feature | Mark Flyer, M.D., CIIP, Maimonides Medical Center, and Serena Mak, M.D.

In today’s fast paced and “consumer-driven” medical environment, there are more demands imposed on clinicians to deliver quick and accurate care. These increasing demands have made it difficult for them to review imaging results in a timely fashion, resulting in potential dire consequences for their patients and medical-legal implications for their organizations.

Home June 04, 2013
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Siemens Healthcare has announced that the U.S. Food and Drug Administration (FDA) recently cleared the company’s CAIPIRINHA (Controlled Aliasing in Volumetric Parallel Imaging Results IN Higher Acceleration) software as part of Siemens’ syngo MR D13A software package for parallel magnetic resonance (MR) imaging. The software helps enable patients with breath-holding difficulties to reduce the amount of time they hold their breath by up to 50 percent without sacrificing imaging resolution or contrast.

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