UltraSPECT, dose management, lower dose SPECT
Feature | Nuclear Imaging | Dave Fornell

Nuclear myocardial perfusion imaging (MPI) with positron emission tomography (PET) and single-photon emission computed tomography (SPECT) have been the gold standard for noninvasive detection of coronary ischemia and infarcts. However, the high radiation doses patients receive are making some providers think twice before referring their patients for nuclear MPI.

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Contego Medical announced the completion of a $5.6 million Series B financing round, led by Hatteras Venture Partners. Hatteras is an early stage venture firm with a focus on medical devices, biopharmaceuticals, diagnostics and related opportunities in human medicine. The round also included Mountain Group Partners, Lookout Capital and Medical Mutual.

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Penn Medicine’s Penn Care at Home program reported a 53 percent reduction in 30-day readmission rates for 130 congestive heart failure patients since implementing software from Health Recovery Solutions. Readmission rates dropped from 8 percent to 3.8 percent over a period from July 2014 to February 2015.

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The Healthcare Information and Management Systems Society (HIMSS) released the results of the 2015 HIMSS Mobile Technology Survey. This year’s study, of more than 200 healthcare provider employees, found that nearly 90 percent of respondents are utilizing mobile devices within their organizations to engage patients in their healthcare. The report also showed that respondents believe that mobile health (mHealth) technologies are beginning to drive cost savings and improve the quality of care delivered.

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On April 17, 2015 the Centers for Medicare and Medicaid Services (CMS) issued a proposed rule to update fiscal year (FY) 2016 Medicare payment policies and rates under the Inpatient Prospective Payment System (IPPS) and the Long-Term Care Hospital (LTCH) Prospective Payment System (PPS). The proposed rule, which would apply to approximately 3,400 acute care hospitals and approximately 435 LTCHs, would affect discharges occurring on or after Oct. 1, 2015.

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EBR Systems Inc. announced it has raised $20 million for clinical studies and regulatory filings, including commitments toward a second quarter closing. EBR Systems is using the funds to build on promising European clinical work; obtain CE Mark for the company’s proprietary wireless pacing system; obtain approval for a U.S. Investigational Device Exemption (IDE) clinical study; and complete development of its second generation system that is smaller and more energy efficient.

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Feature | Dave Fornell

The latest advances in echocardiography were discussed at a special evening symposium at the 2015 American College of Cardiology (ACC) meeting, organized by Methodist Debakey Heart and Vascular Center.

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Cerner Corp. and Qualcomm Life Inc. announced an agreement to extend Cerner’s medical device connectivity capabilities beyond the hospital to the home. Cerner will leverage Qualcomm Life’s U.S. Food and Drug Administration (FDA)-listed 2net Platform and Hub to capture data from medical devices and sensors within a patient’s home, and transmit it to Cerner healthcare clients through Cerner’s CareAware device connectivity platform. Through this initiative, care providers can remotely monitor chronically ill patients in near-real time to enable proactive engagement to potentially reduce the risk of an acute care episode.

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WITS(MD), a provider of medical image workflow solutions, announced the introduction of Image Mover, a mobile application that securely captures medical images from smart devices with a zero-protected health information (PHI) footprint.

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Pingmd debuted its virtual care mobile app, Pingmd 3, at the 2015 Healthcare Information and Management Systems Society (HIMSS) annual conference, April 13-15 in Chicago. The platform allows virtual care coordination using messaging, voice, picture and video in asynchronous and real time communications securely.

Home April 16, 2015
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The U.S. Food and Drug Administration (FDA) approved Amgen’s ivabradine (Corlanor) to reduce hospitalization from worsening heart failure.

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CareDx Inc., a molecular diagnostics company focused on the development and commercialization of clinically differentiated, high-value, non-invasive surveillance solutions for transplant recipients, announced new evidence that the proportion of cell-free DNA (cfDNA) derived from the transplanted organ and found in the bloodstream of the recipient is correlated to the rejection status of the organ. This new biomarker (cfDNA) in combination with AlloMap, the company's molecular diagnostic surveillance solution, provides greater accuracy of identification of rejection in heart transplant recipients than either test alone.

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NEC Display Solutions of America received U.S. Food and Drug Administration 510(K) market clearance of the MultiSync MD322C8 LCD, a high-resolution display for radiology review applications in healthcare organizations.

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Nuance Communications showcased its newest innovations for bringing clinical documentation to smart devices, smart watches and the Internet of things at the 2015 Health Information Management Systems Society (HIMSS) Annual Conference in Chicago this week.

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Siemens Healthcare showcased their healthcare information technology portfolio, including software and hardware supporting clinical workflow and enhanced productivity, at the Healthcare Information and Management Systems Society (HIMSS) 2015 conference, April 13-15 in Chicago.

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