Technology

Ziehm Imaging received U.S. Food and Drug Administration (FDA) clearance to market its new generation Ziehm Vision RFD C-arm for pediatric and other interventional operating room procedures. The Ziehm Vision RFD C-arm offers fully motorized movement on four axes to maximize image quality while minimizing procedural dose. It was cleared for a range of image procedures including specific intended uses in pediatric imaging.

Home February 06, 2014
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St. Jude Medical Nanostim Leadless Pacemaker EP Lab
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The first U.S. implant was announced for St. Jude Medical’s LEADLESS II pivotal trial, designed to evaluate the Nanostim leadless pacemaker for U.S. Food and Drug Administration (FDA) approval. The world’s first retrievable, non-surgical pacemaker was implanted at The Mount Sinai Hospital in New York City by Vivek Reddy, M.D.

Home February 06, 2014
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MRI Systems IMV Medical Information Division
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The average age of installed MRI scanners in the United States has increased from 8.7 years in 2010 to 11.4 years in 2013, according to a new market research report by IMV Medical Information Division.

Home February 06, 2014
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Mercom Capital Group Venture Capital Funding Healthcare IT
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Mercom Capital Group LLC, a global communications and consulting firm, released its annual report on funding and mergers and acquisition (M&A) activity for the healthcare information technology (IT) sector in 2013.

Home February 05, 2014
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GlobalMed CapSure Cloud CT Systems Radiation Dose Management Clinical Decision
Feature

GlobalMed’s CapSure Cloud application can eliminate a second radiation dose by making an initial CT scan available to all healthcare providers involved in a patient’s care. Once the images are uploaded to the secure cloud imaging server from the originating hospital, the sign-on information can be shared with specialists at the receiving hospital so they can view the study. In emergency cases, this means the team at the receiving hospital can be prepared for the patient’s arrival and go directly to the OR.

Home February 05, 2014
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defibrillator-monitors, defibrillator monitor
Feature | Defibrillator Monitors | Dave Fornell

For U.S. hospitals and emergency medical services (EMS) looking to upgrade their aging defibrillator-monitors, new technologies added to these systems enable more feedback to first responders and can help speed door-to-balloon times by transmitting pre-hospital ECGs.

Home February 03, 2014
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News

Percutaneous coronary intervention (PCI) centers are unequal relative to population and heart attack prevalence across the United States, according to a study in the Journal of the American Heart Association. A multi-center team led by James Langabeer II, Ph.D., The University of Texas Health Science Center at Houston, conducted the study.

Home February 03, 2014
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InfoBionic’s MoMe System for cardiac arrhythmia monitoring received CE marking. The MoMe System is a remote patient monitoring platform that can transition between Holter, Event and Mobile Cardiac Telemetry (MCT) modes. The platform leverages cloud computing and proprietary analytics, and delivers on-demand access to patient data for diagnosis.

Home February 03, 2014
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therapeutic hypothermia, Philips InnerCool
Feature | Dave Fornell

Use of therapeutic hypothermia is used to prevent neurological damage in patients who suffer sudden cardiac arrest (SCA), and there are many advocates suggesting a similar approach can help improve outcomes in ST-elevated myocardial infarction (STEMI) patients.

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ImaCor Inc., developer of hemodynamic transesophageal echocardiography (hTEE) technology, released the hTEE QuickStartT mobile application. The app complements ImaCor’s hTEE training program and provides clinicians access to how-to videos, patient case reviews and customer support.

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The U.S. Food and Drug Administration (FDA) issued a Class I Recall of Edwards Lifesciences LLC’s Embol-X Glide Protection System due to deformed cannula trip. Applying force to the tip during insertion or removal may lead to separation and embolization. Use of the recalled product may cause serious adverse health consequences, including death.

Home February 03, 2014
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Feature | Dave Fornell

Stage 2 meaningful use guidelines for electronic medical records (EMRs) suggest use of clinical decision support (CDS) software to help clinicians choose appropriate labs, diagnoses, therapies and imaging exams. A draft policy to replace the sustainable growth rate (SGR) formula now being considered by a joint U.S. Senate Finance and House Committee on Ways and Means Committee might make this suggestion a requirement in the future. The draft policy would deny Medicare payment for exams if the ordering physician did not consult appropriate use criteria (AUC) and require prior authorization for outlier providers.

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Thorne Research Inc. and Itamar Medical Inc. entered into a three-year non-exclusive agreement to co-market Itamar's EndoPAT and WatchPat. EndoPat is a device to assess arterial (endothelial) function, and WatchPAT is a home-based sleep test to diagnose obstructive sleep apnea. The U.S. Food and Drug Administration (FDA) have cleared both.

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CVIS, cardiovascular information system
Feature | Jen Ireland, Ascendian Healthcare Consulting

The push for healthcare to be digitally transformed and paper-free means having access to electronic medical records anytime/anywhere. This effort amplified, has left many cardiology departments struggling to catch up. According to the Administration on Aging people 65+ represented 12.4 percent of the population in the year 2000, but are expected to grow to be 19 percent of the population by 2030. The increase in longevity-on top of advances in medications, less invasive treatments and diagnostic testing will greatly increase demand for cardiology.

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Blackford Analysis, a provider of software products that accelerate comparison of medical images, introduced its products to the Middle Eastern market at the Arab Health Congress 2014 in Dubai. Designed to be integrated directly into any image viewer, such as a PACS, Advanced Visualization Viewer or Universal Viewer, Blackford Analysis’ products work within existing systems to enable instant comparison of multiple image studies.

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