Technology

September 27, 2011 – Calgary Scientific Inc. has received clearance from the U.S. Food and Drug Administration (FDA) to market medical imaging application, ResolutionMD Mobile, as a mobile diagnostic application in the United States. With this secure, highly scalable, server-based software solution, physicians anywhere can rapidly access, view and interact with patient images and reports stored within any healthcare facility, and render a clinical diagnosis using their mobile devices. Prior non-diagnostic versions of this product are currently distributed and licensed under original equipment manufacturer (OEM) agreements with global leaders in medical imaging and information technology. In addition to the recent FDA clearance, ResolutionMD Mobile has also been licensed by Health Canada and bears the CE mark for distribution in Europe.

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Toshiba will showcase its proprietary non-contrast magnetic resonance (MR) angiography imaging techniques and a new ...

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Toshiba will showcase the Vantage Titan 3.0T MR system at the 2011 Radiological Society of North America (RSNA) trade show. The machine is equipped with multi-phase transmission technology, creating the most homogeneous abdominal and pelvic images on 3.0T systems.

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September 27, 2011 — AccessClosure Inc. announced the shipment of its one millionth Mynx unit. The Mynx Vascular Closure Device received U.S. Food and Drug Administration (FDA) approval in May 2007, following with its full commercial launch in September 2007.

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September 27, 2011 – Health 2.0 announced the launch of the Novartis CardioEngagement Challenge, asking multi-disciplinary teams of developers to create an interactive solution enabling patients to better manage their cardiovascular health through a customizable, user-friendly interface.

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September 27, 2011 — Occlutech announced its CEO, Tor Peters, has obtained a favorable ruling from the district court in Düsseldorf in patent litigation initiated personally against him by St. Jude AGA Medical. Occlutech is a European developer of implants for treating structural heart disease.

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September 27, 2011 — AF Stat released updates to the AFib Educator, a free smartphone app and desktop widget designed to help healthcare providers better explain atrial fibrillation (AFib) to their patients.

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September 27, 2011 — A team of physicians, engineers and materials scientists at Children's Hospital Boston and the Massachusetts Institute of Technology (MIT) have created cardiac patches, with cells all beating in time, that could someday help heart attack patients. The devices were created using nanotechnology and tiny gold wires.

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September 27, 2011 — Last week’s inclusion of critical congenital heart disease (CCHD) in the standard list of recommended screenings for new babies by the Department of Health and Human Services (HHS) has received support from the American College of Cardiology (ACC).

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September 27, 2011 — A study in the Sept. 27 issue of the Journal of the American College of Cardiology suggests that early coronary computed tomographic angiography (CCTA) is preferable to rest-stress myocardial perfusion imaging (MPI) when evaluating acute low-risk chest pain in the emergency department.

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Feature | Dave Fornell

The new imaging modality of positron emission tomography (PET)/magnetic resonance imaging (MRI) was introduced to the U.S. market in June. The Siemens Biograph mMR (molecular MR) gained U.S. Food and Drug Administration (FDA) 510(k) clearance as the first dedicated PET/MRI system. It is the only system to combine both modalities into one machine, allowing simultaneous imaging of location, function and metabolic activity of organs in a single image.

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Feature | Dave Fornell

With a growing problem of overcrowded emergency departments, coronary computed tomography angiography (CCTA) may be a solution to address the management of chest pain patients. CCTA is increasingly recognized as an accurate, noninvasive tool to safely assess coronary artery disease. Advocates for the modality say it leads to earlier identification and management of obstructive coronary artery disease (CAD), rapid early discharge, improved flow of overcrowded emergency departments and reduced costs.

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Case Study

Indiana University (IU) Health La Porte Hospital in La Porte, Ind., made the decision to build an advanced EP procedure lab right in the community with holding areas, ancillary workspaces, office space and a clinical area. The vision was for the lab to encompass all aspects of arrhythmia care, beginning at the procedure area and finishing with the outpatient clinic. It also was extremely important that the space was efficient, cost-effective and flexible.

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Feature | Adhir Shroff, M.D., MPH

A review of recent transradial clinical study data.

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The use of the Barbeau test in radial access procedures.
Feature | Radial Access | Stephanie Murray RN, BSN, CCRN-CMC

Staff education is a vital component for the successful transition to a predominantly transradial cardiac catheterization program. Educational efforts must extend beyond the cath lab. A successful program incorporates staff from the pre- and post-procedure units, telemetry unit, intensive care unit (ICU) and any other unit that routinely cares for cardiac catheterization patients.

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