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Tryton Medical Inc. announced that the Nordic-Baltic Bifurcation Study Group will investigate the Tryton Side Branch Stent. The trial is a prospective, controlled, randomized, multicenter clinical study examining the role of final kissing balloon inflations in patient outcomes. A total of 150 patients will receive the Tryton Side Branch Stent with a drug-eluting stent, with evaluation by intravascular optical coherence tomography (OCT) imaging technology.

Home June 13, 2013
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Mirada Medical collaborators has presented new positron emission tomography/magnetic resonance imaging (PET/MRI) research. The software supports both the hardware hybrid scanners and provides validated deformable registration for software based PET/CT (computed tomorgraphy)/MRI.

Home June 13, 2013
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Technology

MIM Software Inc. has introduced a new version of MIM Encore that provides a single platform for viewing positron emission tomography (PET), computed tomography (CT), magnetic resonance imaging (MRI) and nuclear medicine exams. Users will benefit from having all of the imaging data they need available on one workstation. Additionally, integrated quantitative analysis solutions are available for both cardiac and neuro PET and single photon emission computed tomography (SPECT) providing an all-in-one solution for Nuclear Medicine departments.

Home June 13, 2013
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Technology

Siemens Healthcare has introduced the world’s first xSPECT system — combines the high sensitivity of single-photon emission computed tomography (SPECT) with the high specificity of computed tomography (CT), completely integrating the data from the two modalities, to generate high resolution and quantitative images. Meanwhile, Biograph mCT Flow is a new positron emission tomography/computed tomography (PET/CT) system that overcomes the limitations of conventional bed-based PET/CT with FlowMotion. This new technology moves the patient smoothly through the system’s gantry, while continuously acquiring PET data.

Home June 12, 2013
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UltraSPECT announced the installation of its proprietary Wide Beam Reconstruction (WBR) software at nearly 10 healthcare facilities. The installations came as a result of the recent agreement between UltraSPECT and radiopharmaceutical provider PharmaLogic, under which PharmaLogic offers the WBR software as part of its patient-centered approach.

Home June 12, 2013
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Siemens Healthcare has introduced Biograph mCT Flow, a positron emission tomography/computed tomography (PET/CT) system that, for the first time ever, overcomes the limitations of conventional bed-based PET/CT with FlowMotion, a revolutionary new technology that moves the patient smoothly through the system’s gantry, while continuously acquiring PET data. Biograph mCT Flow with FlowMotion takes routine image quality to a new level by enabling imaging protocols based on the organ’s need.

Home June 11, 2013
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Feature | Raissa Rocha

The phrase “doing more with less” is becoming more prevalent in tightening economic environments, and the operating room (OR) is one example of where hospitals are looking to maximize savings. Mobile C-arm units are important for maximizing space in the OR and can provide the image quality needed to visualize anatomy and devices during complex surgical procedures. The latest advances in mobile C-arms aim to provide users with the flexibility and ergonomics that can support accomplishing more in the OR with less.

Home June 11, 2013
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New long-term data from the DIVERGE study, presented at EuroPCR 2013 by Principal Investigator Dr. Stefan Verheye, Antwerp Cardiovascular Centre, ZNA Middelheim Hospital, Belgium, has shown that the use of the Axxess drug-eluting stent (DES) for the treatment of complex coronary bifurcation lesions resulted in low levels of both MACE and VLST over a five-year period. Axxess is now the only dedicated bifurcation stent with a substantial body of supporting data out to five years.

Home June 11, 2013
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Between June and October, 2013, healthcare providers at hospitals and medical centers across the United States and Canada can experience GE Healthcare’s entire line of Centricity* Imaging technologies when the Centricity Imaging IT Tour visits locations in over 30 major markets.

Home June 11, 2013
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eHealth Technologies’ eHealthViewer ZF is a zero footprint viewer that enables clinicians, with any secure browser, to instantly access their patients’ medical images, in diagnostic-quality, right from within their patients’ medical record. The latest enhancement to the eHealthViewer ZF is Image Collaboration. Whether through consultation with a remote specialist or grand rounds with the patients’ clinical care team, the eHealthViewer ZF collaboration tool delivers real-time, fluid image review and interaction for healthcare professionals. Using this singular feature, multiple users at different locations, can interactively view and manipulate radiology and cardiology images with full access to the eHealthViewer ZF advanced toolset.

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Feature

Just a few years ago, integrated positron emission tomography and magnetic resonance (PET/MR) imaging was found only in research institutes, but little by little the technology has expanded into clinical practice. This is especially true for cardiac indications, for which the highly sensitive soft tissue contrast of MR and the functional and metabolic imaging of PET are particularly valuable. New research proves the value of PET/MR compared to PET/computed tomography (CT) in cardiac applications, say researchers at the Society of Nuclear Medicine and Molecular Imaging’s 2013 Annual Meeting.

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Direct Flow Medical Inc. announced that it has received approval from the U.S. Food and Drug Administration (FDA) for an Investigational Device Exemption (IDE) to begin the SALUS feasibility trial of the Direct Flow Medical Transcatheter Aortic Heart Valve System. The device encompasses a transcatheter aortic heart valve with a metal-free frame and flexible, low-profile delivery system that virtually eliminates aortic regurgitation. It is designed to improve the long term survivability of patients by resolving the clinical issues associated with current commercial valves.

Home June 10, 2013
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C. R. Bard Inc. announced the enrollment of the first patient into the Lutonix Below the Knee (BTK) Clinical Trial at The Cardiac and Vascular Institute in Gainesville, Fla. The purpose of this pivotal global, multi-center randomized Investigational Device Exemption (IDE) trial is to compare the safety and effectiveness of the Lutonix 014 Drug Coated PTA Dilatation Catheter to a standard angioplasty balloon catheter for the treatment of critical limb ischemia.

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AngioLight has successfully completed an initial animal study of the AngioLight System at Fu Wai Hospital, a leading cardiovascular center located in Beijing. The study paves the way for AngioLight to go forward in China with full-scale animal and clinical testing of the system, which will begin following the anticipated completion of study protocols, hospital review and required China Food and Drug Administration (CFDA) approvals.

Home June 07, 2013
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Medtronic Inc. announced new data demonstrating that simultaneously pacing the lower chambers of the heart, or biventricular (BiV) pacing with a cardiac resynchronization therapy (CRT) device, significantly improves heart failure symptoms and quality of life in a subset of heart failure patients.

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