Paramedics in Bellingham, Wash., used the Lucas device on patient Nancy Olson, who went into cardiac arrest following a ...
July 29, 2011 – Philips installed a MultiDiagnost Eleva X-ray system at Delray Medical Center, a 493-bed acute care hospital serving southeast Florida, and MultiDiagnost Eleva with 3-D-RX reconstruction technology at West Boca Medical Center, an award-winning facility serving Boca Raton and Palm Beach county regions. The hospitals are part of Tenet Healthcare Corporation, one of the largest investor-owned healthcare delivery systems in the nation.
July 29, 2011 — InspireMD Inc., developer of the MGuard mesh protective stent system, announced that the first patient has been enrolled in the MASTER (MGuard for Acute ST Elevation Reperfusion) randomized trial. It is a multinational, randomized, controlled trial designed to demonstrate MGuard coronary stent's superiority over standard care for heart attack patients.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
July 29, 2011 — Oxygen Biotherapeutics Inc. and privately held Aurum Biosciences Ltd. of Glasgow, Scotland, have signed a letter of intent (LOI) to conduct preclinical research for imaging and therapeutic intervention of acute ischemic stroke. Aurum, using Oxygen’s proprietary Oxycyte PFC (perfluorocarbon) emulsion in combination with Aurum’s proprietary Glasgow Oxygen Level Dependent (GOLD) magnetic resonance imaging (MRI) techniques, will conduct the research.
July 29, 2011 — Boston Scientific Corporation's board of directors has approved a five-year, $150 million investment to expand its commercial presence in China, one of the world's largest and fastest-growing medical device markets.
July 29, 2011 — The U.S. Food and Drug Administration (FDA) this week issued draft guidance that clarifies when changes or modifications to a previously cleared 510(k) device require a new premarket submission.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
July 27, 2011 – Micell Technologies Inc. announced that it has completed patient enrollment in its DESSOLVE II CE mark clinical study of the MiStent drug-eluting coronary stent system. The MiStent DES is an ultra-thin drug-eluting stent distinguished by a rapid-absorbing drug/polymer coating formulation. Enrollment of 183 patients across 26 study centers throughout Europe and New Zealand was accomplished ahead of schedule.
July 27, 2011 – A special panel convened July 21 in Gaithersburg, Md., to review the results of the Excor pediatric ventricular assist device (VAD) investigational device exemption (IDE) clinical trial. The panel convened at the request of Bram Zuckerman, M.D., director, division of cardiovascular devices, Center for Devices and Radiologic Health of the U.S. Food and Drug Administration (FDA).
July 27, 2011 – A new echocardiography remote reading program was introduced to provide expert exam interpretation in all 50 states. The new program, created by USARAD.com, a Joint Commission accredited provider of imaging services, is intended to address the longstanding need for fast, reliable interpretation of echocardiograms for mobile ultrasound companies and other imaging facilities across the nation.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
July 27, 2011 – As the number of interventional procedures to diagnose and treat patients increases worldwide, and the procedures grow in complexity and length, exposure to radiation is a growing concern for both clinicians and patients. Interventional fluoroscopy is the third largest source of radiation from medical procedures, accounting for about 7 percent of the total radiation exposure of Americans in a year, according to a study by the National Council on Radiation Protection. GE’s Innova imaging systems help clinicians reduce radiation exposure without compromising the image quality they need to make confident decisions during interventional procedures.
The U.S. Food and Drug Administration (FDA) is alerting healthcare professionals to stop using CardioGen-82 for cardiac positron emission tomography (PET) scans. The manufacturer, Bracco Diagnostics Inc., has decided to voluntarily recall CardioGen-82 this week after two patients set off radiation detectors at a U.S. border crossings due to strontium contamination.
July 26, 2011 – According to the 2011 Top 20 Best in KLAS Awards: Medical Equipment & Infrastructure report, GE Healthcare’s Logiq E9 has been recognized as the top general imaging ultrasound system in the market. In the same report, GE’s Vivid E9 was awarded a share of the top spot for cardiovascular ultrasound systems.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
July 26, 2011 – The first patient has been enrolled in the LEVANT 2 clinical trial, a global, multi-center, randomized trial evaluating the safety and efficacy of Lutonix’s Moxy drug-coated balloon compared with a standard angioplasty balloon for the treatment of peripheral arterial disease (PAD). The first case was performed at St. John's Hospital in Springfield, Ill. by Jeff Goldstein, M.D.
July 26, 2011 – Cardio Pulmonary Diagnostic LLC in Newark and Hudson County Cardiovascular Care PC in Jersey City, N.J. have selected McKesson’s Practice Complete certified electronic health record (EHR) and practice management system. Built with cloud-computing technology, the integrated solution is designed to help providers improve billing and patient services, assist in accelerating payments and contribute to reductions in information technology costs and regulatory risk.
July 26, 2011 — Concentric Medical Inc. has launched the DAC 070 Catheter, the fourth and largest diameter addition to its distal access catheter (DAC) family to aid clot removal in ischemic stroke patients.