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Saint Louis professor develops new high-flow brain bypass procedure

On the cover of a recent edition of the journal Neurosurgery, the highest circulation medical journal in the field, readers saw an artist's intricate depiction of the high-flow brain bypass technique developed by Saint Louis University professor of neurosurgery, Saleem Abdulrauf, M.D.

15 Apr 2011

Neurovasx receives FDA approval for cPAX Aneurysm Treatment System

The U.S. Food and Drug Administration has approved the cPAX Aneurysm Treatment System for surgery on brain aneurysms that are difficult to manage because of their size and shape.

15 Apr 2011

New Pipeline Embolization Device receives FDA approval for treatment of brain aneurysms

The U.S. Food and Drug Administration today approved a new device that provides neurointerventional surgeons with another tool to treat brain aneurysms without performing open surgery.

7 Apr 2011

FDA approves Covidien's PMA application for Pipeline Embolization Device

Covidien, a leading global provider of healthcare products, today announced that it received Premarket Approval from the U.S. Food and Drug Administration for the Pipeline Embolization Device, indicated for the endovascular treatment of adults with large or giant wide-necked intracranial aneurysms in the internal carotid artery from the petrous to the superior hypophyseal segments.

7 Apr 2011

FDA approves NeuroVasx cPAX Aneurysm Treatment System

NeuroVasx announced today that the FDA has approved the cPAX Aneurysm Treatment System as a Humanitarian Use Device for the treatment of large, giant and wide-neck cerebral aneurysms, which are typically the most difficult to treat. The HDE allows for the treatment of up to 4,000 patients per year in the U.S.

6 Apr 2011

Reverse Medical's ReFlex A+ Catheter receives European CE mark approval

Reverse Medical Corporation announced today that it has received CE Mark for its ReFlex A+ Catheter for intracranial distal access, delivery and aspiration.

5 Apr 2011

Scientia Vascular's PLATO microcatheters granted CE mark

Scientia Vascular, developer of innovative products that are optimized for endovascular access and therapies, announced today that its PLATOTM Microcath has received CE Mark approval, facilitating availability for European neuro, cardio and peripheral endovascular applications.

31 Mar 2011

New research measures direct radiation doses in patients during endovascular procedures

New research published in the April 2011 issue of the Journal of Vascular Surgery®, the official publication of the Society for Vascular Surgery®, directly measured the radiation doses for patients and operators during complex endovascular procedures.

30 Mar 2011

Toshiba introduces new Infinix-i cardiovascular X-ray systems

Accurately navigating and interpreting cardiovascular anatomy for precise device deployment is a challenge to physicians during complex interventional procedures. Providing physicians with greater confidence during these difficult procedures, Toshiba America Medical Systems, Inc. is introducing upgrades to its Infinix-i product line.

28 Mar 2011

FDA approves humanitarian device exemption for Elana Surgical Kit in cerebral bypass

Dutch medical device manufacturer, Elana bv, announced today that it has received approval from the U.S. Food and Drug Administration (FDA) for a humanitarian device exemption (HDE), enabling a lifesaving cerebral bypass. Elana bv is a corporate spin-off from the University Medical Centre Utrecht, the Netherlands.

25 Mar 2011

New platinum coil technology makes minimally invasive surgery for brain aneurysms safer and cheaper

Loyola University Hospital is the first center in the Midwest to use new technology that makes minimally invasive surgery for life-threatening brain aneurysms significantly safer and cheaper.

25 Mar 2011

Longer delays between heart attacks and elective surgeries lowers death rates and subsequent heart attacks

Before undergoing elective surgery, patients should consider waiting longer after a heart attack than is currently recommended, according to a study scheduled for publication in the May issue of the journal, Annals of Surgery.

24 Mar 2011

FDA Neurological Devices Advisory Panel voted to recommend approval for Pipeline Embolization Device

Covidien, a leading global provider of healthcare products, today announced that the U.S. Food and Drug Administration Neurological Devices Advisory Panel voted to recommend approval for Pipeline Embolization Device, intended for the endovascular treatment of large or giant wide-necked intracranial aneurysms in the cavernous and paraclinoid regions of the internal carotid artery.

19 Mar 2011

FDA approves ELANA Surgical Kit for standard bypass surgery in brain

U.S. Food and Drug Administration today approved a surgical kit that allows neurosurgeons to reroute blood flow around an aneurysm or a tumor in the brains of patients at greater risk of stroke during standard bypass surgery.

11 Mar 2011

Volume-based referrals do not necessarily improve patient outcomes

Referring patients to hospitals that have the largest volume of surgical procedures does not necessarily lead to improved outcomes for the overall population, according to the results of a new study in the February issue of the Journal of the American College of Surgeons.

11 Mar 2011

Western Medical installs Toshiba's vascular X-ray system to provide efficiency during diagnostic procedures

To increase diagnostic capabilities and provide patients with the highest quality care, Western Medical Center Santa Ana has installed Toshiba America Medical Systems, Inc.'s Infinix VF-i bi-plane vascular X-ray system with Volume Navigation 3D roadmapping.

28 Feb 2011

New study: Surgeon annual volume linked to decreased in-hospital mortality for aneurysm repairs

A new study in the March 2011 issue of the Journal of Vascular Surgery, the official publication of the Society for Vascular Surgery, has revealed that for open repair of intact elective abdominal aortic aneurysms, surgeon annual volume rather than institutional volume is more strongly associated with decreased in-hospital mortality.

24 Feb 2011

Endologix announces initial PEVAR Trial presentation at 2011 iCON annual meeting

Endologix, developer of minimally invasive treatments for aortic disorders, announced today the presentation of the initial clinical results from the PEVAR Trial at the 2011 iCON annual meeting in Scottsdale, Arizona.

16 Feb 2011

Nfocus Neuromedical's Luna AES receives CE Mark approval to treat brain aneurysms

Nfocus Neuromedical, Inc., an innovative medical device company with a focus on the next generation treatment for brain aneurysms, announced today that its Luna Aneurysm Embolization System received CE Mark for the treatment of patients with brain aneurysms.

15 Feb 2011

PhRMA: 299 medicines under development for prevention and treatment of heart disease and stroke

An American dies of heart disease every 39 seconds, and African Americans suffer a higher death rate from heart disease and stroke than Americans overall. Partly as a result of having the highest prevalence of high blood pressure in the world, African Americans have a 1.5 times greater rate of heart disease death than other Americans and a 1.8 times greater rate of fatal stroke.

1 Feb 2011