An experimental device for removing blood clots in stroke patients dramatically outperformed the standard mechanical treatment, according to research presented by UCLA Stroke Center director Dr. Jeffrey L. Saver at the American Stroke Association’s 2012 international conference in New Orleans…
A research team led by investigators at Mayo Clinic in Florida has found that a small device worn on a patient’s brow can be useful in monitoring stroke patients in the hospital. The device measures blood oxygen, similar to a pulse oximeter, which is clipped onto a finger…
An irregular heartbeat that you don’t even feel but can be picked up by a pacemaker is associated with a significantly increased risk of stroke, says a new McMaster University study…
Collaborative stroke research study in January 2012 Archives of Physical Medicine & Rehabilitation shows bedside clinical evaluation can detect spatial neglect, a common disabling cognitive disorder that impedes recovery for 30 to 50% of stroke survivors. West Orange, NJ. January 3, 2012…
Severely impaired stroke survivors could walk better when a robotic assist system was added to conventional rehabilitation, according to a study in Stroke: Journal of the American Heart Association. Italian researchers evaluated two-year mobility outcomes in 48 stroke survivors who had been discharged from a hospital and were unable to walk at the study’s start…
A simple function that most of us take for granted - swallowing - is the focus of University of Adelaide research which could help thousands of stroke sufferers around the world…
Today, Penumbra, Inc. announced the Shonin approval by the Japanese Ministry of Health, Labor and Welfare of the Penumbra System for revascularization of patients with acute ischemic stroke. Penumbra, together with its exclusive distribution partner, Medico’s Hirata, Inc., will begin immediate commercialization of the device in Japan…
Bioness Inc. announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its NESS L300® Plus System. The device combines the Company’s NESS L300® Foot Drop System with a thigh stimulation cuff, to provide knee flexion and extension in addition to ankle dorsiflexion during gait…
Bioness Inc. announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its NESS L300® Plus System. The device combines the Company’s NESS L300® Foot Drop System with a thigh stimulation cuff, to provide knee flexion and extension in addition to ankle dorsiflexion during gait…
New research from the University of Calgary’s Faculty of Medicine shows that doctors can make a stroke diagnosis using an iPhone application with the same accuracy as a diagnosis at a medical computer workstation. This technology can be particularly useful in rural medical settings…