Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Friday, January 27, 2017

Liquid Agent Puts Stopper to Infectious Brain Aneurysms

I wonder if this solution has addressed the problem that this earlier glue had? Ask your doctor for the safety profile.

FDA issues warning about Covidien brain device that has killed nine - Onyx glue


http://www.medpagetoday.com/Cardiology/PCI/62762?
Delicate mycotic aneurysms, thought to increase a patient's risk of intracranial hemorrhage, might be embolized safely with a liquid agent delivered endovascularly, a retrospective case series showed.
For all nine patients who required treatment for these intracranial aneurysms arising as a rare complication of infective endocarditis, a single rapid injection of Trufill n-butyl cyanoacrylate (n-BCA) -- with immediate microcatheter removal -- successfully blocked them off.
There were no complications associated with using n-BCA to prevent aneurysm bleeding, Muhammad S. Hussain, MD, of Cleveland Clinic, and colleagues reported online in Interventional Neurology.
"Endovascular embolization of infectious intracranial aneurysms with liquid embolics can be performed successfully in critically ill patients requiring immediate open heart surgery and anticoagulation," the authors concluded.
"The reason for cerebral angiography and endovascular embolization of the infectious aneurysms was the presence of intracerebral hemorrhage in four patients and preoperative treatment prior to open heart surgery in five patients since systemic heparinization was required during these surgeries," they noted.
"Early embolization prior to and within a short interval from open heart surgery is feasible." Two of the nine studied patients underwent open heart surgery within the same day as aneurysm embolization. No new hemorrhages were reported within 2 months of n-BCA injection.
Hussain's analysis encompassed nine consecutive patients with infective endocarditis and mycotic aneurysms who received endovascular administration of n-BCA from 2013 through 2015 at the Cleveland Clinic.
"Endovascular approach for embolization is evolving and becoming a more frequently used treatment option for infectious intracranial aneurysms," the authors wrote.
"Due to the parent vessel compromise and irregular morphology of these aneurysms, embolization frequently requires vessel sacrifice. This can be accomplished with coils and/or liquid embolics; however, the distal location and small caliber of the parent artery makes coil embolization not feasible in most cases, in whom endovascular embolization with liquid embolics may be the only treatment option."

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