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.

Wednesday, May 13, 2015

Understanding the ‘Enemy Within’ that Causes Brain Damage after Cardiac Arrest

Does your heart doctor know enough to protect your brain from damage after a heart attack? Would your neurologist know enough when your heart doctor asks for a consult?
http://www.urmc.rochester.edu/news/story/index.cfm?id=4315
A new $1.7 million grant will bring together a team of researchers to study – and ultimately thwart – the chain reaction that occurs in the body after cardiac arrest that can ultimately lead to brain damage and death.
“While the biological sequence of events is triggered by cardiac arrest, the death and disability associated with this event is the result of a broader systemic injury caused by the initial loss of blood flow and subsequent tissue inflammation once blood circulation is restored,” said University of Rochester Medical Center neurologist Marc Halterman, M.D., Ph.D., the principal investigator of the study. “In fact, it is the cumulative effect of this systemic injury on the brain – and not the heart – that ultimately leads to mortality in the disorder.”
Each year, some 400,000 Americans suffer cardiac arrest. Despite improvements in pre-hospital resuscitation and the widespread use of induced hypothermia, which can help protect tissue from damage due to lack of blood flow, fewer than 30,000 (7.6 percent) cardiac arrest patients will ultimately survive to hospital discharge.
Within minutes of resuscitation, a complex sequence of events unfolds throughout the body involving the cardiovascular, immune, and respiratory systems. The tissue damage caused by the cessation and restoration of blood flow combined with pro-inflammatory factors released from the gastrointestinal tract triggers a robust systemic inflammatory response.
These molecular cues in turn activate circulating neutrophils, which serve as the immune system’s “first responders” channeling them to sites of injury where they inadvertently cause further damage. Scientists speculate that this chain of events causes the immune system to go into overdrive and immune cells, including neutrophils, eventually work their way into the central nervous system where they attack and kill brain cells.
“While we typically associate neutrophils with the immune system’s first line of defense against invading pathogens, in the aftermath of a cardiac arrest they may actually act more like the enemy within by adding fuel to the fire,” said Halterman.  
The attack on the brain is delayed and peaks days after arrest; consequently, scientists speculate that by focusing on the early steps in this response they may be able to find a way to head neutrophils off at the pass by preventing their activation and mobilization into tissue that is attempting to recover from the initial effects of the loss of blood flow. The new research will focus primarily on the lungs as a potential site of therapeutic intervention where the activation of neutrophils could be modified or prevented.
Because of the complex, multi-system nature of the project, the research will bring together a team of scientists, including Michael O’Reilly, Ph.D. and Arshad Rahman, Ph.D. with the Department of Pediatrics, and Minsoo Kim, Ph.D. with the Department of Microbiology and Immunology. The National Institute of Neurological Disorders and Stroke (NINDS) will fund work on the project. The initial studies were supported pilot funds from the Schmitt Program on Integrative Brain Research to Halterman and O’Reilly. Additional support will be provided through a recent fellowship from the NINDS awarded to Nguyen Mai, an M.D./Ph.D. student in Halterman’s lab, who played a key role in collecting the preliminary data required for the grant applications.
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