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.

Sunday, November 25, 2018

Influence of Neiromidin® on cognitive functions and neuroplasticity processes in traumatic brain injury

Will this be applicable to stroke? A very simple question. Whom the fuck do we go to to get it answered?

Influence of Neiromidin® on cognitive functions and neuroplasticity processes in traumatic brain injury


I.A. Hryhorova, O.O. Teslenko, A.S. Novak

Abstract


Mild and moderate traumatic brain injury (TBI) is one of the most common diseases in neurotraumatology and an important problem of modern healthcare in all countries. The results of our work give grounds to conduct comprehensive pathogenetic prevention and treatment of detected cognitive impairment in patients already in the acute period of TBI in order to prevent their progression in the future. A higher level of brain glial neurotrophic factor — nerve growth factor beta — in the blood serum of patients receiving Neiromidin® indicated the active influence of the drug on the stimulation of neuroplasticity processes in traumatic brain injury. The demonstrated clinical efficacy of Neiromidin® allows us to recommend its inclusion in the schemes of standard therapy for TBI. And its administration in the acute period of TBI will avoid a progressive cognitive impairment in the future.

Keywords


traumatic brain injury; cognitive impairment; Neiromidin®; neuroplasticity

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