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.

Tuesday, November 20, 2012

Ultra-flexible, thin-film electrode arrays for chronic neural recording and stimulation of brain cavity wall

Tell your researcher  about this to be able to follow neuroplasticity and neurogenesis as it occurs.
https://lirias.kuleuven.be/handle/123456789/362998
Introduction: Brain injuries are a major source of difficult-to-treat deficits and human disability. Brain lesion cavities are seen in stroke, brain trauma, congenital brain disorders and after successful resection of brain tumors and abscesses. Brain computer interfaces offer an exciting new approach to address deficits resulting from brain lesions. The idea is to implant mechanically flexible implants that adopt the shape of the lesion cavity wall and that are covered with electrode contacts for recording neuronal signals and electrical stimulation. This should enable us to interact with the residual intact brain tissue and partially restore functionality by interacting with pathological circuits.
Aim: The aim of this research is to design and develop a highly-flexible, biocompatible electrode array that can be used for long-term recording of neuronal signals.
Methods: Using soft lithography, thin-film (7 micron), net-shaped 4 x 4 electrode arrays were produced. Platinum electrode contacts were separately embedded in 0.4 mm wide square islands that were connected by 0.2 mm long spring-like structures. This design guarantees flexibility and optimal adhesion to curved surfaces (cortical gyri and sulci) and lesion cavities. Platinum contacts were 92 micron in diameter and were placed at a pitch of 675 micron. These electrode arrays were implanted on the sensorimotor cortex of healthy rats for histological assessment of biocompatibility (n=3, ) and for recording evoked potentials (EP, n=4, repeated measurements up to 4 months after implantation). EP recording was performed with peripheral stimulation of fore- and hindlimbs, both ipsi- and contralateral to the electrode array implant.
Results: The electrode arrays adopted the surface of the sensorimotor cortex in rat and chronic implantation induced no overt discomfort. Tissue damage due to the implantation procedure was seen around 300 micron deep, but was comparable to sham implantation procedures. Preliminary data demonstrate that electrophysiological EP responses could be recorded over the 4 month follow-up period.
Conclusion: The design of this electrode array allowed implantation on curved surfaces and can be used for chronic electrophysiological measurements. One of the possible applications is interaction with the lesion cavity wall, in order to restore function.

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