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.

Monday, June 23, 2025

Brain fluid physiology in ischaemic stroke; more than just oedema

 Your competent? doctor has been working on solving this problem for a lot of years, right? Oh no, your doctors have done nothing and haven't initiated research to solve the problem! And your incompetent? board of directors hasn't fired them? 

In my opinion competence is immediately installing protocols upon published research. Does your incompetent? doctor think that is too high a bar? FIRE THEM! And if your doctor is still there after doing nothing your board of directors is completely incompetent!

  • brain edema (1 post to April 2025)
  • Perihematomal edema (3 posts to May 2020)
  • cytotoxic edema (1 post to April 2025)
  • edema (11 posts to May  2012)
  • cerebral edema (14 posts to December 2012)
  • edema progression (2 posts to January 2022)
  • Perihematomal edema (3 posts to May 2020)
  • Brain fluid physiology in ischaemic stroke; more than just oedema


    Published: Volume 22, article number 60, (Cite this article
    You have full access to thisopen accessarticleFluids and Barriers of the CNSAims and scopeSubmit manuscript

    Background

    Cerebrospinal fluid and interstitial fluid dynamics are critical for maintaining homeostasis in the central nervous system. These fluids facilitate waste clearance, micronutrient distribution, and provide a tightly regulated ionic environment. Ischaemic stroke, a leading cause of morbidity and mortality, disrupts this delicate system, compounding the physiological challenges posed by the condition. Despite recent advances in our understanding of the importance of cerebrospinal fluid (CSF) and interstitial fluid (ISF) movement and exchange, the role of this system in stroke pathophysiology remains underexplored.

    Main body

    Emerging evidence indicates that ischaemic stroke acutely alters CSF and ISF movement and exchange, with effects observed at both local and brain-wide levels. In the hyper-acute phase, there is an influx of CSF into perivascular spaces, potentially contributing to early cell swelling. Over time, impaired clearance mechanisms exacerbate ionic and vasogenic oedema, elevating intracranial pressure and further compromising perfusion in the ischaemic penumbra. Mechanistic studies suggest that disruptions in arterial pulsatility, extracellular space microstructure, and aquaporin 4 localisation may underlie these changes. Experimental models have revealed decreased CSF and ISF exchange, movement and outflow in the hours to days following stroke, with implications for waste clearance and secondary injury processes. The interplay between these dynamics and cortical spreading depolarisations, stroke severity, and cerebrovascular physiology adds complexity to understanding the condition’s progression.

    Conclusion

    The disruption of CSF and ISF movement and exchange may represent a significant, yet underappreciated contributor to post-stroke pathology. Addressing these alterations could offer novel therapeutic avenues to mitigate secondary damage, improve central nervous system (CNS) homeostasis, and enhance recovery outcomes. Future research must focus on elucidating the precise mechanisms of CSF and ISF movement and exchange disturbance and exploring targeted interventions to restore normal fluid dynamics in the CNS post-stroke.

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