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.

Saturday, October 12, 2024

The association between serum S100β levels and prognosis in acute stroke patients after intravenous thrombolysis

 So you found an association. WHAT THE FUCK NEEDS TO BE DONE TO PREVENT THE PROBLEMS? That is what good stroke research should be doing. This is useless for stroke recovery!

The association between serum S100β levels and prognosis in acute stroke patients after intravenous thrombolysis

1. S100β levels 24 hours after IVT were independently associated with HT, infarct volume, and prognosis in stroke patients

Evidence Rating Level: 2 (Good)

Intravenous thrombolysis (IVT) is the treatment with the highest level of evidence in acute disabling ischemic stroke however half of these patients do not reach favourable outcomes. S100β is a calcium-binding protein mostly seen in astrocytes meaning an elevation in serum concentrations reflets astrocyte damage. Previous studies have shown that S100β levels in the peripheral blood 48 hours post-stroke was functionally significant at 3 months. Thrombolytic drugs may play a role in elevating S100β as they increase the breakdown of the blood-brain barrier which allows more S100β to enter systemic circulation. This prospective cohort study aimed to look at S100β levels in patients 24 hours after IVT and look for the relationship between S100β and hemorrhagic transformation (HT) and final infarct volume. 1072 blood samples were analyzed. Patients who underwent HT had significantly higher serum S100β levels 24 hours post-IVT (0.237 (0.100–0.801) ng/mL vs. 0.118 (0.050–0.240) ng/mL, P < 0.001). No significant interaction association was found between stroke lateralization and S100β. When looking at infarct volume, the highest S100β levels were independently corelated with larger infarct volumes. The association of infarct volume and S100β levels were similar between dominant and non-dominant hemisphere stroke showing no increased incidence in either outcome. Functionally, higher S100β was associated with higher 24-h and 7-day National Institutes of Health Stroke Scale (NIHSS) scores. Patients with dominant hemisphere strokes and high S100β had higher NIHSS scores. S100β was also significantly elevated in patients with unfavourable outcomes on the modified Rankin Scale (mRS) score (0.140 (0.062–0.393) ng/mL vs. 0.100 (0.050–0.196) ng/mL, P < 0.001). Finally, the highest S100β level was independently predictive of all-cause death within 3 months of IVT. Therefore, S100β levels 24 hours after IVT were independently associated with HT, infarct volume, and prognosis in stroke patients. 

Click to read the study in BMC Medicine

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