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.

Friday, October 13, 2017

Risk Factors for Seizures, Epilepsy After Stroke

Useless since it doesn't give any information on how to prevent seizures and epilepsy.  Maybe treat like this?

Cannabidiol May Reduce Seizures by Half in Hard-to-treat Epilepsy

https://www.medscape.com/viewarticle/886872?src=soc_fb_171012_mscpedt_news_mdscp_mdscp_stroke
Daniel M. Keller, PhD
October 10, 2017
KYOTO, Japan — The rate of seizures or epilepsy after thrombolysis for the treatment of ischemic stroke is similar to the rates in the decades before the use of thrombolysis, a retrospective study shows.
"Hemorrhagic transformation and degree of neurological compromise after thrombolysis, but not before, were independently associated with seizures or post-stroke epilepsy," lead author, Marino Bianchin, MD, PhD, Hospital Clínicas de Porto Alegre, Brazil, reported.
In the new analysis, presented at the XXIII World Congress of Neurology (WCN), researchers also reported several factors potentially associated with unfavorable outcome and found that seizures were among them.
Seizures and epilepsy affect a substantial proportion of patients after they have had a stroke. In fact, stroke is the leading cause of diagnosis of new-onset epilepsy in patients older than 65 years, Dr Bianchin said.
To evaluate the risk factors, the researchers performed a retrospective study of 153 consecutive patients who received thrombolysis using tissue plasminogen activator (tPA) for the treatment of acute ischemic stroke between 2005 and 2011. Patients were followed for at least 2 years after the stroke, and those with epilepsy had at least two prolonged electroencephalograms.
The cohort consisted of 74 women and 79 men, had a mean age of 67.2 ± 13.1 years, and initial and 3-month National Institutes of Health Stroke Scale (NIHSS) mean scores of 10.95 ± 6.25  and 2.09 ± 3.55, respectively.
General health and metabolic variables as well as stroke-specific ones were evaluated as risk factors, including age, sex, ethnicity, hypertension, diabetes mellitus, hypercholesterolemia, smoking, alcohol use, atrial fibrillation, NIHSS score, stroke cause, vascular territories, stroke severity, hemorrhagic transformation, and outcome of thrombolysis.
Response to treatment was assessed by using the NIHSS and modified Rankin Scale (mRS) 3 months after the stroke. A good outcome was considered to be an mRS score of 0 or 1, and a bad outcome was defined as an mRS score of 2 or greater. Bleeding was defined as any central nervous system bleeding according to radiologic criteria.
Of the 153 patients, 21 (13.7%) had seizures and 15 (9.8%) had epilepsy. The researchers found that of the variables evaluated, only hemorrhagic transformation and mRS score of 2 or greater were significant independent risk factors for seizures or for epilepsy.
There was no significant effect of NIHSS score or glucose on admission, systolic blood pressure at onset, diabetes, or hypercholesterolemia.
Table 1. Independent Risk Factors for Seizures or Epilepsy After Thrombolysis
Endpoint
Independent Risk Factors for Seizures
Independent Risk Factors for Epilepsy
Adjusted Odds Ratio (95% Confidence Interval)
P Value
Adjusted Odds Ratio (95% Confidence Interval)
P Value
Hemorrhagic transformation
3.55 (1.11 - 11.34)
.033
3.26 (1.08 - 9.78)
.035
MRS score ≥ 2 at 3 mo after stroke
5.82 (1.45 - 23.42)
.013
3.51 (1.20 - 10.32)
.022
Age, NIHSS score, and seizure were independent risk factors for unfavorable outcome (mRS score of 2 or greater).
Table 2. Independent Risk Factors for Unfavorable Outcome (mRS Score ≥ 2)
Variable
Adjusted Odds Ratio (95% Confidence Interval)
P Value
Age
1.03 (1.01 - 1.06)
.011
NIHSS score
1.08 (1.03 - 1.14)
.001
Hemorrhagic transformation
0.43 (0.21 - 0.90)
.024
Seizure
3.07 (1.22 - 7.75)
.018
Large cortical area (Alberta Stroke Program Early CT score [ASPECTS] ≤ 7)
0.49 (0.26 - 0.96)
.036

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