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 26, 2013

In-transit Preconditioning Study Shows Neutral Effect in Stroke Patients

But does this new one reject this earlier study? Bad study because they are not measuring the correct items, MRIs can't see penumbra damage, you need PET scans for that. 
Does no one in the stroke world have a functioning brain?
Can using a simple blood-pressure cuff limit damage from strokes caused by decreased blood supply to the brain? On the way to the hospital.
 Does your hospital know? Doctor?
http://www.tctmd.com/show.aspx?id=123068
Key Points:
  • Acute stroke patients randomized to treatment with or without remote ischemic preconditioning during EMS transport
  • No effect seen on penumbral salvage, final infarct size, progression, as measured by MRI
  • Nonetheless, tissue-level analysis hints at some neuroprotection, study authors say

By L.A. McKeown
Tuesday, November 26, 2013

Although a prehospital strategy of remote ischemic preconditioning appears safe in patients with acute stroke, magnetic resonance imaging (MRI) results suggest little difference between treated and untreated patients, according to a study published online November 7, 2013, ahead of print in Stroke.
Researchers led by Kristina Dupont Hougaard, MD, of Aarhus University Hospital (Aarhus, Denmark), randomized 443 patients with symptoms of acute stroke (transient ischemic attack, acute ischemic, or hemorrhagic) to IV recombinant tissue plasminogen activator (rtPA) with (n = 247) or without (n = 196) remote ischemic preconditioning between June 2009 and January 2011.
No Clinical Effect Seen
Compared with controls, those randomized to preconditioning had a higher incidence of TIA (17% vs. 8.2%; P = 0.006), and a lower National Institutes of Health (NIH) Stroke Scale score on admission (P = 0.016). However, after reclassification for missing data and other issues, there were no differences in demographic and clinical characteristics between the 2 groups.
At 3 months, there were no differences in penumbral salvage, final infarct size, and infarct growth on MRI between the intervention and control groups (table 1).
Table 1. MRI Results at 3 Months
Median Values
Remote Preconditioning
Controls
P Value
Penumbral Salvage, mL
11.89 (0.53-63.39)
14.10 (1.60-79.82)
0.20
Final Infarct Size, mL
1.63 (0.35-20.09)
1.99 (0.35-16.19)
0.97
Infarct Growth, mL
0 (-0.62 to 8.01)
0.02 (-0.95 to 4.96)
0.79

However, tissue analysis to test for sensitivity to treatment-related effects showed a treatment-dependent change in infarct risk when correcting for the differences in baseline values of mean transit time and perfusion-weighted imaging. Tissue infarct risk by vessel status at arrival and after administration of rtPA showed a reduction of infarct risk in diffusion-weighted imaging-positive tissue at 1 month for patients treated with preconditioning who had no baseline occlusion. In those with persisting occlusion, there also was a reduction of infarct risk except among those with severely prolonged transit times.
Analysis of vessel status at arrival also indicated that in preconditioned patients with no vessel occlusion on admission, there was an overall reduction in the risk of infarction for tissue subjected to preconditioning.
Enough Suggestion of Benefit to Move Ahead
According to the study authors, the patient-level analysis suggests the distribution of diffusion-weighted imaging lesion intensities “seems left shifted for patients treated with [preconditioning] during transportation to the hospital, suggesting a lower degree of cytotoxic edema and therefore potentially less tissue damage when perfusion is promptly restored.” The benefits of the strategy, therefore, “may not be limited to penumbral tissue, but seems to pertain to tissue within the [diffusion-weighted imaging] lesion,” they say.
While any translation of these results into a possible clinical benefit remains unknown, Dr. Hougaard and colleagues say their study is consistent with at least 1 other that has indicated possible neuroprotective effects from remote preconditioning in the poststroke phase in patients with intraarterial stenosis.
The study is limited though by an acknowledged error in randomization. This occurred in the initial period when final consent was not obtained from patients randomized to no preconditioning and as a result those patients were not included in the analysis. “This imbalance may have affected the clinical outcome data but does not affect the tissue-level results in that this approach is inherently adjusted for any imbalance in baseline [perfusion-weighted imaging] and [diffusion-weighted imaging],” they write.
Study Details
Remote preconditioning was performed by ambulance staff during transportation and consisted of 4 inflations of a standard upper limb blood pressure cuff to either 200 or 25 mm Hg above the systolic blood pressure, each lasting 5 minutes and separated by 5 minutes of cuff deflation. Preconditioning also was performed approximately 1 hour before MRI in those patients who participated in the MRI portion of the study. Symptom severity was not assessed prior to preconditioning.

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