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.

Thursday, March 28, 2019

Thrombolysis Works Early Enough for Lacunar Strokes

And just when are you going to change your definition of success to the expectation of success that stroke survivors have? 100% recovery. NOTHING LESS THAN THAT. Stop fucking around with your tyranny of low expectations

Thrombolysis Works Early Enough for Lacunar Strokes

Findings from post hoc analysis of WAKE-UP trial could complicate ED imaging strategy

  • by Contributing Writer, MedPage Today
Stroke patients with lacunar infarcts may also benefit from pharmacological reperfusion with alteplase, according to a post hoc analysis of the WAKE-UP trial.
A favorable outcome(Not according to stroke survivors) at 90 days was numerically more likely when these patients were randomized to alteplase rather than placebo (59% vs 46%, adjusted OR 1.68, 95% CI 0.76-3.69). The distribution of modified Rankin Scale scores also non-significantly shifted to favor the alteplase group by then (adjusted OR 1.94, 95% CI 0.95-3.93).
"While the WAKE-UP trial was not powered to demonstrate the efficacy of treatment in subgroups of patients, the results indicate that the association of IV alteplase with functional outcome does not differ in patients with imaging-defined lacunar infarcts compared with those experiencing other stroke subtypes," wrote Ewgenia Barow, MD, of the University Medical Center Hamburg-Eppendorf Martinistraße in Germany, and colleagues in JAMA Neurology.
Whether thrombosis plays a role in the pathophysiology of lacunar infarctions has been uncertain, clot-dissolving treatment is of questionable help, the investigators noted. Arguments against using alteplase in these patients include concerns about an increased risk of symptomatic intracranial hemorrhage (SICH) and the idea that lacunar strokes are associated with a "more benign" natural history, they added.
Indeed, one death and one SICH were observed within 90 days of alteplase administration, whereas no such events occurred in the placebo group.
The one SICH patient had not been treated for hypertension (with systolic blood pressure reaching 250 mm Hg) on admission nor during infusion. "This patient has to be considered a protocol violation and should not have been treated with IV alteplase owing to uncontrollable hypertension," Barow and colleagues argued.
"The current analysis further tips the scales strongly in favor of treating lacunar strokes.While post hoc, exploratory, and likely underpowered, the study by Barow and colleagues shows no effect modification by stroke subtype," commented Pooja Khatri, MD, of the University of Cincinnati, in an accompanying editorial.
WAKE-UP was a trial of MRI-guided thrombolysis in patients with acute strokes of unknown onset time. Out of the 503 patients enrolled, 108 had acute lacunar infarcts (subcortical ischemic lesions in the territory of a small penetrating artery).
This group was younger than the rest of the WAKE-UP cohort (average age 63 vs 66, P=0.003) and had more men (68.5% vs 63.5%). They were admitted with less severe strokes (NIH Stroke Scale score median 5 vs 6 points, P<0.001) and were less likely to have a history of atrial fibrillation (1.9% vs 14.4%, P<0.001). Lesions were smaller as well (median DWI lesion volume 0.7 vs 3.8 mL, P<0.001).
Within the lacunar infarct subgroup, there were no significant baseline differences between the 50.9% receiving alteplase and the rest assigned to placebo.
Given the new signal that thrombolysis can work in lacunar infarction, it may be logistically harder to select stroke patients for this therapy more than 4.5 hours from last known well, Khatri said.
"The hope has been that we can replace MRI by [one or two] CT imaging strategies as a more cost-effective strategy for identifying these patients, but this now seems more distant," the editorialist wrote. "Emergency departments that have a policy of using CT imaging first will have to take many patients without occlusions visualized on CT angiography to the MRI scanner expeditiously, to avoid missing patients with lacunar infarcts."
It may be that MRI is "the most inclusive and efficient approach for the largest proportion of patients," she stated.
WAKE-UP was funded by a grant from the European Union.
Barow disclosed support from the German Parkinson Society and Actelion Pharmaceuticals Deutschland GmbH.
Khatri disclosed relevant relationships (institutional) with Genentech, Nervive, Cerenovus, Viz.AI, the NIH, the National Institute of Neurological Disorders and Stroke, and Lumosa.
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