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 8, 2016

Thrombectomy Tied to Better Outcomes in Large Core Strokes, Too

Once again failure to even measure how badly the neuronal cascade of death is after these large strokes. Endpoints of stroke research are missing a lot, researchers don't know what they should be doing. With a defined stroke strategy, everyone in the world would be going to the same endpoint. 100% survivor recovery.
http://www.medpagetoday.com/Cardiology/PCI/61282?xid=nl_mpt_DHE_2016-11-08&eun=g424561d0r&pos=1
Stroke patients with large swaths of irreversibly-injured tissue at risk for significant infarct expansion still benefited from endovascular therapy, a single-center study found.
Among individuals with large baseline ischemic cores and mismatch profiles, endovascular therapy was associated with:
  • A favorable shift in the overall distribution of 90-day modified Rankin Scale (mRS) scores (OR 2.56, 95% CI 2.50-8.47)
  • Higher rates of functional independence (mRS scores 0-2; 25% versus 0%, P=0.04)
  • Smaller final infarct volumes (average 87 versus 242 mL, P<0.001)
By 90 days, type 2 parenchymal hematomas occurred at similar rates between control and treatment groups (4% versus 7%, P>0.99), according to Raul G. Nogueira, MD, of Grady Memorial Hospital in Atlanta, and colleagues in their study published online in JAMA Neurology. Also comparable for the two groups, respectively, were risk of hemicraniectomy (7% versus 21%, P=0.10) and mortality (29% versus 48%, P=0.75).
"In properly selected patients, endovascular therapy appears to benefit patients with large core and large mismatch profiles," the investigators concluded.
"Somehow, these patients with malignant profiles did not experience worse outcomes than expected, and they actually benefited from the right therapy, for the right patient, at the right time," agreed David S. Liebeskind, MD, of University of California, Los Angeles, writing in an accompanying editorial.
"The categorical exclusion of large ischemic cores may have been warranted in prior trials to establish the role of endovascular therapy, yet uncertainties or shades of gray abound in the daily triage of patients with such lesions."
"[The authors] challenge the historical tenet of imaging selection that eliminates the only therapeutic opportunity for patients with large ischemic cores and large mismatch imaging profiles to avoid devastating outcomes. Their article builds on mounting data from a variety of approaches with CT and MRI that question the way we use imaging and the process of how we consider optimal therapeutic strategies for patients with stroke," Liebeskind added.
"The results of this study, in combination with other recent reports using different imaging definitions of large infarcts, suggest that individual stroke outcomes and novel opportunities to expand therapeutic benefits of endovascular thrombectomy are undeniably multivariable and informed by multidimensional imaging," he wrote.
Nogueira's group analyzed data retrieved from stroke patients with proximal occlusion on CT angiography and baseline ischemic cores more than 50 mL on CT perfusion imaging (n=56) who got endovascular therapy or medical therapy alone at a tertiary care center from 2011 to 2015. The case-control design matched patients based on age, baseline ischemic core volume on CT perfusion imaging, and glucose levels.
A sensitivity analysis showed that patients with a baseline ischemic core more than 70 mL had a substantial reduction in final infarct volumes (mean 110 versus 319 mL, P<0.001) but no statistically significant improvement in the distribution of mRS scores (P=0.18).
Nogueira reported receiving research support fom Stryker Neurovascular, Covidien, and Penumbra.
Liebeskind reported working as a consultant to Stryker and Medtronic and is employed by the University of California, which holds a patent on retriever devices for stroke.

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