These people must have no brains at all. With all this knowledge out there on the neuronal cascade of death. Why would you expect decent outcomes at 90 days if all you are doing is blowing out the clot via tPA or clot retrieval device?
http://www.medpagetoday.com/Cardiology/Strokes/37252?
For the second time in as many days, researchers' expectations that
endovascular therapy would improve outcomes in patients with acute
ischemic stroke have been dashed.
Compared with intravenous thrombolytic therapy alone, giving
endovascular therapy after thrombolytic therapy did not improve outcomes
in patients with acute ischemic stroke, the Interventional Management
of Stroke (IMS) III investigators reported online in the New England Journal of Medicine and at the International Stroke Conference in Honolulu.
On Wednesday, Italian researchers reported results of a head-to-head trial showing that endovascular therapy did not improve outcomes compared with IV tPA. That study also was reported in NEJM and at the meeting.
IMS III was stopped early, after 656 participants had been
randomized, because the proportion of patients with functional
independence at 90 days did not differ significantly according to
treatment: 40.8% with endovascular therapy versus 38.7% with IV tPA.
After adjustment for National Institutes of Health Stroke Scale
(NIHSS) strata, that's an absolute difference of just 1.5 percentage
points (95% CI -6.1 to 9.1), according to Joseph P. Broderick, MD, of
the University of Cincinnati Neuroscience Institute, and colleagues.
On the flip side, endovascular therapy did not appear to cause any
harm, with similar safety outcomes in both groups, Broderick told MedPage Today.
Broderick said that he and his team expected the combination approach
to improve outcomes by at least 10 percentage points. That's because
the one-two punch combines the advantages of a rapid start with IV tPA
with a means of eliminating large clots that persist after treatment.
Also, studies suggest endovascular therapy is associated with nearly
twice the rate of recanalization of the affected cerebral artery. But
researchers are increasingly learning – from this trial and others --
the limitations of revascularization as a surrogate measure for
efficacy, he said.
In IMS III, patients ages 18 to 82 who received IV tPA within 3 hours
of symptom onset were randomized in a 2:1 fashion to receive additional
endovascular therapy or not. Those in the endovascular group underwent
angiography as quickly as possible, and those with no evidence of a
treatable occlusion received no additional treatment.
Those with a treatable occlusion received endovascular therapy with
intra-arterial tPA or mechanical clot disruption or retrieval, at the
choice of the neurointerventionalist. Angiography had to begin within 5
hours and be completed within 7 hours of symptom onset.
At the time the trial was stopped, there were 434 patients in the endovascular arm and 222 in the IV tPA arm.
The primary outcome measure was functional independence, defined as a
score of 2 or less on the 6-point modified Rankin scale in which higher
scores indicate greater disability.
There were no significant differences in rates of functional
independence in any of the predefined subgroups of patients, including
those with an NIHSS score of 20 or higher and those with a score of 19
or lower.
In addition, there were no differences in mortality at 90 days (19.1%
in the endovascular group versus 21.6% in the IV tPA group, P=0.52) or symptomatic intracranial hemorrhage within 30 hours of initiation of tPA (6.2% and 5.9%, respectively, P=0.83).
However, there was a "trend toward benefit" in patients with more
severe strokes (NIHSS scores of 20 or more), in patients with clots in
the terminal part of the internal carotid artery, and in patients
treated more quickly, Broderick said. He believes future randomized
trials should focus on such patients.
The time to intra-arterial treatment was 32 minutes longer in IMS III
compared with the two pilot studies that preceded it. This may help to
explain the lack of clinical benefit despite substantially better
revascularization with intra-arterial therapy. "We probably did not open
the arteries quickly enough," said Broderick.
American Stroke Association spokesperson Ralph Sacco, MD, head of
neurology at the University of Miami, said he was disappointed by the
results. "We have all had cases where we saw recanalization with
endovascular approaches and then saw recovery. We were hoping for this
to be borne out in the trial," he said.
Sacco told MedPage Today that endovascular technology is
"always improving. Perhaps the use of more modern stent retrievers,
which were used in only a small number of patients in this trial before
it was halted, would provide greater benefit," he said.
( It can improve 100% and still not do any better because it doesn't address the neuronal cascade of death. These people need their scientist title taken away.)
Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 28,987 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke.DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER, BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
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.
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