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, June 1, 2021

EXPRESS: Direct mechanical thrombectomy without intravenous thrombolysis versus bridging therapy for acute ischaemic stroke: a meta-analysis of randomized controlled trials

You have the wrong outcome measured. 'good functional outcome'  IS NOT WHAT SURVIVORS WANT. They want 100% recovery, not your tyranny of low expectations.  Will you be OK with 'good functional outcome' when your children and grandchildren have strokes?

EXPRESS: Direct mechanical thrombectomy without intravenous thrombolysis versus bridging therapy for acute ischaemic stroke: a meta-analysis of randomized controlled trials

First Published May 18, 2021 Research Article 

Background

Direct mechanical thrombectomy (dMT) may result in similar outcomes compared to a bridging approach with intravenous thrombolysis (IVT+MT) in acute ischaemic stroke. Recent randomised controlled trials (RCTs) have varied in their design and non-inferiority margins (NIM).

Aim

We sought to meta-analyse accumulated trial data to assess the difference and non-inferiority in clinical and procedural outcomes between dMT and bridging therapy.

Summary of review

We conducted a systematic review of electronic databases following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Random effects meta-analyses were conducted for the pooled data. The primary outcome was good functional outcome at 90 days (modified Rankin Scale (mRS)≤2). Secondary outcomes included excellent functional outcome (mRS≤1), mortality, any intracranial haemorrhage (ICH), symptomatic ICH, successful reperfusion (TICI2b) and procedure-related complications. Four RCTs comprising 1633 patients (817 dMT, 816 bridging therapy) were included. There were no statistical differences for the 90-day good functional outcome (OR=1.02, 95%CI 0.84-1.25, p=0.54, I2=0%), and the absolute risk difference was 1% (95% CI −4% to 5%). The lower 95% CI falls within the strictest NIM of -10% among included RCTs. dMT reduced the odds of successful reperfusion (OR=0.76, 95%CI 0.60-0.97, p=0.03, I2=0%) and any ICH (OR=0.65, 95%CI 0.49-0.86, p=0.003, I2=38%). There was no difference in the remaining secondary outcomes. The risk of bias for all studies was low.

Conclusion

The combined trial data assessing dMT versus bridging therapy showed no difference in improving good functional outcome. The wide non-inferiority thresholds set by individual trials are in contrast with the clinical consensus on minimally important differences. However, our pooled analysis indicates non-inferiority of dMT with a 4% margin of confidence. The application of these findings is limited to patients presenting directly to MT-capable centres and real-world workflow times may differ against those achieved in a trial setting.

 

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