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.

Monday, February 26, 2024

Blood Pressure Management Following Endovascular Stroke Treatment: A Feasibility Trial and Meta‐Analysis of Outcomes

 Leaders would solve this blood pressure management problem. Obviously no one here is a leader! So don't plan on having a stroke until that is solved. Maybe you want to initiate clinical trials on this yourself before you become the 1 in 4 per WHO that has a stroke.

Up to you, since there is NO LEADERSHIP in stroke nothing will occur in a reasonable amount of time to help stroke survivors. This is why we need survivors in charge

Blood Pressure Management Following Endovascular Stroke Treatment: A Feasibility Trial and Meta‐Analysis of Outcomes

Originally publishedhttps://doi.org/10.1161/SVIN.123.001287Stroke: Vascular and Interventional Neurology. 2024;0:e001287

Abstract

BACKGROUND

Although postprocedure blood pressure (BP) correlates with outcome in patients undergoing endovascular thrombectomy (EVT), the optimal target is unknown.

METHODS

We performed a pilot randomized‐controlled clinical trial enrolling participants with persistently elevated BP after successful EVT. Participants were randomized within 1 hour from the end of EVT to either intensive (systolic BP target <140 mmHg) or standard BP target (systolic BP <180 mmHg) for 48 hours. The main end point was feasibility, which was assessed with the enrollment rate and adherence to allocated BP target. Exploratory end points included neurologic deterioration, functional improvement, intracranial hemorrhage, and flow dynamics detected by transcranial Doppler ultrasonography. We included the outcomes of our trial in an aggregate data meta‐analysis of randomized‐controlled clinical trials evaluating the utility of BP control after successful EVT. The primary outcome of the meta‐analysis was 3‐month good functional outcome, defined as a modified Rankin Scale score of ≤2.

RESULTS

Between October 23, 2020, and February 4, 2023, 221 patients were screened and 30 were randomized (14%; average recruitment of 1.2 participants/month). Participants in the intensive BP arm had a mean±SD systolic BP of 131±18 mm Hg over 48 hours (75% of the readings were <140 mm Hg), whereas participants in the standard BP arm had a mean±SD 48‐hour systolic BP of 139±18 mm Hg (48% of the readings were between 140 and 180 mm Hg). No differences between the 2 groups were documented in any of the predefined exploratory end points. In a meta‐analysis of 5 randomized‐controlled clinical trials involving 1558 participants, intensive BP control was associated with lower probability for 3‐month good functional outcome (odds ratio, 0.66 [95% CI, 0.53–0.82]; I2 = 8%) when compared with standard BP control.

CONCLUSIONS

The natural course of BP normalization following successful recanalization poses challenges to the conduct and success of randomized‐controlled clinical trials evaluating different BP thresholds after EVT. Meta‐analysis of existing trials suggests harm associated with active BP lowering.

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