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 30, 2020

Association of pre-stroke metformin use, stroke severity, and thrombolysis outcome

So that brings up an immediate question. 'Should metformin be immediately given to stroke patients as part of their hyperacute therapy?'  WHOM will answer that question? Specific names needed. You can see the fucking incompetence of all the stroke medical world in that nothing seems to have been done with this in the past 4.5 years.

You could stay forever young (or young for a long time) with this diabetes drug 

Dec. 2015

In this one is this line:The drug, which is cheaply available for just $0.16 a day, works by boosting the number of oxygen molecules released into a cell, which in turn seems to benefit the robustness and longevity of the body’s basic building blocks. (This would seem to be much easier and faster than HBOT. I'm requesting this at my next stroke, my doctor won't know what hit her when I tell her how to treat me.)

My list of 31 things I was going to demand after my next stroke. I guess metformin isn't in there.

 The latest here:

Association of pre-stroke metformin use, stroke severity, and thrombolysis outcome

Laura P Westphal, Roni Widmer, Ulrike Held, Klaus Steigmiller, Christian Hametner, Peter Ringleb, Sami Curtze, Nicolas Martinez-Majander, Marjaana Tiainen, Christian H Nolte, Jan F Scheitz, Hebun Erdur, Alexandros A Polymeris, Christopher Traenka, Ashraf Eskandari, Patrik Michel, Mirjam R Heldner, Marcel Arnold, Andrea Zini, Laura Vandelli, Jonathan M Coutinho, Adrien E Groot, Visnja Padjen, Dejana R Jovanovic, Yannick Bejot, Céline Brenière, Guillaume Turc, Pierre Seners, Alessandro Pezzini, Mauro Magoni, Didier Leys, Sixtine Gilliot, Michael J Scherrer, Georg Kägi, Andreas R Luft, Henrik Gensicke, Paul Nederkoorn, Turgut Tatlisumak, Stefan T Engelter, Susanne Wegener

Abstract

Objective: To evaluate whether pretreatment with metformin (MET) is associated with less stroke severity and better outcome after intravenous thrombolysis (IVT), we analyzed a cohort of 1919 stroke patients with type-2 diabetes in a multicenter exploratory analysis.
Methods: Data from patients with diabetes affected by ischemic stroke treated with IVT were collected within the European Thrombolysis in Ischemic Stroke Patients (TRISP) collaboration. We applied propensity score matching (PSM) to obtain balanced baseline characteristics of patients treated with and without MET.
Results: Of 1919 stroke patients with type-2 diabetes who underwent IVT, 757 (39%) had received MET before stroke (MET+), whereas 1162 (61%) had not (MET-). MET+ patients were younger with a male preponderance. Hypercholesterolemia and pretreatment with statins, antiplatelets or antihypertensives were more common in the MET+ group. After PSM, the two groups were well balanced with respect to demographic and clinical aspects. Stroke severity on admission (NIHSS 10.0 ± 6.7 vs. 11.3 ± 6.5), 3-months degree of independence on modified Rankin Scale (mRS): 2 [IQR 1.0, 4.0] vs. 3 [IQR 1.0, 4.0] as well as mortality (12.5% vs. 18%) were significantly lower in the MET+ group. The frequency of symptomatic intracerebral hemorrhages did not differ between groups. HbA1c levels were well balanced between both groups.
Conclusions: Stroke patients with diabetes on treatment with MET receiving IVT had less severe strokes on admission and a better functional outcome at 3 months. This suggests a protective effect of MET resulting in less severe strokes as well as beneficial thrombolysis outcome.
  • Received April 19, 2019.
  • Accepted in final form January 6, 2020.

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