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, September 4, 2017

Statin intensification sufficient for most with atherosclerotic CVD

Well shit, is this in the USA?  The FDA has basically banned high potency statins due to side effects. Are you that incompetent that you don't know regulations? 

Once again it is up to you to train your doctor.

FDA announces new safety recommendations for high-dose simvastatin June 2011

The latest here:

Statin intensification sufficient for most with atherosclerotic CVD

Christopher Paul Cannon
Christopher P. Cannon
Most individuals with atherosclerotic CVD could reach an LDL level of less than 70 mg/dL with intensification of oral lipid-lowering therapy, with only a small amount requiring a PCSK9 inhibitor, according to a study published in JAMA Cardiology.
Christopher P. Cannon, MD, senior physician at Brigham and Women's Hospital and professor of medicine at Harvard Medical School, and colleagues identified a cohort of 105,269 participants (57% men; mean age, 65 years) with atherosclerotic CVD from a database of U.S. medical and pharmacy claims from 2012 to 2013. For the simulation cohort, the researchers used replacement (in the bootstrapping method) to enter 1 million participants into a Monte Carlo simulation.
Those not receiving statins were given atorvastatin 20 mg. Intensification occurred in the following sequence: up-titration to atorvastatin 80 mg; add-on ezetimibe therapy; add-on alirocumab (Praluent, Sanofi/Regeneron) 75 mg; and up-titration to alirocumab 150 mg.
Before treatment intensification, in the simulation cohort of 1 million patients (55% men; mean age, 66 years), 51.5% used statin monotherapy and 1.7% used statins plus ezetimibe, and 25.2% reached an LDL level of less than 70 mg/dL.
After lipid-lowing treatment intensification, 99.3% could reach an LDL level less than 70 mg/dL, according to the simulation. This level was reached in 67.3% of participants with statin monotherapy, in 18.7% with statins plus ezetimibe and in 14% with an add-on PCSK9 inhibitor.
Sidney C. Smith Jr., MD, FACC, FAHA, FESC
Sidney C. Smith Jr.
“Fundamental to the recommendations for the new nonstatin therapies to lower cholesterol levels will be an exerted program to increase use of intensive statin therapies as recommended by the current 2013 ACC/AHA cholesterol guidelines,” Sidney C. Smith Jr., MD, of the heart and vascular center at the School of Medicine at University of North Carolina, Chapel Hill, and past president of the American Heart Association and the World Heart Federation, wrote in an accompanying editorial. “Too many patients with [atherosclerotic CVD] do not receive intensive statin therapy as recommended. As noted in the VA study, a nearly 50% reduction in cost or $1 billion savings would be the benefit of optimizing intensive statin therapy and adding ezetimibe for those patients with persisting LDL levels above 70 mg/dL.” – by Cassie Homer
Disclosures: Cannon reports receiving grants from Amgen, Arisaph, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Janssen, Merck and Takeda, and consultant fees from Alnylam, Amarin, Amgen, Arisaph, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, GlaxoSmithKline, Kowa, Merck, Lipimedix, Pfizer, Regeneron Pharmaceuticals, Sanofi and Takeda. Please see the study for all other authors’ relevant financial disclosures. Smith reports no relevant financial disclosures.

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