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.

Sunday, April 3, 2016

Statin intolerance is real, researchers find. Another (more costly) drug may get around the problem

I'm back and still as pissed off as ever. These people don't even know the correct problem to solve. You fucking idiots, cholesterol is not the problem, inflammation is, which grabs the cholesterol out of the bloodstream packing it into plaque.  Learn about cause and effect and stop trying to force statins to be the only solution.
https://www.washingtonpost.com/news/to-your-health/wp/2016/04/03/statin-intolerance-is-real-researchers-find-but-another-more-expensive-drug-may-help/
Statins like Lipitor and its generics have revolutionized cardiovascular care for nearly two decades as an effective, inexpensive way to reduce LDL cholesterol, the so-called bad cholesterol in the bloodstream.
Not everyone can take them, though; a significant number of people complain of muscle pain, weakness and cramping so severe that they discontinue the therapy even at the risk of a heart attack or stroke. Their resistance to the medication has been controversial, because in most cases there are no biomarkers for the muscle problems individuals describe. Some researchers have speculated that the problem is psychological, the "nocebo" effect of blaming the medication for the pain.
But a study released Sunday shows for the first time that statin intolerance is very real and that a newer, different kind of drug can have a strong impact on these patients' high cholesterol.
Researchers found that 42.6 percent of people who had complained of muscle pain while taking at least two different statins experienced the same symptoms when given a statin during the study but had no ill effects when administered a placebo. They were then able to reduce their LDL cholesterol levels by more than half when given a PCSK9 inhibitor, evolocumab, for 24 weeks, compared with just a 16.7 percent reduction on ezetimibe, another medication.
The Food and Drug Administration approved PCSK9 inhibitors last year, but only for small groups of people, including those with an inherited disease that dramatically elevates their LDL cholesterol levels.
"This problem of statin intolerance is one of the most vexing problems for both patients and physicians in cardiovascular medicine," Steven E. Nissen, chairman of the Department of Cardiovascular Medicine at the Cleveland Clinic, said in an interview. He said the new study, which he led, offers hope for people who have not been able to take statins because of side effects.
The research was unveiled Sunday at the American College of Cardiology's annual conference and published simultaneously in the medical journal JAMA. It was funded by Amgen, maker of evolocumab, an injectable PCSK9 inhibitor. Nissen has worked with many pharmaceutical companies to determine the efficacy of heart therapies but requires the companies to donate any payments to charity so that he receives no compensation or tax breaks, according to a bio accompanying the study.
Heart disease is the leading killer of Americans, and some 73 million people in the United States have high LDL cholesterol, which can greatly increase their cardiovascular risk. Millions of people take statins to lower their risk. In 2013, the American College of Cardiology and the American Heart Association released new treatment guidelines that would substantially increase the number of people on statins.
Mary Norine Walsh, vice president of the American College of Cardiology and medical director of Heart Failure and Cardiac Transplantation at St. Vincent Heart Center in Indianapolis, called the study "encouraging."
PCSK9 inhibitors, she added, are "going to be, possibly, an option for patients who are statin intolerant."
But that may not happen for a while. In addition to requiring FDA approval, the drugs are much more expensive -- from $10,000 to $15,000 a year. And because evidence of statin intolerance is largely subjective, insurance companies may balk until there are ways to more conclusively prove that patients are unable to take the cheaper drugs.
The two therapies have not yet been compared against each other in a randomized, controlled study, Walsh noted.
In Nissen's study, 491 people who were unable to tolerate various kinds or doses of statins were given atorvastatin (Lipitor) or a placebo at 53 research sites around the world. Their ages ranged from 18 to 80, and they had heart disease, high LDL cholesterol or other risk factors for cardiovascular problems. Overall, 209 suffered side effects from the statins and were put on either evolocumab or ezetemibe (Zetia).
The PCSK9 inhibitor works by blocking a substance that hinders the liver's ability to remove cholesterol from the blood. Ezetemibe, by contrast, decreases cholesterol absorption in the small intestine.
The monthly injections of the PCSK9 inhibitor proved far more effective after 24 weeks, cutting patients' LDL cholesterol by an average of 52.8 percent, compared to 16.7 percent for the other drug.

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