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.

Wednesday, June 21, 2023

Colchicine's Rebirth as Cardiovascular Drug Approved by FDA

Well, didn't your doctor start using this a long time ago? 

AHA: Colchicine Prevents Postop Afib December 2011 

Could Old Gout Drug Offer New CV Benefits? November 2015 

Anti-inflammatory therapy for preventing stroke and other vascular events after ischaemic stroke or transient ischaemic attack November 2017 

The latest here:

Colchicine's Rebirth as Cardiovascular Drug Approved by FDA

Repurposed anti-inflammatory drug may be used alone or in combination with standard meds

 FDA APPROVED colchicine (Lodoco) over a photo of a section of an artery narrowed from atherosclerosis.

The FDA approved colchicine (Lodoco) for cardiovascular prevention in adults with established atherosclerotic disease or multiple risk factors, making it the first anti-inflammatory medicine with such an indication.

The drug is now indicated for reducing the risks of myocardial infarction, stroke, coronary revascularization, and cardiovascular deaths, following regulatory approval of Agepha Pharma's drug application for a new manufacturing process of the decades-old gout medication.

"Approval by the FDA of the first drug to target cardiovascular inflammation is an important step forward for the care of our patients," said Paul Ridker, MD, MPH, of Harvard Medical School and Brigham and Women's Hospital in Boston, in a press releaseopens in a new tab or window from the drug maker. "To treat coronary disease effectively, cardiologists must aggressively reduce inflammation and cholesterol."

Agepha Pharma said its colchicine will be available for prescription in the second half of 2023. The product is to be used at a dose of 0.5 mg orally once daily -- alone or in combination with standard lipid-lowering medications -- for the cardiovascular indication.

At this dose, the alkaloid drug had been found to reduce cardiovascular events by 31% compared with placebo when used with high-intensity statins and other cardiovascular prevention therapies among people with chronic coronary disease in the LoDoCo2 randomized trialopens in a new tab or window (6.8% vs 9.6%, respectively; HR 0.69, 95% CI 0.57-0.83, P<0.001).

"For the first time, patients with residual inflammatory risk, as measured by hs-CRP [high-sensitivity C-reactive protein], will have an FDA-approved treatment option demonstrated to reduce the risk of cardiovascular disease by targeting the inflammatory pathways that influence major cardiac events," said Michael Blaha, MD, MPH, of Johns Hopkins Medicine in Baltimore, in a statement.

Available generically, colchicine is derived from the autumn crocus plant used medicinally for thousands of years in Egypt.

The label for Lodocoopens in a new tab or window warns that concurrent use of strong CYP3A4 inhibitors (e.g., clarithromycin, ketoconazole) or P-glycoprotein inhibitors (e.g., cyclosporine, ranolazine) is contraindicated due to potential excesses in the concentration of colchicine. The drug is also contraindicated in patients with kidney failure or severe liver disease.

People on colchicine have reported blood dyscrasias and neuromuscular toxicity. Moreover, the most common side effects are gastrointestinal symptoms and myalgia.

Due to potential drug-drug interactions, colchicine users should be monitored for muscle pain toxicity if they are also on HMG-Co A reductase inhibitors, fibrates, gemfibrozil, and digoxin. Colchicine can also interact with oral contraceptives like norethindrone/ethinyl estradiol and cause diarrhea, nausea, and cold sweats.

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