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.

Saturday, September 23, 2023

Statin initiation despite already low LDL tied to improved mortality after first stroke

Did your incompetent doctor miss the research that showed that statin initiation improved stroke recovery in the past decades?

1. Statins.

tested in rats from 2003

http://Statins induce angiogenesis, neurogenesis, and synaptogenesis after stroke Statins induce angiogenesis, neurogenesis, and synaptogenesis after stroke  

Simvastatin Attenuates Stroke-induced Splenic Atrophy and Lung Susceptibility to Spontaneous Bacterial Infection in Mice

Or,

Simvastatin attenuates axonal injury after experimental traumatic brain injury and promotes neurite outgrowth of primary cortical neurons 

October 2012

tested in humans, March, 2011

http://www.medwirenews.com/39/91658/Stroke/Acute_statin_therapy_improves_survival_after_ischemic_stroke.html

And now lost even to the Wayback Machine

So I think this below is the actual research;

Association Between Acute Statin Therapy, Survival, and Improved Functional Outcome After Ischemic Stroke April 2011

he latest here:

Statin initiation despite already low LDL tied to improved mortality after first stroke

Key takeaways:

  • In-hospital initiation of statin therapy may lower all-cause death risk in patients with first-time stroke and already low LDL.
  • Statins did not appear to impact risk for secondary stroke or MI.

Researchers in South Korea showed that statin therapy for treatment-naive patients with already low LDL hospitalized for first-time stroke may reduce risk for all-cause death in the following months.

Statin therapy did not affect risk for secondary stroke or MI, according to data published in the Journal of the American Heart Association.

Statins_AdobeStock
In-hospital initiation of statin therapy may lower all-cause death risk in patients with first-time stroke and already low LDL.
Image: Adobe Stock

“A target LDL-C level < 70 mg/dL is recommended to reduce the risk of vascular events in acute ischemic stroke,” Joon-Tae Kim, MD, PhD, of the department of neurology at Chonnam National University Medical School, Chonnam National University Hospital in Gwangju, South Korea, and colleagues wrote. “However, an issue that still needs further research is whether statin treatment could reduce the risk of early vascular events when baseline LDL-C levels are already low, at < 70 mg/dL, at the time of index stroke.”

For this prospective, multicenter study of the nationwide Clinical Research Center for Stroke-Korea registry, researchers assessed 2,850 consecutive patients with first-time acute ischemic stroke and LDL less than 70 mg/dL at baseline without prior statin treatment (mean age, 70 years; 64% men).

The primary outcome was a composite of hemorrhagic or ischemic stroke, MI and all-cause death within 3 months of hospitalization.

Overall, 74.2% of patients with already low LDL received statin therapy during hospitalization for first-time stroke.

The primary composite outcome occurred in 6.7% patients who received statin therapy compared with 21.5% of patients who did not (P < .001), according to the study. After inverse probability of treatment weighting, the rates of the primary composite outcome were 7.64% in the statin group and 13.13% in the no statin group (P < .001), and statin therapy was associated with a nearly 50% reduction in the primary composite outcome (HR = 0.54; 95% CI, 0.42-0.69).

The reduction in occurrence of the primary outcome was mainly driven by lower mean event rates at 3 months for all-cause death (5.51% vs. 12.13%; P < .001) while the rates of stroke (P = .692), hemorrhagic stroke (P = .885) and MI (P = .263) were not significantly different.

“Statins seemed to have considerable effectiveness in reducing the risk of early vascular outcomes, mainly death, which might be related to the pleiotropic effect of statins,” the researchers wrote. “These might include neuroprotection, improved collateral flows, and anti-inflammatory effects, but their effect in reducing the risk of recurrent stroke by reducing atherothrombosis is less substantial in the early periods after acute ischemic stroke.”

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