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, February 24, 2020

Lower target LDL after stroke prevents 25% of events at 5 years

I have no clue what mine is or was, the doctor rattles off some numbers assuming I know what is being talked about. Do you really think your hospital will pick up on this and create a protocol for it?

Lower target LDL after stroke prevents 25% of events at 5 years

During the 5 years after a stroke, targeting LDL of less than 70 mg/dL prevented more than one-quarter of major CV events, recurrent cerebral infarction or urgent carotid revascularization and recurrent cerebral infarction or hemorrhage vs. an LDL target of less than approximately 100 mg/dL.
According to new data from the Treat Stroke to Target trial presented at the International Stroke Conference, the target LDL of less than 70 mg/dL in the 5-year period after stroke was associated with lower risk for the primary endpoint of stroke, MI, new symptoms requiring urgent coronary or carotid revascularization and CV death compared with target LDL of less than 100 ± 10 mg/dL (9.6% vs. 12.9%; HR = 0.74; 95% CI, 0.75-0.94).
The lower target LDL was also associated with reductions in cerebral infarction or urgent carotid revascularization (27%; P = .046), cerebral infarction or intracranial hemorrhage (28%; P = .023), and the primary outcome plus intracranial hemorrhage (25%; P = .022) vs. the higher target LDL.
The findings were simultaneously published in Stroke.
“In patients with ischemic stroke associated with atherosclerotic disease, as compared to a target LDL of 100 mg/dL, targeting LDL of less than 70 mg/dL during 5.3 years avoided one subsequent major vascular event in four and one ischemic stroke or intracranial hemorrhage in four without increasing the risk of intracranial hemorrhage, with a number needed to treat of 30, meaning that if you treat 30 patients you will avoid one stroke,” Pierre Amarenco, MD, of the department of neurology and stroke center at Bichat Hospital, University of Paris, said during the presentation. “This is a very important achievement for future guidelines.”
In other findings, intracranial hemorrhages occurred in 1.2% of patients assigned to LDL less than 70 mg/dL and in 1% of patients assigned to LDL less than 100 ± 10 mg/dL (HR = 1.17; 95% CI, 0.53-2.62).
Patients with proven ischemic stroke
“In a subanalysis, we found a strange result in patients with proven ischemic stroke, having a 37% relative risk reduction and no apparent benefit in patients with transient ischemic attack, that is, no ischemia proven on a brain imaging, with a significant interaction. It’s difficult to explain that,” Amarenco said during his presentation. “Perhaps there is too much noise in the diagnosis of transient ischemic attacks. This is possible and, in future trials, we should concentrate on patients with proven ischemic stroke.”
Perspective
Larry B. Goldstein
Larry B. Goldstein
The primary report was published in the New England Journal of Medicine earlier this year and showed the benefit of treatment with a statin targeting an LDL of approximately 70 mg/dL compared with 100 mg/dL on reducing major vascular events in participants who had an ischemic stroke or TIA related to atherosclerosis within the prior 3 months (22% reduction). The trial was conducted in France and Korea, which started enrollment later and where follow up was shorter (5.3 vs. 2 years).  Although there was no statistical heterogeneity based on country, there was no significant benefit in Korea. An exploratory analysis focused on France found a 26% reduction in major vascular events. The participants from Korea will continue to be followed to determine whether they also benefit. Overall, the results are consistent with exploratory analyses of the SPARCL trial that found a greater benefit with achieving an LDL of approximately 70 mg/dL and support this therapeutic target.
  • Larry B. Goldstein, MD, FAAN, FANA, FAHA
  • Cardiology Today Editorial Board Member
    University of Kentucky

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