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, April 25, 2022

Benefits of ticagrelor, aspirin for stroke outweigh risks over 30 days

So you know what your doctor is considering after your stroke.

Benefits of ticagrelor, aspirin for stroke outweigh risks over 30 days

The benefits of ticagrelor and aspirin outweighed the risk for major hemorrhage in patients with mild to moderate ischemic stroke or at high risk for transient ischemic attack during 30 days of treatment, according to a Neurology study.

“Due to their pharmacological effects, long-term treatment with P2Y12 inhibitors is associated with an increased risk of bleeding, which has triggered interest in defining the duration of therapy with the best benefit-risk profile,” Yongjun Wang, MD, of Beijing Tiantan Hospital and Capital Medical University, and colleagues wrote.

human head, brain highlighted
Source: Adobe Stock.

Researchers sought to determine the short-term benefits and risks of ticagrelor with aspirin in patients with acute mild to moderate ischemic stroke or high-risk TIA in the THALES (The Acute Stroke or Transient Ischemic Attack Treated with Ticagrelor and ASA for Prevention of Stroke and Death) trial.

They analyzed 11,016 patients (5,523 in the ticagrelor-aspirin group, 5,493 in the aspirin-only group; mean age, 65 years; 39% women) and evaluated the cumulative incidence of irreversible efficacy and safety outcomes at various intervals during the 30-day treatment period. Researchers categorized efficacy as major ischemic events, defined as a composite of ischemic stroke or non-hemorrhagic death, and safety as major hemorrhage, defined as a composite of intracranial hemorrhage and fatal bleedings. They classified net clinical impact as the combination of the two.

Results showed the reduction of major ischemic events by ticagrelor occurred in the first week (4.1% vs. 5.3%; absolute risk reduction = 1.15%; 95% CI, 0.36-1.94) and remained through 30 days. In addition, researchers observed an increase in major hemorrhage during the first week, which remained relatively constant in subsequent weeks (absolute risk increase = 0.3%). Cumulative analysis also showed that net clinical impact favored the ticagrelor-aspirin group within the first week (aRR = 0.97%; 95% CI, 0.17-1.77) and remained constant through the treatment period.

“This analysis does not support shortening the 30-day regimen of (dual anti-platelet therapy) with ticagrelor and aspirin, and shorter treatment period has not been studied,” Wang and colleagues wrote.

 

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