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, May 19, 2018

Afib Post-Stroke OAC Tied to Fewer Long-Term Events

I wish this would be written up into an understandable stroke protocol. That way stroke survivors could refer to AFIB101 and ask their doctor how it applies to them. Right now survivors are relying on doctors to know the latest in stroke. That has been proven many times to be completely false, they basically know nothing since medical school.  You're screwed.
https://www.medpagetoday.com/cardiology/arrhythmias/72976?

No increased risk of bleeding complications in Danish registry

  • by Contributing Writer, MedPage Today
Atrial fibrillation (Afib) patients who received post-stroke oral anticoagulation therapy had significantly lower risk of a new thromboembolic event without increased risk of bleeding complications, an observational study from Denmark found.
Over a median of 2.2 years, the risk of a subsequent stroke (adjusted HR 0.81; 95% CI 0.73 to 0.89) and death (adjusted HR 0.68; 95% CI, 0.65 to 0.72) for Afib patients was significantly lower among those treated with oral anticoagulants compared with no antithrombotic therapy, according to Anna Gundlund, MD, of Herlev and Gentofte Hospital in Hellerup, Denmark, and colleagues.
Only 36.3% of Afib patients received oral anticoagulation therapy before their stroke and 52.5% received it after, although treatment rates improved over time, they reported online in JAMA Network Open.
"Our findings suggest a substantial opportunity for improving primary and secondary stroke prophylaxis in high-risk patients with Afib," they wrote.
In the U.S., Afib patients account for a growing proportion of ischemic strokes. Significant underuse of anticoagulation has been reported both in the U.S. and Europe: Nearly 40% of Afib patients who should receive an oral anticoagulant are wrongly given aspirin, a recent analysis of the American College of Cardiology's PINNACLE registry showed.
In this retrospective study of people with Afib from the Danish National Patient Registry, Gundlund and colleagues evaluated 30,626 patients who had a pre-stroke CHA2DS2-VASc score of 1 or higher for men and 2 or higher for women from 2004 to 2017. In 2010, European guidelines changed to recommend oral anticoagulants instead of aspirin for stroke prevention in Afib patients. (The study reflected this change, but even so, the percentage of eligible patients who did not receive any antithrombotic therapy remained about 23% in later years.)
The researchers looked at three groups of patients: those treated with oral anticoagulation therapy, those treated with antiplatelet therapy alone, or those who received no antithrombotic treatment. Patients were a median of 81 years old and 50.8% were female.
During a maximum of 10 years of follow up, 17.5%, 21.2%, and 21.5% of patients experienced a new thromboembolic event and 72.7%, 86.4%, and 86.2% died among those treated with oral anticoagulation therapy, antiplatelet therapy, or no antithrombotic therapy, respectively.
Post-stroke oral anticoagulation was associated not only with lower risk of recurrent thromboembolic events, but no significant difference in bleeding complications compared with no post-stroke antithrombotic therapy (adjusted HR 0.97; 95% CI 0.86 to 1.10).
This analysis expands previous findings about preventive strategies for Afib patients and also "brings focus to a lack of guideline-adherent prescription of oral anticoagulation immediately after stroke," observed Jonathan Hsu, MD, of the University of California San Diego, who was not involved in the study.
"As clinicians, we need to realize that a lack of oral anticoagulation prescription in patients with atrial fibrillation at risk for stroke puts our patients at a disservice, and we need to increase awareness of proper preventative therapies," he told MedPage Today.
The authors listed several limitations to their research. They examined all types of Afib, including Afib secondary to other conditions, which may have influenced physicians' choice of antithrombotic therapy. No information on labile international normalized ratio was available for this population, possibly leading to an overestimation of patients receiving adequate oral anticoagulation therapy, they noted. Results also may have been influenced by patient compliance.
Gundlund reported receiving research funding from Bristol-Myers Squibb. Co-authors reported relationships with Janssen Pharmaceuticals, Daiichi Sankyo, Genentech, AstraZeneca, Bayer Corp, Bristol-Myers Squibb, Boehringer Ingelheim, Novo Nordisk, and Biotronic.

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