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, September 9, 2024

Higher efficacy of intravenous thrombolysis in patients with acute ischemic stroke taking direct oral anticoagulants—A new relevant hypothesis

 I have no clue, so ask your competent? doctor what changes to the initial stroke protocol this will cause. 

Do you prefer your  doctor and hospital  incompetence NOT KNOWING? OR NOT DOING?

Higher efficacy of intravenous thrombolysis in patients with acute ischemic stroke taking direct oral anticoagulants—A new relevant hypothesis

\r\nSenta Frol,
Senta Frol1,2*Janja Pretnar Oblak,Janja Pretnar Oblak1,2Pawel Kermer,Pawel Kermer3,4George NtaiosGeorge Ntaios5Panagiotis Papanagiotou,Panagiotis Papanagiotou6,7Mi&#x;o &#x;abovi
,Mišo Šabovič2,8
  • 1Department of Vascular Neurology, University Medical Center Ljubljana, Ljubljana, Slovenia
  • 2Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
  • 3Department of Neurology, Nordwest-Krankenhaus Sanderbusch, Friesland Kliniken GmbH, Sande, Germany
  • 4University Medical Center Göttingen, Göttingen, Germany
  • 5Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece
  • 6Clinic of Diagnostic and Interventional Neuroradiology, Klinikum Bremen Mitte, Bremen, Germany
  • 7Department of Radiology, Aretaieion University Hospital, National and Kapodistrian University of Athens, Athens, Greece
  • 8Department of Vascular Disorders, University Medical Center Ljubljana, Ljubljana, Slovenia

Introduction

Direct oral anticoagulants (DOACs) have been established as first-line therapy for stroke prevention in patients with non-valvular atrial fibrillation due to their high safety and efficacy, as demonstrated in large randomized controlled trials (RCTs) (14) and real-world data. Despite their efficacy, about 1%−2% of DOAC-treated patients suffer from acute ischemic stroke (AIS) (14). At the same time, intravenous thrombolysis (IVT) is recommended as first-line therapy for AIS patients (5, 6). Currently, alteplase is the preferred thrombolytic agent, while tenecteplase, which is more fibrin-specific and has a longer half-life, has recently been approved for IVT in AIS in Europe (7). However, most international guidelines advise against IVT in DOAC-treated patients who have ingested their medication within 48 h prior to AIS onset, except for dabigatran-treated patients reversed by idarucizumab (5, 8).

Ongoing debates regarding IVT safety in patients on DOACs speculate on possible pathophysiological explanations. It was hypothesized that both direct and indirect thrombin inhibition might reduce disruptions to the blood-brain barrier, thereby lowering the risk of hemorrhage (9, 10). Equally important is the high efficacy of IVT in DOAC-treated patients. Recently, no safety concerns regarding IVT were reported while patients receiving IVT were more likely to have good functional outcomes (11, 12).

In this context, this opinion article discusses about the potentially higher efficacy of IVT in patients on DOACs, a topic which warrants more in-depth exploration, such as enhanced fibrinolytic activity.

More at link.


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