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
- 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) (1–4) and real-world data. Despite their efficacy, about 1%−2% of DOAC-treated patients suffer from acute ischemic stroke (AIS) (1–4). 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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