Why the study?
Direct oral anticoagulants reduce some bleeding risks compared with older anticoagulants but do not eliminate them, making active bleeding presentations to the emergency department a critical clinical scenario requiring optimal management strategies.
Understanding the pathophysiological mechanisms of bleeding in patients on DOACs is essential for establishing appropriate therapies in the emergency department.
Prioritizes mechanistic insights for DOAC bleed management in ED; leaves open targeted therapies pending clinical trials.
Many patients who access in the emergency department for acute bleeding are on anticoagulants; before specific reversal agents were developed, bleeding on anticoagulants was burdened with a substantial increase in morbidity and mortality. Clinical trials demonstrated favourable risk-benefit profiles of direct-acting oral anticoagulants compared with vitamin K antagonists in patients with atrial fibrillation and compared with low molecular weight heparin in patients treated and prevented from venous thromboembolism. Even if they drastically reduced some types of bleeding, particularly intracranial haemorrhage, they have not completely eliminated this risk. The arrival of a patient with active bleeding in the emergency department is always a critical scenario that involves resources and costs. In critical setting, the diagnosis and treatment of bleeding should occurred simultaneously. Understanding the pathophysiological mechanisms that occur during bleeding is essential for establish the most appropriate therapies and improve the standard of care of the haemorrhagic patients.
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Marco et al. (2023) studied this question.
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