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Author Spotlight: Deciphering Coagulation Disorders in Traumatic Brain Injury Patients
Published on: August 4, 2023
COVID-19-associated coagulopathy and antithrombotic agents-lessons after 1 year
Jenneke Leentjens1, Thijs F van Haaps2, Pieter F Wessels3
1Department of Internal Medicine, Radboud Institute for Health Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.
Insights
For hospitalized COVID-19 patients, prophylactic anticoagulation is recommended for the critically ill, while therapeutic doses may benefit non-critically ill patients. Ambulant and post-discharge patients do not routinely require pharmacological thromboprophylaxis.
Area of Science:
- Internal Medicine
- Cardiology
- Infectious Diseases
Background:
- COVID-19 presents a high risk of thrombotic complications due to unique interactions with endothelial cells, inflammation, and coagulation.
- Current guidelines for thrombosis prophylaxis in hospitalized COVID-19 patients lack robust evidence, leading to weak recommendations.
Purpose of the Study:
- To summarize the pathophysiology of COVID-19-associated coagulopathy across different patient groups (ambulant, hospitalized non-critically ill, critically ill, post-discharge).
- To review recent randomized controlled trial data on antithrombotic therapy in critically ill COVID-19 patients.
- To provide evidence-based recommendations for optimal antithrombotic use in COVID-19.
Main Methods:
- Review of the pathophysiology of COVID-19 coagulopathy.
- Analysis of data from randomized controlled trials (RCTs) evaluating antithrombotic therapy in COVID-19 patients.
- Synthesis of evidence for different patient strata: ambulant, hospitalized (non-critically and critically ill), and post-discharge.
Main Results:
- Pharmacological thromboprophylaxis is not routinely recommended for ambulant and post-discharge COVID-19 patients.
- A therapeutic dose of low-molecular-weight heparin may improve outcomes in non-critically ill hospitalized patients.
- Prophylactic dose anticoagulation is recommended for critically ill hospitalized patients, as therapeutic doses do not improve outcomes.
Conclusions:
- Optimal antithrombotic strategies for COVID-19 vary significantly based on disease severity and hospitalization status.
- New RCT data are crucial for refining clinical guidance on antithrombotic therapy for COVID-19 patients.
- Further research is expected to provide more definitive recommendations for managing COVID-19-associated coagulopathy.
Abstract:
COVID-19 is associated with a high incidence of thrombotic complications, which can be explained by the complex and unique interplay between coronaviruses and endothelial cells, the local and systemic inflammatory response, and the coagulation system. Empirically, an intensified dose of thrombosis prophylaxis is being used in patients admitted to hospital with COVID-19 and several guidelines on this topic have been published, although the insufficiency of high quality and direct evidence has led to weak recommendations. In this Viewpoint we summarise the pathophysiology of COVID-19 coagulopathy in the context of patients who are ambulant, admitted to hospital, and critically ill or non-critically ill, and those post-discharge from hospital. We also review data from randomised controlled trials in the past year of antithrombotic therapy in patients who are critically ill. These data provide the first high-quality evidence on optimal use of antithrombotic therapy in patients with COVID-19. Pharmacological thromboprophylaxis is not routinely recommended for patients who are ambulant and post-discharge. A first ever trial in non-critically ill patients who were admitted to hospital has shown that a therapeutic dose of low-molecular-weight heparin might improve clinical outcomes in this population. In critically ill patients, this same treatment does not improve outcomes and prophylactic dose anticoagulant thromboprophylaxis is recommended. In the upcoming months we expect numerous data from the ongoing antithrombotic COVID-19 studies to guide clinicians at different stages of the disease.
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