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To Anticoagulate or Not to Anticoagulate in COVID-19: Lessons after 2 Years
John G Rizk1, Aashish Gupta2, Jose G Lazo3
1Department of Pharmaceutical Health Services Research, University of Maryland School of Pharmacy, Baltimore, Maryland.
Insights
COVID-19 increases blood clot risk, but therapeutic anticoagulation in critically ill patients offers no benefit and increases bleeding. Noncritically ill patients may benefit from heparin, while post-discharge anticoagulation shows promise.
Area of Science:
- Cardiovascular Medicine
- Infectious Diseases
- Hematology
Background:
- Coronavirus disease 2019 (COVID-19) is linked to a hypercoagulable state driven by inflammation, increasing arterial and venous thromboembolism (VTE) risk.
- COVID-19 patients with VTE exhibit higher mortality rates compared to those without, underscoring the need for effective VTE prevention strategies.
- High rates of microvascular and macrovascular thrombosis in COVID-19 necessitate evaluating anticoagulation strategies across different patient populations.
Approach:
- Review of randomized control trials (RCTs) evaluating antithrombotic therapy in COVID-19 patients over the past two years.
- Analysis of findings in critically ill hospitalized patients, noncritically ill hospitalized patients, post-discharge patients, and outpatients.
- Inclusion of data on anticoagulation in pregnant/lactating patients and antiplatelet therapy for COVID-19.
Key Points:
- Therapeutic dose anticoagulation in critically ill COVID-19 patients did not improve outcomes and increased bleeding compared to prophylactic doses.
- Hospitalized noncritically ill COVID-19 patients may experience improved clinical outcomes with therapeutic doses of heparin formulations.
- Anticoagulation with direct oral anticoagulants post-discharge may be beneficial, pending results from ongoing large RCTs.
- Outpatients and non-hospitalized COVID-19 patients generally lack sufficient event burden for antithrombotic therapy consideration.
Conclusions:
- Anticoagulation strategies for COVID-19 vary significantly by patient severity and setting, with critical care patients not benefiting from therapeutic doses.
- Prophylactic anticoagulation and specific formulations like heparin may be beneficial in certain hospitalized COVID-19 patient groups.
- Further research, including ongoing RCTs, is crucial to refine optimal antithrombotic strategies for diverse COVID-19 patient cohorts, including those post-discharge.
Abstract:
A hypercoagulable state associated with coronavirus disease 2019 (COVID-19) has been well documented and is believed to be strongly supported by a proinflammatory state. The hypercoagulable state in turn results in increased incidence of arterial and venous thromboembolism (VTE) seen in hospitalized COVID-19 when compared with hospitalized non-COVID-19 patient cohorts. Moreover, patients with arterial or VTE and COVID-19 have higher mortality compared with COVID-19 patients without arterial or VTE. Prevention of arterial or VTE thus remains an essential question in the management of COVID-19 patients, especially because of high rates of reported microvascular and macrovascular thrombosis. This has prompted multiple randomized control trials (RCTs) evaluating different anticoagulation strategies in COVID-19 patients at various stages of the disease. Herein, we review findings from RCTs in the past 2 years of antithrombotic therapy in critically ill hospitalized patients, noncritically ill hospitalized patients, patients postdischarge from the hospital, and outpatients. RCTs in critically ill patients demonstrated therapeutic dose anticoagulation does not improve outcomes and has more bleeding than prophylaxis dose anticoagulant in these patients. Trials in noncritically ill hospitalized patients showed a therapeutic dose anticoagulation with a heparin formulation might improve clinical outcomes. Anticoagulation with a direct oral anticoagulant posthospital discharge may improve outcomes, although there is a large RCT in progress. Nonhospitalized COVID-19 patients have an insufficient burden of events to be candidates for antithrombotic therapy. Anticoagulation in pregnant and lactating patients with COVID-19, as well as antiplatelet therapy for COVID-19, is also reviewed.
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