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COVID-19-induced coagulopathy: Experience, achievements, prospects
Leonid Dubey1, Olga Dorosh1,2, Nataliya Dubey1
1Danylo Halytsky Lviv National Medical University, Lviv, Ukraine.
Insights
Severe COVID-19 causes coagulopathy, marked by elevated D-dimer (DD), increasing thrombotic risk and mortality. Monitoring DD is crucial for guiding thromboprophylaxis and anticoagulation strategies in patients.
Area of Science:
- Hematology
- Infectious Diseases
- Critical Care Medicine
Background:
- Coagulopathy is a key feature of severe COVID-19, linked to systemic inflammation.
- Hematological changes like elevated D-dimer (DD), prolonged activated partial thromboplastin clotting time (APTT), and prothrombin time (PT) are observed.
- Endothelial dysfunction, hypoxia, and pulmonary congestion contribute to thrombosis and microvascular occlusion in COVID-19 patients.
Purpose of the Study:
- To characterize the coagulopathy associated with COVID-19.
- To investigate the relationship between hematological changes and thrombotic events.
- To determine the prognostic value of DD levels for in-hospital mortality and guide thromboprophylaxis strategies.
Main Methods:
- Observational study analyzing hematological parameters in hospitalized COVID-19 patients.
- Assessment of D-dimer (DD), activated partial thromboplastin clotting time (APTT), prothrombin time (PT), and fibrinogen levels.
- Correlation analysis between hematological markers, disseminated intravascular coagulation (DIC) syndrome, and patient outcomes (mortality, thrombotic events).
Main Results:
- COVID-19-associated coagulopathy primarily manifests as a significant increase in DD without significant changes in platelet count, APTT, or PT.
- Disseminated intravascular coagulation (DIC) syndrome was present in 71.4% of deceased COVID-19 patients versus 0.6% of survivors.
- A DD increase of more than 3-4 times the normal level was associated with higher in-hospital mortality.
Conclusions:
- COVID-19-associated coagulopathy is characterized by increased thrombin formation and local fibrinolysis, primarily indicated by elevated DD.
- Assessment of disease severity and coagulopathy markers like DD is essential for effective thromboprophylaxis and anticoagulation management.
- Consideration for extended thromboprophylaxis or therapeutic anticoagulation post-hospitalization, guided by imaging, is warranted for COVID-19 survivors at risk.
Abstract:
The presence of coagulopathy as part of the systemic inflammatory response syndrome is a characteristic feature of severe coronavirus disease 2019 (COVID-19). Hematological changes (increased D-dimer [DD], prolonged activated partial thromboplastin clotting time [APTT] and prothrombin time [PT], high fibrinogen levels) have been observed in hospitalized patients with COVID-19, which characterize the risk of thrombotic events. Against the background of COVID-19 there is endothelial dysfunction, hypoxia and pulmonary congestion, mediated by thrombosis and microvascular occlusion. Up to 71.4% of patients who died from COVID-19 had disseminated intravascular coagulation syndrome, compared with only 0.6% of survivors. The main manifestation of COVID-19-associated coagulopathy is a significant increase in DD without a decrease in platelet count or prolongation of APTT and PT, indicating increased thrombin formation and the development of local fibrinolysis. An increase in DD levels of more than 3-4 times was associated with higher in-hospital mortality. Therefore, COVID-19 requires assessment of the severity of the disease for further tactics of thromboprophylaxis. The need for continued thromboprophylaxis, or therapeutic anticoagulation, in patients after inpatient treatment for two weeks using imaging techniques to assess of thrombosis assessment.
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