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Updated: Dec 13, 2025

Author Spotlight: A Novel Method for Comprehensive Cell Component Analysis of Cerebral Blood Clots
Published on: July 21, 2023
Emerging evidence of a COVID-19 thrombotic syndrome has treatment implications
Joan T Merrill1, Doruk Erkan2, Jerald Winakur3
1Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA. joan-merrill@omrf.org.
Insights
Coronavirus disease 19 (COVID-19) associated thromboses may not be disseminated intravascular coagulation (DIC). This condition resembles complement-mediated thrombotic microangiopathy (TMA) syndromes, requiring different treatments than standard DIC protocols.
Area of Science:
- Hematology
- Immunology
- Infectious Diseases
Background:
- Increasing reports link coronavirus disease 19 (COVID-19) to thrombotic events.
- Disseminated intravascular coagulation (DIC) is frequently suspected, but atypical features are noted.
Purpose of the Study:
- To differentiate COVID-19 associated thromboses from typical DIC.
- To explore potential similarities with complement-mediated thrombotic microangiopathy (TMA) syndromes.
Main Methods:
- Analysis of key clinical and laboratory features in COVID-19 patients with thrombosis.
- Comparison of COVID-19 thrombotic microangiopathy (TMA) features with established TMA syndromes.
Main Results:
- COVID-19 thromboses show minimal bleeding risk and mild thrombocytopenia.
- Elevated fibrinogen and detection of SARS-CoV-2 and complement in thrombotic areas were observed.
- The disorder's profile diverges significantly from classic DIC.
Conclusions:
- COVID-19 associated thromboses are distinct from DIC and resemble complement-mediated TMA.
- Standard DIC treatments (anticoagulation, antivirals) may be insufficient for these TMA syndromes.
- Ineffective immune responses in COVID-19 may link to severe pneumonia and life-threatening microangiopathy.
Abstract:
Reports of widespread thromboses and disseminated intravascular coagulation (DIC) in patients with coronavirus disease 19 (COVID-19) have been rapidly increasing in number. Key features of this disorder include a lack of bleeding risk, only mildly low platelet counts, elevated plasma fibrinogen levels, and detection of both severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and complement components in regions of thrombotic microangiopathy (TMA). This disorder is not typical DIC. Rather, it might be more similar to complement-mediated TMA syndromes, which are well known to rheumatologists who care for patients with severe systemic lupus erythematosus or catastrophic antiphospholipid syndrome. This perspective has critical implications for treatment. Anticoagulation and antiviral agents are standard treatments for DIC but are gravely insufficient for any of the TMA disorders that involve disorders of complement. Mediators of TMA syndromes overlap with those released in cytokine storm, suggesting close connections between ineffective immune responses to SARS-CoV-2, severe pneumonia and life-threatening microangiopathy.
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