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Published on: April 1, 2015
Impaired fibrinolysis in critically ill COVID-19 patients
Mirjam Bachler1, Johannes Bösch2, Daniel P Stürzel2
1Institute for Sports Medicine, Alpine Medicine and Health Tourism, UMIT-University for Health Sciences, Medical Informatics and Technology, Hall, Austria.
Insights
Critically ill COVID-19 patients exhibit impaired fibrinolysis, a hypofibrinolytic state contributing to thrombosis. This impaired fibrinolysis may stem from a reduced fibrinolytic response, impacting coagulation.
Area of Science:
- Coagulation and Thrombosis
- Critical Care Medicine
- Infectious Diseases
Background:
- Critically ill COVID-19 patients often experience a hypercoagulable state, leading to significant macrovascular and microvascular thrombosis.
- Hypofibrinolysis, or impaired clot breakdown, is suspected as a key factor contributing to this thrombotic tendency.
Purpose of the Study:
- To investigate the fibrinolytic function in critically ill COVID-19 patients using viscoelastic whole blood analysis.
- To compare the fibrinolytic response of COVID-19 patients with that of healthy individuals.
Main Methods:
- Retrospective analysis of 20 critically ill COVID-19 patients and 60 healthy controls.
- Coagulation function assessed using the ClotPro® device, including the TPA test to evaluate fibrinolysis.
- Key parameters measured: lysis time (LT), maximum clot firmness (MCF), and maximum lysis (ML).
Main Results:
- COVID-19 patients demonstrated hypercoagulability across multiple ClotPro® assays (EX, IN, FIB tests).
- A decreased fibrinolytic response was observed in COVID-19 patients, indicated by prolonged TPA test LT and decreased ML in the EX test.
- Patients with impaired fibrinolysis showed elevated fibrinogen, thrombocyte count, and C-reactive protein levels.
Conclusions:
- Critically ill COVID-19 patients present with significantly impaired fibrinolysis.
- This hypofibrinolytic state appears to be, at least partially, driven by a diminished fibrinolytic response, contributing to thrombotic complications.
Background:
Critically ill coronavirus disease 2019 (COVID-19) patients present with a hypercoagulable state with high rates of macrovascular and microvascular thrombosis, for which hypofibrinolysis might be an important contributing factor.
Methods:
We retrospectively analysed 20 critically ill COVID-19 patients at Innsbruck Medical University Hospital whose coagulation function was tested with ClotPro® and compared with that of 60 healthy individuals at Augsburg University Clinic. ClotPro is a viscoelastic whole blood coagulation testing device. It includes the TPA test, which uses tissue factor (TF)-activated whole blood with added recombinant tissue-derived plasminogen activator (r-tPA) to induce fibrinolysis. For this purpose, the lysis time (LT) is measured as the time from when maximum clot firmness (MCF) is reached until MCF falls by 50%. We compared COVID-19 patients with prolonged LT in the TPA test and those with normal LT.
Results:
Critically ill COVID-19 patients showed hypercoagulability in ClotPro assays. MCF was higher in the EX test (TF-activated assay), IN test (ellagic acid-activated assay), and FIB test (functional fibrinogen assay) with decreased maximum lysis (ML) in the EX test (hypofibrinolysis) and highly prolonged TPA test LT (decreased fibrinolytic response), as compared with healthy persons. COVID-19 patients with decreased fibrinolytic response showed higher fibrinogen levels, higher thrombocyte count, higher C-reactive protein levels, and decreased ML in the EX test and IN test.
Conclusion:
Critically ill COVID-19 patients have impaired fibrinolysis. This hypofibrinolytic state could be at least partially dependent on a decreased fibrinolytic response.
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