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. 2023 Sep 16;24(18):14179. doi: 10.3390/ijms241814179

Table 1.

Changes in the fibrinolytic system in specific clinical settings.

Clinical Setting Changes in the Fibrinolytic System
Liver disease
Stable cirrhosis Alcoholic cirrhosis: increased fibrinolysis due to release and defective clearance of tPA
Non-alcoholic steatohepatitis cirrhosis:
hypofibrinolysis due to increased levels of PAI-1
Decompensated cirrhosis and acute-on-chronic liver failure Highly variable, ranging from severely hypofibrinolytic to hyperfibrinolytic
Acute liver failure Profound hypofibrinolysis, uncertain clinical relevance
Liver transplantation Hyperfibrinolysis due to defective clearance of tPA in the anhepatic state and increased release from the donor liver. Antifibrinolytic therapy is recommended during surgery
Trauma
Major trauma Hyperfibrinolysis, hypofibrinolysis, and fibrinolytic shutdown. Antifibrinolytic therapy increases survival after major trauma with haemorrhagic shock if administered less than 3 h after trauma
Brain trauma Variable, both hyperfibrinolysis and hypofibrinolysis. Early antifibrinolytic therapy may be beneficial in mild-to-moderate brain injury
Sepsis Consistent findings of hypofibrinolysis in correlation with organ failure. Increased levels of PAI-1, TAFIa/TAFIa, and fibrinogen, decreased levels of plasminogen
Cardiovascular disease Both stable atherosclerosis and ACS are associated with decreased fibrin clot permeability and prolonged lysis times. Clot structure and lysis time may be prognostic marker for reinfarction or cardiovascular mortality in ACS patients
Venous thromboembolism (VTE)
DVT A high PAI-1 level predisposes to VTE. Patients with recurrent DVT have higher PAI-levels than patients without recurrence of DVT.
PE Patients with PE may have looser clot structure than patients with isolated DVT. In high-risk PE patients, systemic thrombolysis is indicated. In cases of contraindications, catheter-based thrombo-aspiration is an alternative.

Abbreviations: ACS: acute coronary syndrome; DVT: deep vein thrombosis; PAI-1: plasminogen activator inhibitor-1; PE: pulmonary embolism; TAFI: thrombin-activatable fibrinolysis inhibitor; tPA: tissue plasminogen activator; and VTE: venous thromboembolism.