Table 1.
Primary haemostasis | |
Platelet count | Detects risks of bleeding only at extreme levels |
Bleeding time | Generally, does not predict bleeding risk |
Platelet function analyser | Thrombopenia makes the interpretation difficult |
Thromboelastometry | Little experience in cirrhotic patients |
Platelet function assay Aggregometry | Thrombopenia makes the interpretation difficult |
Membrane molecule expression | Specialized laboratory; mostly, in research setting |
Soluble activation markers | |
Platelet adhesion under flow conditions | |
Molecular mechanisms | |
Secondary haemostasis | |
PT and APTT | Insensitive to plasma levels of the anticoagulants |
Thrombin generation | Too complex for use in routine diagnostic laboratories |
Thromboelastometry | No standardization of parameters in cirrhotic patients |
Low predictive positive value | |
Fibrinolysis | |
Fibrinolysis markers | No clear evidence between hyperfibrinolysis and bleeding in cirrhotic patients |
Euglobulin clot lysis time | Not widely available |
PT: Prothrombin time; APTT: Activated partial thromboplastin time.