Table 3.
Differential features of sepsis-associated “DIC” and other thrombo-coagulopathies
“DIC” without hepatic coagulopathy | “DIC” with hepatic coagulopathy | EA-VMTD/DIT without hepatic coagulopathy | True DIC | |
---|---|---|---|---|
Associated disease |
Sepsis Other critical illnesses |
Sepsis Other critical illnesses FHF |
Sepsis Other critical illnesses |
APL |
Mechanism | ||||
Complement activation | + | + | + | No evidence |
Endotheliopathy | + | + | + | No evidence |
Inflammatory path | Activated | Activated | Activated | No evidence |
Activated hemostatic path | ULVWF | ULVWF | ULVWF | Aberrant TF path |
Thrombogenesis | Via micothrombogenesis | Via micothrombogenesis | Via micothrombogenesis | Via fibrinogenesis |
Liver involvement | None | FHF | None | Unlikely to occur |
Pathology | ||||
Coagulation disorder | VMTD | VMTD with FHF | VMTD | Hemorrhagic disorder |
Character of blood clots | Microthrombi | Microthrombi | Microthrmbi | Fibrin clots |
Nature of blood clot | Platelet + ULVWF | Platelet +ULVWF | Platelet +ULVWF | Fibrin meshes |
Hematology | ||||
Platelet | Decreased | Decreased | Decreased | Decreased due to APL |
MAHA | + | + | + | – |
FVIII | Normal/increased | Markedly increased | Normal/increased | Markedly decreased |
PT/aPTT | Normal | Prolonged | Normal | Prolonged |
Fibrinogen | Normal | Decreased | Normal | Decreased |
Clinical Phenotype | MODS | MODS | MODS | Hemorrhagic syndrome |
TTP-like syndrome | TTP-like syndrome | TTP-like syndrome | ||
Chronic “DIC” | Acute “DIC” | EA-VMTD/DIT | ||
FHF | ||||
Correct diagnosis | EA-VMTD/DIT | EA-VMTD/DIT with hepatic coagulopathy | EA-VMTD/DIT | True DIC |
Disease designation | EA-VMTD | EA-VMTD with hepatic coagulopathy | EA-VMTD | Consumption coagulopathy |
Abbreviations: APL acute promyelocytic leukemia, DIC disseminated intravascular coagulation, “DIC” ill-founded DIC, DIT disseminated intravascular microthrombosis, FHF fulminant hepatic failure, MAHA microangiopathic hemolytic anemia, MODS multiorgan dysfunction syndrome, PT prothrombin time, aPTT activated partial thromboplastin time, TTP thrombotic thrombocytopenic purpura, ULVWF unusually large von Willebrand factor multimers, EA-VMTD endotheliopathy-associated vascular microthrombotic disease
aPlease note that “DIC” without hepatic coagulopathy is exactly the same to EA-VMTD/DIT without hepatic coagulopathy, which is also consistent with the thesis that “DIC” is DIT