Skip to main content

Table 3 Differential features of sepsis-associated “DIC” and other thrombo-coagulopathies

From: Sepsis and septic shock: endothelial molecular pathogenesis associated with vascular microthrombotic disease

 

“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

  1. 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
  2. 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