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Table 3 Representative underlying diseases and pathologies that must be differentiated

From: Proposal for new diagnostic criteria for DIC from the Japanese Society on Thrombosis and Hemostasis

Decreased platelet count

1.

Enhancement of platelet destruction and aggregation

 

• Thrombotic microangiopathy (TMA): thrombotic thrombocytopenic purpura (TTP), hemolytic uremic syndrome (HUS), HELLP syndrome, TMA after hematopoietic stem cell transplantation

 

• Heparin-induced thrombocytopenia (HIT)

 

• Idiopathic thrombocytopenic purpura (ITP), systemic lupus erythematosus (SLE), antiphospholipid antibody syndrome (APS)

 

• Extracorporeal circulation

2.

Pathologies that lead to bone marrow suppression/bone marrow failure

 

• Hematopoietic malignancies (acute leukemia, blastic crisis of chronic myelogenous leukemia, myelodysplastic syndrome, multiple myeloma, bone marrow infiltration of malignant lymphoma)

 

• Hemophagocytic syndrome

 

• Solid cancers (with bone marrow infiltration)

 

• Chemotherapy or radiation therapy with bone marrow suppression

 

• Bone marrow suppression due to drugs

 

• Some viral infections

 

• Some blood diseases besides hematopoietic malignancies (aplastic anemia, paroxysmal nocturnal hemoglobinuria, megaloblastic anemia)

3.

Liver failure, cirrhosis, hypersplenism

4.

Sepsis

5.

Bernard-Soulier syndrome, MYH9 disorder (e.g., May-Hegglin disorder), Wiskott-Aldrich syndrome

6.

Dilution

 

• Massive bleeding

 

• Massive transfusion, massive infusion

 

• Pregnancy thrombocytopenia

7.

Pseudo-thrombocytopenia

Elevated FDP

 

1. Thrombosis: deep vein thrombosis, pulmonary thromboembolism

 

2. Massive hydrothorax/ascites

 

3. Large hematoma

 

4. Fibrinolytic therapy

Decreased fibrinogen

 

1. Congenital afibrinogenemia, congenital hypofibrinogenemia, dysfibrinogenemia

 

2. Liver failure, malnutrition

 

3. Drug-induced: L-asparaginase, corticosteroids, fibrinolytic therapy

 

4. False lowering: at the time of administration of drugs with anti-thrombin action (e.g., dabigatran)

Prothrombin time prolongation

 

1. Vitamin K deficiency, oral warfarin

 

2. Liver failure, malnutrition

 

3. Deficiency or inhibitor of extrinsic coagulation factor

 

4. Ingestion of a direct oral anticoagulant

 

5. False prolongation: insufficient blood sample volume, addition of an anti-coagulant

Decreased antithrombin activity

 

1. Liver failure, malnutrition

 

2. Extravasation due to inflammation (e.g., sepsis)

 

3. Degradation by granulocyte elastase (e.g., sepsis)

 

4. Congenital antithrombin deficiency

 

5. Drug-induced: L-asparaginase

Elevated TAT, SF, or F1+2

 

1. Thrombosis: deep vein thrombosis, pulmonary embolism

 

2. Some atrial fibrillation

  1. Note: However, DIC may also occur with the above conditions and diseases