Disseminated Intravascular Coagulation (DIC) Overview
Increased Clotting and Consumption of Clotting Factors
Findings:
• Bleeding
• Recent history of trauma, sepsis, malignancy (Especially acute promyelocytic leukemia) or ABO incompatible blood transfusion
• Thrombocytopenia
• Prolonged PT/PTT
• Low plasma fibrinogen
• Elevated D-Dimer
• Increased thrombin time
• Reduced levels of factors VII, X, V and II
• Reduced levels of antithrombin, protein C and S
Pathophysiology:
• Process is simultaneous coagulation and fibrinolysis
• Procoagulant Exposure → Tissue factor → Fibrinolysis → End organ damage
Clinical Findings:
• Bleeding (64%)
• Renal dysfunction (25%)
• Hepatic dysfunction (19%)
• Respiratory dysfunction (16%)
• Shock (14%)
• Thromboembolism (7%)
• CNS involvement (2%)
Cutaneous Manifestations of DIC:
• Petechiae
• Purpura
• Palpable variants of both
• Acral cyanosis
• Hemorrhagic bullae
• Purpura fulminans
• Subcutaneous dissecting hematoma
• Bleeding from wound or venipuncture sites
Laboratory Findings in DIC:
• Platelet count: ↓
• Fibrinogen: ↓
• PT/INR: ↑
• PTT: ↑
• D-Dimer: ↑
• Peripheral smear: Schistocytes, helmet cells
DDX:
• TMA’s (HUS/TTP/DITMA)
- MAHA + Thrombocytopenia
- Platelet rich microthrombi without significant fibrin clot formation or consumption coagulopathy
- Thrombocytopenia
- Normal coagulation studies
- PBS: + Schistocytes
- MAHA: TTP/HUS > DIC
• Severe Liver Disease:
- Impaired synthesis of coagulation factors
- Reduction of pro/anticoagulants
- Thrombocytopenia - bleeding or thrombosis (Hypersplenism and thrombopoietin deficiency)
• HIT: Heparin-PF4 antibodies/SRA
- + Thrombosis
- + Bleeding
Treatment:
• Treat primary cause
• Correct coagulation abnormalities
- PLT, FFP, Cryoprecipitate
- PLT > 50,000
- Fibrinogen > 150 (Cryoprecipitate to increase > 100mg/dL)
- Heparin if presence of large thrombosis
- Hg > 7
- INR < 2.3
- APTT < 1.5 x normal
Supportive Measures:
• Hemodynamic/Ventilatory support
• Aggressive hydration
• RBC transfusion for bleeding
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