Management of Disseminated Intravascular Coagulation (DIC)
The cornerstone of DIC management is treating the underlying cause while providing appropriate supportive care tailored to the specific DIC subtype (procoagulant, hyperfibrinolytic, or subclinical) and clinical manifestations. 1
Diagnostic Approach
- Diagnosis requires monitoring of:
- Platelet count (decreased, often <50 × 10^9/L)
- Prothrombin time (prolonged PT/INR >14 seconds/>1.1)
- Fibrinogen levels (decreased, <1.5 g/L)
- D-dimer (elevated, >0.5 mg/L)
- Serial measurements are crucial as dynamic changes are hallmarks of DIC 1
- Note: Normal PT/aPTT does not exclude DIC, especially in subclinical forms 1
Treatment Algorithm
Step 1: Treat the Underlying Condition
- Most critical intervention for all DIC types 1, 2
- Examples:
- Early chemotherapy initiation for malignancy-associated DIC
- Immediate ATRA administration for acute promyelocytic leukemia
- Antibiotics for sepsis-induced DIC
- Management of obstetric complications
Step 2: Supportive Care Based on DIC Type and Clinical Presentation
For Bleeding-Predominant DIC:
Platelet transfusion:
Fresh frozen plasma (FFP):
- Administer 15-30 mL/kg with careful monitoring 1
- Consider when there is active bleeding with prolonged PT/INR
Fibrinogen replacement:
- Provide cryoprecipitate or fibrinogen concentrate when levels <1.5 g/L 1
- Particularly important with ongoing hemorrhage
For Thrombosis-Predominant DIC:
- Anticoagulation:
For Organ Failure Type DIC:
Step 3: Ongoing Monitoring and Adjustments
- Regular clinical and laboratory surveillance to assess:
- Improvement/worsening of coagulopathy
- Development of complications
- Response to treatment of underlying condition 1
Special Considerations
Central Line Management
- Use tunneled central venous catheters for long-term access
- Avoid peripherally inserted central catheters (PICCs) due to higher thrombosis risk
- Prefer single-lumen catheters when possible
- Place lines only at compressible sites
- Correct coagulopathy before procedure 1
Common Pitfalls to Avoid
- Overlooking the short lifespan of transfused products in active DIC, requiring more frequent monitoring and replacement 1
- Using antifibrinolytic agents without clear evidence of hyperfibrinolytic DIC 1
- Using recombinant Factor VIIa which carries thrombotic risks and lacks evidence in DIC 1
- Delaying treatment of the underlying disease, which is the most crucial intervention 1
- Misinterpreting normal coagulation screens as excluding DIC 1
- Failing to recognize DIC subtypes which require different management approaches 5
Remember that DIC management should be individualized based on the underlying cause, clinical manifestations (bleeding vs. thrombosis), and severity of laboratory abnormalities, with the primary goal of reducing morbidity and mortality through prompt treatment of the underlying condition.