Heparin Dosing in Disseminated Intravascular Coagulation (DIC)
In DIC, prophylactic-dose heparin (5,000 units subcutaneously every 8-12 hours) should be used for thrombosis prevention in non-bleeding critically ill patients, while therapeutic-dose heparin (continuous infusion at 10 units/kg/hour without targeting aPTT prolongation) is reserved only for cases where thrombosis clearly predominates, such as venous thromboembolism, arterial thrombosis, or severe purpura fulminans with acral ischemia. 1, 2
Clinical Decision Algorithm for Heparin in DIC
Step 1: Treat the Underlying Condition First
- The cornerstone of DIC management is treating the underlying disorder causing DIC—heparin is only adjunctive therapy 1, 2, 3
- Do not delay definitive treatment (e.g., ATRA in acute promyelocytic leukemia) while considering anticoagulation 1
Step 2: Assess for Contraindications to Any Heparin
Absolute contraindications include: 1, 2
- Active bleeding
- Platelet count <20 × 10⁹/L
- Hyperfibrinolytic DIC (markedly elevated fibrinolysis markers)
- History of heparin-induced thrombocytopenia
Step 3: Determine Clinical Phenotype
For Non-Bleeding, Critically Ill Patients (Most Common Scenario)
- Use prophylactic-dose unfractionated heparin: 5,000 units subcutaneously every 8-12 hours 4, 1, 2
- This prevents venous thromboembolism without significantly increasing bleeding risk 2, 3
- Do not use therapeutic doses in this population unless thrombosis develops 1, 3
For Thrombosis-Predominant DIC (Minority of Cases)
Therapeutic heparin is indicated when: 1, 2, 5
- Documented venous or arterial thromboembolism
- Severe purpura fulminans with acral ischemia or vascular skin infarction
- Retained dead fetus with hypofibrinogenemia (prior to labor induction)
- Giant hemangioma with excessive bleeding
- Promyelocytic leukemia with thrombotic features
Dosing for therapeutic anticoagulation in high bleeding risk DIC: 1, 2
- Continuous infusion unfractionated heparin at 10 units/kg/hour
- Do NOT target aPTT prolongation to 1.5-2.5 times control (aPTT is unreliable in DIC due to consumptive coagulopathy)
- Use weight-adjusted dosing without attempting to achieve traditional therapeutic aPTT ranges 1, 2
- The short half-life and reversibility of unfractionated heparin make it preferable in this high-risk setting 2
Choice Between Unfractionated Heparin vs. LMWH
Select unfractionated heparin when: 1, 6
- High bleeding risk exists (allows rapid reversibility with protamine)
- Severe renal impairment present (creatinine clearance <30 mL/min)
- Patient requires continuous renal replacement therapy
- Lower bleeding risk
- Normal renal function
- Solid tumor-associated DIC with thromboembolism (full-dose LMWH for 1 month, then 75% dose for 5 months)
- More predictable pharmacokinetics desired
Critical Monitoring Parameters
For Unfractionated Heparin in DIC:
- Do NOT rely on aPTT for dose adjustment—it is unreliable in DIC due to factor consumption and prolonged baseline values 1, 2
- Use anti-Factor Xa assays instead (target 0.3-0.7 IU/mL for therapeutic dosing) 1, 8
- Monitor platelet count once or twice weekly for heparin-induced thrombocytopenia 1
- Observe clinically for signs of bleeding rather than relying solely on laboratory parameters 2
For LMWH in DIC:
- Check peak anti-Xa levels 4 hours post-injection after the third dose 1
- Monitor platelet count every 24-72 hours in high-risk patients 1
Common Pitfalls to Avoid
Do not use therapeutic-dose heparin in non-bleeding DIC patients without documented thrombosis—this significantly increases bleeding risk without proven benefit on organ dysfunction or mortality 2, 5, 3
Do not target traditional therapeutic aPTT ranges (1.5-2.5 times control) in DIC—the aPTT is already prolonged from consumptive coagulopathy, making it an unreliable monitoring parameter 1, 2
Do not withhold prophylactic heparin in non-bleeding critically ill DIC patients—the thrombotic risk from immobility and critical illness outweighs bleeding risk when platelets are >20 × 10⁹/L 1, 2, 3
Do not use heparin as a substitute for treating the underlying condition—heparin alone does not reverse DIC or improve organ dysfunction 2, 5, 3
Special Populations
Cancer-Associated DIC:
- Use prophylactic heparin unless thromboembolism occurs 1
- If thromboembolism develops, switch to therapeutic LMWH (full dose for 1 month, then 75% dose for 5 months) 1
Acute Promyelocytic Leukemia:
- Early initiation of ATRA is more important than heparin 1
- Consider therapeutic heparin only if thrombotic complications develop 5
Subclinical DIC:
- Prophylactic heparin is beneficial unless hyperfibrinolytic features are present 1