Heparin Dosing for DVT
For an adult patient with confirmed DVT and no renal impairment, initiate low-molecular-weight heparin (LMWH) at weight-based dosing: enoxaparin 1 mg/kg subcutaneously every 12 hours (or 1.5 mg/kg once daily) or dalteparin 200 U/kg once daily, as LMWH is preferred over unfractionated heparin for superior outcomes. 1, 2
Preferred Initial Anticoagulation Strategy
LMWH is the first-line choice over unfractionated heparin (UFH) for DVT treatment based on guideline recommendations (grade 2C evidence). 1 The American College of Chest Physicians guidelines specifically state that LMWH or fondaparinux should be preferred over UFH when bridging to warfarin. 1
LMWH Dosing Options
- Enoxaparin: 1 mg/kg subcutaneously every 12 hours OR 1.5 mg/kg once daily 1, 3
- Dalteparin: 200 U/kg subcutaneously once daily 1
- No routine anti-Xa monitoring required for most patients on standard weight-based LMWH dosing 3
Advantages of LMWH Over UFH
- Reduced mortality and major bleeding compared to UFH during initial DVT treatment 2, 3
- Lower risk of heparin-induced thrombocytopenia (HIT): UFH carries up to 5% HIT risk versus lower rates with LMWH 1
- More predictable pharmacokinetics: LMWH demonstrates better correlation between dose and anticoagulant effect (r=0.59) compared to UFH (r=0.38) 4
- Outpatient treatment feasibility with equivalent safety and efficacy to inpatient UFH therapy 3
Unfractionated Heparin Dosing (When LMWH Contraindicated)
If UFH is necessary (e.g., severe renal impairment with CrCl <30 mL/min), use the following FDA-approved weight-based protocol: 5
Intravenous UFH Protocol
- Initial bolus: 80 units/kg IV 1, 5
- Continuous infusion: 18 units/kg/hour 1, 5
- Target aPTT: 1.5-2.5 times control (corresponding to anti-Factor Xa level 0.3-0.7 IU/mL) 1, 5
- Monitoring frequency: Check aPTT every 4 hours initially, then at appropriate intervals after achieving therapeutic range 5
Subcutaneous UFH Alternative
- Initial dose: 333 units/kg subcutaneously 1
- Maintenance: 250 units/kg subcutaneously every 12 hours 1
- This regimen demonstrated equivalent safety and efficacy to IV UFH in the FIDO trial 1
Critical Safety Monitoring
Platelet Count Surveillance for HIT
- Monitor platelets every 2-3 days from day 4 to day 14 in patients receiving any heparin formulation with HIT risk ≥1% 1, 3
- HIT typically presents with ≥50% platelet decline 5-10 days after heparin initiation (earlier with prior exposure) 1
- Risk is substantially higher with UFH (up to 5%) compared to LMWH, particularly in post-orthopedic surgery patients 1
Additional Laboratory Monitoring
- Baseline assessment: aPTT, INR, platelet count, hematocrit 5
- Ongoing surveillance: Periodic hematocrit and occult blood in stool throughout therapy 5
Renal Impairment Considerations
LMWH accumulation occurs with CrCl <30 mL/min, requiring either: 1, 3
- Dose adjustment of LMWH with anti-Xa monitoring, OR
- Switch to UFH as the preferred alternative since it does not accumulate in renal failure 2, 3
- Contraindication: Fondaparinux is absolutely contraindicated if CrCl <30 mL/min 1
Transition to Oral Anticoagulation
- Initiate warfarin on the same day as starting parenteral anticoagulation 2
- Continue LMWH for minimum 5 days AND until INR 2.0-3.0 for at least 24 hours 2
- Target INR: 2.5 (range 2.0-3.0) 2
- When stopping heparin: No tapering required; discontinue UFH infusion completely before starting LMWH if transitioning between agents 3
Common Pitfalls to Avoid
- Do NOT use intramuscular route due to frequent hematoma formation 5
- Avoid inadequate initial anticoagulation: Failure to achieve aPTT >1.5 times control with UFH is associated with 25% risk of recurrent VTE 6
- Do NOT confuse heparin vial strengths: Verify correct concentration to prevent dosing errors, particularly avoiding confusion with catheter lock flush vials 5
- Ensure proper subcutaneous injection technique: Use deep subcutaneous (intrafat) injection above iliac crest or abdominal fat layer with 25-26 gauge needle 5