Enoxaparin Dosing and Administration
Prophylactic Dosing for DVT Prevention
For DVT prophylaxis in medical and surgical patients, administer enoxaparin 40 mg subcutaneously once daily, starting 2-4 hours preoperatively or within 24 hours of hospital admission, and continuing throughout hospitalization or until the patient is fully ambulatory. 1, 2
Standard Prophylactic Regimens:
- 40 mg subcutaneously once daily is the standard dose for most medical and surgical patients 1, 3, 2
- Duration: entire hospital stay or until full ambulation for medical patients; minimum 7-10 days for surgical patients 1, 2
- Alternative regimen: 30 mg subcutaneously every 12 hours has demonstrated superior efficacy in knee arthroplasty when started 12-24 hours post-surgery 1, 2
Advantages Over Unfractionated Heparin:
- Better bioavailability and longer half-life 1, 3
- More predictable anticoagulation effect 1, 3
- Lower risk of heparin-induced thrombocytopenia and osteopenia 1, 3
- Lower risk of major bleeding 1
Therapeutic Dosing for DVT/PE Treatment
For treatment of established DVT or PE, administer enoxaparin 1 mg/kg subcutaneously every 12 hours, which provides consistent therapeutic anticoagulation with proven efficacy equivalent to unfractionated heparin. 1, 2, 4
Standard Therapeutic Regimens:
- Primary regimen: 1 mg/kg subcutaneously every 12 hours 1, 3, 2, 4
- Alternative regimen: 1.5 mg/kg subcutaneously once daily 1, 3, 2, 4
- Initial treatment duration: typically 5-10 days, overlapping with warfarin until INR >2.0 for 2 consecutive days 1, 2
- For cancer patients: extended treatment for at least 3-6 months, with consideration for dose reduction after the first month 1
Evidence for Equivalence:
Both once-daily and twice-daily therapeutic enoxaparin regimens have been shown to be equivalent to dose-adjusted unfractionated heparin in terms of symptomatic VTE recurrence and major hemorrhage 1, 4. The once-daily regimen offers improved patient compliance, reduced healthcare worker exposure, and potentially lower treatment costs 1.
Dose Adjustments for Special Populations
Severe Renal Impairment (CrCl <30 mL/min):
Dose reduction is mandatory due to 44% reduction in enoxaparin clearance, which significantly increases bleeding risk. 1, 3, 2
- Prophylactic dose: 30 mg subcutaneously once daily 1, 3, 2
- Therapeutic dose: 1 mg/kg subcutaneously every 24 hours 1, 3
- Renal clearance is reduced by 31% in moderate impairment and 44% in severe impairment 1, 3
Obesity (BMI >30 kg/m²):
- Consider intermediate doses: 40 mg subcutaneously every 12 hours 1, 3, 2
- Alternative: weight-based dosing at 0.5 mg/kg subcutaneously every 12 hours 1, 3, 2
- For BMI ≥40 kg/m²: use 0.8 mg/kg subcutaneously every 12 hours for therapeutic dosing 1
- For patients with weight >150 kg at high risk: consider 40 mg every 12 hours for prophylaxis 3
Pregnancy with Class III Obesity:
- Intermediate doses: 0.5 mg/kg subcutaneously every 12 hours for thromboprophylaxis 1
Hepatic Dysfunction:
Enoxaparin is primarily eliminated renally, not hepatically, making it safer than unfractionated heparin in patients with liver dysfunction. 1
- Elevated transaminases (ALT/AST) without coagulopathy do not contraindicate enoxaparin use 1
- Avoid in moderate-to-severe liver disease with hepatic coagulopathy 1
- Elevated liver enzymes alone do not require dose adjustment 1
Critical Timing Considerations with Neuraxial Anesthesia
Avoid enoxaparin administration within 10-12 hours before neuraxial anesthesia or spinal catheter removal to prevent spinal hematoma. 1, 3, 2
Timing Guidelines:
- Prophylactic doses (40 mg once daily): may be started as early as 4 hours after catheter removal but not earlier than 12 hours after the block was performed 1, 3, 2
- Intermediate (40 mg every 12 hours) or therapeutic doses: may be started as early as 4 hours after catheter removal but not earlier than 24 hours after the block 3
- Preoperative timing: start 2-4 hours preoperatively or 10-12 hours preoperatively for neuraxial anesthesia 1, 3
Monitoring Recommendations
Anti-Xa Level Monitoring:
Monitor anti-Xa levels in patients with severe renal impairment on prolonged therapy, targeting 0.5-1.5 IU/mL. 1, 2
- Measure 4-6 hours after dosing, after patient has received 3-4 doses 1
- Target peak anti-Xa level for once-daily therapeutic dosing: 1.0-1.5 IU/mL 1
- Target peak anti-Xa level for twice-daily therapeutic dosing: 0.6-1.0 IU/mL 1
- Also monitor in pregnant patients on therapeutic doses and patients with morbid obesity 3
- Routine monitoring is generally not necessary for most patients 1
Platelet Monitoring:
Monitor platelet counts every 2-3 days from day 4 to day 14 to screen for heparin-induced thrombocytopenia. 1, 2
- Follow-up monitoring: hemoglobin, hematocrit, and platelet count at least every 2-3 days for the first 14 days and every 2 weeks thereafter 1
Baseline Laboratory Testing:
- CBC, renal and hepatic function panel, aPTT, and PT/INR 1
- Always check creatinine clearance before initiating enoxaparin, as this determines dosing more than liver function 1
Common Pitfalls and Caveats
Critical Warnings:
- Failure to properly time enoxaparin administration with spinal/epidural procedures can increase the risk of spinal hematoma 1
- Not adjusting the dose in patients with renal impairment can lead to drug accumulation and increased bleeding risk 1
- Standard fixed dosing may be inadequate in obese patients and excessive in very low-weight patients 1
- Avoid switching between enoxaparin and unfractionated heparin due to increased bleeding risk 1
- Use cautiously with other antiplatelet or anticoagulant medications due to increased bleeding risk 1