Enoxaparin Dosing for DVT and PE Prophylaxis
For DVT and PE prophylaxis, the recommended dose of enoxaparin is 40 mg subcutaneously once daily for most patients. 1
Standard Prophylactic Dosing
- Enoxaparin 40 mg subcutaneously once daily is the standard prophylactic dose for most hospitalized patients at risk of DVT/PE 1
- Duration should be for the length of hospital stay or until fully ambulatory for medical patients, and at least 7-10 days for surgical patients 1
- Enoxaparin offers advantages over unfractionated heparin including better bioavailability, longer half-life, more predictable anticoagulation effect, and lower risk of heparin-induced thrombocytopenia 1
Special Population Dose Adjustments
Renal Impairment
- For patients with severe renal impairment (creatinine clearance <30 mL/min), reduce the dose to 30 mg subcutaneously once daily 1, 2
- Renal clearance of enoxaparin is reduced by 31% in moderate renal impairment and 44% in severe renal impairment 1
- Not adjusting the dose in patients with renal impairment can lead to drug accumulation and increased bleeding risk 1
Obesity
- For patients with obesity (BMI >30 kg/m²), consider intermediate doses (40 mg subcutaneously every 12 hours) or weight-based dosing (0.5 mg/kg subcutaneously every 12 hours) 1
- Standard fixed dosing may be inadequate in obese patients and excessive in very low-weight patients 1
Timing of Administration
- For surgical patients, enoxaparin should be started 2-4 hours preoperatively or 10-12 hours preoperatively 1
- Avoid administration within 10-12 hours before neuraxial anesthesia to reduce risk of spinal hematoma 1
Therapeutic Dosing (for Treatment of Established VTE)
- For treatment of established DVT/PE (not prophylaxis), the recommended doses are:
- In patients with cancer requiring extended treatment, enoxaparin 1 mg/kg twice daily or 1.5 mg/kg once daily is recommended 3
Monitoring Recommendations
- Routine monitoring of anti-Xa levels is not required for prophylactic dosing in most patients 1
- For patients with severe renal impairment on prolonged therapy, consider monitoring anti-Xa levels with a target range of 0.5-1.5 IU/mL 1
- Anti-Xa levels should be measured 4-6 hours after dosing, after the patient has received 3-4 doses 1
- Regular monitoring of platelet count is necessary during treatment due to risk of heparin-induced thrombocytopenia 3
Common Pitfalls and Caveats
- Failure to properly time enoxaparin administration with spinal/epidural procedures can increase the risk of spinal hematoma 1
- Concomitant use with other antiplatelet or anticoagulant medications increases bleeding risk 1, 2
- For patients at very high bleeding risk, consider mechanical prophylaxis with intermittent pneumatic compression devices instead of pharmacological prophylaxis 2