Enoxaparin Dosing in Renal Impairment for VTE Prevention
For patients with impaired renal function (CrCl <30 mL/min), enoxaparin dose should be reduced to 30 mg subcutaneously once daily for thromboprophylaxis to prevent deep vein thrombosis (DVT) and pulmonary embolism (PE). 1
Renal Impairment and Enoxaparin Pharmacokinetics
Renal function significantly impacts enoxaparin clearance:
- Renal clearance of enoxaparin is reduced by 31% in moderate renal impairment (CrCl 30-60 mL/min)
- Renal clearance is reduced by 44% in severe renal impairment (CrCl <30 mL/min) 1
- This reduced clearance leads to drug accumulation and increased bleeding risk if standard doses are used
Dosing Recommendations by Clinical Scenario
For VTE Prophylaxis:
- Normal renal function: 40 mg subcutaneously once daily
- Severe renal impairment (CrCl <30 mL/min): 30 mg subcutaneously once daily 1
For Treatment of Established VTE:
- Normal renal function: 1 mg/kg subcutaneously every 12 hours or 1.5 mg/kg once daily
- Severe renal impairment (CrCl <30 mL/min): Dose reduction required; consider monitoring anti-Xa levels 2
Special Considerations for Cancer Patients
The National Comprehensive Cancer Network (NCCN) specifically recommends:
- LMWHs should be used with caution in patients with renal dysfunction
- Dose adjustments and anti-Xa monitoring may be required in renal dysfunction 2
- For cancer patients with severe renal impairment requiring thromboprophylaxis, the dose should be reduced to 30 mg subcutaneously once daily 2, 1
Monitoring Recommendations
For patients with severe renal impairment:
- Consider monitoring anti-Xa levels, especially with therapeutic dosing
- Target anti-Xa level: 0.5-1.5 IU/mL (measured 4-6 hours after injection) 1
- Laboratory monitoring: Check hemoglobin, hematocrit, and platelet count every 2-3 days for the first 14 days and every 2 weeks thereafter 2
Alternative Anticoagulants
In patients with severe renal dysfunction:
- Unfractionated heparin (UFH) may be preferred in some cases due to its non-renal clearance 1
- If using UFH, monitor aPTT every 4-6 hours during initiation and adjust to maintain aPTT 1.5-2.5 times normal 1
- Consider the increased risk of heparin-induced thrombocytopenia with UFH compared to LMWH
Clinical Pitfalls to Avoid
- Failure to adjust dose: Not reducing enoxaparin dose in renal impairment can lead to bioaccumulation and increased bleeding risk
- Inadequate monitoring: Patients with severe renal impairment may require anti-Xa monitoring
- Overlooking drug interactions: P-glycoprotein inhibitors or inducers can affect enoxaparin levels
- Weight extremes: Consider adjusted dosing for patients with extreme obesity or low body weight
- Assuming all LMWHs are the same: Enoxaparin has different renal clearance characteristics compared to other LMWHs like dalteparin
By following these evidence-based dosing recommendations, clinicians can effectively prevent VTE while minimizing bleeding complications in patients with impaired renal function.