Treatment of Pulmonary Embolism in Older Adults with Enoxaparin
Primary Dosing Recommendation
For older adults with pulmonary embolism and normal renal function (CrCl >30 mL/min), administer enoxaparin 1 mg/kg subcutaneously every 12 hours or 1.5 mg/kg once daily, continuing for a minimum of 5 days and until therapeutic oral anticoagulation is achieved (INR 2.0-3.0 for 2 consecutive days). 1
Critical Age-Specific Considerations
Patients ≥75 Years Old
- Avoid the initial 30 mg IV bolus that is sometimes used in younger patients, as elderly patients have significantly increased bleeding risk 2
- Standard subcutaneous dosing (1 mg/kg every 12 hours) can be used, but heightened vigilance for bleeding complications is essential 2
- The combination of advanced age and any degree of renal impairment represents dual high-risk factors requiring extreme caution 3
Mandatory Renal Function Assessment
- Calculate creatinine clearance (CrCl) using the Cockcroft-Gault formula in ALL older adults before initiating enoxaparin, as near-normal serum creatinine frequently masks reduced renal function in elderly patients, particularly women and those with low body weight 3
Renal Impairment Dosing (Common in Older Adults)
Severe Renal Impairment (CrCl <30 mL/min)
- Reduce enoxaparin to 1 mg/kg subcutaneously once daily (a 50% total daily dose reduction) 3
- Patients with CrCl <30 mL/min have 2.25 times higher odds of major bleeding (OR 2.25,95% CI 1.19-4.27) with standard dosing 3
- Strongly consider switching to unfractionated heparin (UFH) as the preferred alternative, which requires no renal dose adjustment 3
- UFH dosing: 60 U/kg IV bolus (maximum 4000 U) followed by 12 U/kg/hour infusion (maximum 1000 U/hour), adjusted to maintain aPTT at 1.5-2.0 times control 3
Moderate Renal Impairment (CrCl 30-60 mL/min)
- Reduce the enoxaparin dose by 25% (to 75% of standard dose) 3
- Monitor closely for bleeding complications 3
Monitoring in Renal Impairment
- Monitor anti-Xa levels in all patients with CrCl <30 mL/min to prevent drug accumulation 3
- Check peak anti-Xa levels 4 hours after administration, only after 3-4 doses have been given 3
- Target therapeutic anti-Xa range: 0.5-1.0 IU/mL for twice-daily dosing, >1.0 IU/mL for once-daily dosing 3
Duration of Treatment
Standard Bridging to Warfarin
- Continue enoxaparin for minimum 5 days regardless of INR response 1
- Do not discontinue enoxaparin until INR is 2.0-3.0 for 2 consecutive days 1
- Start warfarin on the same day as enoxaparin initiation, preferably within 24 hours 1
- Never switch between enoxaparin and UFH during the same hospitalization, as this increases bleeding risk 3
Alternative: Direct Oral Anticoagulants (DOACs)
- Rivaroxaban and apixaban can be started immediately without enoxaparin bridging 1
- Dabigatran and edoxaban require ≥5 days of enoxaparin before switching 1
Critical Safety Monitoring
Platelet Count Monitoring
- Monitor platelet counts every 2-3 days from day 4 to day 14 to screen for heparin-induced thrombocytopenia (HIT) 1
Bleeding Risk Factors in Older Adults
- Enoxaparin clearance is reduced by 39% in patients with CrCl <30 mL/min 3
- Drug exposure increases by 35% with repeated dosing in renal impairment 3
- Strong linear correlation exists between CrCl and enoxaparin clearance (R=0.85, P<0.001) 3
Contraindications and Alternatives
Absolute Contraindications
- Fondaparinux is absolutely contraindicated when CrCl <30 mL/min and should never be used 3
When to Avoid Enoxaparin Entirely
- Hemodynamically unstable patients (shock/hypotension) should receive intravenous UFH rather than enoxaparin, as LMWH has not been tested in unstable patients 1
- Patients on hemodialysis should have enoxaparin administered 6-8 hours after dialysis completion to minimize bleeding risk at vascular access sites 3
Special Populations
Cancer Patients
- Extended LMWH monotherapy at 75-80% of initial dose for 6 months is superior to warfarin 1
- Continue anticoagulation as long as active malignancy persists 1
Underweight Patients (<55 kg) with Renal Impairment
- Use 30 mg once daily and monitor anti-Xa levels closely, as both factors independently increase bleeding risk 3