What is the recommended dosing of enoxaparin (low molecular weight heparin) for a patient with ST-Elevation Myocardial Infarction (STEMI)?

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Enoxaparin Dosing in STEMI

Standard Dosing for STEMI with Fibrinolytic Therapy

For patients under 75 years receiving fibrinolytic therapy for STEMI, administer a 30 mg IV bolus of enoxaparin followed 15 minutes later by 1 mg/kg subcutaneously every 12 hours, with a maximum of 100 mg for the first two doses. 1

Age-Based Modifications

  • Patients ≥75 years should NOT receive the IV bolus and instead receive 0.75 mg/kg subcutaneously every 12 hours, with a maximum of 75 mg for the first two doses. 1, 2, 3
  • This age-based modification is critical because elderly patients have significantly increased risk of intracranial hemorrhage, as documented in nine randomized trials and meta-analyses. 1

Renal Dosing Adjustments

  • For creatinine clearance <30 mL/min, reduce to 1 mg/kg subcutaneously once daily (instead of twice daily) regardless of age. 1, 2, 3
  • Calculate creatinine clearance in all STEMI patients before initiating enoxaparin, as renal impairment dramatically affects drug clearance. 4
  • Enoxaparin clearance decreases by 31% in moderate renal impairment and 44% in severe renal impairment, leading to significant drug accumulation with standard dosing. 4

Duration of Therapy

  • Continue enoxaparin throughout hospitalization or for up to 8 days. 1, 2, 3
  • Never switch between enoxaparin and unfractionated heparin in either direction - this carries a Class III recommendation (causes harm) due to significantly increased bleeding risk. 1

STEMI with Primary PCI (No Fibrinolysis)

  • Enoxaparin may be used as an alternative to unfractionated heparin for patients undergoing primary PCI, though this is less well-established than its use with fibrinolytic therapy. 1

Critical Safety Considerations

Bleeding Risk Management

  • The ExTRACT-TIMI 25 trial demonstrated that enoxaparin reduces death and recurrent MI compared to UFH, despite slightly higher bleeding rates, resulting in net clinical benefit. 2, 3, 5
  • Major bleeding occurs in approximately 1.9-2.4% of patients with full-dose fibrinolytic therapy. 5
  • Do not administer UFH to patients already on enoxaparin - this "stacking" significantly increases bleeding complications. 6

Common Pitfalls to Avoid

  • Failure to adjust for age ≥75 years - omitting the IV bolus and reducing the subcutaneous dose is mandatory to prevent intracranial hemorrhage. 1, 2, 3
  • Failure to adjust for renal impairment - patients with CrCl <30 mL/min require once-daily dosing to prevent drug accumulation and bleeding. 1, 4
  • Switching anticoagulants - transitioning between enoxaparin and UFH dramatically increases bleeding risk and should be avoided. 1
  • Exceeding maximum doses - the first two subcutaneous doses should not exceed 100 mg in patients <75 years or 75 mg in patients ≥75 years. 2, 3

Evidence Quality

  • These recommendations carry Class I, Level of Evidence A from the ACC/AHA STEMI guidelines, based on nine randomized trials and meta-analyses. 1
  • The ExTRACT-TIMI 25 trial (n=20,506 patients) provides the strongest evidence for enoxaparin superiority over UFH in STEMI with fibrinolytic therapy. 2, 3

References

Guideline

Enoxaparin Dosing in STEMI

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Spotlight on enoxaparin in ST-segment elevation myocardial infarction.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2008

Guideline

Enoxaparin Dosing and Duration for NSTEMI

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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