What is the recommended dose and duration of Enoxaparin (low molecular weight heparin) for the management of Non-ST-Elevation Myocardial Infarction (NSTEMI)?

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Last updated: November 12, 2025View editorial policy

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Enoxaparin Dosing and Duration for NSTEMI

For NSTEMI, administer enoxaparin 1 mg/kg subcutaneously every 12 hours, continued for the duration of hospitalization or until PCI is performed. 1

Standard Dosing Regimen

  • Dose: 1 mg/kg subcutaneously every 12 hours 1
  • Optional IV loading dose: An initial 30 mg intravenous bolus has been used in selected patients, though this is not universally required for NSTEMI 1
  • Duration: Continue throughout hospitalization or until PCI is performed 1

Critical Dose Adjustments

Renal Impairment

  • For creatinine clearance <30 mL/min: Reduce dose to 1 mg/kg subcutaneously once daily (not every 12 hours) 1
  • Calculate creatinine clearance in all patients before initiating enoxaparin, as renal impairment is common in older patients and significantly affects dosing 1
  • Consider switching to UFH as an alternative in severe renal dysfunction 1

Management at Time of PCI

The timing of the last enoxaparin dose relative to PCI determines additional anticoagulation needs:

  • If PCI occurs within 8 hours of last subcutaneous dose: Generally adequate anticoagulation exists; no additional enoxaparin needed 1
  • If PCI occurs 8-12 hours after last dose: Administer additional 0.3 mg/kg IV enoxaparin at time of PCI 1
  • If PCI occurs >12 hours after last dose: Treat as de novo anticoagulation with full-dose regimen 1

Critical Safety Considerations

Avoid "Stacking" Anticoagulants

  • Never administer UFH to patients already on enoxaparin during PCI—this "stacking" significantly increases bleeding risk 1
  • The SYNERGY trial demonstrated increased bleeding complications when patients on upstream enoxaparin received additional UFH at PCI 1

Bleeding Risk Profile

  • Enoxaparin demonstrates superior efficacy compared to UFH in reducing recurrent ischemic events in NSTEMI 1
  • The ESSENCE trial showed sustained benefit at 1 year with reduced recurrent ischemia and need for invasive procedures 1
  • While some studies showed slightly increased TIMI major bleeding with enoxaparin versus UFH, this was often related to improper "stacking" of anticoagulants 1

Evidence Quality

This recommendation carries Level of Evidence A from the 2014 ACC/AHA guidelines for NSTEMI management 1. The guidelines give enoxaparin a Class I recommendation, meaning it is definitively indicated for all NSTEMI patients requiring anticoagulation, regardless of whether an early invasive or ischemia-guided strategy is planned 1.

Common Pitfalls to Avoid

  • Failing to dose-adjust for renal function: Always calculate creatinine clearance before initiating therapy 1
  • Adding UFH during PCI: This increases bleeding without improving outcomes 1
  • Confusing NSTEMI dosing with STEMI dosing: STEMI protocols may include mandatory IV bolus and different timing; NSTEMI does not require the IV bolus 2
  • Continuing enoxaparin beyond hospitalization without clear indication: Duration is until discharge or PCI, not indefinite 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Administration Time for Intravenous Enoxaparin 30 mg Bolus

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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