enoxaparin

Brand: Lovenox

ISMP High Alert Prototype Drug
Drug Class: anticoagulant
Drug Family: anticoagulant
Subclass: low molecular weight heparin (LMWH)
Organ Systems: cardiovascularhematology-oncology

Mechanism of Action

LMWH with high anti-Xa:anti-IIa ratio (3.7:1); more predictable PK than UFH; predominantly inhibits Xa via AT-III.

factor Xa (predominant via AT-III)factor IIa (minor)

Indications

  • DVT/PE treatment and prevention
  • ACS (NSTEMI/STEMI)
  • thromboprophylaxis
  • bridging

Contraindications

  • active major bleeding
  • HIT history (cross-reactivity)
  • severe renal impairment (adjust dose)

Adverse Effects

Common

  • injection site bruising
  • elevated LFTs

Serious

  • major hemorrhage
  • HIT (10x less than UFH)
  • hyperkalemia

Pharmacokinetics (ADME)

Absorption 92% SC bioavailability
Distribution mainly intravascular
Metabolism desulfation/depolymerization (not CYP)
Excretion renal
Half-life 4.5-7 hours
Onset 3-5 hours SC
Peak 3-5 hours
Duration ~12 hours
Protein Binding ~0% plasma
Vd 4.3 L

Drug Interactions

Drug / Agent Mechanism Severity
antiplatelet agents increased bleeding risk major
protamine partial reversal 60-80% only moderate

Nursing Considerations

  1. Therapeutic: 1 mg/kg SC q12h or 1.5 mg/kg SC daily
  2. Prophylactic: 30-40 mg SC daily
  3. Renal dose adjustment: CrCl <30 use 1 mg/kg SC daily for therapeutic
  4. Anti-Xa monitoring in renal impairment, obesity (BMI >40), pregnancy
  5. No routine aPTT monitoring needed

Clinical Pearls

  • More predictable PK vs UFH: no aPTT monitoring routinely needed
  • Lower HIT risk (10x) than UFH: shorter chains bind PF4 less
  • ESSENCE/TIMI 11B: superior to UFH for NSTEMI outcomes

Safety Profile

Pregnancy safe
Lactation use-with-caution
Renal Adjustment Required
Hepatic Adjustment Not required
TDM Not required

Concordance Terms

Cross-referenced clinical concepts — click any term to see all content where it appears.