Bridging Coumadin to Lovenox Prior to Surgery
For patients requiring bridging anticoagulation, stop warfarin 5 days before surgery, start therapeutic-dose enoxaparin when INR falls below 2.0 (typically day 3), give the last enoxaparin dose 24 hours before surgery at half the daily dose, and resume therapeutic enoxaparin 48-72 hours postoperatively for high bleeding risk procedures or 24 hours for low bleeding risk procedures. 1, 2
Pre-Operative Protocol
Warfarin Discontinuation
- Stop warfarin 5 days (5 doses) before the planned surgical procedure to allow INR to decrease to ≤1.5 1
- Check INR the day before surgery; proceed if INR ≤1.5 1
- If INR is 1.5-1.8 on the day before surgery, administer oral vitamin K 1-2.5 mg for reversal 1
Enoxaparin Initiation
- Start therapeutic-dose enoxaparin 36 hours after the last warfarin dose (typically day 3 pre-operatively) when INR falls below 2.0 1, 2
- Use enoxaparin 1 mg/kg subcutaneously twice daily OR 1.5 mg/kg once daily 1, 2
- Give the last pre-operative enoxaparin dose 24 hours before surgery at half the total daily dose (e.g., if using 1 mg/kg twice daily, give only the morning dose; if using 1.5 mg/kg once daily, give 0.75 mg/kg) 1
Critical Timing Consideration
The 24-hour interval before surgery is essential because studies show that >90% of patients receiving enoxaparin 12 hours before surgery have detectable anticoagulant effect, with 34% having therapeutic levels at the time of surgery 1
Post-Operative Protocol
Warfarin Resumption
- Resume warfarin at the usual maintenance dose on the evening of surgery or the next morning, provided adequate hemostasis is achieved 1, 3
- Do not use loading doses (doubling the dose) as this creates management challenges without clear benefit 3
Enoxaparin Resumption Based on Bleeding Risk
For Low-to-Moderate Bleeding Risk Procedures:
- Resume therapeutic-dose enoxaparin 24 hours after surgery 1, 2, 3
- Continue enoxaparin until INR ≥2.0 on two consecutive measurements 1, 3
For High Bleeding Risk Procedures (including spinal surgery, intracranial surgery, or neuraxial anesthesia):
- Wait 48-72 hours before resuming therapeutic-dose enoxaparin 1, 2
- Consider prophylactic-dose enoxaparin (40 mg once daily) during the first 48-72 hours for patients at very high thrombotic risk, then transition to therapeutic dosing 1, 2, 3
- Assess the surgical site for ongoing bleeding, wound drainage, or hematoma before initiating therapeutic anticoagulation 3
INR Monitoring
- Check INR on postoperative day 4 and again on days 7-10 1, 2
- Discontinue enoxaparin only when INR reaches ≥2.0 on two consecutive measurements 1, 2, 3
- Draw blood for INR at least 10-12 hours after the last enoxaparin dose to avoid falsely elevated readings 3
Renal Function Adjustment
Critical for patients with impaired renal function:
- If creatinine clearance <30 mL/min, reduce enoxaparin to once-daily dosing OR consider intravenous unfractionated heparin targeting aPTT 1.5-2.0 times control 1, 2
- Unfractionated heparin should be stopped 4-6 hours before surgery given its 90-minute half-life 1
Alternative: Intermediate-Dose Regimen
For patients where the balance between thrombosis and bleeding risk is particularly concerning, intermediate-dose enoxaparin 40 mg subcutaneously twice daily represents a reasonable alternative with favorable safety profiles in bridging studies 1, 2
Who Actually Needs Bridging?
The decision to bridge depends critically on thromboembolic risk:
Bridge anticoagulation is suggested for: 1
- Mechanical heart valves
- Atrial fibrillation with high thromboembolic risk (CHA₂DS₂-VASc ≥5)
- Recent VTE (<3 months)
- Antiphospholipid syndrome with recurrent thrombosis
- Atrial fibrillation without high thromboembolic risk (CHA₂DS₂-VASc <5)
- Remote VTE (>3 months ago)
- Patients on DOACs (direct oral anticoagulants)
The landmark BRIDGE trial demonstrated that forgoing bridging in atrial fibrillation patients was noninferior for preventing thromboembolism (0.4% vs 0.3%) but superior for preventing major bleeding (1.3% vs 3.2%) 4
Common Pitfalls to Avoid
Major bleeding occurs in up to 20% of patients when therapeutic-dose enoxaparin is given too close to surgery without adequate assessment of hemostasis 1, 2. This is the single most important complication to prevent.
- Never give therapeutic-dose enoxaparin within 24 hours of surgery 1
- Never resume therapeutic-dose enoxaparin within 48-72 hours after high bleeding risk procedures 1, 2
- Never perform neuraxial anesthesia with residual anticoagulant effect 3
- Always reassess renal function postoperatively as it affects enoxaparin dosing 3