Heparin Dosing for Hemodialysis Patients with DVT/PE
For hemodialysis patients with DVT or PE, use unfractionated heparin (UFH) rather than low-molecular-weight heparin (LMWH), with standard therapeutic dosing: 80 units/kg IV bolus followed by 18 units/kg/hour continuous infusion, adjusted to maintain aPTT at 1.5-2.5 times control. 1, 2
Primary Recommendation: Unfractionated Heparin
UFH is the preferred anticoagulant for hemodialysis patients because it does not accumulate in severe renal impairment (CrCl <30 mL/min), unlike LMWHs which are renally eliminated and carry significantly increased bleeding risk. 1, 3
Standard UFH Dosing Protocol
- Initial bolus: 80 units/kg IV (or fixed dose of 5,000-10,000 units) 1, 2
- Continuous infusion: 18 units/kg/hour (or 1,300 units/hour, approximately 30,000-40,000 units/24 hours) 1, 2
- Target aPTT: 1.5-2.5 times control (typically 45-75 seconds) 1, 4
Monitoring Requirements
- Check aPTT 4-6 hours after initial bolus, then 6-10 hours after any dose adjustment, then daily once therapeutic 4
- Monitor platelet count every 2-3 days from day 4 to day 14 to screen for heparin-induced thrombocytopenia 3
- Failure to achieve therapeutic aPTT within 24 hours is associated with 25% recurrence rate versus 2% when therapeutic levels are maintained 1, 5
Duration of Therapy
- Continue UFH for minimum 5 days regardless of INR 4
- Overlap with warfarin for 4-5 days until INR 2.0-3.0 for 2 consecutive days 4, 6
- Do not discontinue heparin before day 5 even if INR becomes therapeutic earlier, as shorter durations increase recurrence risk 4
Why Not LMWH in Hemodialysis Patients?
Enoxaparin and other LMWHs are contraindicated or require extreme caution in hemodialysis patients due to 44% reduction in clearance with severe renal impairment, leading to drug accumulation and significantly increased bleeding risk. 1, 3
Evidence Against LMWH Use
- Renal clearance of enoxaparin is reduced by 31% in moderate renal impairment (CrCl 30-60 mL/min) and 44% in severe renal impairment (CrCl <30 mL/min) 1
- A randomized trial in elderly patients with CrCl <60 mL/min showed substantially higher mortality with tinzaparin versus UFH (11.2% vs 6.3%, P=0.049), leading to early termination 1
- Standard LMWH dosing in severe renal insufficiency is associated with 2-3 fold increased bleeding risk 1
If LMWH Must Be Used
Only if UFH is absolutely contraindicated (e.g., documented HIT without available non-heparin alternatives), use enoxaparin with mandatory dose reduction and anti-Xa monitoring: 1, 3
- Prophylactic dose: 30 mg subcutaneously once daily (instead of 40 mg) 1, 3
- Therapeutic dose: 1 mg/kg subcutaneously every 24 hours (instead of every 12 hours) 1, 3
- Monitor anti-Xa levels 4-6 hours after the 3rd or 4th dose, targeting 0.5-1.5 IU/mL for therapeutic dosing 1, 3
Alternative: Non-Heparin Anticoagulants for HIT
If heparin-induced thrombocytopenia develops, immediately discontinue all heparin and initiate a non-heparin anticoagulant such as argatroban or bivalirudin. 1
- Argatroban or bivalirudin are preferred in hemodialysis patients with HIT because of shorter half-life and ability to monitor effect 1
- Fondaparinux and DOACs should be avoided in severe renal impairment due to accumulation risk 1
- Avoid argatroban in moderate-severe hepatic dysfunction (Child-Pugh B or C) or use reduced doses 1
Critical Pitfalls to Avoid
- Never use standard LMWH dosing in hemodialysis patients without dose adjustment and anti-Xa monitoring - this dramatically increases bleeding risk 1, 3
- Never discontinue heparin before 5 days of therapy even if INR is therapeutic - this increases VTE recurrence 4
- Never fail to achieve therapeutic aPTT within 24 hours - subtherapeutic anticoagulation in the first 24 hours is associated with 25% recurrence rate 1
- Never use tinzaparin in elderly hemodialysis patients - associated with significantly increased mortality 1
Special Circumstances
High-Risk PE with Hemodynamic Instability
- Use UFH rather than LMWH regardless of renal function for easier reversibility and titration 4
- Continue until hemodynamic stability achieved before transitioning to oral anticoagulation 4