Heparin DVT Prophylaxis Dosing
For DVT prophylaxis in adult patients, unfractionated heparin should be administered at 5,000 units subcutaneously every 8 hours, as this three-times-daily regimen provides superior protection compared to twice-daily dosing. 1
Standard Prophylactic Regimen
The recommended dose is 5,000 units subcutaneously every 8 hours for most hospitalized patients requiring VTE prophylaxis. 2, 1
- This TID (three-times-daily) dosing provides more consistent anticoagulant effect and greater reduction in DVT incidence compared to BID (twice-daily) administration 1, 3
- The every-8-hour regimen is specifically recommended by the American Heart Association and is the standard in current guidelines 1
- For cancer patients, 5,000 units every 8 hours is explicitly the preferred regimen given their elevated thrombotic risk 2, 1, 4
Alternative Dosing for Moderate-Risk Patients
- 5,000 units subcutaneously every 12 hours is acceptable for moderate-risk medical patients but provides less robust protection than TID dosing 2, 1, 3
- This BID regimen may be appropriate when bleeding risk is elevated or for patients with fewer VTE risk factors 3
Timing and Duration
Initiate heparin 2 hours before surgery for surgical patients to achieve adequate anticoagulation at the time of greatest thrombotic risk 5, 6
- Continue prophylaxis for at least 7-10 days postoperatively or until the patient is fully ambulatory, whichever is longer 2, 5
- For cancer patients undergoing major abdominal or pelvic surgery, consider extended prophylaxis up to 35 days given persistently elevated thrombotic risk 2, 3
- Medical patients should receive prophylaxis throughout hospitalization until fully ambulatory 2, 4
Special Population Adjustments
Renal Impairment
- UFH is the preferred agent when creatinine clearance is <30 mL/min as it is primarily metabolized by the liver rather than renally excreted 1, 4, 3
- Standard dosing of 5,000 units every 8 hours can be used without dose adjustment in renal failure 1
Low Body Weight Patients (≤50 kg)
- Consider reduced-dose prophylaxis: 5,000 units every 12 hours in critically ill patients weighing ≤50 kg 7
- This reduced dosing strategy is associated with lower bleeding risk (5% vs 12.5%) while maintaining similar VTE protection 7
Obese Patients
- Standard dosing of 5,000 units every 8 hours remains appropriate for obese patients 8
- Higher doses (7,500 units every 8 hours) have not demonstrated clear benefit and may increase bleeding risk 8
Evidence Comparing BID vs TID Dosing
TID dosing (every 8 hours) is superior to BID dosing (every 12 hours) for preventing clinically significant VTE events. 9
- Meta-analysis shows TID heparin demonstrates a trend toward decreased pulmonary embolism (BID 1.5 vs TID 0.5 per 1,000 patient-days, p=0.09) 9
- TID dosing reduces proximal DVT and PE combined (BID 2.3 vs TID 0.9 per 1,000 patient-days, p=0.05) 9
- However, TID dosing carries increased major bleeding risk (BID 0.35 vs TID 0.96 per 1,000 patient-days, p<0.001) 9
Critical Pitfalls to Avoid
Do not use UFH in patients with active or history of heparin-induced thrombocytopenia (HIT) - use a direct thrombin inhibitor or fondaparinux instead 1
- Monitor platelet counts every 2-3 days from day 4 to day 14 in patients with HIT risk ≥1% 1
- Avoid administering anticoagulants within 10-12 hours of neuraxial anesthesia due to spinal hematoma risk 1, 4
- Do not default to BID dosing for high-risk patients (≥2 VTE risk factors, weight >100 kg, cancer patients) as this provides subtherapeutic prophylaxis 3
- Absolute contraindications include active major bleeding, recent CNS hemorrhage, or high-risk intracranial/spinal lesions 3
When UFH is Preferred Over LMWH
- Severe renal impairment (CrCl <30 mL/min) where LMWH accumulates and increases bleeding risk 1, 4, 3
- Need for rapid reversibility with protamine sulfate 1
- Cost considerations in resource-limited settings 1
- History of LMWH-associated adverse reactions 1
High Bleeding Risk Patients
For patients at high risk for bleeding, use mechanical thromboprophylaxis (graduated compression stockings and/or intermittent pneumatic compression) until bleeding risk diminishes, then initiate pharmacologic prophylaxis 2, 3